WO2020261933A1 - Élément de conversion photoélectrique, élément d'imagerie, capteur optique et matériau d'élément de conversion photoélectrique - Google Patents

Élément de conversion photoélectrique, élément d'imagerie, capteur optique et matériau d'élément de conversion photoélectrique Download PDF

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WO2020261933A1
WO2020261933A1 PCT/JP2020/022287 JP2020022287W WO2020261933A1 WO 2020261933 A1 WO2020261933 A1 WO 2020261933A1 JP 2020022287 W JP2020022287 W JP 2020022287W WO 2020261933 A1 WO2020261933 A1 WO 2020261933A1
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substituent
group
photoelectric conversion
conversion element
formula
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PCT/JP2020/022287
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Japanese (ja)
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花木　直幸
知昭 吉岡
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富士フイルム株式会社
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Priority to JP2021527593A priority Critical patent/JP7382404B2/ja
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    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L27/00—Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate
    • H01L27/14—Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation
    • H01L27/144—Devices controlled by radiation
    • H01L27/146—Imager structures
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K39/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic radiation-sensitive element covered by group H10K30/00
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/549—Organic PV cells

Definitions

  • the present invention relates to a photoelectric conversion element, an image sensor, an optical sensor, and a material for a photoelectric conversion element.
  • Patent Document 1 discloses a photoelectric conversion element containing a predetermined compound.
  • a photoelectric conversion element is required to have excellent responsiveness when receiving light.
  • the compound represented by the formula (1) described later is a compound represented by the formula (2) described later, a compound represented by the formula (3) described later, or a compound represented by the formula (4) described later.
  • the present invention it is possible to provide a photoelectric conversion element having excellent responsiveness. Further, according to the present invention, it is possible to provide a material for an image sensor, an optical sensor, and a photoelectric conversion element.
  • the "substituent” includes a group exemplified by the substituent W described later, unless otherwise specified.
  • the substituent W is, for example, a halogen atom (fluorine atom, chlorine atom, bromine atom, iodine atom, etc.), an alkyl group (including a cycloalkyl group, a bicycloalkyl group, and a tricycloalkyl group), an alkenyl group (including a cycloalkyl group, a bicycloalkyl group, and an alkenyl group).
  • a halogen atom fluorine atom, chlorine atom, bromine atom, iodine atom, etc.
  • an alkyl group including a cycloalkyl group, a bicycloalkyl group, and a tricycloalkyl group
  • an alkenyl group including a cycloalkyl group, a bicycloalkyl group, and an alkenyl group.
  • each of the above-mentioned groups may further have a substituent (for example, one or more groups of each of the above-mentioned groups) if possible.
  • a substituent for example, one or more groups of each of the above-mentioned groups
  • an alkyl group which may have a substituent is also included as a form of the substituent W.
  • the substituent W has a carbon atom
  • the number of carbon atoms of the substituent W is, for example, 1 to 20.
  • the number of atoms other than the hydrogen atom of the substituent W is, for example, 1 to 30.
  • the number of carbon atoms of the alkyl group is preferably 1 to 20, more preferably 1 to 10, and even more preferably 1 to 6.
  • the alkyl group may be linear, branched, or cyclic. Examples of the alkyl group include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a t-butyl group, an n-hexyl group, a cyclopentyl group and the like.
  • the alkyl group may be, for example, a cycloalkyl group, a bicycloalkyl group, or a tricycloalkyl group, and may have a cyclic structure thereof as a partial structure.
  • the substituent that the alkyl group may have is not particularly limited, and examples thereof include a substituent W, and an aryl group (preferably 6 to 18 carbon atoms, more preferably). 6), a heteroaryl group (preferably 5 to 18, more preferably 5 to 6 carbon atoms), or a halogen atom (preferably a fluorine atom or a chlorine atom).
  • the above-mentioned alkyl group is preferable as the alkyl group portion of the alkoxy group.
  • the above-mentioned alkyl group is preferable as the alkyl group moiety in the alkylthio group.
  • the substituent that the alkoxy group may have includes the same examples as the substituent in the alkyl group that may have a substituent.
  • the substituent which the alkylthio group may have includes the same examples as the substituent in the alkyl group which may have a substituent.
  • the alkenyl group may be linear, branched chain, or cyclic.
  • the alkenyl group preferably has 2 to 20 carbon atoms.
  • the substituent which the alkenyl group may have includes the same examples as the substituent in the alkyl group which may have a substituent.
  • the alkynyl group may be linear, branched chain, or cyclic.
  • the alkynyl group preferably has 2 to 20 carbon atoms.
  • the substituent which the alkynyl group may have includes the same examples as the substituent in the alkyl group which may have a substituent.
  • the aryl group is preferably an aryl group having 6 to 18 ring members, unless otherwise specified.
  • the aryl group may be monocyclic or polycyclic.
  • the aryl group is preferably, for example, a phenyl group, a naphthyl group, an anthryl group, or a phenanthrenyl group.
  • the substituent which the aryl group may have is not particularly limited, and examples thereof include a substituent W, and an alkyl group which may have a substituent (preferably).
  • the number of carbon atoms is preferably 1 to 10), and a methyl group is more preferable.
  • the heteroaryl group includes a hetero atom such as a nitrogen atom, a sulfur atom, an oxygen atom, a selenium atom, a tellurium atom, a phosphorus atom, a silicon atom, and / or a boron atom.
  • a heteroaryl group having a monocyclic or polycyclic ring structure is preferable.
  • the number of carbon atoms in the ring member atom of the heteroaryl group is not particularly limited, and is preferably 3 to 18 and more preferably 3 to 5.
  • the number of heteroatoms in the ring member atom of the heteroaryl group is not particularly limited, and is preferably 1 to 10, more preferably 1 to 4, and even more preferably 1 to 2.
  • the number of ring members of the heteroaryl group is not particularly limited, and is preferably 5 to 8, more preferably 5 to 7, and even more preferably 5 to 6.
  • the heteroaryl group includes a fryl group, a pyridyl group, a quinolyl group, an isoquinolyl group, an acridinyl group, a phenanthridinyl group, a pteridinyl group, a pyrazinyl group, a quinoxalinyl group, a pyrimidinyl group, a quinazolyl group, a pyridadinyl group, a synnolinyl group and a phthalazinyl group.
  • the substituent the substituent
  • the silyl group which may have a substituent includes, for example, a group represented by —Si ( RS1 ) ( RS2 ) ( RS3 ).
  • R S1 , R S2 , and R S3 independently have an alkyl group which may have a substituent, an alkoxy group which may have a substituent, an alkylthio group which may have a substituent, and a substituent.
  • the numerical range represented by using “-” means a range including the numerical values before and after "-" as the lower limit value and the upper limit value.
  • the hydrogen atom may be a light hydrogen atom (ordinary hydrogen atom) or a deuterium atom (double hydrogen atom or the like).
  • the photoelectric conversion element of the present invention is a photoelectric conversion element having a conductive film, a photoelectric conversion film, and a transparent conductive film in this order, and the photoelectric conversion film is a compound represented by the formula (1) (hereinafter referred to as a compound). , Also referred to as "specific compound”), and n-type semiconductor materials.
  • a compound represented by the formula (1)
  • specific compound also referred to as "specific compound”
  • n-type semiconductor materials n-type semiconductor materials.
  • the specific compound Since the specific compound has such a characteristic structure, it is presumed that the responsiveness of the photoelectric conversion element is excellent when the specific compound is used for the photoelectric conversion element. Further, the photoelectric conversion element having a photoelectric conversion film manufactured by using a specific compound is also excellent in heat resistance. It is believed that this is due to the rigid structure of the particular compound.
  • the excellent responsiveness and / or heat resistance of the obtained photoelectric conversion element is also simply referred to as "the effect of the present invention is excellent".
  • FIG. 1 shows a schematic cross-sectional view of an embodiment of the photoelectric conversion element of the present invention.
  • the photoelectric conversion element 10a shown in FIG. 1 includes a conductive film (hereinafter, also referred to as a lower electrode) 11 that functions as a lower electrode, an electron blocking film 16A, a photoelectric conversion film 12 containing a specific compound described later, and an upper electrode. It has a structure in which functional transparent conductive films (hereinafter, also referred to as upper electrodes) 15 are laminated in this order.
  • FIG. 2 shows a configuration example of another photoelectric conversion element.
  • FIGS. 1 and 2 has a configuration in which an electron blocking film 16A, a photoelectric conversion film 12, a hole blocking film 16B, and an upper electrode 15 are laminated in this order on a lower electrode 11.
  • the stacking order of the electron blocking film 16A, the photoelectric conversion film 12, and the hole blocking film 16B in FIGS. 1 and 2 may be appropriately changed depending on the application and characteristics.
  • the photoelectric conversion element 10a it is preferable that light is incident on the photoelectric conversion film 12 via the upper electrode 15. Further, when the photoelectric conversion element 10a (or 10b) is used, a voltage can be applied. In this case, it is preferable that the lower electrode 11 and the upper electrode 15 form a pair of electrodes, and a voltage of 1 ⁇ 10 -5 to 1 ⁇ 10 7 V / cm is applied between the pair of electrodes. From the viewpoint of performance and power consumption, the applied voltage is more preferably 1 ⁇ 10 -4 to 1 ⁇ 10 7 V / cm, further preferably 1 ⁇ 10 -3 to 5 ⁇ 10 6 V / cm.
  • the voltage application method it is preferable to apply the voltage so that the electron blocking film 16A side serves as the cathode and the photoelectric conversion film 12 side serves as the anode in FIGS. 1 and 2.
  • a voltage can be applied by the same method.
  • the photoelectric conversion element 10a (or 10b) can be suitably applied to an image sensor application.
  • the photoelectric conversion film is a film containing a specific compound.
  • the specific compound will be described in detail.
  • R a1 and R a2 each independently represent a hydrogen atom or a substituent.
  • substituent W which includes a halogen atom, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and a substituent.
  • An alkylthio group which may have a substituent, a silyl group which may have a substituent, an aryl group which may have a substituent, or a heteroaryl group which may have a substituent is preferable.
  • R a1 and R a2 are each independently preferably a hydrogen atom.
  • R a1 when a plurality of R a1 is present, R a1 may have respectively be the same or different where there exist a plurality. In the formula (1), when a plurality of R a2 are present, R a2 may have respectively be the same or different where there exist a plurality.
  • the 5-membered ring containing X 1 and Y 1 is an aromatic hetero ring
  • the 5-membered ring containing X 2 and Y 2 is an aromatic hetero ring.
  • it is preferable that one of X 1 and Y 1 represents -CR a1 and the other represents -O-, -S-, or -Se-.
  • Ra3 may have a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, an alkylthio group which may have a substituent, and a substituent.
  • R a3 when a plurality of R a3 is present, R a3 may have respectively be the same or different where there exist a plurality.
  • Ar 1 to Ar 4 each independently represent an aromatic ring group which may have a substituent.
  • the aromatic ring group may be monocyclic or polycyclic.
  • the aromatic ring group has one or more (preferably 1 to 3) heteroatoms (nitrogen atom, sulfur atom, oxygen atom, selenium atom, tellurium atom, phosphorus atom, silicon atom, and / or boron atom, etc.) as ring member atoms. ) May or may not be included.
  • the number of ring members of the aromatic ring group is preferably 5 to 18.
  • the monocyclic aromatic ring group includes, for example, a benzene ring group, a frill ring group, a pyridine ring group, a pyrazine ring group, a pyrimidine ring group, and a pyridazine ring group.
  • a polycyclic aromatic ring group is a group formed by condensing single rings having aromaticity.
  • a polycyclic aromatic ring group two or more of the ring member atoms of each monocycle (monocycle having aromaticity) constituting the polycyclic aromatic ring are other singles constituting the polycyclic aromatic ring group. It is also a ring member atom of a ring (a single ring having aromaticity).
  • the aromatic ring group is a polycyclic aromatic ring group
  • the polycyclic aromatic ring group includes, for example, a naphthalene ring group, an anthracene ring group, a quinoline ring group, an isoquinolin ring group, an acrydin ring group, and phenanthridin.
  • Ring group pteridine ring group, quinoxaline ring group, quinazoline ring group, cinnoline ring group, phthalazine ring group, benzoxazole ring group, benzothiazole ring group, benzimidazole ring group, indazole ring group, benzoisooxazole ring group, benzoiso Thiazole ring group, benzofuran ring group, benzothiophene ring group, benzoselenophen ring group, dibenzofuran ring group, dibenzothiophene ring group, dibenzoselenophen ring group, thienothiophene ring group, thienopyrol ring group, dithienopyrrole ring group, indol ring group , Imidazopyridine ring group, and carbazole ring group.
  • the substituent that the aromatic ring group in Ar 1 and Ar 2 may have is not L 1 . Further, the substituent that the aromatic ring group in Ar 2 may have is not Ar 1 . Similarly, the substituent that the aromatic ring group in Ar 3 and Ar 3 may have is not L 2 . Further, the substituent that the aromatic ring group in Ar 3 may have is not Ar 4 . Further, Ar 1 and Ar 2 are directly bonded to each other by a single bond specified in the formula (1). Similarly, Ar 3 and Ar 4 are directly bonded to each other by a single bond specified in the formula (1).
  • Examples of the substituent which the aromatic ring group in Ar 1 to Ar 4 may have include the substituent W, and among them, a halogen atom, an alkyl group which may have a substituent, and a substituent are included.
  • a aryl group which may have a substituent or a heteroaryl group which may have a substituent is preferable.
  • the aromatic ring group further has an aromatic ring group as a substituent.
  • Examples of the above-mentioned "aromatic ring group as a substituent” include the above-mentioned monocyclic aromatic ring group and polycyclic aromatic ring group.
  • the aromatic ring group further has an aromatic ring group as a substituent
  • one or more of these aromatic ring groups may have further different substituents.
  • the different substituents of each of these aromatic ring groups may be bonded to each other. That is, these aromatic ring groups may be bonded to each other by forming a further different ring between them.
  • the further different ring formed between these aromatic ring groups is a non-aromatic ring.
  • the aromatic ring group A further has an aromatic ring group B as a substituent
  • the aromatic ring group A may further have a substituent A
  • the aromatic ring group B further contains a substituent B. You may have.
  • Substituent A and substituent B may be bonded to each other to form a further different ring (non-aromatic ring) between the aromatic ring group A and the aromatic ring group B.
  • aromatic ring groups are bonded to each other by forming a further different ring (non-aromatic ring) between them, for example, these aromatic ring groups jointly form a fluorene ring group.
  • Ar 1 to Ar 4 preferably Ar 1 and / or Ar 4
  • Ar 2 and Ar 3 are preferably a monocyclic aromatic ring group which may have a substituent, and more preferably a benzene ring group which may have a substituent. Further, from the viewpoint that the effect of the present invention is more excellent, it is preferable that at least one of Ar 1 and Ar 2 is a benzene ring group which may have a substituent, and at least one of Ar 3 and Ar 4 has a substituent. It is also preferable that it is a benzene ring group which may have. As will be described later, Ar 1 and Ar 2 may have a bond via L 1 in addition to the single bond specified in the equation (1).
  • Ar 1 and Ar 2 are benzene ring groups which may have a substituent
  • Ar 1 and Ar 2 have a bond via L 1
  • Ar 1 and Ar 2 are jointly used.
  • a fluorene ring group which may have a substituent may be formed.
  • Ar 3 and Ar 4 may have a bond via L 2 in addition to the single bond specified in the formula (1).
  • Ar 3 and Ar 4 are benzene ring groups which may have a substituent
  • Ar 3 and Ar 4 have a bond via L 2
  • Ar 3 and Ar 4 are jointly used.
  • a fluorene ring group which may have a substituent may be formed.
  • Ar 1 and Ar 4 are polycyclic aromatic ring groups which may have substituents or groups represented by the formula (R), respectively. It is preferable to have it.
  • the number of ring members of the polycyclic aromatic ring group is preferably 9 to 18.
  • Examples of the polycyclic aromatic ring group are as described above, and a naphthalene ring group or a benzothiophene ring group is preferable.
  • * 1 and * 2 independently represent the coupling positions. Specifically, in Ar 1 which is a group represented by the formula (R), * 1 represents the bonding position with Ar 2 and * 2 represents the bonding position with (L 1 ) m 1 . In Ar 4 which is a group represented by the formula (R), * 1 represents a bond position with Ar 3 and * 2 represents a bond position with (L 2 ) m 2 . However, as described later, m1 and m2 may be 0. In Ar 1 which is a group represented by the formula (R), when m1 is 0, * 2 does not exist. In Ar 4 which is a group represented by the formula (R), when m2 is 0, * 2 does not exist.
  • Ar X represents a monocyclic aromatic ring group which may have a substituent other than Ar Y.
  • Examples of the monocyclic aromatic ring group are as described above, and among them, a benzene ring group is preferable.
  • Ar Y represents an aromatic ring group which may have a substituent.
  • Examples of the aromatic ring group of Ar Y include the above-mentioned monocyclic aromatic ring group and the above-mentioned polycyclic aromatic ring group, and among them, the benzene ring group is preferable.
  • the monocyclic aromatic ring group in Ar X and the aromatic ring group in Ar Y have ring-membered atoms bonded to each other by a single bond.
  • Examples of the substituent that the monocyclic aromatic ring group in Ar X may have other than Ar Y and the substituent that the aromatic ring group in Ar Y may have include the substituent W. It is also preferable that the monocyclic aromatic ring group in Ar X has no substituent other than Ar Y. Further, the substituent which the aromatic ring group may have in Ar Y has a halogen atom, an alkyl group which may have a substituent, an aryl group which may have a substituent, or a substituent. Heteroaryl groups may be preferred. However, the substituent that the monocyclic aromatic ring group in Ar X may have other than Ar Y and the substituent that the aromatic ring group in Ar Y may have do not bond to each other. That is, Ar X and Ar Y are not combined except for the single bond specified in the formula (R). For example, the group represented by the formula (R) does not include a fluorene ring group.
  • m1 and m2 independently represent 0 or 1, respectively.
  • L 1 and L 2 independently form -S-, -O-, -Se- , -SiR a4 R a5- , -NR a6- , or -CR a7 R a8- , respectively.
  • R a4 to R a8 are independently hydrogen atom, halogen atom, alkyl group which may have a substituent, alkoxy group which may have a substituent, and an alkylthio group which may have a substituent.
  • L 1 and L 2 each independently, -CR a7 R a8 - preferably, R a7 and R a8 are -CR a7 R a8 is an alkyl group which may have a substituent - are more preferred, -C (CH 3 ) 2 -is more preferable.
  • L 1 is directly bonded to each aromatic ring group in Ar 1 and Ar 2 .
  • L 2 is directly attached to the respective aromatic ring groups in Ar 3 and Ar 4 .
  • the compound represented by the formula (1) is represented by the compound represented by the formula (2), the compound represented by the formula (3), or the compound represented by the formula (4). It is preferably a compound. Among them, the compound represented by the formula (1) is more preferably the compound represented by the formula (3).
  • Y 3 and Y 4 independently represent -O-, -S-, or -Se-, respectively.
  • R 1 to R 4 independently have a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and a substituent. It represents an alkylthio group which may have a substituent, a silyl group which may have a substituent, an aryl group which may have a substituent, or a heteroaryl group which may have a substituent.
  • Ar 1 to Ar 4 each independently represent an aromatic ring group which may have a substituent.
  • m1 and m2 independently represent 0 or 1, respectively.
  • L 1 and L 2 independently form -S-, -O-, -Se- , -SiR a4 R a5- , -NR a6- , or -CR a7 R a8- , respectively.
  • R a4 to R a8 independently have a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and a substituent.
  • alkylthio group which may have a substituent a silyl group which may have a substituent, an alkenyl group which may have a substituent, an alkynyl group which may have a substituent, an aryl group which may have a substituent, Alternatively, it represents a heteroaryl group which may have a substituent.
  • m1 represents 0, L 1 is absent, and Ar 1 and Ar 2 are connected only by a single bond, which is specified in the above formula (2).
  • m2 represents 0, L 2 does not exist, and Ar 3 and Ar 4 are connected only by the single bond specified in the above equation (2).
  • Ar 1 to Ar 4 , m1, m2, L 1 , L 2 and R a4 to R a8 in the formula (2) are Ar 1 to Ar 4 , m1, m2, L 1 , in the formula (1). It is the same as L 2 and R a4 to R a8 , respectively.
  • Y 3 and X 3 independently represent -O-, -S-, or -Se-, respectively.
  • R 1 to R 3 and R 5 are independently a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and a substituent, respectively.
  • Ar 1 to Ar 4 each independently represent an aromatic ring group which may have a substituent.
  • m1 and m2 independently represent 0 or 1, respectively.
  • L 1 and L 2 independently form -S-, -O-, -Se- , -SiR a4 R a5- , -NR a6- , or -CR a7 R a8- , respectively.
  • R a4 to R a8 independently have a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and a substituent.
  • alkylthio group which may have a substituent a silyl group which may have a substituent, an alkenyl group which may have a substituent, an alkynyl group which may have a substituent, an aryl group which may have a substituent, Alternatively, it represents a heteroaryl group which may have a substituent.
  • m1 represents 0, L 1 is absent, and Ar 1 and Ar 2, are connected only by a single bond, which is specified in the above formula (3).
  • m2 represents 0, L 2 does not exist, and Ar 3 and Ar 4 are connected only by the single bond specified in the above equation (3).
  • Ar 1 to Ar 4 , m1, m2, L 1 , L 2 and R a4 to R a8 in the formula (3) are Ar 1 to Ar 4 , m1, m2, L 1 , L 1 in the formula (1). It is the same as L 2 and R a4 to R a8 , respectively.
  • X 3 and X 4 independently represent -O-, -S-, or -Se-, respectively.
  • R 1 to R 2 and R 5 to R 6 independently have a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, and an alkoxy group which may have a substituent.
  • Ar 1 to Ar 4 each independently represent an aromatic ring group which may have a substituent.
  • m1 and m2 independently represent 0 or 1, respectively.
  • L 1 and L 2 independently form -S-, -O-, -Se- , -SiR a4 R a5- , -NR a6- , or -CR a7 R a8- , respectively.
  • R a4 to R a8 independently have a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an alkoxy group which may have a substituent, and a substituent.
  • alkylthio group which may have a substituent a silyl group which may have a substituent, an alkenyl group which may have a substituent, an alkynyl group which may have a substituent, an aryl group which may have a substituent, Alternatively, it represents a heteroaryl group which may have a substituent.
  • m1 represents 0, L 1 is absent, and Ar 1 and Ar 2, are connected only by a single bond which is expressly in the formula (4).
  • m2 represents 0, L 2 does not exist, and Ar 3 and Ar 4 are connected only by the single bond specified in the above equation (4).
  • Ar 1 ⁇ Ar 4 in, m1, m2, L 1, L 2 and,, R a4 ⁇ R a8 are, Ar 1 ⁇ Ar 4 in the formula (1), m1, m2, L 1, It is the same as L 2 and R a4 to R a8 , respectively.
  • the molecular weight of the specific compound is not particularly limited, and is preferably 425 to 1200, more preferably 450 to 900. When the molecular weight is 1200 or less, the vapor deposition temperature does not rise and the decomposition of the compound is unlikely to occur. When the molecular weight is 425 or more, the glass transition point of the vapor-deposited film is not lowered, and the heat resistance of the photoelectric conversion element is improved.
  • the specific compound may be used alone or in combination of two or more.
  • the specific compound is particularly useful as a material for a photoelectric conversion film used in an image sensor or an optical sensor.
  • the specific compound can also be used as a coloring material, a liquid crystal material, an organic semiconductor material, a charge transport material, a pharmaceutical material, and a fluorescence diagnostic agent material.
  • the specific compound is preferably a compound having an ionization potential of -5.0 to -6.0 eV in a single membrane in terms of matching the energy level with the n-type semiconductor material described later.
  • the maximum absorption wavelength of the specific compound is not particularly limited, and is preferably in the range of, for example, 300 to 500 nm.
  • the maximum absorption wavelength is a value measured in a solution state (solvent: chloroform) by adjusting the absorption spectrum of the specific compound to a concentration such that the absorbance becomes 0.5 to 1.
  • the maximum absorption wavelength of the photoelectric conversion film is not particularly limited, and is preferably in the range of, for example, 300 to 700 nm.
  • the photoelectric conversion film contains an n-type semiconductor material as a component other than the above-mentioned specific compound.
  • the n-type semiconductor material is an acceptor-type organic semiconductor material (compound), and refers to an organic compound having a property of easily accepting electrons. More specifically, the n-type semiconductor material refers to an organic compound having a higher electron affinity than the specific compound when used in contact with the above-mentioned specific compound.
  • the electron affinity of the n-type semiconductor material is preferably 3.0 to 5.0 eV.
  • the n-type semiconductor material includes, for example, fullerenes selected from the group consisting of fullerene and derivatives thereof, condensed aromatic carbocyclic compounds (for example, naphthalene derivatives, anthracene derivatives, phenanthrene derivatives, tetracene derivatives, pyrene derivatives, perylene derivatives, and , Fluolanthene derivative); 5- to 7-membered heterocyclic compound having at least one nitrogen atom, oxygen atom, and sulfur atom (eg, pyridine, pyrazine, pyrimidine, pyridazine, triazine, quinoline, quinoxalin, quinazoline, phthalazine) , Synnoline, Isoquinolin, Pteridine, Aclysine, Phenazine, Phenantroline, Tetrazole, Pyrazole, Imidazole, and Thiazole, etc.); Polyarylene compounds; Fluorene compounds; Cyclop
  • the n-type semiconductor material preferably contains fullerenes selected from the group consisting of fullerenes and derivatives thereof.
  • fullerenes include fullerenes C60, fullerenes C70, fullerenes C76, fullerenes C78, fullerenes C80, fullerenes C82, fullerenes C84, fullerenes C90, fullerenes C96, fullerenes C240, fullerenes C540, and mixed fullerenes.
  • the fullerene derivative include compounds in which a substituent is added to the fullerene.
  • the substituent is preferably an alkyl group, an aryl group, or a heterocyclic group.
  • the fullerene derivative the compound described in JP-A-2007-123707 is preferable.
  • the thickness) ⁇ 100) in terms of a single layer is preferably 15 to 100% by volume, more preferably 35 to 100% by volume.
  • An organic dye may be used as the n-type semiconductor material in place of the n-type semiconductor material described in the upper row or together with the n-type semiconductor material described in the upper row.
  • an organic dye By using an organic dye as the n-type semiconductor material, it is easy to control the absorption wavelength (maximum absorption wavelength) of the photoelectric conversion element in an arbitrary wavelength range.
  • the organic pigments include, for example, cyanine pigments, styryl pigments, hemicyanine pigments, merocyanine pigments (including zero methine merocyanin (simple merocyanin)), rodacianin pigments, allopolar pigments, oxonols pigments, hemioxonor pigments, squalium pigments, croconium pigments, etc.
  • the n-type semiconductor material contains an organic dye
  • the film thickness) ⁇ 100) in terms of a single layer is preferably 15 to 100% by volume, more preferably 35 to 100% by volume.
  • the molecular weight of the n-type semiconductor material is preferably 200 to 1200, more preferably 200 to 1000.
  • the photoelectric conversion film preferably has a bulk heterostructure formed in a state where a specific compound and an n-type semiconductor material are mixed.
  • the bulk heterostructure is a layer in which a specific compound and an n-type semiconductor material are mixed and dispersed in a photoelectric conversion film.
  • the bulk heterostructure is described in detail in paragraphs [0013] to [0014] of JP-A-2005-303266.
  • the film thickness of the n-type semiconductor material (thickness in terms of a single layer) ⁇ 100) is preferably 15 to 75% by volume, more preferably 35 to 75% by volume.
  • the photoelectric conversion film is substantially composed of a specific compound and an n-type semiconductor material. Substantially means that the total content of the specific compound and the n-type semiconductor material is 95% by mass or more with respect to the total mass of the photoelectric conversion film.
  • the n-type semiconductor material contained in the photoelectric conversion film may be used alone or in combination of two or more.
  • the photoelectric conversion film containing a specific compound is a non-luminescent film, and has characteristics different from those of an organic electroluminescent device (OLED: Organic Light Emitting Diode).
  • the non-emission film is intended to be a film having an emission quantum efficiency of 1% or less, and an emission quantum efficiency of 0.5% or less is preferable, and 0.1% or less is more preferable.
  • the photoelectric conversion film can be formed mainly by a dry film forming method.
  • the dry film forming method includes, for example, a physical vapor deposition method such as a vapor deposition method (particularly a vacuum vapor deposition method), a sputtering method, an ion plating method, an MBE (Molecular Beam Epitaxy) method, and a CVD method such as plasma polymerization. (Chemical Vapor Deposition) method can be mentioned. Of these, the vacuum deposition method is preferable.
  • the manufacturing conditions such as the degree of vacuum and the vapor deposition temperature can be set according to a conventional method.
  • the thickness of the photoelectric conversion film is preferably 10 to 1000 nm, more preferably 50 to 800 nm, further preferably 50 to 500 nm, and particularly preferably 50 to 300 nm.
  • the electrodes are made of a conductive material.
  • the conductive material include metals, alloys, metal oxides, electrically conductive compounds, and mixtures thereof. Since light is incident from the upper electrode 15, it is preferable that the upper electrode 15 is transparent to the light to be detected.
  • the material constituting the upper electrode 15 is, for example, antimony or fluorine-doped tin oxide (ATO: Antimony Tin Oxide, FTO: Fluorine topped Tin Oxide), tin oxide, zinc oxide, indium oxide, indium tin oxide (ITO: Conductive metal oxides such as Indium Tin Oxide) and indium zinc oxide (IZO); metal thin films such as gold, silver, chromium, and nickel; these metals and conductive metal oxides Mixtures or laminates; and organic conductive materials such as polyaniline, polythiophene, and polypyrrole, and the like. Of these, conductive metal oxides are preferable from the viewpoints of high conductivity and transparency.
  • the sheet resistance is preferably 100 to 10000 ⁇ / ⁇ .
  • the degree of freedom in the range of film thickness that can be thinned is large.
  • Increasing the light transmittance is preferable because it increases the light absorption in the photoelectric conversion film and increases the photoelectric conversion ability.
  • the film thickness of the upper electrode 15 is preferably 5 to 100 nm, more preferably 5 to 20 nm.
  • the lower electrode 11 may be transparent or may reflect light without being transparent, depending on the intended use.
  • the materials constituting the lower electrode 11 are, for example, antimony or fluorine-doped tin oxide (ATO, FTO), tin oxide, zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO).
  • Conductive metal oxides such as gold, silver, chromium, nickel, titanium, tungsten, and metals such as aluminum, oxides of these metals, or conductive compounds such as nitrides (as an example, titanium nitride (TiN)). ); Mixtures or laminates of these metals and conductive metal oxides; and organic conductive materials such as polyaniline, polythiophene, and polypyrrole.
  • the method for forming the electrode is not particularly limited and can be appropriately selected depending on the electrode material. Specifically, a wet method such as a printing method and a coating method; a physical method such as a vacuum deposition method, a sputtering method, and an ion plating method; and a chemical method such as CVD and a plasma CVD method. , Etc. can be mentioned.
  • a wet method such as a printing method and a coating method
  • a physical method such as a vacuum deposition method, a sputtering method, and an ion plating method
  • a chemical method such as CVD and a plasma CVD method.
  • Etc. can be mentioned.
  • the electrode material is ITO
  • methods such as an electron beam method, a sputtering method, a resistance heating vapor deposition method, a chemical reaction method (sol-gel method, etc.), and a dispersion of indium tin oxide can be mentioned.
  • the photoelectric conversion element of the present invention preferably has one or more intermediate layers in addition to the photoelectric conversion film between the conductive film and the transparent conductive film.
  • the intermediate layer include a charge blocking film.
  • the charge blocking film include an electron blocking film and a hole blocking film. Each film will be described in detail below.
  • the electron blocking film is a donor organic semiconductor material (compound), and for example, the following p-type organic semiconductors can be used.
  • One type of p-type organic semiconductor may be used alone, or two or more types may be used.
  • the p-type organic semiconductor is, for example, a triarylamine compound (for example, N, N'-bis (3-methylphenyl)-(1,1'-biphenyl) -4,4'-diamine (TPD), 4,4.
  • TPD triarylamine
  • '-Bis [N- (naphthyl) -N-phenyl-amino] biphenyl ( ⁇ -NPD) a compound described in paragraphs [0128] to [0148] of JP2011-228614A, JP-A-2011-176259.
  • JP2011-228614A JP-A-2011-176259.
  • Pyrazole compounds polyarylene compounds, condensed aromatic carbocyclic compounds (eg, naphthalene derivatives, anthracene derivatives, phenanthrene derivatives, tetracene derivatives, pentacene derivatives, pyrene derivatives, perylene derivatives, and fluorantene derivatives. Body), porphyrin compounds, phthalocyanine compounds, triazole compounds, oxadiazole compounds, imidazole compounds, polyarylalkane compounds, pyrazolone compounds, amino-substituted calcon compounds, oxazole compounds, fluorenone compounds, silazane compounds, and nitrogen-containing heterocyclic compounds.
  • condensed aromatic carbocyclic compounds eg, naphthalene derivatives, anthracene derivatives, phenanthrene derivatives, tetracene derivatives, pentacene derivatives, pyrene derivatives, perylene derivatives, and fluorantene derivatives
  • Examples thereof include a metal complex having as a ligand.
  • Examples of the p-type organic semiconductor include compounds having a smaller ionization potential than the n-type semiconductor material, and if this condition is satisfied, the organic dye exemplified as the n-type semiconductor material can also be used.
  • a polymer material can also be used as the electron blocking film.
  • the polymer material include polymers such as phenylene vinylene, fluorene, carbazole, indole, pyrrole, pyrrole, picolin, thiophene, acetylene, and diacetylene, and derivatives thereof.
  • the electron blocking film may be composed of a plurality of films.
  • the electron blocking film may be made of an inorganic material.
  • Inorganic materials that can serve as electron blocking films include, for example, calcium oxide, chromium oxide, copper oxide, manganese oxide, cobalt oxide, nickel oxide, copper oxide, gallium copper oxide, strontium oxide copper, niobium oxide, molybdenum oxide, and indium copper oxide. , Indium silver oxide, and iridium oxide.
  • the hole blocking film is an acceptor-type organic semiconductor material (compound), and the above-mentioned n-type semiconductor material can be used.
  • the method for producing the charge blocking film is not particularly limited, and examples thereof include a dry film forming method and a wet film forming method.
  • the dry film forming method include a vapor deposition method and a sputtering method.
  • the vapor deposition method may be any of a physical vapor deposition (PVD) method and a chemical vapor deposition (CVD) method, and a physical vapor deposition method such as a vacuum vapor deposition method is preferable.
  • Examples of the wet film forming method include an inkjet method, a spray method, a nozzle printing method, a spin coating method, a dip coating method, a casting method, a die coating method, a roll coating method, a bar coating method, and a gravure coating method. From the viewpoint of precision patterning, the inkjet method is preferable.
  • the thickness of the charge blocking film is preferably 3 to 200 nm, more preferably 5 to 100 nm, and even more preferably 5 to 30 nm, respectively.
  • the photoelectric conversion element may further have a substrate.
  • the type of substrate used is not particularly limited, and examples thereof include a semiconductor substrate, a glass substrate, and a plastic substrate.
  • the position of the substrate is not particularly limited, and usually, a conductive film, a photoelectric conversion film, and a transparent conductive film are laminated on the substrate in this order.
  • the photoelectric conversion element may further have a sealing layer.
  • the performance of the photoelectric conversion material may be significantly deteriorated due to the presence of deterioration factors such as water molecules. Therefore, the entire photoelectric conversion film is coated with a ceramic such as a dense metal oxide, metal nitride, or metal nitride that does not allow water molecules to permeate, or a sealing layer such as diamond-like carbon (DLC: Diamond-like Carbon). The above deterioration can be prevented by coating and sealing.
  • the sealing layer may be selected and manufactured as a material in accordance with paragraphs [0210] to [0215] of JP2011-082508.
  • An image sensor is an element that converts optical information of an image into an electric signal.
  • a plurality of photoelectric conversion elements are arranged on a matrix in the same plane, and each photoelectric conversion element (pixel) has an optical signal. Is converted into an electric signal, and the electric signal can be sequentially output to the outside of the image sensor for each pixel. Therefore, each pixel is composed of one or more photoelectric conversion elements and one or more transistors.
  • FIG. 3 is a schematic cross-sectional view showing a schematic configuration of an image pickup device for explaining an embodiment of the present invention.
  • This image pickup element is mounted on an image pickup element such as a digital camera and a digital video camera, an electronic endoscope, and an image pickup module such as a mobile phone.
  • the imaging element 20a shown in FIG. 3 includes a photoelectric conversion element 10a (green photoelectric conversion element 10a) of the present invention, a blue photoelectric conversion element 22, and a red photoelectric conversion element 24, and these include a direction in which light is incident. Are laminated.
  • the photoelectric conversion element 10a is the photoelectric conversion element of the present invention, and is mainly used as a green photoelectric conversion element by controlling the absorption wavelength so that green light can be received. Examples of the method of controlling the absorption wavelength of the photoelectric conversion element of the present invention include a method of using an organic dye suitable as an n-type semiconductor material.
  • the image sensor 20a is a so-called laminated body type color-separated image sensor.
  • the wavelength spectra detected by the photoelectric conversion element 10a, the blue photoelectric conversion element 22, and the red photoelectric conversion element 24 are different from each other. That is, the blue photoelectric conversion element 22 and the red photoelectric conversion element 24 correspond to photoelectric conversion elements that receive light having a wavelength different from the light received (absorbed) by the photoelectric conversion element 10a.
  • the photoelectric conversion element 10a can mainly receive green light
  • the blue photoelectric conversion element 22 can mainly receive blue light
  • the red photoelectric conversion element can mainly receive red light.
  • the green light is intended to be light having a wavelength in the range of 500 to 600 nm
  • the blue light is intended to be light in the wavelength range of 400 to 500 nm
  • the red light is intended to be light in the wavelength range of 600 to 700 nm.
  • the photoelectric conversion element 10a mainly absorbs green light, but blue light and red light pass through the photoelectric conversion element 10a.
  • the blue light is mainly absorbed, but the red light is transmitted through the blue photoelectric conversion element 22.
  • the red photoelectric conversion element 24 is absorbed by the red photoelectric conversion element 24.
  • the image sensor 20a which is a laminated color-separated image sensor, one pixel can be composed of three light receiving units of green, blue, and red, and a large area of the light receiving unit can be obtained.
  • the configurations of the blue photoelectric conversion element 22 and the red photoelectric conversion element 24 are not particularly limited.
  • a photoelectric conversion element having a configuration in which silicon is used to separate colors according to the difference in light absorption length may be used.
  • the blue photoelectric conversion element 22 and the red photoelectric conversion element 24 may both be made of silicon.
  • the photoelectric conversion element 10a mainly receives the green light having the middle wavelength, and the remaining blue light. And red light can be easily separated.
  • blue light is easily absorbed near the surface of silicon, and red light reaches a relatively deep position in silicon. Can invade.
  • blue light is mainly received by the blue photoelectric conversion element 22 existing at a shallower position
  • red light is mainly received by the red photoelectric conversion element 24 existing at a deeper position.
  • the blue photoelectric conversion element 22 and the red photoelectric conversion element 24 have a conductive film, an organic photoelectric conversion film having a maximum absorption maximum for blue light or red light, and a transparent conductive film formation in this order.
  • a photoelectric conversion element (blue photoelectric conversion element 22 or red photoelectric conversion element 24) may be used.
  • the blue photoelectric conversion element 22 may be the photoelectric conversion element of the present invention in which the absorption wavelength is controlled so that the blue light has an absorption maximum.
  • the red photoelectric conversion element 24 may be the photoelectric conversion element of the present invention in which the absorption wavelength is controlled so that the red light has an absorption maximum.
  • the photoelectric conversion element, the blue photoelectric conversion element, and the red photoelectric conversion element of the present invention are arranged in this order from the incident side of the light, but the present invention is not limited to this, and the arrangement is not limited to this. You may.
  • the blue photoelectric conversion element, the photoelectric conversion element of the present invention, and the red photoelectric conversion element may be arranged in this order from the side where the light is incident.
  • the green photoelectric conversion element may be used as a photoelectric conversion element other than the photoelectric conversion element of the present invention, and the blue photoelectric conversion element and / or the red photoelectric conversion element may be used as the photoelectric conversion element of the present invention.
  • the configuration in which the photoelectric conversion elements of the three primary colors of blue, green, and red are stacked has been described, but the number of layers (2 colors) or 4 layers (4 colors) or more is large. It doesn't matter.
  • the photoelectric conversion element 10a of the present invention may be arranged on the arranged blue photoelectric conversion element 22 and the red photoelectric conversion element 24. If necessary, a color filter that further absorbs light having a predetermined wavelength may be arranged on the incident side of the light.
  • the form of the image sensor is not limited to that shown in FIG. 3 and the above-mentioned form, and may be another form.
  • the photoelectric conversion element, the blue photoelectric conversion element, and the red photoelectric conversion element of the present invention may be arranged at the same in-plane position.
  • the photoelectric conversion element may be used in a single layer.
  • a blue, red, and green color filters may be arranged on the photoelectric conversion element 10a of the present invention to separate colors.
  • the photoelectric conversion element of the present invention may be used by the photoelectric conversion element alone, or may be used as a line sensor in which the photoelectric conversion element is arranged in a straight line, or a two-dimensional sensor in which the photoelectric conversion element is arranged on a plane.
  • the present invention also includes the invention of a material for a photoelectric conversion element.
  • the material for a photoelectric conversion element of the present invention is a material used for manufacturing a photoelectric conversion element (preferably a photoelectric conversion element for an image sensor or an optical sensor) containing a compound (specific compound) represented by the formula (1).
  • a photoelectric conversion element preferably a photoelectric conversion element for an image sensor or an optical sensor
  • the compound represented by the formula (1) in the material for a photoelectric conversion element is the same as the compound represented by the above formula (1), and the preferable conditions are also the same. It is preferable that each of the specific compounds contained in the material for the photoelectric conversion element is used for producing the photoelectric conversion film of the photoelectric conversion film contained in the photoelectric conversion element.
  • the content of the specific compound contained in the material for the photoelectric conversion element is preferably 30 to 100% by mass, more preferably 70 to 100% by mass, and 99 to 100% by mass, respectively, of the total mass of the material for the photoelectric conversion element. More preferred.
  • the specific compound contained in the material for the photoelectric conversion element may be one kind alone or two or more kinds.
  • Titanium tetrachloride (12.4 g, 65.3 mmol) was dissolved in THF (tetrahydrofuran, 455 mL) in a 1000 mL three-necked flask under a nitrogen atmosphere. Further, after the liquid temperature in the flask was set to ⁇ 10 ° C., zinc powder (8.54 g, 131 mmol) was added to the flask. THF of intermediate 7a (2.42 g, 10.9 mmol; synthesized according to the synthetic method of S4j described in Supporting information of Chemistry A European Journal 2015, 21, 12871-12875) while heating and refluxing the obtained mixture. The (200 mL) solution was added over 5 hours.
  • THF tetrahydrofuran
  • reaction product was purified by silica gel column chromatography to obtain 1.73 g of Intermediate 7b. Yield 84%.
  • the measurement results of the intermediate 7b by ESI-MS were as follows.
  • a dehydrated THF (7 mL) solution of tributyltin chloride (2.6 g, 7.9 mmol) was added dropwise to the solution while maintaining the internal temperature of the solution at ⁇ 66 ° C. or lower, and then the solution was added to room temperature (7 mL). The temperature was returned to 23 ° C.) and reacted at room temperature for 1 hour to obtain a reaction solution.
  • Water (50 mL) was measured in a 300 mL Erlenmeyer flask, and the obtained reaction solution was added thereto to stop the reaction.
  • the reaction product contained in the obtained liquid was extracted with ethyl acetate.
  • the organic phase containing the reaction product obtained by the extraction treatment was dried over sodium sulfate and concentrated under reduced pressure.
  • the photoelectric conversion element includes a lower electrode 11, an electron blocking film 16A, a photoelectric conversion film 12, a hole blocking film 16B, and an upper electrode 15.
  • an amorphous ITO is formed on a glass substrate by a sputtering method to form a lower electrode 11 (thickness: 30 nm), and the following compound (B-1) is further vacuumed on the lower electrode 11.
  • An electron blocking film 16A was formed by forming a film by a heat vapor deposition method.
  • a photoelectric conversion film 12 having a bulk heterostructure of 200 nm was formed by co-depositing and forming a film by a vacuum vapor deposition method so as to have a temperature of 100 nm and 100 nm (photoelectric conversion film forming step). Further, the following compound (B-2) was formed on the photoelectric conversion film 12 to form a hole blocking film 16B (thickness: 10 nm).
  • an amorphous ITO was formed on the hole blocking film 16B by a sputtering method to form an upper electrode 15 (transparent conductive film) (thickness: 10 nm).
  • a SiO film is formed on the upper electrode 15 as a sealing layer by a vacuum vapor deposition method, and then an aluminum oxide (Al 2 O 3 ) layer is formed on the SiO film by an ALCVD (Atomic Layer Chemical Vapor Deposition) method to form a photoelectric conversion element.
  • ALCVD Atomic Layer Chemical Vapor Deposition
  • the responsiveness of each of the obtained elements (A) was evaluated. A voltage is applied so that the electric field intensity of 1.0 ⁇ 10 5 V / cm in each element (A), was irradiated with light of 400nm from the upper electrode (transparent conductive film) side. Assuming that the value of the photocurrent 10 milliseconds after the start of irradiation was 100%, the time required for the photocurrent to reach 97% or more was calculated. The responsiveness of each element (A) was evaluated by a relative value when the value of the element (A) of Example 1 (the time required for the photocurrent to reach 97% or more) was set to 1.
  • Evaluation was performed with a relative value of 0.5 or less as A, a value larger than 0.5 and 1 or less as B, a value larger than 1 and 2 or less as C, and a value larger than 2 as D. Practically, A or B is preferable, and A is more preferable. The results are shown in Table 1.
  • Table 1 below shows the results of tests conducted using photoelectric conversion elements manufactured using each compound.
  • Table 1 below shows the results of tests conducted using photoelectric conversion elements manufactured using each compound.
  • the column "Formula (3)” indicates whether or not the specific compound used corresponds to the compound represented by the formula (3). If this requirement is met, it is designated as A, and if it is not met, it is designated as B.
  • the photoelectric conversion element of the present invention using a specific compound for the photoelectric conversion film has excellent responsiveness. It was also confirmed that the photoelectric conversion element of the present invention is also excellent in heat resistance.
  • the photoelectric conversion element using the compound R-1 in which the aromatic ring group corresponding to Ar 1 and Ar 4 in the formula (1) does not exist has insufficient responsiveness.
  • the heat resistance was also inferior to that of the photoelectric conversion element of the present invention.
  • the photoelectric conversion element using the compound R-2 having a mother nucleus having a structure different from that of the specific compound had insufficient responsiveness.
  • the heat resistance was also inferior to that of the photoelectric conversion element of the present invention.
  • the group corresponding to the group represented by Ar 1 or Ar 4 in the formula (1) in the specific compound is represented by a polycyclic aromatic ring group which may have a substituent or a formula (R). It was confirmed that the obtained photoelectric conversion element has more excellent heat resistance in the case of a group (see the results of Examples 2, 3, 6, 7, 8 and the like).

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  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
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Abstract

La présente invention concerne un élément de conversion photoélectrique ayant une excellente sensibilité, et concerne également un élément d'imagerie, un capteur optique et un matériau d'élément de conversion photoélectrique. Cet élément de conversion photoélectrique comprend, dans l'ordre donné, un film conducteur (11), un film de conversion photoélectrique (12) et un film conducteur transparent (15). Le film de conversion photoélectrique contient un composé représenté par la formule (1) et un matériau semi-conducteur de type n.
PCT/JP2020/022287 2019-06-28 2020-06-05 Élément de conversion photoélectrique, élément d'imagerie, capteur optique et matériau d'élément de conversion photoélectrique WO2020261933A1 (fr)

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