JP2010153764A - Photoelectric conversion element, imaging element, and method of manufacturing the photoelectric conversion element - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a photoelectric conversion element which can be improved in photoelectric conversion efficiency with a configuration of a photoelectric conversion layer containing only one kind of organic material, to provide an imaging element, and to provide a method of manufacturing the photoelectric conversion element. <P>SOLUTION: The photoelectric conversion element includes a pair of electrodes and the photoelectric conversion layer provided between the pair of electrodes, and the photoelectric conversion layer contains only an organic compound of one kind of donor-acceptor linked structure as an organic compound and is formed in a state that the temperature of the layer is held at room temperature or below when formed. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to a photoelectric conversion element, an imaging element, and a method for manufacturing a photoelectric conversion element.

  2. Description of the Related Art Conventionally, there is a photoelectric conversion element having a configuration in which a photoelectric conversion layer is provided between a pair of electrodes and electric charges such as electrons and holes are generated by applying an electric field between the electrodes. Examples of such photoelectric conversion elements include those shown in the following patent documents.

JP 2002-76027 A JP-A-6-326338

  In Patent Document 1, a photoelectric conversion layer of a photoelectric conversion element has a bulk hetero structure in which a plurality of organic materials are simultaneously deposited, and the photoelectric conversion efficiency is improved by controlling the fine structure. However, Patent Document 1 does not describe increasing the efficiency of a photoelectric conversion element including a photoelectric conversion layer including only one organic material.

  Patent Document 2 aims to improve carrier conversion speed and photoelectric conversion efficiency by spontaneously polarizing an organic material forming a photoelectric conversion layer using corona discharge and increasing molecular orientation. However, the photoelectric conversion efficiency is only about 2%, and the effect is not sufficient. Further, there is no description about increasing the efficiency of a photoelectric conversion element including a photoelectric conversion layer containing only one organic material.

  The present invention has been made in view of the above circumstances, and the object thereof is a photoelectric conversion element and an imaging element capable of realizing improvement in photoelectric conversion efficiency with a configuration of a photoelectric conversion layer containing only one kind of organic material. And it is providing the manufacturing method of a photoelectric conversion element.

  The present invention is a photoelectric conversion element comprising a pair of electrodes and a photoelectric conversion layer provided between the pair of electrodes, wherein the photoelectric conversion layer is one kind of donor-acceptor connection structure as an organic compound. And a photoelectric conversion element formed in a state where the temperature of the layer is lower than room temperature when the photoelectric conversion layer is formed.

  Moreover, this invention is an image pick-up element provided with the said photoelectric conversion element.

Furthermore, the present invention is a method for producing a photoelectric conversion element comprising a pair of electrodes and a photoelectric conversion layer provided between the pair of electrodes,
This is a method for producing a photoelectric conversion element, wherein an organic compound having a donor-acceptor connection structure is used as the organic compound, and the photoelectric conversion layer is formed in a state where the temperature of the organic compound is lower than room temperature.

  According to the present invention, it is not necessary to form the photoelectric conversion layer with a plurality of organic materials, and the photoelectric conversion efficiency can be improved by forming the photoelectric conversion layer with only one kind of organic material.

  ADVANTAGE OF THE INVENTION According to this invention, the photoelectric conversion element which can implement | achieve the improvement of a photoelectric conversion efficiency with the structure of the photoelectric converting layer containing only one type of organic material, the manufacturing method of a photoelectric conversion element is provided. be able to.

Sectional schematic diagram showing an example of the configuration of a photoelectric conversion element having a charge blocking layer Energy diagram showing the state of the intermediate level in the charge blocking layer having the two-layer structure shown in FIG. The figure explaining the combination of the material of each layer when the charge blocking layer shown in FIG. 1 is a three-layer structure Cross-sectional schematic diagram of a photoelectric conversion element having a three-layer structure electron blocking layer and a three-layer structure hole blocking layer Energy diagram for explaining the state of carrier movement through the intermediate level of the charge blocking layer when a voltage is applied to the photoelectric conversion element of FIG. Cross-sectional schematic diagram showing schematic configuration of photoelectric conversion element Sectional schematic diagram which shows the modification of the photoelectric conversion element of the structure shown by FIG. Sectional schematic diagram which shows schematic structure of the other example of the photoelectric conversion element of this embodiment Sectional schematic diagram which shows the modification of the photoelectric conversion element shown by FIG. Sectional schematic diagram which shows schematic structure of the other example of the photoelectric conversion element of this embodiment Cross-sectional schematic diagram showing a modification of the photoelectric conversion element shown in FIG. Cross-sectional schematic diagram for one pixel for explaining another configuration example of the image sensor 12 is a schematic cross-sectional view of the intermediate layer shown in FIG. Cross-sectional schematic diagram for one pixel for explaining another configuration example of the image sensor Cross-sectional schematic diagram for one pixel of a solid-state image sensor for explaining another configuration example of the image sensor Cross-sectional schematic diagram of a solid-state image sensor for explaining another configuration example of the image sensor Partial surface schematic diagram for explaining another configuration example of the image sensor XX cross-sectional schematic diagram of the image sensor shown in FIG. The figure which shows the specific structural example of the signal reading part shown in FIG. Graph showing spectral absorption spectrum Graph showing fluorescence absorption spectrum Graph showing fluorescence spectrum Graph showing spectral absorption spectrum

  The photoelectric conversion element is a photoelectric conversion element provided with a pair of electrodes and a photoelectric conversion layer provided between the pair of electrodes, and the photoelectric conversion layer is one kind of donor-acceptor connection as an organic compound. It includes only an organic compound having a structure, and is formed in a state where the temperature of the layer is lower than room temperature when the photoelectric conversion layer is formed.

  As a result of intensive studies, the present inventor, when producing a photoelectric conversion layer, in the state where the temperature of the base substrate for forming the photoelectric conversion film is at least a temperature lower than room temperature, It has been found that when an organic compound having a donor-acceptor linking structure is formed, the photoelectric conversion efficiency of the photoelectric conversion element can be improved by changing the molecular association of the formed layer.

  Here, the donor-acceptor linking structure referred to in the present invention refers to a structure having a donor part and an acceptor part in the same molecule and the compound having an asymmetric structure. At this time, the donor-acceptor linking structure is first defined as (donor)-(linking group)-(acceptor) as a general formula, and a 5-membered or 6-membered nitrogen-containing heterocycle is formed as the general formula of the donor part. An atomic group that has aniline as a partial skeleton. The linking group has one or more methine chains, and the acceptor has a double bond C with an electron-withdrawing group.

  Note that as long as the temperature of the layer can be cooled to a temperature lower than room temperature when the photoelectric conversion layer is formed, the means for cooling the layer is not limited to the method of cooling the base substrate to be formed. When forming the photoelectric conversion layer, the temperature of the layer is preferably less than 25 ° C, and more preferably in the range of 0 ° C to -170 ° C.

  The molecular association of a layer is determined by the correlation between the molecular kinetic energy and the orientation energy due to the molecular dipole moment. When the photoelectric conversion layer is formed of an organic material having a dipole moment, the donor part (acceptor part) of the molecule contained in the organic compound of the donor-acceptor linked structure constituting the layer is cooled by cooling the base substrate. It seems that the correlation between the acceptor part (donor part) of the molecule is strengthened, and as a result, the state of the molecular association of the layer is oriented in a more ordered direction and the charge separation is promoted. .

  The dipole moment shows a small value in a material having a symmetrical skeleton of the chemical formula, and shows a large value in an organic compound having a donor-acceptor connection structure.

  As the organic compound having a donor-acceptor connection structure, an organic material having a dipole moment of 0 D (Debye) or more is preferable, and an organic material having a dipole moment of 1.0 D or more is particularly preferable.

By forming a photoelectric conversion layer consisting only of an organic compound having a donor-acceptor connection structure on a base substrate cooled to a temperature below the room temperature, it is not necessary to mix a plurality of organic compounds, and a single layer organic compound A photoelectric conversion element with high photoelectric conversion efficiency can be obtained.
It is preferable that an electric field applied to the photoelectric conversion layer through a pair of electrodes is 1.0E ⁺⁴ V / cm to 1.0E ⁺⁷ V / cm.

  As an organic compound having a donor-acceptor linking structure, a dipole moment greater than 0D, in particular, a 4H pyran compound, a donor-acceptor direct-coupled compound, or a merocyanine compound of 1.0D or more is preferably used.

  Examples of the organic compound having a donor-acceptor linking structure of 1.0D or more include those represented by the following chemical formula.

The organic compound having a donor-acceptor linking structure is preferably a compound including a partial structure represented by the following general formula (1).
General formula (1)

In the formula, X represents O, S, or N—R ₁₀ . R ₁₀ represents a hydrogen atom or a substituent. R ^x and R ^y each independently represent a hydrogen atom or a substituent, and at least one of them represents an electron withdrawing group. R ^x and R ^y may be linked to form a ring. R represents a bond, a hydrogen atom or a substituent, and at least one is a bond (-). nr represents an integer of 1 to 4. When nr is 2 or more, R may be the same or different. The Rs at the 2nd and 3rd positions may be linked to each other at the 5th and 6th positions to form a ring.

  The compound containing a partial structure represented by the general formula (1) used in the present invention, particularly a 4H pyran compound, will be described in detail.

As the substituent represented by R ₁₀ , those described as the substituent W below are applied. Further, the substituent represented by R ^x, R ^y is the following substituent group W is applied, at least one of R ^x, R ^y is an electron withdrawing group. It is preferable that the total of Sp ² carbons contained in R ^x and R ^y is 3 or more.

As the substituent W, a halogen atom, an alkyl group (including a cycloalkyl group, a bicycloalkyl group, and a tricycloalkyl group), an alkenyl group (including a cycloalkenyl group and a bicycloalkenyl group), an alkynyl group, an aryl group, and a heterocyclic group (May be referred to as a heterocyclic group), cyano group, hydroxy group, nitro group, carboxy group, alkoxy group, aryloxy group, silyloxy group, heterocyclic oxy group, acyloxy group, carbamoyloxy group, alkoxycarbonyloxy group, Aryloxycarbonyloxy group, amino group (including anilino group), ammonio group, acylamino group, aminocarbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, alkyl and arylsulfonylamino , Mercapto group, alkylthio group, arylthio group, heterocyclic thio group, sulfamoyl group, sulfo group, alkyl and arylsulfinyl group, alkyl and arylsulfonyl group, acyl group, aryloxycarbonyl group, alkoxycarbonyl group, carbamoyl group, aryl and Heterocyclic azo group, imide group, phosphino group, phosphinyl group, phosphinyloxy group, phosphinylamino group, phosphono group, silyl group, hydrazino group, ureido group, boronic acid group (-B (OH) ₂ ), Examples thereof include a phosphato group (—OPO (OH) ₂ ), a sulfato group (—OSO ₃ H), and other known substituents.

  When R is a bond, it is preferably located at the 2-position and / or 6-position of the X-containing 6-membered ring in the general formula (1), more preferably at the 2-position or 6-position. When R represents a hydrogen atom or a substituent, it is preferably located at the 2, 3, 5 position of the X-containing 6-membered ring. In the case where Rs are connected to form a ring, examples of the ring include the same rings as those described above that W can form a ring together. nr represents an integer of 1 to 4, and nr is preferably 1 or 2. When nr is 1, R is preferably a bond, and when nr is 2, two Rs are both bonds or one is preferably a bond, more preferably one. One is a bond.

  Specific examples of the compound including the partial structure represented by the general formula (1) are shown below, but the present invention is not limited to these.

  As the 4H pyran compound, for example, a compound represented by the following chemical formula can be used.

As a donor-acceptor direct connection type compound, the compound shown by following General formula (2) is included.
General formula (2)

In the formula, Z ₁₁ represents an atomic group necessary for forming a 5- or 6-membered ring. L ₁ , L ₂ and L ₃ each represents an unsubstituted methine group or a substituted methine group. D ₁ represents an atomic group. n represents an integer of 0 or more.

The D ₁ may be represented by the following general formula (2-2).
General formula (2-2)

In the formula, R _{1 to} R ₆ each independently represent a hydrogen atom or a substituent. R ₁ and R ₂ , R ₃ and R ₄ , R ₅ and R ₆ , R ₂ and R ₅ , and R ₄ and R ₆ may be bonded to each other to form a ring.
The D ₁ may be represented by the following general formula (2-3).
General formula (2-3)

In formula, R < ₁₁ > -R < ₁₄ >, R < ₂₀ > -R < ₂₄ >, R < ₃₀ > -R < ₃₄ > represents a hydrogen atom or a substituent each independently. R _{10 to} R ₁₄ , R _{20 to} R ₂₄ , and R _{30 to} R ₃₄ may be bonded to each other to form a ring.
The ring formed by the Z ₁₁ can be a functional group represented by the following general formula (2-4).
General formula (2-4)

R _{41 to} R ₄₄ each independently represents a hydrogen atom or a substituent.
The ring formed by the Z ₁₁ can be a functional group represented by the following general formula (2-5).
Formula (2-5)

R ₄₁ , R ₄₄ and R _{45 to} R ₄₈ each independently represent a hydrogen atom or a substituent.
It can be set as the photoelectric conversion element whose n in the said General formula (2) is 0.
Wherein L _1, L _2, L ₃ can be a photoelectric conversion element is a unsubstituted methine group, respectively.

As the substituent W in the general formula (2), a halogen atom, an alkyl group (including a cycloalkyl group, a bicycloalkyl group, and a tricycloalkyl group), an alkenyl group (including a cycloalkenyl group and a bicycloalkenyl group), and an alkynyl group , Aryl group, heterocyclic group (may be referred to as heterocyclic group), cyano group, hydroxy group, nitro group, carboxy group, alkoxy group, aryloxy group, silyloxy group, heterocyclic oxy group, acyloxy group, carbamoyloxy Group, alkoxycarbonyloxy group, aryloxycarbonyloxy group, amino group (including anilino group), ammonio group, acylamino group, aminocarbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, Alkyl and Ally Sulfonylamino group, mercapto group, alkylthio group, arylthio group, heterocyclic thio group, sulfamoyl group, sulfo group, alkyl and arylsulfinyl group, alkyl and arylsulfonyl group, acyl group, aryloxycarbonyl group, alkoxycarbonyl group, carbamoyl group , Aryl and heterocyclic azo groups, imide groups, phosphino groups, phosphinyl groups, phosphinyloxy groups, phosphinylamino groups, phosphono groups, silyl groups, hydrazino groups, ureido groups, boronic acid groups (-B (OH) ₂ ), a phosphato group (—OPO (OH) ₂ ), a sulfato group (—OSO ₃ H), and other known substituents.

  More specifically, W represents the following (1) to (48).

(1) Halogen atom For example, fluorine atom, chlorine atom, bromine atom, iodine atom

(2) Alkyl group represents a linear, branched or cyclic substituted or unsubstituted alkyl group. They also include (2-a) to (2-e).

(2-a) alkyl group Preferably an alkyl group having 1 to 30 carbon atoms (for example, methyl, ethyl, n-propyl, isopropyl, t-butyl, n-octyl, eicosyl, 2-chloroethyl, 2-cyanoethyl, 2-ethylhexyl) )

(2-b) cycloalkyl group Preferably, the substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms (for example, cyclohexyl, cyclopentyl, 4-n-dodecylcyclohexyl).

(2-c) Bicycloalkyl group Preferably, the substituted or unsubstituted bicycloalkyl group having 5 to 30 carbon atoms (for example, bicyclo [1,2,2] heptan-2-yl, bicyclo [2,2,2] Octane-3-yl)

(2-d) Tricycloalkyl group Preferably, it is a substituted or unsubstituted tricycloalkyl group having 7 to 30 carbon atoms (for example, 1-adamantyl).

(2-e) A polycyclic cycloalkyl group having a larger ring structure In addition, an alkyl group (for example, an alkyl group of an alkylthio group) in a substituent described below represents an alkyl group of such a concept, Group and alkynyl group.

(3) Alkenyl group represents a linear, branched, or cyclic substituted or unsubstituted alkenyl group. They include (3-a) to (3-c).

(3-a) Alkenyl group Preferably it is a C2-C30 substituted or unsubstituted alkenyl group (for example, vinyl, allyl, prenyl, geranyl, oleyl).

(3-b) Cycloalkenyl group Preferably, the substituted or unsubstituted cycloalkenyl group having 3 to 30 carbon atoms (for example, 2-cyclopenten-1-yl, 2-cyclohexen-1-yl)

(3-c) Bicycloalkenyl group A substituted or unsubstituted bicycloalkenyl group, preferably a substituted or unsubstituted bicycloalkenyl group having 5 to 30 carbon atoms (for example, bicyclo [2,2,1] hept-2-ene -1-yl, bicyclo [2,2,2] oct-2-en-4-yl)

(4) Alkynyl group Preferably, the substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms (for example, ethynyl, propargyl, trimethylsilylethynyl group)

(5) Aryl group Preferably, it is a C6-C30 substituted or unsubstituted aryl group (for example, phenyl, p-tolyl, naphthyl, m-chlorophenyl, o-hexadecanoylaminophenyl, ferrocenyl).

(6) Heterocyclic group Preferably, it is a monovalent group obtained by removing one hydrogen atom from a 5- or 6-membered substituted or unsubstituted aromatic or non-aromatic heterocyclic compound, more preferably carbon. It is a 5- or 6-membered aromatic heterocyclic group of formula 3 to 50.
(For example, 2-furyl, 2-thienyl, 2-pyrimidinyl, 2-benzothiazolyl. In addition, a cationic heterocyclic group such as 1-methyl-2-pyridinio and 1-methyl-2-quinolinio may be used)

(7) Cyano group

(8) Hydroxy group

(9) Nitro group

(10) Carboxy group

(11) Alkoxy group Preferably, the substituted or unsubstituted alkoxy group having 1 to 30 carbon atoms (for example, methoxy, ethoxy, isopropoxy, t-butoxy, n-octyloxy, 2-methoxyethoxy)

(12) Aryloxy group Preferably, the substituted or unsubstituted aryloxy group having 6 to 30 carbon atoms (for example, phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, 2-tetradecanoyl) Aminophenoxy)

(13) Silyloxy group Preferably, the silyloxy group having 3 to 20 carbon atoms (for example, trimethylsilyloxy, t-butyldimethylsilyloxy)

(14) Heterocyclic oxy group Preferably, the substituted or unsubstituted heterocyclic oxy group having 2 to 30 carbon atoms (for example, 1-phenyltetrazol-5-oxy, 2-tetrahydropyranyloxy)

(15) Acyloxy group, preferably a formyloxy group, a substituted or unsubstituted alkylcarbonyloxy group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyloxy group having 6 to 30 carbon atoms (for example, formyloxy, acetyloxy , Pivaloyloxy, stearoyloxy, benzoyloxy, p-methoxyphenylcarbonyloxy)

(16) Carbamoyloxy group Preferably, the substituted or unsubstituted carbamoyloxy group having 1 to 30 carbon atoms (for example, N, N-dimethylcarbamoyloxy, N, N-diethylcarbamoyloxy, morpholinocarbonyloxy, N, N- Di-n-octylaminocarbonyloxy, Nn-octylcarbamoyloxy)

(17) Alkoxycarbonyloxy group Preferably, the substituted or unsubstituted alkoxycarbonyloxy group having 2 to 30 carbon atoms (for example, methoxycarbonyloxy, ethoxycarbonyloxy, t-butoxycarbonyloxy, n-octylcarbonyloxy)

(18) Aryloxycarbonyloxy group Preferably, the substituted or unsubstituted aryloxycarbonyloxy group having 7 to 30 carbon atoms (for example, phenoxycarbonyloxy, p-methoxyphenoxycarbonyloxy, pn-hexadecyloxyphenoxycarbonyl) Oxy)

(19) Amino group Preferably, an amino group, a substituted or unsubstituted alkylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted anilino group having 6 to 30 carbon atoms (for example, amino, methylamino, dimethylamino, Anilino, N-methyl-anilino, diphenylamino)

(20) Ammonio group Preferably, an ammonio group, an ammonio group substituted with 1 to 30 carbon atoms or an unsubstituted alkyl, aryl, or heterocyclic ring (for example, trimethylammonio, triethylammonio, diphenylmethylammonio)

(21) Acylamino group Preferably, a formylamino group, a substituted or unsubstituted alkylcarbonylamino group having 1 to 30 carbon atoms, a substituted or unsubstituted arylcarbonylamino group having 6 to 30 carbon atoms (for example, formylamino, acetyl) Amino, pivaloylamino, lauroylamino, benzoylamino, 3,4,5-tri-n-octyloxyphenylcarbonylamino)

(22) Aminocarbonylamino group Preferably, the substituted or unsubstituted aminocarbonylamino having 1 to 30 carbon atoms (for example, carbamoylamino, N, N-dimethylaminocarbonylamino, N, N-diethylaminocarbonylamino, morpholinocarbonylamino) )

(23) Alkoxycarbonylamino group Preferably, the substituted or unsubstituted alkoxycarbonylamino group having 2 to 30 carbon atoms (for example, methoxycarbonylamino, ethoxycarbonylamino, t-butoxycarbonylamino, n-octadecyloxycarbonylamino, N- Methyl-methoxycarbonylamino)

(24) Aryloxycarbonylamino group Preferably, the substituted or unsubstituted aryloxycarbonylamino group having 7 to 30 carbon atoms (for example, phenoxycarbonylamino, p-chlorophenoxycarbonylamino, mn-octyloxyphenoxycarbonylamino) )

(25) Sulfamoylamino group Preferably, the substituted or unsubstituted sulfamoylamino group having 0 to 30 carbon atoms (for example, sulfamoylamino, N, N-dimethylaminosulfonylamino, Nn-octylamino) Sulfonylamino)

(26) Alkyl or arylsulfonylamino group Preferably, the substituted or unsubstituted alkylsulfonylamino having 1 to 30 carbon atoms, or the substituted or unsubstituted arylsulfonylamino having 6 to 30 carbon atoms (for example, methylsulfonylamino, butylsulfonyl) Amino, phenylsulfonylamino, 2,3,5-trichlorophenylsulfonylamino, p-methylphenylsulfonylamino)

(27) Mercapto group

(28) Alkylthio group Preferably, it is a C1-C30 substituted or unsubstituted alkylthio group (for example, methylthio, ethylthio, n-hexadecylthio).

(29) Arylthio group Preferably, the substituted or unsubstituted arylthio having 6 to 30 carbon atoms (for example, phenylthio, p-chlorophenylthio, m-methoxyphenylthio)

(30) Heterocyclic thio group Preferably, the substituted or unsubstituted heterocyclic thio group having 2 to 30 carbon atoms (for example, 2-benzothiazolylthio, 1-phenyltetrazol-5-ylthio)

(31) Sulfamoyl group Preferably, the substituted or unsubstituted sulfamoyl group having 0 to 30 carbon atoms (for example, N-ethylsulfamoyl, N- (3-dodecyloxypropyl) sulfamoyl, N, N-dimethylsulfamoyl) N-acetylsulfamoyl, N-benzoylsulfamoyl, N- (N′-phenylcarbamoyl) sulfamoyl)

(32) Sulfo group

(33) an alkyl or arylsulfinyl group, preferably a substituted or unsubstituted alkylsulfinyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfinyl group having 6 to 30 carbon atoms (for example, methylsulfinyl, ethylsulfinyl, phenylsulfinyl, p-methylphenylsulfinyl)

(34) an alkyl or arylsulfonyl group, preferably a substituted or unsubstituted alkylsulfonyl group having 1 to 30 carbon atoms, a substituted or unsubstituted arylsulfonyl group having 6 to 30 carbon atoms, such as methylsulfonyl, ethylsulfonyl, phenylsulfonyl, p-methylphenylsulfonyl)

(35) Acyl group Preferably, it is a formyl group, a substituted or unsubstituted alkylcarbonyl group having 2 to 30 carbon atoms, a substituted or unsubstituted arylcarbonyl group having 7 to 30 carbon atoms, a substituted or unsubstituted group having 4 to 30 carbon atoms. Heterocyclic carbonyl groups bonded to carbonyl groups at substituted carbon atoms (eg, acetyl, pivaloyl, 2-chloroacetyl, stearoyl, benzoyl, pn-octyloxyphenylcarbonyl, 2-pyridylcarbonyl, 2-furylcarbonyl )

(36) Aryloxycarbonyl group Preferably, it is a substituted or unsubstituted aryloxycarbonyl group having 7 to 30 carbon atoms (for example, phenoxycarbonyl, o-chlorophenoxycarbonyl, m-nitrophenoxycarbonyl, pt-butylphenoxycarbonyl). )

(37) Alkoxycarbonyl group Preferably, the substituted or unsubstituted alkoxycarbonyl group having 2 to 30 carbon atoms (for example, methoxycarbonyl, ethoxycarbonyl, t-butoxycarbonyl, n-octadecyloxycarbonyl)

(38) Carbamoyl group Preferably, the substituted or unsubstituted carbamoyl having 1 to 30 carbon atoms (for example, carbamoyl, N-methylcarbamoyl, N, N-dimethylcarbamoyl, N, N-di-n-octylcarbamoyl, N- (Methylsulfonyl) carbamoyl)

(39) Aryl and heterocyclic azo group Preferably, the substituted or unsubstituted arylazo group having 6 to 30 carbon atoms, or the substituted or unsubstituted heterocyclic azo group having 3 to 30 carbon atoms (for example, phenylazo, p-chlorophenylazo , 5-ethylthio-1,3,4-thiadiazol-2-ylazo)

(40) Imido group, preferably N-succinimide, N-phthalimide

(41) Phosphino group Preferably, the substituted or unsubstituted phosphino group having 2 to 30 carbon atoms (for example, dimethylphosphino, diphenylphosphino, methylphenoxyphosphino)

(42) Phosphinyl group Preferably, the substituted or unsubstituted phosphinyl group having 2 to 30 carbon atoms (for example, phosphinyl, dioctyloxyphosphinyl, diethoxyphosphinyl).

(43) Phosphinyloxy group Preferably, the substituted or unsubstituted phosphinyloxy group having 2 to 30 carbon atoms (for example, diphenoxyphosphinyloxy, dioctyloxyphosphinyloxy)

(44) Phosphinylamino group Preferably, the substituted or unsubstituted phosphinylamino group having 2 to 30 carbon atoms (for example, dimethoxyphosphinylamino, dimethylaminophosphinylamino)

(45) Phosphor group

(46) Silyl group Preferably, the substituted or unsubstituted silyl group having 3 to 30 carbon atoms (for example, trimethylsilyl, triethylsilyl, triisopropylsilyl, t-butyldimethylsilyl, phenyldimethylsilyl)

(47) Hydrazino group Preferably a substituted or unsubstituted hydrazino group having 0 to 30 carbon atoms (for example, trimethylhydrazino)

(48) Ureido group Preferably, the substituted or unsubstituted ureido group having 0 to 30 carbon atoms (for example, N, N-dimethylureido)

  Two Ws can also form a ring together. Examples of such a ring include an aromatic or non-aromatic hydrocarbon ring, a heterocyclic ring, and a polycyclic fused ring formed by further combining them. For example, benzene ring, naphthalene ring, anthracene ring, phenanthrene ring, fluorene ring, triphenylene ring, naphthacene ring, biphenyl ring, pyrrole ring, furan ring, thiophene ring, imidazole ring, oxazole ring, thiazole ring, pyridine ring, pyrazine ring, Pyrimidine ring, pyridazine ring, indolizine ring, indole ring, benzofuran ring, benzothiophene ring, isobenzofuran ring, quinolidine ring, quinoline ring, phthalazine ring, naphthyridine ring, quinoxaline ring, quinoxazoline ring, isoquinoline ring, carbazole ring, phenant Examples include lysine ring, acridine ring, phenanthroline ring, thianthrene ring, chromene ring, xanthene ring, phenoxathiin ring, phenothiazine ring, and phenazine ring.

Among the above-described substituents W, those having a hydrogen atom may be substituted with the above groups by removing this. Examples of such substituents include a —CONHSO ₂ — group (sulfonylcarbamoyl group, carbonylsulfamoyl group), —CONHCO— group (carbonylcarbamoyl group), —SO ₂ NHSO ₂ — group (sulfonylsulfamoyl group). ). More specifically, alkylcarbonylaminosulfonyl group (for example, acetylaminosulfonyl), arylcarbonylaminosulfonyl group (for example, benzoylaminosulfonyl group), alkylsulfonylaminocarbonyl group (for example, methylsulfonylaminocarbonyl), arylsulfonylamino A carbonyl group (for example, p-methylphenylsulfonylaminocarbonyl) is mentioned.

The compound represented by the general formula (2) used in the present invention will be described in detail.
In the general formula (2), Z ₁₁ represents an atomic group necessary for forming a 5- or 6-membered ring. L ₁ , L ₂ and L ₃ each represents an unsubstituted methine group or a substituted methine group. D ₁ represents an atomic group. n represents an integer of 0 or more.

Z ₁₁ represents an atomic group necessary for forming a 5- or 6-membered ring, and the ring formed is preferably one that is usually used as an acidic nucleus in a merocyanine dye, and specific examples thereof include the following: Can be mentioned.

(A) 1,3-dicarbonyl nucleus: For example, 1,3-indandione nucleus, 1,3-cyclohexanedione, 5,5-dimethyl-1,3-cyclohexanedione, 1,3-dioxane-4,6- Zeon etc.
(B) pyrazolinone nucleus: for example 1-phenyl-2-pyrazolin-5-one, 3-methyl-1-phenyl-2-pyrazolin-5-one, 1- (2-benzothiazoyl) -3-methyl-2 -Pyrazolin-5-one and the like.
(C) Isoxazolinone nucleus: For example, 3-phenyl-2-isoxazolin-5-one, 3-methyl-2-isoxazolin-5-one and the like.
(D) Oxindole nucleus: For example, 1-alkyl-2,3-dihydro-2-oxindole and the like.
(E) 2,4,6-triketohexahydropyrimidine nucleus: for example, barbituric acid or 2-thiobarbituric acid and its derivatives. Examples of the derivatives include 1-alkyl compounds such as 1-methyl and 1-ethyl, 1,3-dialkyl compounds such as 1,3-dimethyl, 1,3-diethyl and 1,3-dibutyl, 1,3-diphenyl, 1,3-diaryl compounds such as 1,3-di (p-chlorophenyl) and 1,3-di (p-ethoxycarbonylphenyl), 1-alkyl-1-aryl compounds such as 1-ethyl-3-phenyl, Examples include 1,3-di (2-pyridyl) 1,3-diheterocyclic substituents and the like.
(F) 2-thio-2,4-thiazolidinedione nucleus: for example, rhodanine and derivatives thereof. Examples of the derivatives include 3-alkylrhodanine such as 3-methylrhodanine, 3-ethylrhodanine and 3-allylrhodanine, 3-arylrhodanine such as 3-phenylrhodanine, and 3- (2-pyridyl) rhodanine. And the like.

(G) 2-thio-2,4-oxazolidinedione (2-thio-2,4- (3H, 5H) -oxazoledione nucleus: for example, 3-ethyl-2-thio-2,4-oxazolidinedione and the like.
(H) Tianaphthenone nucleus: For example, 3 (2H) -thianaphthenone-1,1-dioxide and the like.
(I) 2-thio-2,5-thiazolidinedione nucleus: for example, 3-ethyl-2-thio-2,5-thiazolidinedione and the like.
(J) 2,4-thiazolidinedione nucleus: for example, 2,4-thiazolidinedione, 3-ethyl-2,4-thiazolidinedione, 3-phenyl-2,4-thiazolidinedione, etc. (k) thiazolin-4-one nucleus : For example, 4-thiazolinone, 2-ethyl-4-thiazolinone and the like.
(L) 2,4-imidazolidinedione (hydantoin) nucleus: for example, 2,4-imidazolidinedione, 3-ethyl-2,4-imidazolidinedione, etc.
(M) 2-thio-2,4-imidazolidinedione (2-thiohydantoin) nucleus: for example, 2-thio-2,4-imidazolidinedione, 3-ethyl-2-thio-2,4-imidazolidinedione etc.
(N) Imidazolin-5-one nucleus: for example, 2-propylmercapto-2-imidazolin-5-one and the like.
(O) 3,5-pyrazolidinedione nucleus: for example, 1,2-diphenyl-3,5-pyrazolidinedione, 1,2-dimethyl-3,5-pyrazolidinedione and the like.
(P) Benzothiophen-3-one nucleus: for example, benzothiophen-3-one, oxobenzothiophen-3-one, dioxobenzothiophen-3-one and the like.
(Q) Indanone nucleus: For example, 1-indanone, 3-phenyl-1-indanone, 3-methyl-1-indanone, 3,3-diphenyl-1-indanone, 3,3-dimethyl-1-indanone, and the like.

The ring formed by Z ₁₁ is preferably a 1,3-dicarbonyl nucleus, a pyrazolinone nucleus, a 2,4,6-triketohexahydropyrimidine nucleus (including a thioketone body), 2-thio-2,4-thiazolidine. Dione nucleus, 2-thio-2,4-oxazolidinedione nucleus, 2-thio-2,5-thiazolidinedione nucleus, 2,4-thiazolidinedione nucleus, 2,4-imidazolidinedione nucleus, 2-thio-2, 4-imidazolidinedione nucleus, 2-imidazoline-5-one nucleus, 3,5-pyrazolidinedione nucleus, benzothiophene-3-one nucleus, indanone nucleus, more preferably 1,3-dicarbonyl nucleus, 2,4,6-triketohexahydropyrimidine nucleus (including thioketone), 3,5-pyrazolidinedione nucleus, benzothiophen-3-one nucleus, indanone nucleus More preferred are a 1,3-dicarbonyl nucleus and a 2,4,6-triketohexahydropyrimidine nucleus (including a thioketone body), and particularly preferred is a 1,3-indandione nucleus.

A preferable ring formed by Z ₁₁ is represented by the following formula.

Z ³ represents an atomic group necessary for forming a 5- to 6-membered ring. Z ³ can be selected from the ring formed by Z ₁₁ described above, preferably 1,3-dicarbonyl nucleus, 2,4,6-triketohexahydropyrimidine nucleus (including thioketone body), Particularly preferred is a 1,3-indandione nucleus.
The case where the ring formed by Z ₁₁ is a group represented by the general formula (2-4) or a group represented by the general formula (2-5) is preferable.
In the case of the group represented by the general formula (2-4), R _{41 to} R ₄₄ each independently represents a hydrogen atom or a substituent. As the substituent, those exemplified as the substituent W can be applied. Further, R _{41 to} R ₄₄ that are adjacent to each other can be bonded to form a ring, and R ₄₂ and R ₄₃ are bonded to form a ring (for example, a benzene ring, a pyridine ring, or a pyrazine ring). The case is preferred. R _{41 to} R ₄₄ are preferably all hydrogen atoms.
The case where the group represented by the general formula (2-4) is a group represented by the general formula (2-5) is preferable.
In the case of the group represented by the general formula (2-5), R ₄₁ , R ₄₄ and R _{45 to} R ₄₈ each independently represent a hydrogen atom or a substituent. As the substituent, those exemplified as the substituent W can be applied. R ₄₁ , R ₄₄ , and R _{45 to} R ₄₈ are preferably all hydrogen atoms.

L ₁ , L ₂ and L ₃ each independently represent an unsubstituted methine group or a substituted methine group. Examples of the substituent of the substituted methine group include the above-described substituent W, and it is preferable that all of L ₁ , L ₂ and L ₃ are unsubstituted methine groups.

  n represents an integer of 0 or more, preferably 0 or more and 3 or less, and more preferably 0. When n is increased, the absorption wavelength region can be made longer, or the thermal decomposition temperature is lowered. N = 0 is preferable in that it has appropriate absorption in the visible region and suppresses thermal decomposition during vapor deposition.

D ₁ represents an atomic group. The D ₁ is preferably a group containing —NR ^a (R ^b ), and more preferably, the D ₁ represents a divalent arylene group to which —NR ^a (R ^b ) is bonded. R ^a and R ^b each independently represent a hydrogen atom or a substituent, and R ^a , R ^b and L may form a ring. R ^a and R ^b may be bonded to each other to form a ring (preferably a 5-membered or 6-membered ring, more preferably a 6-membered ring), and each of R ^a and R ^b is L A ring (preferably a 5-membered or 6-membered ring, more preferably a 6-membered ring) may be formed by combining with the substituents therein. Examples of the substituent represented by R ^a and R ^b include the above-described substituent W, and are preferably an aliphatic hydrocarbon group, an aryl group, and a heterocyclic group.
D ₁ is preferably a divalent arylene group (preferably a phenylene group) having an amino group bonded to the para position. The amino group may be substituted, and the substituent of the amino group may be bonded to the substituent of the aryl group in the arylene group (preferably the benzene ring of the phenyl group) to form a ring. Examples of the substituent of the amino group include the substituent W described above, and an aliphatic hydrocarbon group, an aryl group, or a heterocyclic group is preferable.

When R ^a and R ^b are an aliphatic hydrocarbon group, an aryl group or a heterocyclic group, an alkyl group, an alkenyl group, an aryl group, an alkoxy group, an aryloxy group, an acyl group, an alkoxycarbonyl group, Aryloxycarbonyl group, acylamino group, sulfonylamino group, sulfonyl group, silyl group, aromatic heterocyclic group, more preferably alkyl group, alkenyl group, aryl group, alkoxy group, aryloxy group, silyl group, aromatic A heterocyclic group, more preferably an alkyl group, an aryl group, an alkoxy group, an aryloxy group, a silyl group, and an aromatic heterocyclic group. As specific examples, those exemplified for the substituent W can be applied.

R ^a and R ^b are preferably an alkyl group, an aryl group, or an aromatic heterocyclic group. R ¹ and R ² are particularly preferably an alkyl group, an alkylene group that is linked to L to form a ring, or an aryl group, and more preferably an alkyl group having 1 to 8 carbon atoms that is linked to L to be 5 to 6 members. An alkylene group forming a ring, or a substituted or unsubstituted phenyl group.

It is also preferred that D ₁ is a group represented by the general formula (2-8), (2-9) or (2-10).
Formula (2-8)

In the formula, R _{51 to} R ₅₄ each independently represent hydrogen or a substituent. R ₅₂ and R ₅₃ , or R ₅₁ and R ₅₂ may be linked to form a ring.
Formula (2-9)

In the formula, R _{61 to} R ₆₄ each independently represent hydrogen or a substituent. R ₆₂ and R ₆₃ , or R ₆₁ and R ₆₂ may be linked to form a ring.
Formula (2-10)

_Wherein, R 71 _{to R 73} each independently represent a hydrogen or a substituent. R ₇₂ and R ₇₃ may be linked to form a ring.

The group represented by the general formula (2-2) or (2-3) is more preferably used as the D ₁ .
In general formula (2-2), R _{1 to} R ₆ each independently represents a hydrogen atom or a substituent. R ₁ and R ₂ , R ₃ and R ₄ , R ₅ and R ₆ , R ₂ and R ₅ , and R ₄ and R ₆ may be bonded to each other to form a ring.
Examples of the substituent in R _{1 to} R ₄ include the above-described substituent W. Preferably, R _{1 to} R ₄ are a hydrogen atom, or R ₂ and R ₅ or R ₄ or R ₆ form a 5-membered ring. Yes, and more preferably, any of R _{1 to} R ₄ is a hydrogen atom.
Examples of the substituent in R ₅ and R ₆ include the above-described substituent W. Among the substituents, a substituted or unsubstituted aryl group is preferable. As the substituent of the substituted aryl group, an alkyl group (for example, a methyl group, Ethyl group) and aryl groups (for example, phenyl group, naphthylene group, phenanthryl group, anthryl group) are preferable. R ₅ and R ₆ are preferably a phenyl group, an alkyl-substituted phenyl group, a phenyl-substituted phenyl group, a naphthylene group, a phenanthryl group, and an anthryl group.
In General Formula (2-3), R _{10 to} R ₁₄ , R _{20 to} R ₂₄ , and R _{30 to} R ₃₄ each independently represent a hydrogen atom or a substituent. R _{10 to} R ₁₄ , R _{20 to} R ₂₄ , and R _{30 to} R ₃₄ may be bonded to each other to form a ring.
Examples of the substituent represented by R _{11 to} R ₁₄ , R _{20 to} R ₂₄ , and R _{30 to} R ₃₄ include the substituent W. Preferably, the substituent is an alkyl group (for example, a methyl group or an ethyl group), an aryl group ( For example, a phenyl group). Among _them, preferred is a case R _{20, R 30} is the substituent group, and the other _{R 11 ~R 14, R 21 ~R} 24, R 31 ~R 34 is more preferably be a hydrogen atom.

  Specific examples of the compound represented by the general formula (2) are shown below, but the present invention is not limited thereto.

As the merocyanine compound, for example, a compound represented by the following general formula (3) can be used.
General formula (3)

In the general formula (3), Z ₁ represents an atomic group forming a 5-membered or 6-membered nitrogen-containing heterocycle. However, the case where Z ₁ is an atomic group forming a thiazoline nucleus and a thiazole nucleus is excluded. Za represents an atomic group forming a 5-membered or 6-membered ring. R ₁ represents a hydrogen atom, an alkyl group, an alkenyl group, an aryl group, or a heterocyclic group. L _{11 to} L ₁₄ represent a methine group, may have a substituent, and may form a ring with another methine group. p ₁ represents 0 or 1. n ₁ represents an integer of 0 to 4, and when n ₁ is 2 or more, the plurality of L ₁₃ and L ₁₄ may be the same or different. M ₁ represents an ion for neutralizing the electric charge, and m ₁ represents a number necessary for neutralizing the electric charge.

Z ₁ represents an atomic group forming a specific 5-membered or 6-membered nitrogen-containing heterocyclic ring. The 5- or 6-membered nitrogen-containing heterocycle formed is preferably an oxazole nucleus having 3 to 25 carbon atoms (hereinafter referred to as C number) (for example, 2-3-ethyloxazolyl, 2-3-sulfopropyloxa Zolyl, 2-3-sulfopropylbenzoxazolyl, 2-3-ethylbenzoxazolyl, 2-3-sulfopropyl-γ-naphthoxazolyl, 2-3-ethyl-α-naphthoxazolyl , 2-3-methyl-β-naphthoxazolyl, 2-3-sulfopropyl-β-naphthoxazolyl, 2-5-chloro-3-ethyl-α-naphthoxazolyl, 2-5-chloro -3-ethylbenzoxazolyl, 2-5-chloro-3-sulfopropylbenzoxazolyl, 2-5,6-dichloro-3-sulfopropylbenzoxazolyl, 2-5-bromo-3-sulfo Propylbenzoxazolyl, 2-3-ethyl-5-phenylbenzoxazolyl, 2-5-phenyl-3-sulfopropylbenzoxazolyl, 2-5- (4-bromophenyl) -3-sulfobutyl Benzoxazolyl, 2-5- (1-pyrrolyl) -3-sulfopropylbenzoxazolyl, 2-5,6-dimethyl-3-sulfopropylbenzoxazolyl, 2-3-ethyl-5-methoxy Benzoxazolyl, 2-3-ethyl-5-sulfobenzoxazolyl, etc.), C 3-25 imidazole nucleus (for example, 2-1,3-diethylimidazolyl, 2-5,6- Dichloro-1,3-diethylbenzimidazolyl, 2-5,6-dichloro-3-ethyl-1-sulfopropylbenzimidazolyl, 2-5-chloro-6-cyano- , 3-diethylbenzimidazolyl, 2-5-chloro-1,3-diethyl-6-trifluoromethylbenzimidazolyl, etc.), an indolenine nucleus having 10 to 30 carbon atoms (for example, 3,3-dimethyl-1- Pentylindolenine, 3,3, -dimethyl-1-sulfopropylindolenine, 5-carboxy-1,3,3-trimethylindolenine, 5-carbamoyl-1,3,3-trimethylindolenine, 1,3 3, -trimethyl-4,5-benzoindolenine, etc.), C 9-25 quinoline nuclei (for example, 2-1-ethylquinolyl, 2-1-sulfobutylquinolyl, 4-1-pentylquino) , 4-1-sulfoethylquinolyl, 4-1-methyl-7-chloroquinolyl, etc.), C 3-25 selenazo Nuclei (for example, 2-3methylbenzoselenazolyl), pyridine nuclei having 5 to 25 carbon atoms (for example, 2-pyridyl and the like), and other oxazoline nuclei, Examples include a selenazoline nucleus, a tellurazoline nucleus, a tellurazole nucleus, a benzotelrazole nucleus, an imidazoline nucleus, an imidazo [4,5-quinoxaline] nucleus, an oxadiazole nucleus, a thiadiazole nucleus, a tetrazole nucleus, a pyrimidine nucleus, and a pyrrolidine nucleus.

These nitrogen-containing heterocycles may be substituted, and as a substituent (hereinafter referred to as “substituent W”), a halogen atom, an alkyl group (including a cycloalkyl group, a bicycloalkyl group, and a tricycloalkyl group), An alkenyl group (including a cycloalkenyl group and a bicycloalkenyl group), an alkynyl group, an aryl group, a heterocyclic group (also referred to as a heterocyclic group), a cyano group, a hydroxy group, a nitro group, a carboxy group, an alkoxy group, Aryloxy group, silyloxy group, heterocyclic oxy group, acyloxy group, carbamoyloxy group, alkoxycarbonyl group, aryloxycarbonyl group, amino group (including anilino group), ammonio group, acylamino group, aminocarbonylamino group, alkoxycarbonyl Amino group, aryloxycarbonylamino group, sulf Moylamino group, alkyl and arylsulfonylamino group, mercapto group, alkylthio group, arylthio group, heterocyclic thio group, sulfamoyl group, sulfo group, alkyl and arylsulfinyl group, alkyl and arylsulfonyl group, acyl group, aryloxycarbonyl group, Alkoxycarbonyl group, carbamoyl group, aryl and heterocyclic azo group, imide group, phosphino group, phosphinyl group, phosphinyloxy group, phosphinylamino group, phosphono group, silyl group, hydrazino group, ureido group, boronic acid group (-B _(OH) 2), phosphato group (-OPO _(OH) 2), a sulfato group (-OSO ₃ H), and other known substituents.

  These heterocycles may be further condensed. Preferred examples of the condensed ring include a benzene ring, a benzofuran ring, a pyridine ring, a pyrrole ring, an indole ring and a thiophene ring, and a benzene ring is preferred. These rings may further have a substituent.

More preferably, the 5- or 6-membered nitrogen-containing heterocyclic ring formed by Z ₁ is an oxazole nucleus, an oxazoline nucleus, a benzimidazole nucleus, an indolenine nucleus, or a pyrrolidine nucleus, and more preferably an oxazole nucleus or an indolenine nucleus. And most preferably an indolenine nucleus, a benzoxazole nucleus or a naphthoxazole nucleus.

R ₁ represented by the general formula (3) is a hydrogen atom or an alkyl group (preferably having 1 to 20 carbon atoms, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, benzyl, 3 -Sulfopropyl, 4-sulfobutyl, 3-methyl-3-sulfopropyl, 2'-sulfobenzyl, carboxymethyl, 5-carboxypentyl), an alkenyl group (preferably C2-20, for example, vinyl, allyl), An aryl group (preferably having 6 to 20 carbon atoms, such as phenyl, 2-chlorophenyl, 4-methoxyphenyl, 3-methylphenyl, 1-naphthyl), a heterocyclic group (preferably having 1 to 20 carbon atoms, such as pyridyl, Thienyl, furyl, thiazolyl, imidazolyl, pyrazolyl, pyrrolidino, piperidino, morpholino), more preferably Kill group (preferably an alkyl group having a C number of 1 to 6).

L _{11 to} L ₁₄ each represent a methine group and may have a substituent (preferred examples of the substituent are the same as the examples of the substituent on Z ₁ ), and the substituent is preferably an alkyl group or a halogen atom. Nitro group, alkoxy group, aryl group, nitro group, heterocyclic group, aryloxy group, acylamino group, carbamoyl group, sulfo group, hydroxy group, carboxy group, alkylthio group, cyano group, etc. An alkyl group is preferred. L ₁₃ and L ₁₄ are preferably an unsubstituted methine group or an alkyl group (preferably having a C number of 1 to 6), and more preferably an unsubstituted methine group.
L ₁₃ and L ₁₄ may be linked to each other to form a ring, and preferred examples of the ring formed include a cyclohexene ring, a cyclopentene ring, a benzene ring, and a thiophene ring.

p1 is 0 or 1, preferably 0. n1 represents an integer of 0 to 4, more preferably 0 to 3, and still more preferably 0 or 1. When n1 is 2 or more, the plurality of L ₁₃ and L ₁₄ may be the same or different.

  M1 represents an ion for neutralizing the electric charge, and m1 represents a number necessary for neutralizing the electric charge.

  The ring formed by Za may be any ring, but is preferably a heterocyclic ring (preferably a 5- or 6-membered heterocyclic ring). Here, any heterocyclic ring may be used, but an acidic nucleus of a general merocyanine dye is preferable. Preferred Za represents the remaining atomic group necessary for forming an acidic nucleus.

  For example, the acidic nucleus mentioned here is “The Theory of the Photographic Process” 4th edition, edited by James, McMillan Publishing Company, 1977, pp. 197-200. Are listed. Specifically, acidic nuclei are disclosed in U.S. Pat. Nos. 3,567,719, 3,575,869, 3,804,634, 3,837,862, 4,002,480. No. 4,925,777, JP-A-3-167546, US Pat. No. 5,994,051, US Pat. No. 5,747,236, and the like.

The acidic nucleus is preferred when forming a heterocycle (preferably a 5- or 6-membered nitrogen-containing heterocycle) composed of carbon, nitrogen, and / or chalcogen (typically oxygen, sulfur, selenium, and tellurium) atoms. More preferably, when forming a 5- or 6-membered nitrogen-containing heterocycle consisting of carbon, nitrogen, and / or chalcogen (typically oxygen, sulfur, selenium, and tellurium) atoms.
Specific examples of the acidic nucleus include the following nuclei.

  2-pyrazolin-5-one, pyrazolidin-3,5-dione, imidazolin-5-one, hydantoin, 2 or 4-thiohydantoin, 2-iminooxazolidine-4-one, 2-oxazolin-5-one, 2- Thioxazolidine-2,5-dione, 2-thiooxazoline-2,4-dione, isoxazoline-5-one, 2-thiazoline-4-one, thiazolidine-4-one, thiazolidine-2,4-dione, rhodanine , Thiazolidine-2,4-dithione, isorhodanine, indan-1,3-dione, thiophen-3-one, thiophen-3-one-1,1-dioxide, indoline-2-one, indoline-3-one, 2 -Oxoindazolinium, 3-oxoindazolinium, 5,7-dioxo-6,7-dihydrothiazolo [ 3,2-a] pyrimidine, cyclohexane-1,3-dione, 3,4-dihydroisoquinolin-4-one, 1,3-dioxane-4,6-dione, barbituric acid, 2-thiobarbituric acid, Chroman-2,4-dione, indazolin-2-one, pyrido [1,2-a] pyrimidine-1,3-dione, pyrazolo [1,5-b] quinazolone, pyrazolo [1,5-a] benzimidazole , Pyrazolopyridone, 1,2,3,4-tetrahydroquinoline-2,4-dione, 3-oxo-2,3-dihydrobenzo [d] thiophene-1,1-dioxide, 3-dicyanomethine-2,3- Dihydrobenzo [d] thiophene-1, 1-dioxide nucleus.

  These acidic nuclei may be condensed with a ring or may be substituted with a substituent (for example, the aforementioned W).

  Za is more preferably hydantoin, 2 or 4-thiohydantoin, 2-oxazoline-5-one, 2-thiooxazoline-2, 4-dione, thiazolidine-2, 4-dione, rhodanine, thiazolidine-2, 4- Dithione, barbituric acid, 2-thiobarbituric acid, particularly preferably hydantoin, 2 or 4-thiohydantoin, 2-oxazolin-5-one, rhodanine, barbituric acid, 2-thiobarbituric acid Most preferred is rhodanine.

  Specific examples of the compound represented by the general formula (3) are described below.

A configuration of a photoelectric conversion element and an imaging element for describing an embodiment of the present invention will be described.
The material combination of the present invention is preferably included in the following photoelectric conversion film, but the material other than the material combination of the present invention used for the photoelectric conversion layer including the photoelectric conversion film, and further the photoelectric conversion element including the photoelectric conversion film The following describes a preferable configuration of the imaging element including the other components such as the film used in the above and the photoelectric conversion element.

A configuration capable of providing a photoelectric conversion element capable of effectively reducing dark current by suppressing injection of charges (electrons, holes) from the electrode into the photoelectric conversion layer will be described below.
The photoelectric conversion element is a photoelectric conversion element including a pair of electrodes and a photoelectric conversion layer disposed between the pair of electrodes, and from one of the pair of electrodes between one of the pair of electrodes and the photoelectric conversion layer. When providing the first charge blocking layer that suppresses the injection of charges into the photoelectric conversion layer, the first charge blocking layer has a single layer structure by forming the first charge blocking layer into a multi-layer structure. Can suppress dark current more. Further, in the configuration in which a second charge blocking layer for suppressing charge injection from the other of the pair of electrodes to the photoelectric conversion layer is provided between the other of the pair of electrodes and the photoelectric conversion layer, By making the charge blocking layer have a multilayer structure, dark current can be suppressed more than when the second charge blocking layer has a single layer structure. Furthermore, when at least two of the plurality of layers constituting each of the first charge blocking layer and the second charge blocking layer are made of different materials, the dark current suppressing effect can be further improved. Furthermore, when at least two of the plurality of layers are a layer made of an inorganic material and a layer made of an organic material, the dark current suppressing effect can be improved.

FIG. 1 is a schematic cross-sectional view illustrating an example of a configuration of a photoelectric conversion element having a charge blocking layer.
In FIG. 1, reference numeral 200 is a photoelectric conversion layer, reference numeral 202 is a charge blocking layer having a two-layer structure, and reference numerals 202 a and 202 b are layers constituting the charge blocking layer 202. Reference numerals 201 and 204 are electrodes.

  For example, when the electrode 204 is an electrode on the light incident side, the electrode 204 is preferably made of a highly transparent material because light needs to enter the photoelectric conversion layer 200. A transparent conductive oxide (TCO) is mentioned as an electrode with high transparency. In addition, since the electrode 201 may need to transmit light below the electrode 201 as in the configuration of the imaging element described later, it is preferable that the electrode 201 is similarly formed of a highly transparent material. Even when the electrode 201 is a light incident side electrode, the electrode 204 and the electrode 201 are preferably made of a highly transparent material.

  The charge blocking layer 202 is a layer for suppressing the movement of charges from the electrode 204 to the photoelectric conversion layer 200 when a voltage is applied to the electrode 201 and the electrode 204. When the charge blocking layer 202 has a single layer structure, the material itself constituting the charge blocking layer 202 has an intermediate level (impurity level, etc.), and charges (electrons, holes) are transmitted through the intermediate level. The dark current increases. Therefore, in this configuration example, the charge blocking layer 202 has a two-layer structure instead of a single layer in order to prevent an increase in dark current.

  By forming an interface between the layers 202a and 202b constituting the charge blocking layer 202, discontinuity occurs in the intermediate levels existing in the layers 202a and 202b, and carriers move through the intermediate levels. Since it becomes difficult, it is thought that dark current can be suppressed. However, if the layers 202a and 202b are made of the same material, the intermediate levels existing in the layers 202a and 202b may be exactly the same. Therefore, the layers 202a and 202b are configured to further enhance the dark current suppression effect. It is preferable to use different materials.

  FIG. 2 is an energy diagram showing the state of the intermediate level in the charge blocking layer having the two-layer structure shown in FIG. 1. FIG. 2A shows the case where the layers 202a and 202b are made of the same material. ) Shows a case where the layers 202a and 202b are made of different materials.

  When the materials of the layers 202a and 202b are the same, an interface is generated as described above, so that dark current can be suppressed as compared with a single-layer structure. However, as shown in FIG. 2 (a), when the intermediate levels (S1, S2) of the layers 202a and 202b are at the same energy position, the charge passing through the intermediate levels of the layers 202a and 202b is reduced. Movement (indicated by an arrow in the figure) occurs.

  Here, if the materials of the layers 202a and 202b are different, for example, as shown in FIG. 2B, the intermediate level (S20) of the layer 202b is higher than the intermediate level (S10) of the layer 202a. Since the high energy position is reached, the difference in energy level becomes a barrier, and the movement of charges is suppressed accordingly. In this way, by forming the two layers constituting the charge blocking layer 202 from different materials, the position of the intermediate level of each layer can be reliably dispersed, and thereby the carrier movement via the intermediate level The effect which suppresses is raised.

  FIG. 1 shows an example in which the photoelectric conversion element has one charge blocking layer. In FIG. 1, when voltage is applied to the electrode 201 and the electrode 204 between the electrode 201 and the photoelectric conversion layer 200. Even when a charge blocking layer for suppressing the movement of charges from the electrode 201 to the photoelectric conversion layer 200 is provided, by making this charge blocking layer a two-layer structure, dark current can be suppressed, Furthermore, dark current can be further suppressed by making the two layers of materials different from each other.

  In the above description, the charge blocking layer 202 has an example of a two-layer structure, but this may have a structure of three or more layers. In this case, if at least two of the layers constituting the charge blocking layer are made of different materials, the intermediate level step can be reliably formed inside the charge blocking layer as described above. . For example, when the charge blocking layer has a three-layer structure, as shown in FIG. 3A, the lowermost layer and the uppermost layer are made of material A, and the intermediate layer between them is made of material B different from material A. good. Alternatively, as shown in FIG. 3B, the lowermost layer may be the material B, and the intermediate layer and the uppermost layer may be the material A. Alternatively, as shown in FIG. 3C, the lowermost layer and the intermediate layer may be made of the material A, and the uppermost layer may be made of the material B. Alternatively, as shown in FIG. 3D, the lowermost layer may be a material C different from materials A and B, the intermediate layer may be a material B, and the uppermost layer may be a material A.

  FIG. 4 is a schematic cross-sectional view showing another example of a photoelectric conversion element (a photoelectric conversion element having a three-layered electron blocking layer and a three-layered hole blocking layer). FIG. 5 is an energy diagram for explaining the state of charge transfer through the electron blocking layer and the hole blocking intermediate level when a voltage is applied to the photoelectric conversion element of FIG.

  The photoelectric conversion element of FIG. 4 has a structure in which a pixel electrode (transparent electrode) 190 is provided on a transparent substrate 180, and an electron blocking layer 192 (192a to 192c) having a three-layer structure is laminated on the transparent electrode 190. ), A photoelectric conversion layer 200, and a hole blocking layer 203 (having a structure in which the layers 203a to 203c are stacked) are sequentially stacked, and a counter electrode 300 is further provided thereon. Has a structure. At least two of the layers 192a to 192c are made of different materials. Here, the materials of the layers 192a to 192c are different from each other. Similarly, at least two of the layers 203a to 203c are made of different materials. Here, the materials of the layers 203a to 203c are different from each other.

  With such a configuration, as shown in FIG. 5, when a voltage is applied, the energy levels of the intermediate levels (S5, S6, S7) of each layer in the electron blocking layer 192 are different, and the step becomes an energy barrier. This makes it difficult for electrons to move. Similarly, the energy level of the intermediate level (S8, S9, S10) of each layer in the hole blocking layer 203 is different, and the step becomes an energy barrier, which makes it difficult for holes to move.

Next, effects other than the contents relating to the intermediate level will be described regarding the formation of a plurality of blocking layers.
The method of shifting the intermediate level existing in each layer by stacking as described so far suppresses dark current by “inhibiting the transport of injected charge”, but the multi-layering of the blocking layer “ It also has the effect of reducing dark current by “suppressing charge injection”.

  To suppress the injection of charge from the electrode, “enlarge the energy barrier between the electrode and the layer in contact with it”, “homogeneous blocking layer, and the electrode is below the blocking layer (photoelectric conversion layer) It is important to avoid being close to each other.

  The former is a solution method of setting an energy injection barrier, and the latter is a physical structure in which an electrode material enters a minute defect of a film, and a photoelectric conversion layer and an electrode are close to each other to form a leak point. This is a solution technique that prevents the

  When the blocking layer has a multi-layer structure, the layer in contact with the electrode of the plurality of layers is set so that there is an energy barrier difference from the electrode, and the layer not in contact with the electrode has a charge transporting property and is uniform. The layers can be set so as to prevent the occurrence of leaks, and the functions can be divided and provided in each layer.

  By using an inorganic material layer made of an inorganic material as a blocking layer in contact with the electrode, and using an organic material layer made of an organic material as a blocking layer in the lower layer (between the inorganic material layer and the photoelectric conversion layer), darkness becomes more prominent. It is possible to suppress the current and prevent the reading of the signal charge.

  That is, in FIG. 1, the layer 202a is an inorganic material layer and the layer 202b is an organic material layer. In FIGS. 3B and 3D, A is an inorganic material layer and B is an organic material layer. 3 (c), B is an inorganic material layer, A is an organic material layer, 192c and 203a are inorganic material layers in FIG. 4, and 192a, 192b, 203b, and 203c are organic material layers, Dark current is more remarkably suppressed, and reading of signal charges is not hindered.

  As the inorganic material constituting the inorganic material layer, any of Si, Mo, Ce, Li, Hf, Ta, Al, Ti, Zn, W, and Zr is preferably used. Alternatively, an oxide is preferably used as the inorganic material. It is particularly preferable to use SiO as the oxide.

  In order to prevent charge injection from the electrode, the inorganic material layer needs to have an ionization energy Ip that causes an energy barrier between the work functions of adjacent electrodes, and preferably has a larger Ip. . However, if the charge blocking layer is only this inorganic material layer alone, if the layer thickness is thin, a leak portion will be generated between the electrode and the photoelectric conversion layer, so that a sufficient injection preventing effect cannot be obtained. And the signal charge is difficult to read out.

  Therefore, in addition to this inorganic material layer, it is important to provide an organic material layer below it. The organic material layer has a charge transport property sufficient to transport signal charges generated in the photoelectric conversion layer, is a uniform layer, and is a material with few carriers that cause dark current generated from the material. desirable.

  As a result, the blocking layer can be made uniform and thick without increasing the dark current derived from the blocking layer and without reducing the photoelectric conversion efficiency. It becomes possible to suppress.

  Next, organic material candidates constituting the hole blocking layer and the electron blocking layer will be described.

(Hole blocking layer)
An electron-accepting organic material can be used for the hole blocking layer.
Examples of the electron-accepting material include 1,3-bis (4-tert-butylphenyl-1,3,4-oxadiazolyl) phenylene (OXD-7) and other oxadiazole derivatives, anthraquinodimethane derivatives, and diphenylquinone derivatives. , Bathocuproine, bathophenanthroline, and derivatives thereof, triazole compounds, tris (8-hydroxyquinolinato) aluminum complexes, bis (4-methyl-8-quinolinato) aluminum complexes, distyrylarylene derivatives, silole compounds, etc. Can do. Moreover, even if it is not an electron-accepting organic material, it can be used if it is a material which has sufficient electron transport property. Porphyrin compounds and styryl compounds such as DCM (4-dicyanomethylene-2-methyl-6- (4- (dimethylaminostyryl))-4H pyran) and 4H pyran compounds can be used.

  The thickness of the hole blocking layer is preferably 10 nm to 200 nm, more preferably 30 nm to 150 nm, and particularly preferably 50 nm to 100 nm. This is because if the thickness is too thin, the dark current suppressing effect is lowered, and if it is too thick, the photoelectric conversion efficiency is lowered.

  Specific examples of the hole blocking material candidate include materials represented by the following HB-1 to HB-5 and BCP. Ea represents the electron affinity of the material, and lp represents the ionization potential of the material.

  The selection range of the material actually used for the hole blocking layer is determined by the material of the adjacent electrode and the material of the adjacent photoelectric conversion layer. The ionization potential (Ip) is 1.3 eV or more larger than the work function (Wf) of the material of the adjacent electrode, and Ea is equal to or larger than the electron affinity (Ea) of the material of the adjacent photoelectric conversion layer. Things are good.

(Electronic blocking layer)
An electron donating organic material can be used for the electron blocking layer. Specifically, in a low molecular material, N, N′-bis (3-methylphenyl)-(1,1′-biphenyl) -4,4′-diamine (TPD) or 4,4′-bis [N Aromatic diamine compounds such as-(naphthyl) -N-phenyl-amino] biphenyl (α-NPD), oxazole, oxadiazole, triazole, imidazole, imidazolone, stilbene derivative, pyrazoline derivative, tetrahydroimidazole, polyarylalkane, butadiene 4,4 ', 4 "tris (N- (3-methylphenyl) N-phenylamino) triphenylamine (m-M
TDATA), porphine, tetraphenylporphine copper, phthalocyanine, copper phthalocyanine, titanium phthalocyanine oxide, and other polyphyllin compounds, triazole derivatives, oxazizazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives, pyrazolone derivatives, phenylenediamine derivatives, annealing amine derivatives , Amino-substituted chalcone derivatives, oxazole derivatives, styryl anthracene derivatives, fluorenone derivatives, hydrazone derivatives, silazane derivatives, and the like, and polymer materials include phenylene vinylene, fluorene, carbazole, indole, pyrene, pyrrole, picoline, thiophene, Polymers such as acetylene and diacetylene, and derivatives thereof can be used. Even if it is not an electron-donating compound, it can be used as long as it has a sufficient hole transporting property.

  The thickness of the electron blocking layer is preferably 10 nm to 200 nm, more preferably 30 nm to 150 nm, and particularly preferably 50 nm to 100 nm. This is because if the thickness is too thin, the dark current suppressing effect is lowered, and if it is too thick, the photoelectric conversion efficiency is lowered.

  Specific examples of the electron blocking material candidate include materials represented by the following EB-1 to EB-5, TPD, and m-MTDATA.

  The selection range of the material actually used for the electron blocking layer is defined by the material of the adjacent electrode and the material of the adjacent photoelectric conversion layer. The electron affinity (Ea) is 1.3 eV or more larger than the work function (Wf) of the material of the adjacent electrode, and has an Ip equivalent to or smaller than the ionization potential (Ip) of the material of the adjacent photoelectric conversion layer. Things are good.

  According to such a configuration example, since the charge blocking layer has a multi-layer structure instead of the single charge blocking layer conventionally used, when an external electric field is applied to the photoelectric conversion layer from the electrode Carrier injection can be suppressed, and the photoelectric current / dark current ratio of the photoelectric conversion element can be greatly improved.

  Next, a configuration example of a photoelectric conversion element having a charge blocking layer having a plurality of structures will be described with reference to FIGS.

The charge blocking layer has a “hole blocking layer” with a large hole injection barrier from the adjacent electrode and a high ability to transport electrons as photocurrent carriers, and a large electron injection barrier from the adjacent electrode and a photocurrent. There is an “electron blocking layer” having a high ability to transport holes as carriers. In organic light-emitting elements and the like, a blocking layer using an organic material has already been used in order to prevent carriers from penetrating the light-emitting layer, as disclosed in JP-A-11-339966 and JP-A-2002-329582. By sandwiching an organic blocking layer between the electrode and the photoelectric conversion layer in the photoelectric conversion portion, it is possible to improve the photoelectric conversion efficiency and the response speed without decreasing the S / N ratio when an external voltage is applied.

  As the material used for the hole blocking layer, a material whose ionization potential is higher than the work function of the material of the adjacent electrode and whose electron affinity is higher than the electron affinity of the material of the adjacent photoelectric conversion layer is used. It is done. As a material used for the electron blocking layer, a material whose electron affinity is lower than the work function of the material of the adjacent electrode and whose ionization potential is lower than the ionization potential of the material of the adjacent photoelectric conversion layer is used. . Specific examples thereof are as described in the above configuration example.

  Hereinafter, the structure of the photoelectric conversion element including the photoelectric conversion unit having such a charge blocking layer will be specifically described.

  First, a configuration having a hole blocking layer will be described.

FIG. 6 is a schematic cross-sectional view illustrating a schematic configuration of the photoelectric conversion element.
6 includes a pair of electrodes 100 and 102 facing each other, a photoelectric conversion layer 101 made of an organic material formed between the electrodes 100 and 102, and a photoelectric conversion layer 101 and an electrode 100. A photoelectric conversion unit including a hole blocking layer 103 formed therebetween is included.

  As illustrated, the hole blocking layer 103 has a three-layer structure in which each of the material layers 103a to 103c is stacked. As described above, it is preferable that at least two of the material layers 103a to 103c are made of different materials. Further, the hole blocking layer 103 may have a multilayer structure.

  In the photoelectric conversion element illustrated in FIG. 6, light enters from above the electrode 102, and thus the electrode 102 serves as a light incident side electrode. Further, the photoelectric conversion element shown in FIG. 6 has the electrodes 100, 100 such that holes out of charges (holes and electrons) generated in the photoelectric conversion layer 101 are moved to the electrode 102 and electrons are moved to the electrode 100. A voltage is applied to 102 (that is, electrode 100 is an electrode for extracting electrons).

  The material of the hole blocking layer 103 has an ionization potential equal to or higher than the work function of the material of the adjacent electrode 100 and the electron affinity equal to or higher than the electron affinity of the material of the adjacent photoelectric conversion layer 101. Used. By providing the hole blocking layer 103 between the electrode 100 and the photoelectric conversion layer 101, electrons generated in the photoelectric conversion layer 101 are moved to the electrode 100 when a voltage is applied to the electrodes 100 and 102. In addition, the injection of holes from the electrode 100 to the photoelectric conversion layer 101 can be suppressed. And since the hole blocking layer 103 has a three-layer structure, the effect of suppressing the injection of holes from the electrode 100 to the photoelectric conversion layer 101 via the intermediate level is enhanced.

  The thickness of the whole hole blocking layer 103 is best 10 nm to 200 nm. This is because electrons generated in the photoelectric conversion layer 101 need to be moved to the electrode 100, and if this thickness is too large, the blocking property is improved, but the external quantum efficiency is lowered.

A value obtained by dividing the voltage applied to the electrodes 100 and 102 from the outside by the total thickness of the hole blocking layer 103 and the photoelectric conversion layer 101 (corresponding to the distance between the electrode 100 and the electrode 102) is 1.0. It is preferable that it is * 10 < ⁵ > V / cm to 1.0 * 10 < ⁷ > V / cm.

  In the photoelectric conversion element illustrated in FIG. 6, since it is necessary to make light incident on the photoelectric conversion layer 101, the electrode 102 is preferably a transparent electrode. Transparent means that 80% or more of visible light having a wavelength in the range of about 420 nm to about 660 nm is transmitted.

  Furthermore, although the photoelectric conversion element shown in FIG. 6 will be described later, since it may be necessary to transmit light below the electrode 100, the electrode 100 is also preferably a transparent electrode, and the hole blocking layer 103 is also transparent. It is preferable that

  FIG. 7 is a schematic cross-sectional view showing a modification of the photoelectric conversion element shown in FIG. In the photoelectric conversion element shown in FIG. 6, among the charges (holes and electrons) generated in the photoelectric conversion layer 101, the electrons are moved to the electrode 102, and the holes are moved to the electrode 100. When voltage is applied (that is, when the electrode 102 is an electrode for extracting electrons), the hole blocking layer 103 is interposed between the electrode 102 and the photoelectric conversion layer 101 as shown in FIG. What is necessary is just to make it the structure which provided (it has 3 layer structure which laminated | stacked material layer 103a-103c). In this case, the hole blocking layer 103 needs to be transparent. With such a configuration, dark current can be suppressed.

  6, the material layer 103c is a layer made of an inorganic material, and the material layers 103c103a and 103b are layers made of an organic material. In FIG. 7, the material layer 103a is a layer made of an inorganic material, and the material layers 103b and 103c are As described above, it is more prominent by adopting a configuration in which an organic material layer is disposed between the inorganic material layer and the inorganic material layer and the photoelectric conversion layer at the electrode interface, such as a layer made of an organic material. In addition, it is possible to suppress dark current and prevent reading of signal charges.

  Next, a configuration having an electron blocking layer will be described.

FIG. 8 is a schematic cross-sectional view illustrating a schematic configuration of another example of the photoelectric conversion element (an example having an electron blocking layer). In FIG. 8, the same components as those in FIG. 6 are denoted by the same reference numerals.
The photoelectric conversion element illustrated in FIG. 8 is formed between a pair of opposing electrodes 100 and 102, a photoelectric conversion layer 101 formed between the electrode 100 and the electrode 102, and a photoelectric conversion layer 101 and the electrode 102. And a photoelectric conversion unit including the electron blocking layer 104 (having a three-layer structure in which the material layers 104a to 104c are stacked). As described above, it is preferable that at least two of the material layers 104a to 104c are made of different materials. The electron blocking layer 104 may have a multi-layer structure.

  In the photoelectric conversion element illustrated in FIG. 8, light enters from above the electrode 102, and thus the electrode 102 serves as an electrode on the light incident side. Further, in the photoelectric conversion element shown in FIG. 8, among the charges (holes and electrons) generated in the photoelectric conversion layer 101, the holes are moved to the electrode 102, and the electrons are moved to the electrode 100. A voltage is applied to 102 (that is, electrode 100 is an electrode for extracting electrons).

  As the material of the electron blocking layer 104, a material whose electron affinity is lower than the work function of the material of the adjacent electrode 102 and whose ionization potential is lower than the ionization potential of the material of the adjacent photoelectric conversion layer 101 is used. It is done. By providing the electron blocking layer 104 between the electrode 102 and the photoelectric conversion layer 101, holes generated in the photoelectric conversion layer 101 are moved to the electrode 102 when a voltage is applied to the electrodes 100 and 102. In addition, electrons can be prevented from being injected from the electrode 102 into the photoelectric conversion layer 101.

  The thickness of the electron blocking layer 104 is best from 10 nm to 200 nm. This is because holes generated in the photoelectric conversion layer 101 need to be moved to the electrode 102. If the thickness is too large, the blocking property is improved, but the external quantum efficiency is lowered.

Further, a value obtained by dividing the voltage applied from the outside to the electrodes 100 and 102 by the total thickness of the electron blocking layer 104 and the photoelectric conversion layer 101 (corresponding to the distance between the electrode 100 and the electrode 102) is 1.0 ×. It is preferably 10 ⁵ V / cm to 1.0 × 10 ⁷ V / cm.

  In the photoelectric conversion element shown in FIG. 8, since it is necessary to make light incident on the photoelectric conversion layer 101, the electrode 102 and the electron blocking layer 104 are preferably transparent.

  Further, although the photoelectric conversion element shown in FIG. 8 will be described later, since it may be necessary to transmit light below the electrode 100, the electrode 100 is also preferably a transparent electrode.

  FIG. 9 is a schematic cross-sectional view showing a modification of the photoelectric conversion element having the structure shown in FIG. In the photoelectric conversion element illustrated in FIG. 8, among the charges (holes and electrons) generated in the photoelectric conversion layer 101, the electrons are moved to the electrode 102, and the holes are moved to the electrode 100. When voltage is applied (that is, when the electrode 102 is an electrode for extracting electrons), an electron blocking layer 104 is provided between the electrode 100 and the photoelectric conversion layer 101 as shown in FIG. What is necessary is just to use the provided structure. With such a configuration, dark current can be suppressed.

  8, the material layer 104a is a layer made of an inorganic material, and the material layers 104b and 104c are layers made of an organic material. In FIG. 9, the material layer 104c is a layer made of an inorganic material, and the material layers 104a and 104b are As described above, it is more prominent by adopting a configuration in which an organic material layer is disposed between the inorganic material layer and the inorganic material layer and the photoelectric conversion layer at the electrode interface, such as a layer made of an organic material. In addition, it is possible to suppress dark current and prevent reading of signal charges.

  Next, a configuration having an electron blocking layer and a hole blocking layer will be described.

  FIG. 10 is a schematic cross-sectional view illustrating a schematic configuration of another example of a photoelectric conversion element (an example having a photoelectric conversion unit having both an electron blocking layer and a hole blocking layer). 10, the same components as those in FIGS. 6 and 8 are denoted by the same reference numerals.

  The photoelectric conversion element illustrated in FIG. 10 is formed between a pair of opposed electrodes 100 and 102, a photoelectric conversion layer 101 formed between the electrodes 100 and 102, and a photoelectric conversion layer 101 and the electrode 100. And a photoelectric conversion unit including the hole blocking layer 103 (103a to 103c) and the electron blocking layer 104 (104a to 104c) formed between the photoelectric conversion layer 101 and the electrode 102.

  In the photoelectric conversion element illustrated in FIG. 10, light enters from above the electrode 102, and thus the electrode 102 serves as a light incident side electrode. Further, in the photoelectric conversion element shown in FIG. 10, among the charges (holes and electrons) generated in the photoelectric conversion layer 101, the holes are moved to the electrode 102, and the electrons are moved to the electrode 100. A voltage is applied to 102 (that is, electrode 100 is an electrode for extracting electrons).

The voltage applied to the electrodes 100 and 102 from the outside is the sum of the thickness of the hole blocking layer 103, the thickness of the electron blocking layer 104, and the thickness of the photoelectric conversion layer 101 (corresponding to the distance between the electrode 100 and the electrode 102). The divided value is preferably 1.0 × 10 ⁵ V / cm to 1.0 × 10 ⁷ V / cm.

  According to such a configuration, charge injection from both the electrode 100 and the electrode 102 can be suppressed, and dark current can be effectively suppressed.

FIG. 11 is a schematic cross-sectional view showing a modification of the photoelectric conversion element shown in FIG.
In the photoelectric conversion element shown in FIG. 10, among the charges (holes and electrons) generated in the photoelectric conversion layer 101, the electrons move to the electrode 102, and the holes move to the electrode 100. When a voltage is applied (that is, when the electrode 102 is an electrode for extracting electrons), an electron blocking layer 104 is provided between the electrode 100 and the photoelectric conversion layer 101 as shown in FIG. The hole blocking layer 103 may be provided between the electrode 102 and the photoelectric conversion layer 101.

  With such a configuration, charge injection from both the electrode 100 and the electrode 102 can be suppressed, and dark current can be effectively suppressed.

  Hereinafter, a configuration example of an imaging element using the photoelectric conversion element illustrated in FIG. 11 will be described. In the following description, reference will be made to FIGS. Also in each figure, similarly to the above configuration example, both the hole blocking layer and the electron blocking layer have a multi-layer structure. However, in FIG. 12 to FIG. 16, for the convenience of drawing, each blocking layer is not drawn with being divided into a plurality of layers.

  FIG. 12 is a schematic cross-sectional view of one pixel of the image sensor. 13 is a schematic cross-sectional view of the intermediate layer shown in FIG. This image sensor has a large number of one pixel shown in FIG. 12 arranged in an array on the same plane, and one pixel data of image data can be generated by a signal obtained from the one pixel.

  One pixel of the image sensor shown in FIG. 12 includes an n-type silicon substrate 1, a transparent insulating film 7 formed on the n-type silicon substrate 1, a first electrode film 11 formed on the insulating film 7, And a photoelectric conversion unit including the intermediate layer 12 formed on the one electrode film 11 and the second electrode film 13 formed on the intermediate layer 12, and an opening is provided on the photoelectric conversion unit. A light shielding film 14 is formed, and the light receiving region of the intermediate layer 12 is limited by the light shielding film 14. A transparent insulating film 15 is formed on the light shielding film 14 and the second electrode film 13. In addition, the structure of the photoelectric conversion element demonstrated previously can be employ | adopted for the photoelectric conversion part formed on the insulating film 7. FIG.

  As shown in FIG. 13, the intermediate layer 12 is formed by laminating an undercoat / electron blocking layer 122, a photoelectric conversion layer 123, and a hole blocking / buffer layer 124 in this order on the first electrode film 11. Composed. The electron blocking layer 122 and the hole blocking / buffer layer 124 are each composed of a plurality of layers as described above.

  The photoelectric conversion layer 123 generates charges including electrons and holes in response to incident light from above the second electrode film 13, and has a lower electron mobility than the hole mobility, The vicinity of the second electrode film 13 includes a material having characteristics that generate more electrons and holes than the vicinity of the electrode film 11. A typical example of such a material for the photoelectric conversion film is an organic material. In the configuration of FIG. 12, the photoelectric conversion layer 123 uses a material that absorbs green light and generates electrons and holes corresponding thereto. Since the photoelectric conversion layer 123 can be used in common for all pixels, it may be a single-layer film, and does not need to be separated for each pixel.

  The photoelectric conversion layer 123 can be preferably realized by a combination of the materials of the present invention. The organic material constituting the other photoelectric conversion layer 123 can include at least one of an organic p-type semiconductor and an organic n-type semiconductor. As the organic p-type semiconductor and the organic n-type semiconductor, any of quinacridone derivatives, naphthalene derivatives, anthracene derivatives, phenanthrene derivatives, tetracene derivatives, pyrene derivatives, perylene derivatives, and fluoranthene derivatives can be particularly preferably used.

  The organic p-type semiconductor (compound) is a donor-type organic semiconductor (compound), which is mainly represented by a hole-transporting organic compound and refers to an organic compound having a property of easily donating electrons. More specifically, an organic compound having a smaller ionization potential when two organic materials are used in contact with each other. Therefore, any organic compound can be used as the donor organic compound as long as it is an electron-donating organic compound. For example, triarylamine compounds, benzidine compounds, pyrazoline compounds, styrylamine compounds, hydrazone compounds, triphenylmethane compounds, carbazole compounds, polysilane compounds, thiophene compounds, phthalocyanine compounds, cyanine compounds, merocyanine compounds, oxonol compounds, polyamine compounds, indoles Compounds, pyrrole compounds, pyrazole compounds, polyarylene compounds, condensed aromatic carbocyclic compounds (naphthalene derivatives, anthracene derivatives, phenanthrene derivatives, tetracene derivatives, pyrene derivatives, perylene derivatives, fluoranthene derivatives), nitrogen-containing heterocyclic compounds The metal complex etc. which it has as can be used. Not limited to this, as described above, any organic compound having an ionization potential smaller than that of the organic compound used as the n-type (acceptor property) compound may be used as the donor organic semiconductor.

  Organic n-type semiconductors (compounds) are acceptor organic semiconductors (compounds), which are mainly represented by electron-transporting organic compounds and refer to organic compounds that easily accept electrons. More specifically, the organic compound having the higher electron affinity when two organic compounds are used in contact with each other. Therefore, as the acceptor organic compound, any organic compound can be used as long as it is an electron-accepting organic compound. For example, condensed aromatic carbocyclic compounds (naphthalene derivatives, anthracene derivatives, phenanthrene derivatives, tetracene derivatives, pyrene derivatives, perylene derivatives, fluoranthene derivatives), 5- to 7-membered heterocyclic compounds containing nitrogen atoms, oxygen atoms, and sulfur atoms (E.g. pyridine, pyrazine, pyrimidine, pyridazine, triazine, quinoline, quinoxaline, quinazoline, phthalazine, cinnoline, isoquinoline, pteridine, acridine, phenazine, phenanthroline, tetrazole, pyrazole, imidazole, thiazole, oxazole, indazole, benzimidazole, benzotriazole, Benzoxazole, benzothiazole, carbazole, purine, triazolopyridazine, triazolopyrimidine, tetrazaindene, o Metal complexes having as ligands, such as sadiazole, imidazopyridine, pyralidine, pyrrolopyridine, thiadiazolopyridine, dibenzazepine, tribenzazepine), polyarylene compounds, fluorene compounds, cyclopentadiene compounds, silyl compounds, and nitrogen-containing heterocyclic compounds. Etc. Note that the present invention is not limited thereto, and as described above, any organic compound having an electron affinity higher than that of the organic compound used as the donor organic compound may be used as the acceptor organic semiconductor.

  Any p-type organic dye or n-type organic dye may be used, but preferably a cyanine dye, a styryl dye, a hemicyanine dye, a merocyanine dye (including zero methine merocyanine (simple merocyanine)), three nuclei Merocyanine dye, 4-nuclear merocyanine dye, rhodacyanine dye, complex cyanine dye, complex merocyanine dye, allopolar dye, oxonol dye, hemioxonol dye, squalium dye, croconium dye, azamethine dye, coumarin dye, arylidene dye, anthraquinone dye, triphenyl Methane dye, azo dye, azomethine dye, spiro compound, metallocene dye, fluorenone dye, fulgide dye, perylene dye, phenazine dye, phenothiazine dye, quinone dye, indigo Dye, diphenylmethane dye, polyene dye, acridine dye, acridinone dye, diphenylamine dye, quinacridone dye, quinophthalone dye, phenoxazine dye, phthaloperylene dye, porphyrin dye, chlorophyll dye, phthalocyanine dye, metal complex dye, condensed aromatic carbocyclic dye (Naphthalene derivatives, anthracene derivatives, phenanthrene derivatives, tetracene derivatives, pyrene derivatives, perylene derivatives, fluoranthene derivatives).

  Next, the metal complex compound will be described. The metal complex compound is a metal complex having a ligand having at least one nitrogen atom or oxygen atom or sulfur atom coordinated to the metal, and the metal ion in the metal complex is not particularly limited, but preferably beryllium ion, magnesium Ion, aluminum ion, gallium ion, zinc ion, indium ion, or tin ion, more preferably beryllium ion, aluminum ion, gallium ion, or zinc ion, and still more preferably aluminum ion or zinc ion. There are various known ligands contained in the metal complex. For example, “Photochemistry and Photophysics of Coordination Compounds” published by Springer-Verlag H. Yersin in 1987, “Organometallic Chemistry— Examples of the ligands described in “Basics and Applications—” published by Akio Yamamoto, 1982, etc.

  The ligand is preferably a nitrogen-containing heterocyclic ligand (preferably having 1 to 30 carbon atoms, more preferably 2 to 20 carbon atoms, particularly preferably 3 to 15 carbon atoms, and a monodentate ligand. Or a bidentate or higher ligand, preferably a bidentate ligand such as a pyridine ligand, a bipyridyl ligand, a quinolinol ligand, a hydroxyphenylazole ligand (hydroxyphenyl) Benzimidazole, hydroxyphenylbenzoxazole ligand, hydroxyphenylimidazole ligand)), alkoxy ligand (preferably 1-30 carbon atoms, more preferably 1-20 carbon atoms, particularly preferably carbon 1-10, for example, methoxy, ethoxy, butoxy, 2-ethylhexyloxy, etc.), aryloxy ligands Preferably it has 6 to 30 carbon atoms, more preferably 6 to 20 carbon atoms, particularly preferably 6 to 12 carbon atoms, such as phenyloxy, 1-naphthyloxy, 2-naphthyloxy, 2,4,6-trimethylphenyl Oxy, 4-biphenyloxy, etc.), heteroaryloxy ligands (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, such as pyridyl. Oxy, pyrazyloxy, pyrimidyloxy, quinolyloxy, etc.), alkylthio ligands (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, such as methylthio, Ethylthio, etc.), arylthio ligands (preferably having 6 to 30 carbon atoms, more preferred) Has 6 to 20 carbon atoms, particularly preferably 6 to 12 carbon atoms, such as phenylthio, etc.), a heterocyclic substituted thio ligand (preferably 1 to 30 carbon atoms, more preferably 1 to carbon atoms). 20, particularly preferably 1 to 12 carbon atoms, such as pyridylthio, 2-benzimidazolylthio, 2-benzoxazolylthio, 2-benzthiazolylthio and the like, or siloxy ligand (preferably Has 1 to 30 carbon atoms, more preferably 3 to 25 carbon atoms, particularly preferably 6 to 20 carbon atoms, and examples thereof include a triphenylsiloxy group, a triethoxysiloxy group, and a triisopropylsiloxy group. More preferably a nitrogen-containing heterocyclic ligand, an aryloxy ligand, a heteroaryloxy group, or a siloxy ligand, Preferably, a nitrogen-containing heterocyclic ligand, an aryloxy ligand, or a siloxy ligand is used.

  The intermediate layer 12 can be preferably realized by having the combination material of the present invention. In addition, the semiconductor device includes a p-type semiconductor layer and an n-type semiconductor layer, at least one of the p-type semiconductor and the n-type semiconductor is an organic semiconductor, and the p-type semiconductor and the n-type semiconductor are interposed between the semiconductor layers. The case where the photoelectric conversion layer which has a bulk heterojunction structure layer containing a type semiconductor is contained is preferable. In such a case, by including a bulk heterojunction structure in the intermediate layer 12, the disadvantage that the carrier diffusion length of the photoelectric conversion layer 123 is short can be compensated, and the photoelectric conversion efficiency of the photoelectric conversion layer 123 can be improved. The bulk heterojunction structure is described in detail in Japanese Patent Application Laid-Open No. 2005-303266 (Japanese Patent Application No. 2004-080639).

  The photoelectric conversion layer included in the intermediate layer 12 includes a p-type semiconductor layer, an n-type semiconductor layer (preferably a mixed / dispersed (bulk heterojunction structure) layer), and includes a p-type semiconductor and an n-type semiconductor. It is preferable that the organic compound whose orientation is controlled is included in at least one of the above, and more preferably, the organic compound whose orientation is controlled is included in both the p-type semiconductor and the n-type semiconductor. As this organic compound, those having π-conjugated electrons are preferably used, and it is more preferable that the π-electron plane is oriented at an angle close to parallel rather than perpendicular to the substrate (electrode substrate). The angle with respect to the substrate is preferably 0 ° or more and 80 ° or less, more preferably 0 ° or more and 60 ° or less, further preferably 0 ° or more and 40 ° or less, and further preferably 0 ° or more and 20 ° or less. Particularly preferably, it is 0 ° or more and 10 ° or less, and most preferably 0 ° (that is, parallel to the substrate). As described above, the organic compound layer whose orientation is controlled may be partially included in the entire intermediate layer 12, but preferably the proportion of the portion whose orientation is controlled with respect to the entire intermediate layer 12 is 10%. This is the case, more preferably 30% or more, further preferably 50% or more, more preferably 70% or more, particularly preferably 90% or more, and most preferably 100%. In such a state, by controlling the orientation of the organic compound contained in the intermediate layer 12, the shortcoming of the carrier diffusion length of the photoelectric conversion element layer is compensated, and the photoelectric conversion efficiency of the photoelectric conversion film is improved. .

  In the case where the orientation of the organic compound is controlled, it is more preferable that the heterojunction plane (for example, the pn junction plane) is not parallel to the substrate. It is more preferable that the heterojunction plane is oriented not at a parallel to the substrate (electrode substrate) but at an angle close to perpendicular. The angle with respect to the substrate is preferably 10 ° or more and 90 ° or less, more preferably 30 ° or more and 90 ° or less, further preferably 50 ° or more and 90 ° or less, and further preferably 70 ° or more and 90 ° or less. Particularly preferably, it is 80 ° or more and 90 ° or less, and most preferably 90 ° (that is, perpendicular to the substrate). The organic compound layer whose heterojunction surface is controlled as described above may be partially included in the entire intermediate layer 12. Preferably, the proportion of the portion whose orientation is controlled with respect to the entire intermediate layer 12 is 10% or more, more preferably 30% or more, more preferably 50% or more, still more preferably 70% or more, and particularly preferably 90%. % Or more, most preferably 100%. In such a case, the area of the heterojunction surface in the intermediate layer 12 increases, the amount of carriers of electrons, holes, electron-hole pairs, etc. generated at the interface increases, and the photoelectric conversion efficiency can be improved. In the above-described photoelectric conversion layer in which the orientation of both the heterojunction plane and the π-electron plane of the organic compound is controlled, the photoelectric conversion efficiency can be particularly improved. These states are described in detail in Japanese Patent Application Laid-Open No. 2006-086493 (Japanese Patent Application No. 2004-079931). In terms of light absorption, the thickness of the organic dye layer is preferably as large as possible, but considering the ratio that does not contribute to charge separation, the thickness of the organic dye layer is preferably 30 nm to 300 nm, more preferably 50 nm to 250 nm, Especially preferably, it is 80 nm or more and 200 nm or less.

  The intermediate layer 12 containing these organic compounds is formed by a dry film forming method or a wet film forming method. Specific examples of the dry film forming method include a vacuum vapor deposition method, a sputtering method, an ion plating method, a physical vapor deposition method such as an MBE method, or a CVD method such as plasma polymerization. As the wet film forming method, a casting method, a spin coating method, a dipping method, an LB method, or the like is used.

In the case where a polymer compound is used as at least one of the p-type semiconductor (compound) and the n-type semiconductor (compound), it is preferable to form the film by a wet film forming method that is easy to prepare. When a dry film formation method such as vapor deposition is used, it is difficult to use a polymer because it may be decomposed, and an oligomer thereof can be preferably used instead. On the other hand, when a low molecule is used, a dry film forming method is preferably used, and a vacuum deposition method is particularly preferably used. The vacuum deposition method is basically based on the method of heating compounds such as resistance heating deposition method and electron beam heating deposition method, shape of deposition source such as crucible and boat, degree of vacuum, deposition temperature, base temperature, deposition rate, etc. It is a parameter. In order to make uniform deposition possible, it is preferable to perform deposition by rotating the substrate. The degree of vacuum is preferably higher, and vacuum deposition is performed at 10 ⁻⁴ Torr or less, preferably 10 ⁻⁶ Torr or less, particularly preferably 10 ⁻⁸ Torr or less. It is preferable that all steps during the vapor deposition are performed in a vacuum, and basically the compound is not directly in contact with oxygen and moisture in the outside air. The above-described conditions for vacuum deposition need to be strictly controlled because they affect the crystallinity, amorphousness, density, density, etc. of the organic film. It is preferable to use PI or PID control of the deposition rate using a film thickness monitor such as a quartz crystal resonator or an interferometer. When two or more kinds of compounds are vapor-deposited simultaneously, a co-evaporation method, a flash vapor deposition method, or the like can be preferably used.

  In the photoelectric conversion layer 123 made of an organic material, if light is incident from above the second electrode 13 in the above-described configuration, a large number of electrons and holes generated by light absorption are generated in the vicinity of the second electrode 13, In general, it does not occur so much in the vicinity of the first electrode 11. This is because most of the light near the absorption peak wavelength of the photoelectric conversion layer 123 is absorbed in the vicinity of the second electrode 13, and the light absorption rate decreases as the distance from the vicinity of the second electrode 13 increases. Is attributed. For this reason, unless the electrons or holes generated in the vicinity of the second electrode 13 are efficiently moved to the silicon substrate, the photoelectric conversion efficiency is lowered, resulting in a decrease in sensitivity of the element. Further, since the signal due to the light wavelength strongly absorbed in the vicinity of the second electrode 13 is reduced, as a result, the so-called broadening of the spectral sensitivity is caused.

  Further, in the photoelectric conversion layer 123 made of an organic material, the electron mobility is generally much smaller than the hole mobility. Furthermore, it is known that the electron mobility in the photoelectric conversion layer 123 made of an organic material is easily affected by oxygen, and that the electron mobility is further reduced when the photoelectric conversion layer 123 is exposed to the atmosphere. For this reason, when the electrons are moved to the silicon substrate 1, if the movement distance of the electrons generated in the vicinity of the second electrode 13 in the photoelectric conversion layer 123 is long, a part of the electrons is deactivated during the movement of the electrons. As a result, the sensitivity is lowered and the spectral sensitivity is broadened.

  In order to prevent a decrease in sensitivity and a broadening of spectral sensitivity, it is effective to efficiently move electrons or holes generated in the vicinity of the second electrode 13 to the silicon substrate 1. A problem is how to handle electrons or holes generated in the conversion layer 123.

  Since the solid-state imaging device 1000 includes the photoelectric conversion layer 123 having the above-described characteristics, as described above, holes are collected by the first electrode film 11 which is an electrode opposite to the light incident side electrode. By using this, the external quantum efficiency can be increased, and the sensitivity can be improved and the spectral sensitivity can be sharpened. Therefore, in the solid-state imaging device 1000, the first electrode is formed such that electrons generated in the photoelectric conversion layer 123 move to the second electrode film 13 and holes generated in the photoelectric conversion layer 123 move to the first electrode film 11. A voltage is applied to the film 11 and the second electrode film 13.

  One function of the undercoat / electron blocking layer 122 is to relieve unevenness on the first electrode film 11. When the first electrode film 11 has irregularities, or when dust adheres to the first electrode film 11, a low molecular organic material is deposited thereon to form the photoelectric conversion layer 123. It is easy to form a fine crack in the photoelectric conversion layer 123, that is, a portion where the photoelectric conversion layer 123 is formed only thin. At this time, if the second electrode film 13 is further formed thereon, the crack portion is covered by the second electrode film 13 and close to the first electrode film 11, so that a DC short circuit and an increase in leakage current are likely to occur. In particular, when TCO is used as the second electrode film 13, the tendency is remarkable. For this reason, the unevenness | corrugation can be relieve | moderated by providing the undercoat film | membrane and electron blocking layer 122 on the 1st electrode film 11 previously, and these can be suppressed.

  It is important that the undercoat / electron blocking layer 122 is a homogeneous and smooth film. In particular, when obtaining a smooth film, preferred materials include organic polymer materials such as polyaniline, polythiophene, polypyrrole, polycarbazole, PTPDES, and PTPDEK, and they can also be formed by spin coating.

  The electron blocking layer 122 is provided in order to reduce dark current caused by the injection of electrons from the first electrode film 11, and the electrons from the first electrode film 11 are injected into the photoelectric conversion layer 123. Stop.

  The hole blocking / buffer layer 124 is provided as a hole blocking layer in order to reduce dark current caused by injection of holes from the second electrode film 13. In addition to the function of blocking the injection into the photoelectric conversion layer 123, in some cases, the second electrode film 13 is formed to reduce the damage given to the photoelectric conversion layer 123.

  When the second electrode film 13 is formed on the photoelectric conversion layer 123, high-energy particles existing in the apparatus used for forming the second electrode film 13, such as sputtered particles and secondary electrons in the case of sputtering, When Ar particles, oxygen negative ions, or the like collide with the photoelectric conversion layer 123, the photoelectric conversion layer 123 may be altered, and performance degradation such as an increase in leakage current or a decrease in sensitivity may occur. As one method for preventing this, it is preferable to provide the buffer film 124 on the photoelectric conversion layer 123.

  Returning to FIG. 12, in the n-type silicon substrate 1, a p-type semiconductor region (hereinafter abbreviated as p region) 4, an n-type semiconductor region (hereinafter abbreviated as n region) 3, and a p-region 2 are formed in this order. A high-concentration p region (referred to as a p + region) 6 is formed on the surface portion of the p region 4 that is shielded by the light shielding film 14, and the p + region 6 is surrounded by the n region 5.

  The depth of the pn junction surface between the p region 4 and the n region 3 from the surface of the n-type silicon substrate 1 is a depth that absorbs blue light (about 0.2 μm). Therefore, the p region 4 and the n region 3 absorb blue light, generate holes corresponding thereto, and form a photodiode (B photodiode) that accumulates the holes. Holes generated in the B photodiode are accumulated in the p region 4.

  The depth of the pn junction surface between the p region 2 and the n-type silicon substrate 1 from the surface of the n-type silicon substrate 1 is a depth that absorbs red light (about 2 μm). Therefore, the p region 2 and the n-type silicon substrate 1 absorb red light, generate holes corresponding to the red light, and form a photodiode (R photodiode) that accumulates the holes. Holes generated in the R photodiode are accumulated in the p region 2.

  The p + region 6 is electrically connected to the first electrode film 11 via a connection portion 9 formed in an opening opened in the insulating film 7, and is connected to the first electrode film 11 via the connection portion 9. Accumulate the collected holes. The connection portion 9 is electrically insulated by the insulating film 8 except for the first electrode film 11 and the p + region 6.

  The holes accumulated in the p region 2 are converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) made of a p-channel MOS transistor formed in the n-type silicon substrate 1 and accumulated in the p region 4. The generated holes are converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed in the n region 3, and the electrons accumulated in the p + region 6 5 is converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed in 5 and output to the outside of the solid-state imaging device 1000. These MOS circuits constitute the signal readout section in the claims. Each MOS circuit is connected to a signal readout pad (not shown) by wiring 10. If extraction electrodes are provided in the p region 2 and the p region 4 and a predetermined reset potential is applied, each region is depleted, and the capacitance of each pn junction becomes an infinitely small value. Thereby, the capacity | capacitance produced in a joint surface can be made very small.

  With such a configuration, for example, G light can be photoelectrically converted by the photoelectric conversion layer 123, and B light and R light can be photoelectrically converted by the B photodiode and the R photodiode in the n-type silicon substrate 1. Also, since G light is first absorbed at the top, color separation between B-G and G-R is excellent. This is a great advantage over a solid-state imaging device in which three PDs are stacked in a silicon substrate and all BGR light is separated in the silicon substrate. In the following description, the part (B photodiode and R photodiode) that performs photoelectric conversion made of an inorganic material formed in the n-type silicon substrate 1 of the solid-state imaging device 1000 is also referred to as an inorganic layer.

  In addition, light that has passed through the photoelectric conversion layer 123 is absorbed between the n-type silicon substrate 1 and the first electrode film 11 (for example, between the insulating film 7 and the n-type silicon substrate 1), and according to the light. It is also possible to form an inorganic photoelectric conversion portion made of an inorganic material that generates and accumulates the charges. In this case, a MOS circuit for reading a signal corresponding to the charge accumulated in the charge accumulation region of the inorganic photoelectric conversion unit is provided in the n-type silicon substrate 1, and the wiring 10 is also connected to this MOS circuit. It ’s fine.

The first electrode film 11 plays a role of collecting holes generated and moved in the photoelectric conversion layer 123. The first electrode film 11 is separated for each pixel, whereby image data can be generated. In the configuration shown in FIG. 12, since the n-type silicon substrate 1 also performs photoelectric conversion, the first electrode film 11 preferably has a visible light transmittance of 60% or more, more preferably 90%. preferable. In the case where the photoelectric conversion region does not exist below the first electrode film 11, the first electrode film 11 may be low in transparency. As a material, any of ITO, IZO, ZnO ₂ , SnO ₂ , TiO ₂ , FTO, Al, Ag, and Au can be most preferably used. Details of the first electrode film 11 will be described later.

The second electrode film 13 has a function of discharging electrons generated and moved in the photoelectric conversion layer 123. The second electrode film 13 can be used in common for all pixels. For this reason, in the solid-state imaging device 1000, the second electrode film 13 is a single-layer film common to all pixels. Since the second electrode film 13 needs to make light incident on the photoelectric conversion layer 123, it is necessary to use a material having high transparency to visible light. The second electrode film 13 preferably has a visible light transmittance of 60% or more, and more preferably 90%. As a material, any of ITO, IZO, ZnO ₂ , SnO ₂ , TiO ₂ , FTO, Al, Ag, and Au can be most preferably used. Details of the second electrode film 13 will be described later.

  As the inorganic layer, a pn junction or a pin junction of a compound semiconductor such as crystalline silicon, amorphous silicon, or GaAs is generally used. In this case, since color separation is performed based on the light penetration depth of silicon, the spectral range detected by each stacked light receiving unit is broad. However, color separation is significantly improved by using the photoelectric conversion layer 123 as an upper layer as shown in FIG. 12, that is, by detecting light transmitted through the photoelectric conversion layer 123 in the depth direction of silicon. In particular, as shown in FIG. 12, when G light is detected by the photoelectric conversion layer 123, light transmitted through the photoelectric conversion layer 123 becomes B light and R light. Only light is used and color separation is improved. Even when the photoelectric conversion layer 123 detects B light or R light, color separation is remarkably improved by appropriately selecting the depth of the pn junction surface of silicon.

  The structure of the inorganic layer is preferably npn or pnpn from the light incident side. In particular, by providing a p layer on the surface and increasing the surface potential, holes generated in the vicinity of the surface and dark current can be trapped and dark current can be reduced. preferable.

  12 shows a configuration in which one photoelectric conversion unit is stacked above the n-type silicon substrate 1, but a configuration in which a plurality of photoelectric conversion units are stacked above the n-type silicon substrate 1 is also possible. is there. A configuration in which a plurality of photoelectric conversion units are stacked will be described in a later configuration example. In this case, the light detected by the inorganic layer may be one color, and preferable color separation can be achieved. Further, when detecting four colors of light with one pixel of the solid-state imaging device 1000, for example, a configuration in which one color is detected with one photoelectric conversion unit and three colors are detected with an inorganic layer, A structure in which two photoelectric conversion units are stacked to detect two colors and two colors are detected in the inorganic layer, three photoelectric conversion units are stacked to detect three colors, and one color is detected in the inorganic layer Configuration etc. can be considered. Further, the solid-state imaging device 1000 may be configured to detect only one color with one pixel. In this case, the p region 2, the n region 3, and the p region 4 are eliminated in FIG.

  The inorganic layer will be described in more detail. Preferred configurations of the inorganic layer include a photoconductive type, a pn junction type, a Schottky junction type, a PIN junction type, an MSM (metal-semiconductor-metal) type light receiving element, and a phototransistor type light receiving element. In particular, as shown in FIG. 12, a plurality of first conductivity type regions and second conductivity type regions opposite to the first conductivity type are alternately stacked in a single semiconductor substrate. In addition, it is preferable to use an inorganic layer formed by forming each bonding surface of the first conductivity type region and the second conductivity type region to a depth suitable for mainly photoelectrically converting light in a plurality of different wavelength bands. . As the single semiconductor substrate, single crystal silicon is preferable, and color separation can be performed using absorption wavelength characteristics depending on the depth direction of the silicon substrate.

As the inorganic semiconductor, an InGaN-based, InAlN-based, InAlP-based, or InGaAlP-based inorganic semiconductor can also be used. The nGaN-based inorganic semiconductor is adjusted so as to have a maximum absorption value in the blue wavelength range by appropriately changing the composition of In. That is, the composition is In _x Ga _1-x N (0 ≦ X <1). Such a compound semiconductor is manufactured using a metal organic chemical vapor deposition method (MOCVD method). A nitride semiconductor InAlN system using Al, which is the same group 13 raw material as Ga, can also be used as a short wavelength light receiving section in the same manner as the InGaN system. It is also possible to use InAlP or InGaAlP lattice-matched to the GaAs substrate.

  The inorganic semiconductor may have a buried structure. The embedded structure means a structure in which both ends of the short wavelength light receiving part are covered with a semiconductor different from the short wavelength light receiving part. The semiconductor covering both ends is preferably a semiconductor having a band gap wavelength shorter than or equivalent to the band gap wavelength of the short wavelength light receiving part.

  As the material of the first electrode film 11 and the second electrode film 13, a metal, an alloy, a metal oxide, an electrically conductive compound, or a mixture thereof can be used. As metal materials, Li, Na, Mg, K, Ca, Rb, Sr, Cs, Ba, Fr, Ra, Sc, Ti, Y, Zr, Hf, V, Nb, Ta, Cr, Mo, W, Mn Tc, Re, Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt, Cu, Ag, Au, Zn, Cd, Al, Ga, In, Tl, Si, Ge, Sn, Pb, P , As, Sb, Bi, Se, Te, Po, Br, I, At, B, C, N, F, O, S, and N may be mentioned, but particularly preferred Are Al, Pt, W, Au, Ag, Ta, Cu, Cr, Mo, Ti, Ni, Pd, and Zn.

  The first electrode film 11 takes out holes from the hole transport photoelectric conversion layer or the hole transport layer contained in the intermediate layer 12 and collects the holes, thereby collecting the hole transport photoelectric conversion layer and the hole transport. It is selected in consideration of adhesion to adjacent layers such as a layer, electron affinity, ionization potential, and stability. The second electrode film 13 takes out electrons from the electron transport photoelectric conversion layer or the electron transport layer included in the intermediate layer 12 and discharges the electrons, so that the second electrode film 13 has an adjacent layer such as an electron transport photoelectric conversion layer and an electron transport layer. Is selected in consideration of adhesion, electron affinity, ionization potential, stability, and the like. Specific examples of these include conductive metal oxides such as tin oxide, zinc oxide, indium oxide and indium tin oxide (ITO), or metals such as gold, silver, chromium and nickel, and these metals and conductive metal oxides. Inorganic conductive materials such as copper iodide and copper sulfide, organic conductive materials such as polyaniline, polythiophene and polypyrrole, silicon compounds and laminates of these with ITO, etc. In particular, ITO and IZO are preferable from the viewpoints of productivity, high conductivity, transparency, and the like.

  Various methods are used for producing the electrode depending on the material. For example, in the case of ITO, an electron beam method, a sputtering method, a resistance heating vapor deposition method, a chemical reaction method (sol-gel method, etc.), a coating of a dispersion of indium tin oxide, etc. A film is formed by this method. In the case of ITO, UV-ozone treatment, plasma treatment, etc. can be performed.

  The conditions for forming a transparent electrode film (transparent electrode film) will be described. The silicon substrate temperature at the time of forming the transparent electrode film is preferably 500 ° C. or lower, more preferably 300 ° C. or lower, further preferably 200 ° C. or lower, and further preferably 150 ° C. or lower. Further, a gas may be introduced during the formation of the transparent electrode film, and basically the gas species is not limited, but Ar, He, oxygen, nitrogen and the like can be used. Further, a mixed gas of these gases may be used. In particular, in the case of an oxide material, oxygen defects are often introduced, so that oxygen is preferably used.

  Further, the preferable range of the surface resistance of the transparent electrode film differs depending on whether it is the first electrode film 11 or the second electrode film 13. When the signal readout part has a CMOS structure, the surface resistance of the transparent conductive film is preferably 10000Ω / □ or less, more preferably 1000Ω / □ or less. If the signal reading unit has a CCD structure, the surface resistance is preferably 1000Ω / □ or less, and more preferably 100Ω / □ or less. When used for the second electrode film 13, it is preferably 1000000 Ω / □ or less, more preferably 100000 Ω / □ or less.

Particularly preferable as a material for the transparent electrode film are ITO, IZO, SnO ₂ , ATO (antimony-doped tin oxide), ZnO, AZO (Al-doped zinc oxide), GZO (gallium-doped zinc oxide), TiO ₂ , FTO (fluorine). Doped tin oxide). The light transmittance of the transparent electrode film is preferably 60% or more, more preferably 80% or more, more preferably 90% or more, at the absorption peak wavelength of the photoelectric conversion film included in the photoelectric conversion part including the transparent electrode film. More preferably, it is 95% or more.

  Further, when a plurality of intermediate layers 12 are stacked, the first electrode film 11 and the second electrode film 13 are each photoelectrically connected from the photoelectric conversion film located closest to the light incident side to the photoelectric conversion film located farthest. It is necessary to transmit light having a wavelength other than the light detected by the conversion layer, and it is preferable to use a material that transmits light of 90%, more preferably 95% or more with respect to visible light.

  The second electrode film 13 is preferably made plasma-free. By creating the second electrode film 13 free of plasma, the influence of plasma on the substrate can be reduced, and the photoelectric conversion characteristics can be improved. Here, plasma free means that no plasma is generated during the formation of the second electrode film 13, or the distance from the plasma generation source to the substrate is 2 cm or more, preferably 10 cm or more, more preferably 20 cm or more, It means a state in which the plasma reaching the substrate is reduced.

  Examples of apparatuses that do not generate plasma during the formation of the second electrode film 13 include an electron beam vapor deposition apparatus (EB vapor deposition apparatus) and a pulse laser vapor deposition apparatus. Regarding EB deposition equipment or pulse laser deposition equipment, “Surveillance of Transparent Conductive Films” supervised by Yutaka Sawada (published by CMC, 1999), “New Development of Transparent Conductive Films II” supervised by Yutaka Sawada (published by CMC, 2002) ), "Transparent conductive film technology" by the Japan Society for the Promotion of Science (Ohm Co., 1999), and the references attached thereto, etc. can be used. Hereinafter, a method of forming a transparent electrode film using an EB vapor deposition apparatus is referred to as an EB vapor deposition method, and a method of forming a transparent electrode film using a pulse laser vapor deposition apparatus is referred to as a pulse laser vapor deposition method.

  For an apparatus that can realize a state in which the distance from the plasma generation source to the substrate is 2 cm or more and the arrival of plasma to the substrate is reduced (hereinafter referred to as a plasma-free film forming apparatus), for example, an opposed target sputtering Equipment, arc plasma deposition, etc. are considered, and these are supervised by Yutaka Sawada "New development of transparent conductive film" (published by CMC, 1999), and supervised by Yutaka Sawada "New development of transparent conductive film II" (published by CMC) 2002), “Transparent conductive film technology” (Ohm Co., 1999) by the Japan Society for the Promotion of Science, and references and the like attached thereto can be used.

  When a transparent conductive film such as TCO is used as the second electrode film 13, a DC short circuit or an increase in leakage current may occur. One reason for this is considered to be that fine cracks introduced into the photoelectric conversion layer 123 are covered by a dense film such as TCO, and conduction between the first electrode film 11 on the opposite side is increased. Therefore, in the case of an electrode having a poor film quality such as Al, an increase in leakage current is unlikely to occur. By controlling the film thickness of the second electrode film 13 with respect to the film thickness of the photoelectric conversion layer 123 (that is, the crack depth), an increase in leakage current can be largely suppressed. The thickness of the second electrode film 13 is desirably 1/5 or less of the thickness of the photoelectric conversion layer 123, preferably 1/10 or less.

  Usually, when the conductive film is made thinner than a certain range, the resistance value is rapidly increased. However, in the solid-state imaging device 1000, the sheet resistance is preferably 100 to 10,000 Ω / □, and the film thickness can be reduced. The degree of freedom is large. Further, the thinner the transparent conductive thin film is, the less light is absorbed, and the light transmittance is generally increased. The increase in light transmittance is very preferable because it increases the light absorption in the photoelectric conversion layer 123 and increases the photoelectric conversion ability. In consideration of the suppression of leakage current, the increase in the resistance value of the thin film, and the increase in transmittance due to the thinning, the thickness of the transparent conductive thin film is preferably 5 to 100 nm, more preferably 5 to 20 nm. Something is desirable.

  The material of the transparent electrode film is preferably one that can be formed by a plasma-free film forming apparatus, an EB vapor deposition apparatus, and a pulse laser vapor deposition apparatus. For example, a metal, an alloy, a metal oxide, a metal nitride, a metal boride, an organic conductive compound, a mixture thereof, and the like are preferable. Specific examples include tin oxide, zinc oxide, indium oxide, and indium zinc oxide. (IZO), indium tin oxide (ITO), conductive metal oxides such as indium tungsten oxide (IWO), metal nitrides such as titanium nitride, metals such as gold, platinum, silver, chromium, nickel, aluminum, and these A mixture or laminate of a metal and a conductive metal oxide, an inorganic conductive material such as copper iodide or copper sulfide, an organic conductive material such as polyaniline, polythiophene or polypyrrole, a laminate of these and ITO, Etc. Also, supervised by Yutaka Sawada “New Development of Transparent Conductive Film” (published by CMC, 1999), supervised by Yutaka Sawada “New Development of Transparent Conductive Film II” (published by CMC, 2002), “Transparent by Japan Society for the Promotion of Science” Those described in detail in “Technology of Conductive Film” (Ohm Co., 1999) may be used.

  In this configuration example, two photodiodes are arranged in a direction perpendicular to the incident direction of incident light, instead of stacking two photodiodes in an n-type silicon substrate with the inorganic layer having the configuration shown in FIG. Thus, two colors of light are detected in the n-type silicon substrate.

FIG. 14 is a schematic cross-sectional view of one pixel of the image sensor.
One pixel of the solid-state imaging device 2000 shown in FIG. 14 includes an n-type silicon substrate 17, a first electrode film 30 formed above the n-type silicon substrate 17, an intermediate layer 31 formed on the first electrode film 30, And a photoelectric conversion part comprising the second electrode film 32 formed on the intermediate layer 31, and a light shielding film 34 having an opening is formed on the photoelectric conversion part. Therefore, the light receiving area of the intermediate layer 31 is limited. A transparent insulating film 33 is formed on the light shielding film 34.

  The first electrode film 30, the intermediate layer 31, and the second electrode film 32 have the same configuration as the first electrode film 11, the intermediate layer 12, and the second electrode film 13.

  On the surface of the n-type silicon substrate 17 below the opening of the light shielding film 34, a photodiode composed of the n region 19 and the p region 18 and a photodiode composed of the n region 21 and the p region 20 are formed on the surface of the n-type silicon substrate 17. It is formed side by side. An arbitrary direction on the surface of the n-type silicon substrate 17 is a direction perpendicular to the incident direction of incident light.

  Above the photodiode composed of the n region 19 and the p region 18, a color filter 28 that transmits B light through a transparent insulating film 24 is formed, and a first electrode film 30 is formed thereon. A color filter 29 that transmits R light through a transparent insulating film 24 is formed above the photodiode composed of the n region 21 and the p region 20, and a first electrode film 30 is formed thereon. The periphery of the color filters 28 and 29 is covered with a transparent insulating film 25.

  The photodiode composed of the n region 19 and the p region 18 absorbs the B light transmitted through the color filter 28 and generates holes corresponding thereto, and accumulates the generated holes in the p region 18. The photodiode composed of the n region 21 and the p region 20 absorbs the R light transmitted through the color filter 29 and generates holes corresponding thereto, and accumulates the generated holes in the p region 20.

  A p + region 23 is formed on the surface of the p-type silicon substrate 17 that is shielded by the light shielding film 34, and the p + region 23 is surrounded by the n region 22.

  The p + region 23 is electrically connected to the first electrode film 30 via a connection portion 27 formed in an opening opened in the insulating films 24 and 25, and the first electrode film is connected via the connection portion 27. The holes collected at 30 are accumulated. The connecting portion 27 is electrically insulated by the insulating film 26 except for the first electrode film 30 and the p + region 23.

  The holes accumulated in the p region 18 are converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed in the n-type silicon substrate 17 and accumulated in the p region 20. The generated holes are converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed in the n-type silicon substrate 17, and the holes accumulated in the p + region 23 are The signal is converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed in the n region 22 and output to the outside of the solid-state imaging device 2000. These MOS circuits constitute the signal readout section in the claims. Each MOS circuit is connected to a signal readout pad (not shown) by wiring 35.

  The signal reading unit may be constituted by a CCD and an amplifier instead of the MOS circuit. That is, the holes accumulated in the p region 18, the p region 20, and the p + region 23 are read out to the CCD formed in the n-type silicon substrate 17, transferred to the amplifier by the CCD, and transferred from the amplifier to the holes. A signal reading unit that outputs a corresponding signal may be used.

  As described above, the signal reading unit includes a CCD and a CMOS structure, but CMOS is preferable in terms of power consumption, high-speed reading, pixel addition, partial reading, and the like.

  In FIG. 14, the color filters 28 and 29 perform color separation of the R light and the B light. However, the color filters 28 and 29 are not provided, and the depths of the pn junction surfaces of the p region 20 and the n region 21 are as follows. The depths of the pn junction surfaces of the p region 18 and the n region 19 may be adjusted to absorb the R light and the B light with the respective photodiodes. In this case, the light transmitted through the intermediate layer 31 is absorbed between the n-type silicon substrate 17 and the first electrode film 30 (for example, between the insulating film 24 and the n-type silicon substrate 17), and according to the light. It is also possible to form an inorganic photoelectric conversion portion made of an inorganic material that generates and accumulates the charges. In this case, a MOS circuit for reading a signal corresponding to the charge accumulated in the charge accumulation region of the inorganic photoelectric conversion unit is provided in the n-type silicon substrate 17, and the wiring 35 is also connected to this MOS circuit. It ’s fine.

  Alternatively, a single photodiode provided in the n-type silicon substrate 17 may be used, and a plurality of photoelectric conversion units may be stacked above the n-type silicon substrate 17. Further, a plurality of photodiodes provided in the n-type silicon substrate 17 may be provided, and a plurality of photoelectric conversion units may be stacked above the n-type silicon substrate 17. If there is no need to produce a color image, a single photodiode provided in the n-type silicon substrate 17 and only one photoelectric conversion unit may be stacked.

FIG. 15 is a schematic cross-sectional view of one pixel for explaining another configuration example of the imaging element. In this configuration example, the inorganic layer having the configuration shown in FIG. 12 is not provided, and a plurality (here, three) of photoelectric conversion layers are stacked above the silicon substrate.
A solid-state imaging device 3000 shown in FIG. 15 includes a first electrode film 56, an intermediate layer 57 stacked on the first electrode film 56, and a second electrode film 58 stacked on the intermediate layer 57 above the silicon substrate 41. An R photoelectric conversion unit including the first electrode film 60, an intermediate layer 61 stacked on the first electrode film 60, and a B photoelectric conversion unit including the second electrode film 62 stacked on the intermediate layer 61, The first electrode film 64, the intermediate layer 65 stacked on the first electrode film 64, and the G photoelectric conversion portion including the second electrode film 66 stacked on the intermediate layer 65 are respectively included in the first electrode The film is laminated in this order with the film facing the silicon substrate 41 side.

  A transparent insulating film 48 is formed on the silicon substrate 41, an R photoelectric conversion portion is formed thereon, a transparent insulating film 59 is formed thereon, a B photoelectric conversion portion is formed thereon, and A transparent insulating film 63 is formed thereon, a G photoelectric conversion portion is formed thereon, a light shielding film 68 having an opening is formed thereon, and a transparent insulating film 67 is formed thereon. .

  The first electrode film 64, the intermediate layer 65, and the second electrode film 66 included in the G photoelectric conversion unit have the same configuration as the first electrode film 11, the intermediate layer 12, and the second electrode film 13 illustrated in FIG. .

  The first electrode film 60, the intermediate layer 61, and the second electrode film 62 included in the B photoelectric conversion unit have the same configuration as the first electrode film 11, the intermediate layer 12, and the second electrode film 13 illustrated in FIG. . However, the photoelectric conversion layer included in the intermediate layer 61 uses a material that absorbs blue light and generates electrons and holes according to the blue light.

  The first electrode film 56, the intermediate layer 57, and the second electrode film 58 included in the R photoelectric conversion unit have the same configuration as the first electrode film 11, the intermediate layer 12, and the second electrode film 13 illustrated in FIG. . However, the photoelectric conversion layer included in the intermediate layer 57 uses a material that absorbs red light and generates electrons and holes corresponding thereto.

  The respective electron and hole blocking layers included in the intermediate layers 61 and 57 have signal charges in the relationship between the HOMO and LUMO energy levels of the respective photoelectric conversion films and the HOMO and LUMO levels of the respective blocking layers in contact therewith. It is preferable to select an appropriate material and configuration so that an energy barrier does not occur during the transportation of the material.

  P + regions 43, 45, and 47 are formed in portions of the silicon substrate 41 that are shielded by the light-shielding film 68, and each region is surrounded by n regions 42, 44, and 46.

  The p + region 43 is electrically connected to the first electrode film 56 via a connection portion 54 formed in an opening opened in the insulating film 48, and is connected to the first electrode film 56 via the connection portion 54. Accumulate the collected holes. The connecting portion 54 is electrically insulated by the insulating film 51 except for the first electrode film 56 and the p + region 43.

  The p + region 45 is electrically connected to the first electrode film 60 through a connection portion 53 formed in an opening formed in the insulating film 48, the R photoelectric conversion portion, and the insulating film 59. Then, holes collected by the first electrode film 60 are accumulated. The connection portion 53 is electrically insulated by the insulating film 50 except for the first electrode film 60 and the p + region 45.

  The p + region 47 is electrically connected to the first electrode film 64 through the insulating film 48, the R photoelectric conversion portion, the insulating film 59, the B photoelectric conversion portion, and the connection portion 52 formed in the opening opened in the insulating film 63. And the holes collected by the first electrode film 64 are accumulated through the connection portion 52. The connecting portion 52 is electrically insulated by the insulating film 49 except for the first electrode film 64 and the p + region 47.

  The holes accumulated in the p + region 43 are converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed in the n region 42 and accumulated in the p + region 45. The holes are converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed in the n region 44, and the holes accumulated in the p + region 47 are converted into the n region 46. The signal is converted into a signal corresponding to the amount of charge by a MOS circuit (not shown) formed of a p-channel MOS transistor formed therein and output to the outside of the solid-state imaging device 300. These MOS circuits constitute the signal readout section in the claims. Each MOS circuit is connected to a signal readout pad (not shown) by wiring 55. The signal reading unit may be constituted by a CCD and an amplifier instead of the MOS circuit. That is, the holes accumulated in the p + regions 43, 45, and 47 are read out to the CCD formed in the silicon substrate 41, transferred to the amplifier by the CCD, and a signal corresponding to the holes is output from the amplifier. A simple signal reading unit may be used.

  Note that light transmitted through the intermediate layers 57, 61, and 65 is received between the silicon substrate 41 and the first electrode film 56 (for example, between the insulating film 48 and the silicon substrate 41), and in response to the light. It is also possible to form an inorganic photoelectric conversion portion made of an inorganic material that generates and accumulates the charges. In this case, a MOS circuit for reading a signal corresponding to the charge accumulated in the charge accumulation region of the inorganic photoelectric conversion unit is provided in the silicon substrate 41, and the wiring 55 may be connected to this MOS circuit. .

  As described above, a configuration in which a plurality of photoelectric conversion layers are stacked on a silicon substrate can be realized by a configuration as shown in FIG.

  In the above description, the photoelectric conversion layer that absorbs B light can absorb light of at least 400 to 500 nm, and preferably has a peak wavelength absorptance of 50% or more in that wavelength region. Means. The photoelectric conversion layer that absorbs G light means that it can absorb light of at least 500 to 600 nm, and preferably has a peak wavelength absorptance of 50% or more in that wavelength region. The photoelectric conversion layer that absorbs R light means that it can absorb light of at least 600 to 700 nm, and preferably has an absorption factor of a peak wavelength in the wavelength region of 50% or more.

  In the case of the configuration shown in FIGS. 12 and 15, a pattern in which colors are detected in the order of BGR, BRG, GBR, GRB, RBG, and RGB from the upper layer is conceivable. Preferably, the uppermost layer is G. In the case of the configuration shown in FIG. 14, when the upper layer is the R layer, the lower layer is the same BG layer, and when the upper layer is the B layer, the lower layer is the same plane and the upper layer is the G layer. A combination of the lower layer and the BR layer on the same plane is possible. Preferably, the upper layer is a G layer and the lower layer is a BR layer on the same plane.

  FIG. 16 is a schematic cross-sectional view illustrating a configuration example of another imaging element. In FIG. 16, a cross section for two pixels in a pixel portion, which is a portion that detects light and accumulates charges, wiring connected to an electrode in the pixel portion, bonding PAD connected to the wiring, and the like are formed. The cross section with the peripheral circuit part which is a part to be performed is also shown.

  In the n-type silicon substrate 413 of the pixel portion, a p region 421 is formed on the surface portion, an n region 422 is formed on the surface portion of the p region 421, and a p region 423 is formed on the surface portion of the n region 422. N region 424 is formed on the surface of p region 423.

  The p region 421 accumulates red (R) component holes photoelectrically converted by a pn junction with the n-type silicon substrate 413. The potential change in the p region 421 due to the accumulation of R component holes is read out from the MOS transistor 426 formed in the n-type silicon substrate 413 to the signal readout PAD 427 through the metal wiring 419 connected thereto. .

  The p region 423 accumulates blue (B) component holes photoelectrically converted by the pn junction with the n region 422. The potential change in the p region 423 due to the accumulation of the B component holes is read out from the MOS transistor 426 ′ formed in the n region 422 to the signal readout PAD 427 through the metal wiring 419 connected thereto.

  In the n region 424, a hole accumulation region 425 composed of a p region for accumulating green (G) component holes generated in the photoelectric conversion layer 123 stacked above the n-type silicon substrate 413 is formed. The potential change in the hole accumulation region 425 due to the accumulation of the G component holes is caused by the signal reading PAD 427 from the MOS transistor 426 ″ formed in the n region 424 through the metal wiring 419 connected thereto. Is read out. Usually, the signal readout PAD 427 is provided separately for each transistor from which each color component is read out.

  Here, the p region, the n region, the transistor, the metal wiring, and the like are schematically shown. However, the structure of each is not limited to this, and an optimal one is appropriately selected. Since the B light and R light are separated according to the depth of the silicon substrate, it is important to select the depth from the surface of the silicon substrate such as a pn junction and the doping concentration of each impurity. A technique used in a normal CMOS image sensor can be applied to a CMOS circuit serving as a signal readout unit. A circuit configuration that reduces the number of transistors in the pixel portion, such as a low noise readout column amplifier or a CDS circuit, can be applied.

  A transparent insulating film 412 mainly composed of silicon oxide, silicon nitride, or the like is formed on the n-type silicon substrate 413, and a transparent insulating film mainly composed of silicon oxide, silicon nitride, or the like is formed on the insulating film 412. 411 is formed. The thickness of the insulating film 412 is preferably as small as possible, and is 5 μm or less, preferably 3 μm or less, more preferably 2 μm or less, and further preferably 1 μm or less.

  In the insulating films 411 and 412, a plug 415 mainly composed of, for example, tungsten is formed to electrically connect the first electrode film 414 and the p region 425 as the hole accumulation region. The plug 415 is insulated. The film 411 and the insulating film 412 are relay-connected by a pad 416. The pad 416 is preferably made mainly of aluminum. In the insulating film 412, the above-described metal wiring 419, gate electrodes of the transistors 426, 426 ', 426 "and the like are also formed. It is preferable that a barrier layer including a metal wiring is provided. The plug 415 is provided for each pixel.

  A light shielding film 417 is provided in the insulating film 411 in order to prevent noise caused by the generation of electric charges due to the pn junction of the n region 424 and the p region 425. As the light shielding film 417, a film mainly composed of tungsten, aluminum, or the like is usually used. In the insulating film 411, a bonding PAD 420 (PAD for supplying power from the outside) and a signal readout PAD 427 are formed, and a metal wiring for electrically connecting the bonding PAD 420 and a first electrode film 414 described later. (Not shown) is also formed.

  A transparent first electrode film 414 is formed on the plug 415 of each pixel in the insulating film 411. The first electrode film 414 is divided for each pixel, and the light receiving area is determined by this size. The first electrode film 414 is biased through the wiring from the bonding PAD 420. A structure in which holes can be accumulated in the hole accumulation region 425 by applying a negative bias to the first electrode film 414 with respect to a second electrode film 405 described later is preferable.

  An intermediate layer 12 having the same structure as that shown in FIG. 12 is formed on the first electrode film 414, and a second electrode film 405 is formed thereon.

  On the second electrode film 405, a protective film 404 mainly composed of silicon nitride having a function of protecting the intermediate layer 12 is formed. An opening is formed in the protective film 404 at a position that does not overlap with the first electrode film 414 in the pixel portion, and an opening is formed in a part of the bonding PAD 420 in the insulating film 411 and the protective film 404. A wiring 418 made of aluminum or the like for electrically connecting the second electrode film 405 exposed by the two openings and the bonding PAD 420 to apply a potential to the second electrode film 405 is formed inside the opening and the protective film. 404 is formed. As a material of the wiring 418, an alloy containing aluminum such as Al—Si or Al—Cu alloy can be used.

  A protective film 403 mainly composed of silicon nitride or the like for protecting the wiring 418 is formed on the wiring 418. An infrared cut dielectric multilayer film 402 is formed on the protective film 403, and an infrared cut dielectric is formed. An antireflection film 401 is formed on the body multilayer film 402.

  The first electrode film 414 performs the same function as the first electrode film 11 shown in FIG. The second electrode film 405 performs the same function as the second electrode film 13 shown in FIG.

  With the above configuration, it is possible to perform color imaging by detecting light of BGR three colors with one pixel. In the configuration of FIG. 16, R and B are used as common values in two pixels, and only the G value is used separately. However, since the sensitivity of G is important when generating an image, such a configuration is used. Even so, it is possible to generate a good color image.

  The solid-state imaging device described above can be applied to imaging devices such as digital cameras, video cameras, facsimile machines, scanners, and copying machines. It can also be used as an optical sensor such as a bio or chemical sensor.

In addition, the materials mentioned as the insulating film described in the above configuration examples are SiOx, SiNx, BSG, PSG, BPSG, Al ₂ O ₃ , MgO, GeO, NiO, CaO, BaO, Fe ₂ O ₃ , Y ₂ O. ₃ , metal oxides such as TiO ₂ , metal fluorides such as MgF ₂ , LiF, AlF ₃ , and CaF _{2. The} most preferred materials are SiOx, SiNx, BSG, PSG, and BPSG.

  Note that in the above configuration example, reading of signals from other than the photoelectric conversion layer may use either holes or electrons. That is, as described above, holes are accumulated in the inorganic photoelectric conversion unit provided between the semiconductor substrate and the photoelectric conversion unit stacked on the semiconductor substrate, or in the photodiode formed in the semiconductor substrate. It is good also as a structure which reads the signal according to a hole with a signal read-out part, accumulate | stores an electron with an inorganic photoelectric conversion part or the photodiode formed in a semiconductor substrate, and the signal according to this electron is read with a signal read-out part. It is good also as a structure to read.

  In the above configuration example, the photoelectric conversion unit provided above the silicon substrate uses the configuration shown in FIG. 13, but the configuration shown in FIGS. 1, 6 to 9, etc. may be used. Is possible. According to the configuration shown in FIG. 13, since electrons and holes can be blocked, the dark current suppressing effect is high. When the electrode opposite to the light incident side is an electron extraction electrode, the connecting portion 9 is connected to the second electrode 13 in FIG. 12, and the connecting portion 27 is connected to the second electrode in FIG. 15, the connection portion 54 may be connected to the second electrode 58, the connection portion 53 may be connected to the second electrode 62, and the connection portion 52 may be connected to the second electrode 66.

  The imaging device described in the above configuration example has a configuration in which a large number of one pixel shown in FIGS. 12 to 16 is arranged in an array on the same plane, and RGB color signals can be obtained by the single pixel. The one pixel can be considered as a photoelectric conversion element that converts RGB light into an electrical signal. For this reason, it can be said that the imaging element has a configuration in which a large number of photoelectric conversion elements as shown in FIGS. 12 to 16 are arranged in an array on the same plane.

  FIG. 17 is a partial surface schematic diagram for explaining another configuration example of the imaging element. 18 is a schematic cross-sectional view taken along line XX of the image sensor shown in FIG. In FIG. 17, the microlens 14 is not shown.

  A p-well layer 2 is formed on the n-type silicon substrate 1. Hereinafter, the n-type silicon substrate 1 and the p-well layer 2 are collectively referred to as a semiconductor substrate. A color filter 13r that mainly transmits R light, a color filter 13g that mainly transmits G light, and a color filter that mainly transmits B light in a row direction on the same plane above the semiconductor substrate and in a column direction perpendicular thereto. A number of three types of color filters 13b are arranged.

  A known material can be used for the color filter 13r, but such a material transmits R light. A known material can be used for the color filter 13g, but such a material transmits G light. A known material can be used for the color filter 13b, but such a material transmits B light.

  As the arrangement of the color filters 13r, 13g, 13b, a color filter arrangement (Bayer arrangement, vertical stripe, horizontal stripe, etc.) used in a known single-plate solid-state imaging device can be adopted.

  A transparent electrode 11r is formed above the n region 4r, a transparent electrode 11g is formed above the n region 4g, and a transparent electrode 11b is formed above the n region 4b. The transparent electrodes 11r, 11g, and 11b are divided corresponding to the color filters 13r, 13g, and 13b, respectively. The transparent electrodes 11r, 11g, and 11b have the same functions as the lower electrode 11 in FIG.

  On each of the transparent electrodes 11r, 11g, and 11b, a photoelectric conversion film 12 having a single configuration common to each of the color filters 13r, 13g, and 13b is formed.

  On the photoelectric conversion film 12, an upper electrode 13 having a single configuration common to each of the color filters 13r, 13g, and 13b is formed.

  A photoelectric conversion element corresponding to the color filter 13r is formed by the transparent electrode 11r, the upper electrode 13 facing the transparent electrode 11r, and a part of the photoelectric conversion film 12 sandwiched therebetween. Hereinafter, since this photoelectric conversion element is formed on a semiconductor substrate, it is referred to as an R photoelectric conversion element.

  A photoelectric conversion element corresponding to the color filter 13g is formed by the transparent electrode 11g, the upper electrode 13 facing the transparent electrode 11g, and a part of the photoelectric conversion film 12 sandwiched therebetween. Hereinafter, this photoelectric conversion element is referred to as a G photoelectric conversion element.

  A photoelectric conversion element corresponding to the color filter 13b is formed by the transparent electrode 11b, the upper electrode 13 facing the transparent electrode 11b, and a part of the photoelectric conversion film 12 sandwiched therebetween. Hereinafter, this photoelectric conversion element is referred to as a B photoelectric conversion element.

  A high concentration n-type impurity region (hereinafter referred to as n + region) 4r for accumulating charges generated in the photoelectric conversion film 12 of the photoelectric conversion element on the R substrate is formed in the n region in the p-well layer 2. Yes. In order to prevent light from entering the n + region 4r, it is preferable to provide a light shielding film on the n + region 4r.

  In the n region in the p-well layer 2, an n + region 4g for accumulating charges generated in the photoelectric conversion film 12 of the photoelectric conversion element on the G substrate is formed. In order to prevent light from entering the n + region 4g, it is preferable to provide a light shielding film on the n + region 4g.

  In the n region in the p-well layer 2, an n + region 4b for accumulating charges generated in the photoelectric conversion film 12 of the photoelectric conversion element on the B substrate is formed. In order to prevent light from entering the n + region 4b, it is preferable to provide a light shielding film on the n + region 4b.

  A contact portion 6r made of a metal such as aluminum is formed on the n + region 4r, and a transparent electrode 11r is formed on the contact portion 6r. The n + region 4r and the transparent electrode 11r are electrically connected by the contact portion 6r. ing. The contact portion 6r is embedded in the insulating layer 5 that is transparent to visible light and infrared light.

  A contact portion 6g made of a metal such as aluminum is formed on the n + region 4g, and a transparent electrode 11g is formed on the contact portion 6g. The n + region 4g and the transparent electrode 11g are electrically connected by the contact portion 6g. ing. The contact portion 6g is embedded in the insulating layer 5.

  A contact portion 6b made of a metal such as aluminum is formed on the n + region 4b, and a transparent electrode 11b is formed on the contact portion 6b. The n + region 4b and the transparent electrode 11b are electrically connected by the contact portion 6b. ing. The contact portion 6 b is embedded in the insulating layer 5.

  Signals for reading out signals corresponding to the electric charges generated in the R photoelectric conversion elements and accumulated in the n + regions 4r in the regions other than the n + regions 4r, 4g, 4b formed in the p-well layer 2 A readout unit 5r, a signal readout unit 5g for reading out signals corresponding to the charges generated in the G photoelectric conversion element and accumulated in the n + region 4g, and a signal readout unit 5g generated in the B photoelectric conversion element and accumulated in the n + region 4b. And a signal reading unit 5b for reading out signals corresponding to the charges. Each of the signal reading units 5r, 5g, and 5b can adopt a known configuration using a CCD or a MOS circuit. In order to prevent light from entering the signal readout units 5r, 5g, 5b, it is preferable to provide a light shielding film on the signal readout units 5r, 5g, 5b.

  FIG. 19 is a diagram illustrating a specific configuration example of the signal reading unit 5r illustrated in FIG. 19, the same components as those in FIGS. 17 and 18 are denoted by the same reference numerals. Note that the signal readout units 5r, 5g, and 5b have the same configuration, and thus the description of the signal readout units 5g and 5b is omitted.

  The signal readout section 5r has a reset transistor 43 whose drain is connected to the n + region 4r, its source connected to the power supply Vn, and an output transistor 42 whose gate is connected to the drain of the reset transistor 43 and whose source is connected to the power supply Vcc. A row selection transistor 41 whose source is connected to the drain of the output transistor 42 and whose drain is connected to the signal output line 45; a reset transistor 46 whose drain is connected to the n region 3r and whose source is connected to the power supply Vn; The output transistor 47 whose gate is connected to the drain of the reset transistor 46, the source is connected to the power supply Vcc, and the row selection transistor 48 whose source is connected to the drain of the output transistor 47 and whose drain is connected to the signal output line 49. With.

  By applying a bias voltage between the transparent electrode 11r and the upper electrode 13, a charge is generated according to the light incident on the photoelectric conversion film 12, and the charge moves to the n + region 4r through the transparent electrode 11r. The charge accumulated in the n + region 4r is converted into a signal corresponding to the amount of charge by the output transistor. Then, a signal is output to the signal output line 45 by turning on the row selection transistor 41. After the signal is output, the charge in the n + region 4r is reset by the reset transistor 43.

  Thus, the signal reading unit 5r can be configured by a known MOS circuit including three transistors.

  Returning to FIG. 18, the protective layers 15 and 16 having a two-layer structure for protecting the photoelectric conversion element on the substrate are formed on the photoelectric conversion film 12, and the color filters 13 r, 13 g, and 13 b are formed on the protective layer 16. Has been.

  The image sensor 100 is manufactured by forming the color filters 13r, 13g, 13b and the like after the photoelectric conversion film 12 is formed. However, the color filters 13r, 13g, 13b include a photolithography process and a baking process. When an organic material is used as the photoelectric conversion film 12, if the photolithography process or the baking process is performed with the photoelectric conversion film 12 exposed, the characteristics of the photoelectric conversion film 12 are deteriorated. In the imaging device 100, protective layers 15 and 16 are provided in order to prevent the deterioration of the characteristics of the photoelectric conversion film 12 due to such a manufacturing process.

The protective layer 15 is preferably an inorganic layer made of an inorganic material formed by the ALCVD method. The ALCVD method is an atomic layer CVD method, can form a dense inorganic layer, and can be an effective protective layer for the photoelectric conversion layer 9. The ALCVD method is also known as the ALE method or ALD method. The inorganic layer formed by the ALCVD method is preferably made of Al ₂ O ₃ , SiO ₂ , TiO ₂ , ZrO ₂ , MgO, HfO ₂ , Ta ₂ O ₅ , more preferably made of Al ₂ O ₃ , SiO ₂ , Most preferably, it consists of Al ₂ O ₃ .

  The protective layer 16 is formed on the protective layer 15 in order to further improve the protective performance of the photoelectric conversion film 12, and is preferably an organic layer made of an organic polymer. Parylene is preferable as the organic polymer, and parylene C is more preferable. The protective layer 16 may be omitted, and the arrangement of the protective layer 15 and the protective layer 16 may be reversed. The protection effect of the photoelectric conversion film 12 is particularly high in the configuration shown in FIG.

  When a predetermined bias voltage is applied to the transparent electrode 11r and the upper electrode 13, charges generated in the photoelectric conversion film 12 constituting the photoelectric conversion element on the R substrate move to the n + region 4r via the transparent electrode 11r and the contact portion 6r. , Accumulated here. Then, a signal corresponding to the electric charge accumulated in the n + region 4r is read by the signal reading unit 5r and output to the outside of the image sensor 100.

  Similarly, when a predetermined bias voltage is applied to the transparent electrode 11g and the upper electrode 13, charges generated in the photoelectric conversion film 12 constituting the photoelectric conversion element on the G substrate are transferred to the n + region 4g via the transparent electrode 11g and the contact portion 6g. Go to and accumulate here. Then, a signal corresponding to the electric charge accumulated in the n + region 4g is read out by the signal reading unit 5g and output to the outside of the image sensor 100.

  Similarly, when a predetermined bias voltage is applied to the transparent electrode 11b and the upper electrode 13, charges generated in the photoelectric conversion film 12 constituting the photoelectric conversion element on the B substrate are transferred to the n + region 4b via the transparent electrode 11b and the contact portion 6b. Go to and accumulate here. Then, a signal corresponding to the electric charge accumulated in the n + region 4b is read by the signal reading unit 5b and output to the outside of the image sensor 100.

  As described above, the image sensor 100 generates the R component signal corresponding to the charge generated in the R photoelectric conversion element, the G component signal corresponding to the charge generated in the G photoelectric conversion element, and the B photoelectric conversion element. A B component signal corresponding to the electric charge can be output to the outside. Thereby, a color image can be obtained. With this format, the photoelectric conversion unit becomes thin, so that the resolution is improved and the false color can be reduced. Moreover, since the aperture ratio can be increased regardless of the lower circuit, high sensitivity is possible, and the microlens can be omitted, which is effective in omitting the number of components.

  In this example, the organic photoelectric conversion film has a maximum absorption wavelength in the high green light region and needs to have an absorption region in the entire visible light, but can be preferably realized by the specified material of the present invention.

  As mentioned above, although the structural example using the photoelectric conversion element of this invention as an image pick-up element was described, since the photoelectric conversion element of this invention shows high photoelectric conversion efficiency, even if it uses it as a solar cell, it shows high performance. A preferable element configuration for use as a solar cell is the combination of the photoelectric conversion material described in the present invention with the configuration described in the non-patent document (Adv. Mater., 17, 66 (2005)), etc. Can be applied.

  Hereinafter, the present invention will be described in detail with reference to examples, but the present invention is of course not limited to these examples.

  The organic compounds used in Examples and Comparative Examples are shown below. The value of the dipole moment was measured using molecular modeling software “CAChe (registered trademark)” manufactured by Fujitsu Limited.

(Example 1, Comparative Example 1)
Washed ITO (glass) substrate placed in a deposition apparatus, under reduced pressure below the vacuum degree ^1.0E -4 Pa. After depositing organic compound A as a charge blocking layer, organic compound 1 having a controlled substrate temperature is deposited, and then patterned on an organic thin film while maintaining a vacuum (a mask having a light receiving area of 2 mm × 2 mm) ) And 100 nm of Al was vapor-deposited to produce a photoelectric conversion element. Glass sealing was performed using a UV curable resin without exposing the substrate to the atmosphere.

  The structure of an Example and a comparative example is shown below. The photoelectric conversion elements of Examples and Comparative Examples are basically the same as the configuration shown in FIG. 1, and have a configuration in which a single blocking layer and a photoelectric conversion layer are provided between electrodes. In addition, the number in a parenthesis shows thickness (unit: nm), and shows the cooling temperature at the time of film-forming about the organic compounds 1-6. RT means room temperature, and is 25 ° C. here, for example.

Example 1-1: ITO / organic compound A (100) / organic compound 1 [0 ° C. film formation] (50) / Al (100)
Example 1-2: ITO / organic compound A (100) / organic compound 1 [-15 ° C. film formation] (50) / Al (100)
(Example 1-3): ITO / organic compound A (100) / organic compound 1 [−25 ° C. film formation] (50) / Al (100)
Example 1-4: ITO / organic compound A (100) / organic compound 1 [-45 ° C. film formation] (50) / Al (100)
(Comparative Example 1): ITO / organic compound A (100) / organic compound 1 [RT film formation] (50) / Al (100)

For the above Examples and Comparative Examples, the maximum sensitivity wavelength (meaning the highest external quantum efficiency (sensitivity) at a wavelength of 300 nm to 800 nm) at an in-film electric field strength of 5.0E ⁺⁵ (V / cm). External quantum efficiency (relative value) was measured. Each external quantum efficiency is shown below. The relative value is a relative value when the comparative example is 1.
(Example 1-1) 1.8
(Example 1-2) 5
(Example 1-3) 15
(Example 1-4) 3
(Comparative Example 1) 1

(Example 2, comparative example 2)
An organic compound 2 having a controlled substrate temperature is formed in the same procedure as in Example 1 and Comparative Example 1 above, and a charge blocking layer SiO is deposited thereon, and then amorphous ITO is formed by sputtering to produce photoelectric. A conversion element was produced.
(Example 2): ITO / organic compound A (100) / organic compound 2 [-25 ° C. film formation] (50) / SiO (40) / ITO (5)
(Comparative Example 2): ITO / organic compound A (100) / organic compound 2 [RT film formation] (50) / SiO (40) / ITO (5)

About the said Example and comparative example, the external quantum efficiency (relative value) in the maximum sensitivity wavelength in in-film electric field intensity | strength is 5.0E ^{+ 5} (V / cm) was measured. Each external quantum efficiency is shown below.
(Example 2) 6
(Comparative Example 2) 1

(Example 3, Comparative Example 3)
An organic compound 3 having a controlled substrate temperature is formed in the same procedure as in Example 1 and Comparative Example 1 above, a charge blocking layer SiO is deposited thereon, an amorphous ITO film is formed by sputtering, and the photoelectric A conversion element was produced.
(Example 3): ITO / organic compound A (100) / organic compound 3 [-25 ° C. film formation] (50) / SiO (40) / ITO (5)
(Comparative Example 3): ITO / organic compound A (100) / organic compound 3 [RT film formation] (50) / SiO (40) / ITO (5)

About the said Example and comparative example, the external quantum efficiency (relative value) in the maximum sensitivity wavelength in in-film electric field intensity | strength is 5.0E ^{+ 5} (V / cm) was measured. Each external quantum efficiency is shown below.
(Example 3) 2.5
(Comparative Example 3) 1

(Example 4, comparative example 4)
An organic compound 4 having a controlled substrate temperature is formed in the same procedure as in Example 1 and Comparative Example 1, and a charge blocking layer SiO is deposited thereon, then amorphous ITO is formed by sputtering and photoelectric conversion is performed. An element was produced.
(Example 4): ITO / organic compound A (100) / organic compound 4 [-25 ° C. film formation] (50) / SiO (40) / ITO (5)
(Comparative Example 4): ITO / organic compound A (100) / organic compound 4 [RT film formation] (50) / SiO (40) / ITO (5)

About the said Example and comparative example, the external quantum efficiency (relative value) in the maximum sensitivity wavelength in in-film electric field intensity | strength is 5.0E ^{+ 5} (V / cm) was measured. Each external quantum efficiency is shown below.
(Example 4) 1.8
(Comparative Example 4) 1

(Comparative Example 5)
An organic compound 5 in which the substrate temperature was controlled in the same procedure as in Example 1 and Comparative Example 1 was formed, and Al was deposited to a thickness of 100 nm to produce a photoelectric conversion element.
(Comparative Example 5-1): ITO / organic compound A (100) / organic compound 5 [-25 ° C. film formation] (50) / Al (100)
(Comparative Example 5-2): ITO / organic compound A (100) / organic compound 5 [RT film formation] (50) / Al (100)

About the said Example and comparative example, the external quantum efficiency (relative value) in the maximum sensitivity wavelength in in-film electric field intensity | strength is 5.0E ^{+ 5} (V / cm) was measured. Each external quantum efficiency is shown below.
(Comparative Example 5-1) 1
(Comparative Example 5-2) 1

(Comparative Example 6)
An organic compound 6 having a controlled substrate temperature is formed in the same procedure as in Example 1 and Comparative Example 1, and after depositing a charge blocking layer SiO thereon, amorphous ITO is formed by sputtering and photoelectric conversion is performed. An element was produced.
(Comparative Example 6-1): ITO / organic compound A (100) / organic compound 6 [-25 ° C. film formation] (50) / SiO (40) / ITO (5)
(Comparative Example 6-2): ITO / organic compound A (100) / organic compound 6 [RT film formation] (50) / SiO (40) / ITO (5)

About the said Example and comparative example, the external quantum efficiency (relative value) in the maximum sensitivity wavelength in in-film electric field intensity | strength is 5.0E ^{+ 5} (V / cm) was measured. Each external quantum efficiency is shown below.
(Comparative Example 6-1) 1
(Comparative Example 6-2) 1

  According to this measurement, the organic compounds 1 to 4 having a dipole moment larger than 0 are vapor-deposited with the substrate temperature set to 0 ° C. or lower, and the external quantum efficiency is higher than that of vapor-deposited at room temperature. It turns out that it improves. Also, organic compounds 5 and 6 having a dipole moment of 0 had no effect on the external quantum efficiency regardless of whether or not the substrate temperature was lowered by cooling during film formation.

  In addition, high photoelectric conversion efficiency can be obtained even in cooling film formation with liquid nitrogen (substrate temperature: -170 ° C.), and good in cooling film formation with liquid helium (substrate temperature: estimated −250 ° C.). Result can be obtained.

  Next, the effect of increasing the temperature at a predetermined speed after cooling after the formation of the photoelectric conversion layer is verified.

  In each of Examples 1 to 4 and Comparative Examples 5-1 and 6-1, the film was formed by controlling the substrate temperature to a low temperature, and then the temperature was raised to room temperature at 5 ° C./min. Forming.

(Example 5)
In Example 5, the organic compound 1 whose substrate temperature was controlled in the same procedure as in Example 1 was formed, and then the temperature was raised at 1 ° C./1 min when returning to room temperature. Produced.
Example 5-1 ITO / Organic Compound A (100) / Organic Compound 1 [-25 ° C. Film Formation] (50) / Al (100)

About the said Example 5-1 and the said Example 1-3, the external quantum efficiency (relative value) in the maximum sensitivity wavelength in in-film electric field strength is 5.0E ^{+ 5} (V / cm) was measured. Each external quantum efficiency is shown below.
(Example 1-3) 15
(Example 5-1) 23

  Thereby, after forming the film in a state where the photoelectric conversion layer is lower than room temperature, by slowly returning to the room temperature, by minimizing the influence of changing the state of the molecular association of the layer in the direction of disordering, It can be seen that the charge separation was maintained in an accelerated state.

  Here, when raising the temperature, the temperature is preferably increased at 5 ° C./min or less, and more preferably 1 ° C./min or less. However, when raising the temperature, it is preferable to raise the temperature at 0.1 ° C./min or more from the viewpoint of production suitability (the temperature rise time is too fast for the production speed).

  Next, a description will be given of a spectral absorption spectrum and a fluorescence spectrum when the organic compound having a donor-acceptor connection structure is formed on the substrate while keeping the substrate temperature at room temperature or lower. Here, the organic compound 1 of Example 1 is used.

FIG. 20 is a graph showing a spectral absorption spectrum. In this graph, the horizontal axis indicates the wavelength of light (nm) and the vertical axis indicates the absorbance (Absorbance), and normalization is performed at the top peak.
As shown in FIG. 20, in the organic compound formed by cooling to −25 ° C., the spectrum waveform shifts to the longer wavelength side compared to the organic compound formed at room temperature. That is, when the photoelectric conversion layer is formed, if the substrate temperature is controlled to x ° C. and y ° C. (x ° C.> y ° C.), the waveform at y ° C. is higher than the waveform at x ° C. in the spectral absorption spectrum. It means having a long wave spectrum. Specifically, the inclined region on the long wave side from the peak at which the absorbance reaches the maximum value is significantly shifted to the long wave side.

FIG. 21 is a graph showing a fluorescence spectrum. In this graph, the wavelength of light (nm) is shown on the horizontal axis, and the fluorescence intensity (PL Intensity) is shown on the vertical axis, and normalization is performed at the top peak.
As shown in FIG. 21, in the organic compound formed by cooling to −25 ° C., the spectrum waveform shifts to the short wavelength side as compared with the organic compound formed at room temperature. That is, when the photoelectric conversion layer is formed, if the substrate temperature is controlled to x ° C. and y ° C. (x ° C.> y ° C.), the waveform at y ° C. is shorter than the waveform at x ° C. in the fluorescence spectrum. Means having a normalized spectrum. The inclined region on the short wave side from the peak at which the fluorescence intensity reaches the maximum value is significantly shifted to the short wave side.

The organic compound having a donor-acceptor linking structure preferably has a spectral absorption spectrum peak value λ _MAX of 350 nm to 700 nm.

FIG. 22 is a graph showing a fluorescence spectrum. In this graph, the horizontal axis indicates the wavelength of light (nm), and the vertical axis indicates the fluorescence intensity (PL Intensity). In FIG. 22, the organic compound 1 is used here.
As shown in FIG. 22, when the fluorescence spectrum intensity is measured at the same film thickness (50 nm), the cooled organic compound film has a larger fluorescence spectrum intensity. That is, when the film is formed by controlling the substrate temperature to x ° C. and y ° C. (x ° C.> y ° C.) when forming the photoelectric conversion layer, the waveform at y ° C. is more than the waveform at x ° C. The fluorescence spectrum intensity increases.

  FIG. 23 is a graph showing a spectral absorption spectrum. In this graph, the horizontal axis indicates the wavelength of light (nm), and the vertical axis indicates the absorbance (Absorbance). In this measurement, the organic compound 1 is used for both an organic compound formed by cooling and an organic compound formed at room temperature. As shown in FIG. 23, according to the above spectral absorption measurement, the layer containing the organic compound has the substrate temperature at the time of forming the layer containing the organic compound at x ° C., y ° C. (x ° C.> y ° C. ), The waveform at y ° C. is larger than the waveform at x ° C. in the absorbance at the same film thickness. Thereby, not only the effect of improving the quantum conversion efficiency but also the light absorption ability is increased by increasing the absorbance by cooling, thereby reducing the total film thickness at the time of formation. Furthermore, the effect that power consumption can be reduced can also be obtained.

The present invention includes the following configurations.
(1) A photoelectric conversion element comprising a pair of electrodes and a photoelectric conversion layer provided between the pair of electrodes,
The photoelectric conversion element formed in the state in which the said photoelectric converting layer contains only the organic compound of one kind of donor-acceptor connection structure as an organic compound, and made the temperature of the layer smaller than room temperature at the time of the formation of the said photoelectric converting layer.
(2) The photoelectric conversion element according to (1) above,
The photoelectric conversion element whose dipole moment of the said organic compound is 1.0 D or more.
(3) The photoelectric conversion element according to (1) or (2) above,
The photoelectric conversion element whose peak value (lambda) _MAX of the spectral absorption spectrum of the said organic compound is 350 nm-700 nm.
(4) The photoelectric conversion element according to any one of (1) to (3) above,
Furthermore, a photoelectric conversion element including a charge blocking layer provided between the electrode and the photoelectric conversion layer.
(5) The photoelectric conversion element according to any one of (1) to (4) above,
Of the pair of electrodes, a photoelectric conversion element in which a light incident side electrode is a transparent electrode.
(6) The photoelectric conversion element according to any one of (1) to (5) above,
The photoelectric conversion element whose electric field applied to an organic photoelectric conversion element through the pair of electrodes is 1.0E ⁺⁴ V / cm to 1.0E ⁺⁷ V / cm.
(7) The photoelectric conversion element according to any one of (1) to (6) above,
Spectral absorption measurement is performed on a layer formed by controlling the substrate temperature at x ° C. and y ° C. (x ° C.> y ° C.) when the layer containing the organic compound forms the layer containing the organic compound. A photoelectric conversion element having a spectrum in which the waveform at y ° C. is longer than the waveform at x ° C. in the spectral absorption spectrum.
(8) The photoelectric conversion element according to any one of (1) to (7) above,
When the layer containing the organic compound is measured for fluorescence with respect to the layer formed by controlling the substrate temperature at x ° C. and y ° C. (x ° C.> y ° C.) when the layer containing the organic compound is formed. A photoelectric conversion element having a spectrum in which the waveform at y ° C. is shorter than the waveform at x ° C. in the fluorescence spectrum.
(9) The photoelectric conversion element according to any one of (1) to (8) above,
The photoelectric conversion element whose said organic compound is a compound containing the partial structure shown by following General formula (1).
General formula (1)

（式中、ＸはＯ、Ｓ、Ｎ−Ｒ_１０を表す。Ｒ_１０は水素原子又は置換基を表す。Ｒ^ｘ、Ｒ^ｙはそれぞれに独立に、水素原子又は置換基を表し、少なくとも一方は電子求引基を表す。また、Ｒ^ｘ、Ｒ^ｙは連結して環を形成してもよい。Ｒは結合手、水素原子又は置換基を表すが、少なくとも１つは結合手（−）である。ｎｒは１〜４の整数を表す。ｎｒが２以上のときはＲは同じでも異なってもよい。２位と３位のＲ同士、５位と６位のＲ同士はそれぞれ互いに連結して環を形成してもよい。）

(Wherein, X is O, S, ^.R represents an is _{.R 10} representing the _{N-R 10} a hydrogen atom or a substituent x, independently each ^{R y,} represents a hydrogen atom or a substituent, at least one of R ^x and R ^y may be linked to form a ring, R represents a bond, a hydrogen atom or a substituent, but at least one is a bond (-). Nr represents an integer of 1 to 4. When nr is 2 or more, Rs may be the same or different, and Rs at the 2nd and 3rd positions are connected to each other at the 5th and 6th positions. To form a ring.)

(10) The photoelectric conversion element according to (1) to (8) above,
The photoelectric conversion element whose said organic compound is a compound shown by following General formula (2).
General formula (2)

(In the formula, Z ₁₁ represents an atomic group necessary for forming a 5- or 6-membered ring. L ₁ , L ₂ and L ₃ each represents an unsubstituted methine group or a substituted methine group. D ₁ represents an atom. Represents a group, and n represents an integer of 0 or more.)
(11) The photoelectric conversion element according to (1) to (8) above,
The photoelectric conversion element whose said organic compound is a compound shown by following General formula (3).
General formula (3)

(In the formula, Z ₁ represents an atomic group forming a 5- or 6-membered nitrogen-containing heterocyclic ring. Za represents an atomic group necessary to form a 6-membered ring. R ₁ represents a hydrogen atom or an alkyl group. , an alkenyl group, an aryl group or a heterocyclic group .L ₁₁ ~L ₁₄ represents a methine group which may have a substituent, may be formed with other methine group and ring .p _1, Is 0 or 1, preferably 0. n ₁ represents an integer of 0 to 4, more preferably 0 to 3, and still more preferably 0 or 1. When n ₁ is 2 or more, A plurality of L ₁₃ and L ₁₄ may be the same or different, M ₁ represents an ion for neutralizing charge, m ₁ represents a number necessary for charge neutralization, where Z ₁ represents a thiazoline nucleus and a thiazole nucleus. Except for atomic groups that form
(12) The photoelectric conversion device according to any one of (1) to (11), wherein the layer containing the organic compound has a substrate temperature when the layer containing the organic compound is formed. When the spectral absorption measurement is carried out by controlling each at x ° C. and y ° C. (x ° C.> y ° C.), the waveform at y ° C. in the absorbance at the same film thickness is more than that at x ° C. Large photoelectric conversion element.
(13) The photoelectric conversion device according to any one of (1) to (12), wherein the layer containing the organic compound forms a layer having the same film thickness containing the organic compound. When the substrate temperature is controlled to x ° C. and y ° C. (x ° C.> y ° C.), a photoelectric conversion element having a fluorescence spectrum intensity greater than that when the waveform at y ° C. is x ° C.
(14) The photoelectric conversion element according to any one of (1) to (13) above,
A photoelectric conversion element formed by raising the temperature at 5 ° C./min or less after lowering the temperature of the layer below room temperature when forming the photoelectric conversion layer.
(15) An imaging device comprising the photoelectric conversion device according to any one of (1) to (14).
(16) A method for producing a photoelectric conversion element comprising a pair of electrodes and a photoelectric conversion layer provided between the pair of electrodes,
The manufacturing method of the photoelectric conversion element which forms the said photoelectric converting layer in the state which made the temperature of the said organic compound into temperature lower than room temperature using the organic compound of one type of donor-acceptor connection structure as an organic compound.
(17) The method for producing a photoelectric conversion element according to (16) above,
A method for manufacturing a photoelectric conversion element, which is formed by increasing the temperature at 5 ° C./min or less after the temperature of the layer is made lower than room temperature when forming the photoelectric conversion layer.

11 Lower electrode 12 Photoelectric conversion film 13 Upper electrode 180 Transparent substrate 190 Pixel electrode 192 (192a to 192c) Three-layered electron blocking layer 200 Photoelectric conversion layer 203 (203a to 203c) Three-layered hole blocking layer 204 Electrode 300 Counter electrode

Claims (17)

A photoelectric conversion element comprising a pair of electrodes and a photoelectric conversion layer provided between the pair of electrodes,
The photoelectric conversion element formed in the state in which the said photoelectric converting layer contains only the organic compound of one kind of donor-acceptor connection structure as an organic compound, and made the temperature of the layer smaller than room temperature at the time of the formation of the said photoelectric converting layer. The photoelectric conversion device according to claim 1,
The photoelectric conversion element whose dipole moment of the said organic compound is 1.0 D or more. The photoelectric conversion element according to claim 1 or 2,
The photoelectric conversion element whose peak value (lambda) _MAX of the spectral absorption spectrum of the said organic compound is 350 nm-700 nm. The photoelectric conversion element according to any one of claims 1 to 3, wherein
Furthermore, a photoelectric conversion element including a charge blocking layer provided between the electrode and the photoelectric conversion layer. The photoelectric conversion device according to claim 1, wherein
Of the pair of electrodes, a photoelectric conversion element in which a light incident side electrode is a transparent electrode. The photoelectric conversion element according to any one of claims 1 to 5,
The photoelectric conversion element whose electric field applied to the said photoelectric converting layer through the said pair of electrode is 1.0E ^{+ 4} V / cm-1.0E ^{+ 7} V / cm. The photoelectric conversion device according to claim 1, wherein
Spectral absorption measurement is performed on a layer formed by controlling the substrate temperature at x ° C. and y ° C. (x ° C.> y ° C.) when the layer containing the organic compound forms the layer containing the organic compound. A photoelectric conversion element having a spectrum in which the waveform at y ° C. is longer than the waveform at x ° C. in the spectral absorption spectrum. The photoelectric conversion element according to any one of claims 1 to 7,
When the layer containing the organic compound is measured for fluorescence with respect to the layer formed by controlling the substrate temperature at x ° C. and y ° C. (x ° C.> y ° C.) when the layer containing the organic compound is formed. A photoelectric conversion element having a spectrum in which the waveform at y ° C. is shorter than the waveform at x ° C. in the fluorescence spectrum. The photoelectric conversion element according to any one of claims 1 to 8,
The photoelectric conversion element whose said organic compound is a compound containing the partial structure shown by following General formula (1).
General formula (1)

(Wherein, X is O, S, ^.R represents an is _{.R 10} representing the _{N-R 10} a hydrogen atom or a substituent x, independently each ^{R y,} represents a hydrogen atom or a substituent, at least one of R ^x and R ^y may be linked to form a ring, R represents a bond, a hydrogen atom or a substituent, but at least one is a bond (-). Nr represents an integer of 1 to 4. When nr is 2 or more, Rs may be the same or different, and Rs at the 2nd and 3rd positions are connected to each other at the 5th and 6th positions. To form a ring.) The photoelectric conversion device according to claim 1, wherein
The photoelectric conversion element whose said organic compound is a compound shown by following General formula (2).
General formula (2)

(In the formula, Z ₁₁ represents an atomic group necessary for forming a 5- or 6-membered ring. L ₁ , L ₂ and L ₃ each represents an unsubstituted methine group or a substituted methine group. D ₁ represents an atom. Represents a group, and n represents an integer of 0 or more.) The photoelectric conversion device according to claim 1, wherein
The photoelectric conversion element whose said organic compound is a compound shown by following General formula (3).
General formula (3)

(In the formula, Z ₁ represents an atomic group forming a 5- or 6-membered nitrogen-containing heterocyclic ring. Za represents an atomic group necessary to form a 6-membered ring. R ₁ represents a hydrogen atom or an alkyl group. , an alkenyl group, an aryl group or a heterocyclic group .L ₁₁ ~L ₁₄ represents a methine group which may have a substituent, may be formed with other methine group and ring .p _1, Is 0 or 1, preferably 0. n ₁ represents an integer of 0 to 4, more preferably 0 to 3, and still more preferably 0 or 1. When n ₁ is 2 or more, A plurality of L ₁₃ and L ₁₄ may be the same or different, M ₁ represents an ion for neutralizing charge, m ₁ represents a number necessary for charge neutralization, where Z ₁ represents a thiazoline nucleus and a thiazole nucleus. Except for atomic groups that form The photoelectric conversion element according to any one of claims 1 to 11,
When the layer containing the organic compound is formed by controlling the substrate temperature at the time of forming the layer containing the organic compound at x ° C. and y ° C. (x ° C.> y ° C.) and measuring the spectral absorption. In addition, in the absorbance at the same film thickness, a photoelectric conversion element having a waveform at y ° C. larger than that at x ° C. The photoelectric conversion element according to any one of claims 1 to 12,
When the layer containing the organic compound is formed by controlling the substrate temperature to x ° C. and y ° C. (x ° C.> y ° C.) when forming the layer having the same film thickness containing the organic compound, y A photoelectric conversion element having a fluorescence spectrum intensity greater than that at x ° C. The photoelectric conversion element according to any one of claims 1 to 13,
A photoelectric conversion element formed by raising the temperature at 5 ° C./min or less after lowering the temperature of the layer below room temperature when forming the photoelectric conversion layer.   The image pick-up element provided with the photoelectric conversion element as described in any one of Claim 1 to 14. A method for producing a photoelectric conversion element comprising a pair of electrodes and a photoelectric conversion layer provided between the pair of electrodes,
The manufacturing method of the photoelectric conversion element which forms the said photoelectric converting layer in the state which made the temperature of the said organic compound into temperature lower than room temperature using the organic compound of one type of donor-acceptor connection structure as an organic compound. It is a manufacturing method of the photoelectric conversion element according to claim 16,
A method for manufacturing a photoelectric conversion element, which is formed by increasing the temperature at 5 ° C./min or less after the temperature of the layer is made lower than room temperature when forming the photoelectric conversion layer.

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