WO2017086115A1 - Photoelectric conversion element and solid-state image capture device - Google Patents
Photoelectric conversion element and solid-state image capture device Download PDFInfo
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- WO2017086115A1 WO2017086115A1 PCT/JP2016/081867 JP2016081867W WO2017086115A1 WO 2017086115 A1 WO2017086115 A1 WO 2017086115A1 JP 2016081867 W JP2016081867 W JP 2016081867W WO 2017086115 A1 WO2017086115 A1 WO 2017086115A1
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- photoelectric conversion
- atom
- conversion element
- electrode
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Images
Classifications
-
- 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
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices 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; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/08—Semiconductor devices 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; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof in which radiation controls flow of current through the device, e.g. photoresistors
- H01L31/10—Semiconductor devices 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; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof in which radiation controls flow of current through the device, e.g. photoresistors characterised by at least one potential-jump barrier or surface barrier, e.g. phototransistors
-
- 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 disclosure relates to, for example, a photoelectric conversion element using an organic semiconductor and a solid-state imaging device including the photoelectric conversion element.
- CCD Charge Coupled Device
- CMOS Complementary Metal Oxide Semiconductor
- Patent Document 1 discloses an organic photosensitive device in which external quantum efficiency is improved by constituting a blocking layer and a charge transport layer with a subphthalocyanine compound.
- a photoelectric conversion element is provided between a first electrode and a second electrode arranged to face each other, and between the first electrode and the second electrode, and has a conjugate plane and is included in the conjugate plane.
- a photoelectric conversion layer including a conjugated compound having a first atom in which the substituent R is directly bonded in a direction substantially perpendicular to the conjugate plane.
- the substituent R is attached to the first atom.
- the bond angle of the second atom that has the second atom directly bonded and the third atom directly bonded to the second atom and forms a bond with the first atom and the third atom is fixed.
- the solid-state imaging device includes each pixel including one or a plurality of organic photoelectric conversion units, and the solid-state imaging device according to the embodiment of the present disclosure as the organic photoelectric conversion unit.
- the photoelectric conversion layer between the first electrode and the second electrode that are arranged to face each other has a conjugate plane and is included in the conjugate plane.
- the substituent R of the conjugated compound has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom And a molecular structure in which the bond angle of the second atom forming the bond is fixed.
- the substituent is added to the first atom that is included in the conjugate plane and has a bond angle substantially perpendicular to the conjugate plane. Since the photoelectric conversion layer is formed using a conjugated compound in which R is directly bonded, the degree of freedom of rotation of the substituent R is reduced, and the occurrence of migration of the conjugated compound is suppressed. Therefore, the heat resistance of the photoelectric conversion layer is improved, and a photoelectric conversion element having high heat resistance and a solid-state imaging device including the photoelectric conversion element can be provided. Note that the effects described here are not necessarily limited, and may be any effects described in the present disclosure.
- FIG. 4A It is sectional drawing showing schematic structure of the photoelectric conversion element which concerns on embodiment of this indication. It is a schematic diagram showing the structure of the conjugated compound used for the organic photoelectric converting layer of this indication. It is a top view showing the formation positional relationship of an organic photoelectric converting layer, a protective film (upper electrode), and a contact hole. It is sectional drawing showing the example of 1 structure of an inorganic photoelectric conversion part. It is other sectional drawing of the inorganic photoelectric conversion part shown to FIG. 4A. It is sectional drawing showing the structure (lower side electron extraction) of the electric charge (electron) storage layer of an organic photoelectric conversion part. It is sectional drawing for demonstrating the manufacturing method of the photoelectric conversion element shown in FIG.
- FIG. 6A It is sectional drawing showing the process of following FIG. 6B. It is sectional drawing showing the process of following FIG. 7A. It is sectional drawing showing the process of following FIG. 7B. It is sectional drawing showing the process of following FIG. 8A. It is sectional drawing showing the process of following FIG. 8B. It is principal part sectional drawing explaining the effect
- FIG. 1 illustrates a cross-sectional configuration of a photoelectric conversion element (photoelectric conversion element 10) according to an embodiment of the present disclosure.
- the photoelectric conversion element 10 constitutes one pixel in a solid-state imaging device (described later) such as a CCD image sensor or a CMOS image sensor.
- a pixel transistor including transfer transistors Tr1 to 3 described later
- a multilayer wiring layer multilayer wiring
- one organic photoelectric conversion unit 11G that selectively detects light in different wavelength ranges and performs photoelectric conversion, and two inorganic photoelectric conversion units 11B and 11R are in the vertical direction.
- the organic photoelectric conversion unit 11G has a conjugate plane, is included in the conjugate plane, and has an atom M (the first M) in which the substituent R is directly bonded in a direction substantially perpendicular to the conjugate plane. Formed by using a conjugated compound having the above-mentioned atoms).
- the photoelectric conversion element 10 has a laminated structure of one organic photoelectric conversion unit 11G and two inorganic photoelectric conversion units 11B and 11R. With this, red (R) and green (G) are obtained with one element. , Blue (B) color signals are acquired.
- the organic photoelectric conversion unit 11G is formed on the back surface (surface S1) of the semiconductor substrate 11, and the inorganic photoelectric conversion units 11B and 11R are embedded in the semiconductor substrate 11.
- the organic photoelectric conversion unit 11G is an organic photoelectric conversion element that generates an electron-hole pair by absorbing light in a selective wavelength range (here, green light) using an organic semiconductor.
- the organic photoelectric conversion unit 11G has a configuration in which the organic photoelectric conversion layer 17 is sandwiched between a pair of electrodes (lower electrode 15a and upper electrode 18) for extracting signal charges.
- the lower electrode 15a and the upper electrode 18 are electrically connected to conductive plugs 120a1 and 120b1 embedded in the semiconductor substrate 11 through a wiring layer and a contact metal layer, as will be described later.
- the organic photoelectric conversion layer 17 of the present embodiment is a specific example of the “organic semiconductor layer” in the present disclosure.
- interlayer insulating films 12 and 14 are formed on the surface S1 of the semiconductor substrate 11, and the interlayer insulating film 12 is opposed to respective conductive plugs 120a1 and 120b1 described later. Through-holes are provided in the regions to be conducted, and conductive plugs 120a2 and 120b2 are embedded in the respective through-holes.
- wiring layers 13a and 13b are embedded in regions facing the conductive plugs 120a2 and 120b2, respectively.
- a lower electrode 15 a is provided on the interlayer insulating film 14, and a wiring layer 15 b electrically separated by the lower electrode 15 a and the insulating film 16 is provided.
- the organic photoelectric conversion layer 17 is formed on the lower electrode 15 a, and the upper electrode 18 is formed so as to cover the organic photoelectric conversion layer 17.
- a protective layer 19 is formed on the upper electrode 18 so as to cover the surface thereof.
- a contact hole H is provided in a predetermined region of the protective layer 19, and a contact metal layer 20 that fills the contact hole H and extends to the upper surface of the wiring layer 15b is formed on the protective layer 19.
- the conductive plug 120a2 functions as a connector together with the conductive plug 120a1, and together with the conductive plug 120a1 and the wiring layer 13a, forms a charge (electron) transmission path from the lower electrode 15a to the green power storage layer 110G described later.
- the conductive plug 120b2 functions as a connector together with the conductive plug 120b1, and together with the conductive plug 120b1, the wiring layer 13b, the wiring layer 15b, and the contact metal layer 20, provides a discharge path for charges (holes) from the upper electrode 18. To form.
- the conductive plugs 120a2 and 120b2 are desirably formed of a laminated film of a metal material such as titanium (Ti), titanium nitride (TiN) and tungsten in order to function as a light shielding film.
- a metal material such as titanium (Ti), titanium nitride (TiN) and tungsten in order to function as a light shielding film.
- the use of such a laminated film is desirable because contact with silicon can be ensured even when the conductive plugs 120a1 and 120b1 are formed as n-type or p-type semiconductor layers.
- the interlayer insulating film 12 is made of an insulating film having a small interface state in order to reduce the interface state with the semiconductor substrate 11 (silicon layer 110) and to suppress the generation of dark current from the interface with the silicon layer 110. Desirably configured.
- an insulating film for example, a stacked film of a hafnium oxide (HfO 2 ) film and a silicon oxide (SiO 2 ) film can be used.
- the interlayer insulating film 14 is composed of, for example, a single layer film made of one of silicon oxide, silicon nitride, silicon oxynitride (SiON), or the like, or a laminated film made of two or more of these. .
- the insulating film 16 is formed of, for example, a single layer film made of one of silicon oxide, silicon nitride, silicon oxynitride (SiON), or the like, or a laminated film made of two or more of these.
- the surface of the insulating film 16 is flattened, and has a shape and a pattern substantially free of steps from the lower electrode 15a.
- the insulating film 16 has a function of electrically separating the lower electrodes 15a of each pixel when the photoelectric conversion element 10 is used as a pixel of a solid-state imaging device.
- the lower electrode 15a is provided in a region covering the light receiving surfaces facing the light receiving surfaces of the inorganic photoelectric conversion portions 11B and 11R formed in the semiconductor substrate 11.
- the lower electrode 15a is made of a light-transmitting conductive film, for example, ITO (Indium Tin Oxide).
- ITO Indium Tin Oxide
- a tin oxide (SnO 2 ) -based material to which a dopant is added, or a zinc oxide-based material obtained by adding a dopant to aluminum zinc oxide (ZnO) May be used.
- zinc oxide-based material examples include aluminum zinc oxide (AZO) to which aluminum (Al) is added as a dopant, gallium zinc oxide (GZO) to which gallium (Ga) is added, and indium zinc oxide to which indium (In) is added. (IZO).
- AZO aluminum zinc oxide
- GZO gallium zinc oxide
- Indium zinc oxide to which indium (In) is added.
- IZO indium zinc oxide
- CuI, InSbO 4 , ZnMgO, CuInO 2 , MgIN 2 O 4 , CdO, ZnSnO 3, or the like may be used.
- signal charges are taken out from the lower electrode 15a, the lower electrode 15a is separated for each pixel in a solid-state imaging device described later using the photoelectric conversion element 10 as a pixel. Formed.
- the organic photoelectric conversion layer 17 includes one or both of an organic p-type semiconductor and an organic n-type semiconductor, and photoelectrically converts light in a selective wavelength range while transmitting light in other wavelength ranges. is there.
- the organic photoelectric conversion layer 17 has a maximum absorption wavelength in a range of 450 nm or more and 650 nm or less, for example.
- the organic photoelectric conversion layer 17 has a conjugate plane (conjugate plane P) including the atoms M as shown in FIG. 2, for example, and the atoms M are substantially perpendicular to the conjugate plane P. It is formed using a conjugated compound having a substituent R at a so-called axial position.
- the substituent R is directly bonded to the atom M.
- the substituent R has an atom A (second atom) directly bonded to the atom M and an atom B (third atom) directly bonded to the atom A, and forms a bond with the atom M and the atom B.
- the bond angle of the atom A that is, the bond angle of the atom A formed by the bond between the atom M and the atom A and the bond between the atom B and the atom A is fixed. This bond angle is determined by the hybrid orbital formed by the substituent R.
- the degree of freedom of rotation of the substituent R with respect to the atom M is reduced, and the occurrence of migration in the molecule of the conjugated compound is suppressed.
- an atom having a valence of 3 or more is preferable, and for example, any one of carbon (C), nitrogen (N), and sulfur (S) is preferable.
- C carbon
- N nitrogen
- S sulfur
- specific substituents R include linear, branched, or cyclic alkyl groups having 1 to 80 carbon atoms, perfluoroalkyl groups, aromatic compounds, heterocyclic compounds, aromatic compounds and heterocyclic compounds. Examples include condensed conjugated compounds, acyl groups, cyano groups, and nitro groups.
- linear, branched, or cyclic alkyl groups having 1 to 80 carbon atoms, perfluoroalkyl groups, and aromatic compounds include phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, and triphenylene. , Rubrene, fullerene and derivatives thereof.
- heterocyclic compound examples include aniline, pyrrole, triallylamine, imidazole, triazole, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, And furan and derivatives thereof.
- examples of the substituent R include a substituent in which an angle formed by an atom M, an atom bonded to M, and an adjacent atom is fixed by a hybrid orbital formed by the molecule, such as a trimethylsilyl group.
- a trimethylsilyl group such as a trimethylsilyl group.
- conjugated compound examples include a subphthalocyanine derivative represented by the following formula (1).
- R1 to R12 are each independently a hydrogen atom, halogen atom, linear, branched, or cyclic alkyl group, aryl group, partial fluoroalkyl group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group.
- R 1 to R 12 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon Z1 to Z3 are each independently a nitrogen atom or CR13, and each R13 is independently a hydrogen atom, a halogen atom, a linear, branched or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- Perfluoroalkyl group silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, acylamino A group, an acyloxy group, a carboxy group, a carboxamide group, a carboalkoxy group, an acyl group, a sulfonyl group, a cyano group, and a nitro group, and M1 is boron or a divalent or trivalent metal.
- a phthalocyanine derivative represented by the following formula (2) can be given.
- R14 to R29 are each independently a hydrogen atom, halogen atom, linear, branched, or cyclic alkyl group, aryl group, partial fluoroalkyl group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group.
- any adjacent R14 to R29 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon.
- Z4 to Z7 are each independently a nitrogen atom or CR30, and each R30 is independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- M2 is boron or a divalent or trivalent metal.
- examples of the conjugated compound include a subporphyrin derivative represented by the following formula (3).
- R31 to R36 are each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, a partial fluoroalkyl group, a perfluoroalkyl group, a silylalkyl group, a silylalkoxy group, an arylsilyl group.
- R 31 to R 36 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon.
- Z8 to Z10 are each independently a nitrogen atom or CR37, and R37 is each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- M3 is boron or a divalent or trivalent metal.
- examples of the conjugated compound include porphyrin derivatives represented by the following formula (4).
- R38 to R45 are each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, a partial fluoroalkyl group, a perfluoroalkyl group, a silylalkyl group, a silylalkoxy group, an arylsilyl group.
- any adjacent R38 to R45 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon.
- Z11 to Z14 are each independently a nitrogen atom or CR46, and each R46 is independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- M4 is boron or a divalent or trivalent metal.
- quinacridone and derivatives thereof, fullerene and derivatives thereof, and the like may be used in addition to the conjugated compound.
- the conjugated compound functions as an organic n-type semiconductor
- the quinacridone derivative functions as an organic p-type semiconductor.
- the upper electrode 18 is composed of a conductive film having the same optical transparency as the lower electrode 15a.
- the upper electrode 18 may be separated for each pixel, or may be formed as a common electrode for each pixel.
- the thickness of the upper electrode 18 is, for example, 10 nm to 200 nm.
- the protective layer 19 is made of a light-transmitting material.
- the protective layer 19 is a single-layer film made of any of silicon oxide, silicon nitride, silicon oxynitride, or the like, or a laminated film made of two or more of them. It is.
- the thickness of the protective layer 19 is, for example, 100 nm to 30000 nm.
- the contact metal layer 20 is made of, for example, any one of titanium, tungsten, titanium nitride, aluminum and the like, or a laminated film made of two or more of them.
- FIG. 3 shows a planar configuration of the organic photoelectric conversion layer 17, the protective layer 19 (upper electrode 18), and the contact hole H.
- the peripheral edge e2 of the protective layer 19 (the same applies to the upper electrode 18) is located outside the peripheral edge e1 of the organic photoelectric conversion layer 17, and the protective layer 19 and the upper electrode 18 are organic photoelectric photoelectric. It is formed to protrude outward from the conversion layer 17.
- the upper electrode 18 is formed so as to cover the upper surface and side surfaces of the organic photoelectric conversion layer 17 and to extend onto the insulating film 16.
- the protective layer 19 is formed in a planar shape equivalent to the upper electrode 18 so as to cover the upper surface of the upper electrode 18.
- the contact hole H is provided in a region of the protective layer 19 that is not opposed to the organic photoelectric conversion layer 17 (region outside the peripheral edge e1), and exposes a part of the surface of the upper electrode 18.
- the distance between the peripheral portions e1 and e2 is not particularly limited, but is, for example, 1 ⁇ m to 500 ⁇ m.
- one rectangular contact hole H is provided along the edge of the organic photoelectric conversion layer 17.
- the shape and number of the contact holes H are not limited to this, and other shapes (for example, , Circular, square, etc.) or a plurality of them may be provided.
- a planarizing film 21 is formed on the protective layer 19 and the contact metal layer 20 so as to cover the entire surface.
- an on-chip lens 22 (microlens) is provided on the planarization film 21, an on-chip lens 22 (microlens) is provided.
- the on-chip lens 22 focuses light incident from above on the light receiving surfaces of the organic photoelectric conversion unit 11G and the inorganic photoelectric conversion units 11B and 11R.
- the multilayer wiring layer 51 is formed on the surface S2 side of the semiconductor substrate 11, the light receiving surfaces of the organic photoelectric conversion unit 11G and the inorganic photoelectric conversion units 11B and 11R are arranged close to each other. Thus, it is possible to reduce the variation in sensitivity between the colors depending on the F value of the on-chip lens 22.
- the photoelectric conversion element 10 of the present embodiment signal charges (electrons) are taken out from the lower electrode 15a. Therefore, in the solid-state imaging device using this as a pixel, the upper electrode 18 may be used as a common electrode. In this case, the transmission path including the contact hole H, the contact metal layer 20, the wiring layers 15b and 13b, and the conductive plugs 120b1 and 120b2 may be formed in at least one place for all the pixels.
- the semiconductor substrate 11 is, for example, formed by embedding inorganic photoelectric conversion portions 11B and 11R and a green power storage layer 110G in a predetermined region of an n-type silicon (Si) layer 110.
- the semiconductor substrate 11 is also embedded with conductive plugs 120a1 and 120b1 serving as a transmission path for charges (electrons or holes (holes)) from the organic photoelectric conversion unit 11G.
- the back surface (surface S1) of the semiconductor substrate 11 can be said to be a light receiving surface.
- a plurality of pixel transistors (including transfer transistors Tr1 to Tr3) corresponding to the organic photoelectric conversion unit 11G and the inorganic photoelectric conversion units 11B and 11R are formed on the surface (surface S2) side of the semiconductor substrate 11.
- a plurality of pixel transistors (including transfer transistors Tr1 to Tr3) corresponding to the organic photoelectric conversion unit 11G and the inorganic photoelectric conversion units 11B and 11R are formed.
- a peripheral circuit composed of a logic circuit or the like
- Examples of the pixel transistor include a transfer transistor, a reset transistor, an amplification transistor, and a selection transistor.
- Each of these pixel transistors is composed of, for example, a MOS transistor, and is formed in a p-type semiconductor well region on the surface S2.
- a circuit including such a pixel transistor is formed for each of the red, green, and blue photoelectric conversion units.
- Each circuit may have a three-transistor configuration including a total of three transistors including a transfer transistor, a reset transistor, and an amplifying transistor, among these pixel transistors.
- a transistor configuration may be used.
- the transfer transistors Tr1 to Tr3 are shown and described.
- pixel transistors other than the transfer transistor can be shared between photoelectric conversion units or between pixels. Further, a so-called pixel sharing structure that shares a floating diffusion can also be applied.
- the transfer transistors Tr1 to Tr3 are configured to include gate electrodes (gate electrodes TG1 to TG3) and floating diffusions (FDs 113, 114, and 116).
- the transfer transistor Tr1 transfers the signal charge corresponding to green (electrons in the present embodiment) generated in the organic photoelectric conversion unit 11G and accumulated in the green power storage layer 110G to a vertical signal line Lsig described later. It is.
- the transfer transistor Tr2 transfers the signal charge (electrons in the present embodiment) corresponding to blue generated and accumulated in the inorganic photoelectric conversion unit 11B to a vertical signal line Lsig described later.
- the transfer transistor Tr3 transfers signal charges (electrons in the present embodiment) corresponding to red color generated and accumulated in the inorganic photoelectric conversion unit 11R to a vertical signal line Lsig described later.
- the inorganic photoelectric conversion units 11B and 11R are photodiodes having pn junctions (Photo-Diodes), and are formed in the order of the inorganic photoelectric conversion units 11B and 11R from the surface S1 side on the optical path in the semiconductor substrate 11.
- the inorganic photoelectric conversion unit 11B selectively detects blue light and accumulates signal charges corresponding to blue. For example, from a selective region along the surface S1 of the semiconductor substrate 11, It is formed to extend over a region near the interface with the multilayer wiring layer 51.
- the inorganic photoelectric conversion unit 11R selectively detects red light and accumulates signal charges corresponding to red.
- the inorganic photoelectric conversion unit 11R is formed over a lower layer (surface S2 side) than the inorganic photoelectric conversion unit 11B.
- blue (B) is a color corresponding to a wavelength range of 450 nm to 495 nm
- red (R) is a color corresponding to a wavelength range of 620 nm to 750 nm, for example, and the inorganic photoelectric conversion units 11B and 11R are respectively It is only necessary that light in a part or all of the wavelength range can be detected.
- FIG. 4A shows a detailed configuration example of the inorganic photoelectric conversion units 11B and 11R.
- FIG. 4B corresponds to a structure in another cross section of FIG. Note that in this embodiment, a case where electrons are read out as signal charges out of a pair of electrons and holes generated by photoelectric conversion (when an n-type semiconductor region is used as a photoelectric conversion layer) will be described.
- “+ (plus)” superscripted on “p” and “n” represents a high p-type or n-type impurity concentration.
- the gate electrodes TG2 and TG3 of the transfer transistors Tr2 and Tr3 are also shown.
- the inorganic photoelectric conversion unit 11B includes, for example, a p-type semiconductor region (hereinafter simply referred to as a p-type region, also referred to as an n-type) 111p serving as a hole accumulation layer, and an n-type photoelectric conversion layer serving as an electron accumulation layer. (N-type region) 111n.
- a p-type semiconductor region hereinafter simply referred to as a p-type region, also referred to as an n-type
- N-type photoelectric conversion layer serving as an electron accumulation layer.
- N-type region 111n.
- Each of the p-type region 111p and the n-type photoelectric conversion layer 111n is formed in a selective region in the vicinity of the surface S1, and a part thereof is bent so as to extend to reach the interface with the surface S2. .
- the p-type region 111p is connected to a p-type semiconductor well region (not shown) on the surface S1 side.
- the n-type photoelectric conversion layer 111n is connected to the FD 113 (n-type region) of the blue transfer transistor Tr2. Note that a p-type region 113p (hole accumulation layer) is formed in the vicinity of the interface between each end of the p-type region 111p and the n-type photoelectric conversion layer 111n on the surface S2 side and the surface S2.
- the inorganic photoelectric conversion unit 11R is formed by sandwiching an n-type photoelectric conversion layer 112n (electron storage layer) between p-type regions 112p1 and 112p2 (hole storage layer) (stacking of pnp). Having structure). A part of the n-type photoelectric conversion layer 112n is bent and extended so as to reach the interface with the surface S2. The n-type photoelectric conversion layer 112n is connected to the FD 114 (n-type region) of the red transfer transistor Tr3. A p-type region 113p (hole accumulation layer) is formed at least near the interface between the end of the n-type photoelectric conversion layer 111n on the surface S2 side and the surface S2.
- FIG. 5 shows a detailed configuration example of the green power storage layer 110G.
- a description will be given of a case where electrons out of the pair of electrons and holes generated by the organic photoelectric conversion unit 11G are read from the lower electrode 15a side as signal charges.
- FIG. 5 also shows the gate electrode TG1 of the transfer transistor Tr1 among the pixel transistors.
- the green power storage layer 110G includes an n-type region 115n that serves as an electron storage layer.
- a part of the n-type region 115n is connected to the conductive plug 120a1, and accumulates electrons transmitted from the lower electrode 15a side through the conductive plug 120a1.
- the n-type region 115n is also connected to the FD 116 (n-type region) of the green transfer transistor Tr1.
- a p-type region 115p (hole accumulation layer) is formed in the vicinity of the interface between the n-type region 115n and the surface S2.
- the conductive plug 120a1 is electrically connected to the lower electrode 15a of the organic photoelectric conversion unit 11G and is connected to the green power storage layer 110G.
- the conductive plug 120b1 is electrically connected to the upper electrode 18 of the organic photoelectric conversion unit 11G, and serves as a wiring for discharging holes.
- Each of these conductive plugs 120a1 and 120b1 is made of, for example, a conductive semiconductor layer and is embedded in the semiconductor substrate 11.
- the conductive plug 120a1 may be n-type (because it becomes an electron transmission path), and the conductive plug 120b1 may be p-type (because it becomes a hole transmission path).
- the conductive plugs 120a1 and 120b1 may be, for example, those in which a conductive film material such as tungsten is embedded in the through via.
- the via side surface be covered with an insulating film such as silicon oxide (SiO 2 ) or silicon nitride (SiN).
- a multilayer wiring layer 51 is formed on the surface S2 of the semiconductor substrate 11.
- a plurality of wirings 51 a are arranged via an interlayer insulating film 52.
- the multilayer wiring layer 51 is formed on the side opposite to the light receiving surface, and a so-called back-illuminated solid-state imaging device can be realized.
- a support substrate 53 made of silicon is bonded to the multilayer wiring layer 51.
- the photoelectric conversion element 10 can be manufactured as follows, for example. 6A to 8C show a method for manufacturing the photoelectric conversion element 10 in the order of steps. 8A to 8C show only the main configuration of the photoelectric conversion element 10. Note that the manufacturing method of the photoelectric conversion element 10 described below is merely an example, and the manufacturing method of the photoelectric conversion element 10 (and the photoelectric conversion element 30 described later) according to the embodiment of the present disclosure is limited to the following example. is not.
- the semiconductor substrate 11 is formed. Specifically, a so-called SOI substrate in which a silicon layer 110 is formed on a silicon substrate 1101 with a silicon oxide film 1102 interposed therebetween is prepared. The surface of the silicon layer 110 on the silicon oxide film 1102 side is the back surface (surface S1) of the semiconductor substrate 11. 6A and 6B, the structure shown in FIG. 1 is shown upside down. Subsequently, as shown in FIG. 6A, conductive plugs 120 a 1 and 120 b 1 are formed in the silicon layer 110.
- the conductive plugs 120a1 and 120b1 are formed by, for example, forming a through via in the silicon layer 110 and then burying the barrier metal such as silicon nitride and tungsten as described above in the through via. Can do.
- a conductive impurity semiconductor layer may be formed by ion implantation into the silicon layer 110.
- the conductive plug 120a1 is formed as an n-type semiconductor layer
- the conductive plug 120b1 is formed as a p-type semiconductor layer.
- inorganic photoelectric conversion units 11B and 11R each having a p-type region and an n-type region as shown in FIG.
- the semiconductor substrate 11 is formed.
- a multilayer wiring layer 51 is formed by forming a plurality of layers of wirings 51 a via the interlayer insulating film 52. Subsequently, after a support substrate 53 made of silicon is pasted on the multilayer wiring layer 51, the silicon substrate 1101 and the silicon oxide film 1102 are peeled off from the surface S1 side of the semiconductor substrate 11, and the surface S1 of the semiconductor substrate 11 is removed. Expose.
- the organic photoelectric conversion unit 11G is formed on the surface S1 of the semiconductor substrate 11. Specifically, first, as shown in FIG. 7A, on the surface S1 of the semiconductor substrate 11, the interlayer insulating film 12 made of the laminated film of the hafnium oxide film and the silicon oxide film as described above is formed. For example, after forming a hafnium oxide film by an ALD (atomic layer deposition) method, a silicon oxide film is formed by, for example, a plasma CVD (Chemical Vapor Deposition) method.
- ALD atomic layer deposition
- a silicon oxide film is formed by, for example, a plasma CVD (Chemical Vapor Deposition) method.
- contact holes H1a and H1b are formed at positions facing the conductive plugs 120a1 and 120b1 of the interlayer insulating film 12, and the conductive plugs made of the above-described materials so as to embed these contact holes H1a and H1b, respectively.
- 120a2 and 120b2 are formed.
- the conductive plugs 120a2 and 120b2 may be formed so as to extend to a region where light shielding is desired (so as to cover the region where light shielding is desired), or a light shielding layer may be formed in a region separated from the conductive plugs 120a2 and 120b2. May be.
- the interlayer insulating film 14 made of the above-described material is formed by, for example, a plasma CVD method.
- a plasma CVD method it is desirable to planarize the surface of the interlayer insulating film 14 by, for example, a CMP (Chemical Mechanical Polishing) method.
- contact holes are respectively opened at positions of the interlayer insulating film 14 facing the conductive plugs 120a2 and 120b2, and the wiring layers 13a and 13b are formed by embedding the above-described materials.
- a lower electrode 15 a is formed on the interlayer insulating film 14. Specifically, first, the above-described transparent conductive film is formed over the entire surface of the interlayer insulating film 14 by, eg, sputtering. Thereafter, the lower electrode 15a is removed by removing a selective portion using, for example, dry etching or wet etching using a photolithography method (exposure, development, post-bake, etc. of the photoresist film). Form. At this time, the lower electrode 15a is formed in a region facing the wiring layer 13a. Further, when the transparent conductive film is processed, the transparent conductive film is also left in the region facing the wiring layer 13b, so that the wiring layer 15b constituting a part of the hole transmission path is formed together with the lower electrode 15a. Form.
- an insulating film 16 is formed.
- the insulating film 16 made of the above-described material is formed by, for example, a plasma CVD method so as to cover the entire surface of the semiconductor substrate 11 so as to cover the interlayer insulating film 14, the lower electrode 15a, and the wiring layer 15b.
- the formed insulating film 16 is polished by, for example, a CMP method so that the lower electrode 15a and the wiring layer 15b are exposed from the insulating film 16, and the lower electrode 15a and the insulating film 16 are insulated. Steps between the films 16 are alleviated (preferably planarized).
- the organic photoelectric conversion layer 17 is formed on the lower electrode 15a.
- the above-described subphthalocyanine derivative and quinacridone derivative are patterned by, for example, vacuum deposition.
- another organic layer such as an electron blocking film
- the method for forming the organic photoelectric conversion layer 17 is not necessarily limited to the method using the vacuum deposition method as described above, and other methods such as a printing technique may be used.
- the upper electrode 18 and the protective layer 19 are formed.
- the upper electrode 18 made of the above-described transparent conductive film is formed over the entire surface of the substrate so as to cover the upper surface and side surfaces of the organic photoelectric conversion layer 17 by, for example, vacuum deposition or sputtering. Note that the characteristics of the organic photoelectric conversion layer 17 are likely to fluctuate due to the influence of moisture, oxygen, hydrogen, etc., and therefore it is desirable that the upper electrode 18 be formed with the organic photoelectric conversion layer 17 by a consistent vacuum process.
- the protective layer 19 made of the above-described material is formed by, for example, a plasma CVD method so as to cover the upper surface of the upper electrode 18.
- the upper electrode 18 is processed.
- a contact hole H is formed in the protective layer 19 by, for example, etching using a photolithography method.
- the contact hole H is desirably formed in a region not facing the organic photoelectric conversion layer 17.
- the contact metal layer 20 made of the above-described material is formed using, for example, a sputtering method. At this time, the contact metal layer 20 is formed on the protective layer 19 so as to bury the contact hole H and extend to the upper surface of the wiring layer 15b. Finally, after the planarization film 21 is formed over the entire surface of the semiconductor substrate 11, the on-chip lens 22 is formed on the planarization film 21, thereby completing the photoelectric conversion element 10 shown in FIG.
- FIG. 10 schematically shows a flow of signal charge (electron) acquisition based on incident light.
- signal charge electron
- the green light Lg is selectively detected (absorbed) by the organic photoelectric conversion unit 11G and subjected to photoelectric conversion.
- electrons Eg out of the generated electron-hole pairs are taken out from the lower electrode 15a side, and then transferred to the green power storage layer 110G via the transmission path A (the wiring layer 13a and the conductive plugs 120a1 and 120a2). Accumulated.
- the accumulated electron Eg is transferred to the FD 116 during a read operation.
- the holes Hg are discharged from the upper electrode 18 side through the transmission path B (contact metal layer 20, wiring layers 13b and 15b, and conductive plugs 120b1 and 120b2).
- signal charges are accumulated as follows. That is, in the present embodiment, for example, a predetermined negative potential VL ( ⁇ 0 V) is applied to the lower electrode 15a, and a potential VU ( ⁇ VL) lower than the potential VL is applied to the upper electrode 18. .
- the potential VL is applied to the lower electrode 15a from the wiring 51a in the multilayer wiring layer 51 through the transmission path A, for example.
- the potential VL is applied to the upper electrode 18 from the wiring 51a in the multilayer wiring layer 51 through the transmission path B, for example.
- the electrode 15a side It is led to the electrode 15a side (holes are led to the upper electrode 18 side).
- the electrons Eg are extracted from the lower electrode 15a and accumulated in the green power storage layer 110G (specifically, the n-type region 115n) via the transmission path A.
- the potential VL of the lower electrode 15a connected to the green power storage layer 110G also varies.
- the amount of change in the potential VL corresponds to the signal potential (here, the potential of the green signal).
- the transfer transistor Tr1 is turned on, and the electron Eg stored in the green power storage layer 110G is transferred to the FD.
- a green signal based on the amount of received light of the green light Lg is read out to a vertical signal line Lsig described later through another pixel transistor (not shown).
- the reset transistor and transfer transistor Tr1 are turned on, and the FD 116, which is the n-type region, and the power storage region (n-type region 115n) of the green power storage layer 110G are reset to the power supply voltage VDD, for example. .
- electrons Er corresponding to the incident red light are accumulated in the n-type region (n-type photoelectric conversion layer 112n), and the accumulated electrons Er are transferred to the FD 114 during the read operation. Transferred. Holes are accumulated in a p-type region (not shown).
- the p-type region (a hole accumulation layer of the inorganic photoelectric conversion unit 11B (see FIG. 3)).
- the hole concentration of the p-type region 111p tends to increase. For this reason, generation of dark current at the interface between the p-type region 111p and the interlayer insulating film 12 can be suppressed.
- the transfer transistors Tr2 and Tr3 are turned on, and the electrons Eb and Er accumulated in the n-type photoelectric conversion layers 111n and 112n are transferred to the FDs 113 and 114, respectively. Is done.
- a blue signal based on the amount of received light of the blue light Lb and a red signal based on the amount of received light of the red light Lr are read out to a vertical signal line Lsig described later through another pixel transistor (not shown).
- the reset transistor (not shown) and the transfer transistors Tr2 and Tr3 are turned on, and the FDs 113 and 114, which are n-type regions, are reset to, for example, the power supply voltage VDD.
- the organic photoelectric conversion unit 11G in the vertical direction and the inorganic photoelectric conversion units 11B and 11R, the red, green and blue color lights are separated and detected without providing a color filter. A signal charge can be obtained. Thereby, it is possible to suppress light loss (sensitivity reduction) due to color light absorption of the color filter and generation of false color associated with pixel interpolation processing.
- the photoelectric conversion element formed by using a general subphthalocyanine or its derivative as shown in the following formula (5) as a material of the photoelectric conversion layer has a problem that it has excellent external quantum efficiency and spectral characteristics but has low heat resistance. was there.
- heat treatment such as reflow soldering causes a change in color, a decrease in device characteristics such as electrical characteristics, or deformation or destruction.
- This low heat resistance is considered to be due to the high degree of freedom of rotation of the substituent R ′ by the linker X bonded to boron (B) having a bond angle in a direction perpendicular to the conjugate plane of the subphthalocyanine.
- This substituent R ′ is bonded to boron (B) via the linker X.
- the linker X generally includes, for example, oxygen (O). Since these are divalent atoms, the bond angle is not fixed, and the substituent R ′ bonded to the linker X rotates relatively freely. It becomes possible.
- the subphthalocyanine or its derivative as shown in the formula (5) in the photoelectric conversion layer undergoes migration within the molecule by the above-described soldering or heating under a high temperature environment, and the subphthalocyanine in the photoelectric conversion layer Changes occur in the aggregation and orientation of molecules. As a result, it is considered that the device characteristics change or decrease, or deform or break.
- a subphthalocyanine derivative in which a substituent R is directly bonded to an atom M (for example, boron (B)) having a bond angle in a direction perpendicular to the conjugate plane P or a subphthalocyanine derivative.
- the organic photoelectric conversion layer 17 is formed using a conjugated compound having an atom M having a bond angle in a direction perpendicular to the conjugated plane P.
- the substituent R has a molecular structure in which the bond angle of the atom A formed by the bond between the atom M and the atom A and the bond between the atom B and the atom A is fixed.
- conjugated compounds other than subphthalocyanine derivatives include phthalocyanine derivatives, subporphyrin derivatives, and porphyrin derivatives. This reduces the rotational freedom of the substituent R bonded to the atom M having a bond angle perpendicular to the conjugate plane P of the subphthalocyanine derivative and other conjugated compounds, and suppresses the occurrence of migration due to temperature rise. It becomes possible to do.
- the organic photoelectric conversion layer 17 is a conjugated compound having a substituent having a low degree of rotational freedom for the atom M having a bond angle in the direction perpendicular to the conjugate plane P.
- the organic photoelectric conversion layer 17 was formed. Thereby, generation
- FIG. 12 illustrates an overall configuration of a solid-state imaging device (solid-state imaging device 1) using the photoelectric conversion element 10 (or the photoelectric conversion element 30) described in the above embodiment for each pixel.
- the solid-state imaging device 1 is a CMOS image sensor, and has a pixel unit 1a as an imaging area on a semiconductor substrate 11, and, for example, a row scanning unit 131 and a horizontal selection unit 133 in a peripheral region of the pixel unit 1a.
- the peripheral circuit unit 130 includes a column scanning unit 134 and a system control unit 132.
- the pixel unit 1a has, for example, a plurality of unit pixels P (corresponding to the photoelectric conversion element 10) arranged two-dimensionally in a matrix.
- a pixel drive line Lread (specifically, a row selection line and a reset control line) is wired for each pixel row, and a vertical signal line Lsig is wired for each pixel column.
- the pixel drive line Lread transmits a drive signal for reading a signal from the pixel.
- One end of the pixel drive line Lread is connected to an output end corresponding to each row of the row scanning unit 131.
- the row scanning unit 131 is configured by a shift register, an address decoder, or the like, and is a pixel driving unit that drives each unit pixel P of the pixel unit 1a, for example, in units of rows.
- a signal output from each unit pixel P of the pixel row that is selectively scanned by the row scanning unit 131 is supplied to the horizontal selection unit 133 through each of the vertical signal lines Lsig.
- the horizontal selection unit 133 is configured by an amplifier, a horizontal selection switch, and the like provided for each vertical signal line Lsig.
- the column scanning unit 134 includes a shift register, an address decoder, and the like, and drives the horizontal selection switches in the horizontal selection unit 133 in order while scanning. By the selective scanning by the column scanning unit 134, the signal of each pixel transmitted through each of the vertical signal lines Lsig is sequentially output to the horizontal signal line 135 and transmitted to the outside of the semiconductor substrate 11 through the horizontal signal line 135. .
- the circuit portion including the row scanning unit 131, the horizontal selection unit 133, the column scanning unit 134, and the horizontal signal line 135 may be formed directly on the semiconductor substrate 11, or provided in the external control IC. It may be. In addition, these circuit portions may be formed on another substrate connected by a cable or the like.
- the system control unit 132 receives a clock given from the outside of the semiconductor substrate 11, data for instructing an operation mode, and the like, and outputs data such as internal information of the solid-state imaging device 1.
- the system control unit 132 further includes a timing generator that generates various timing signals, and the row scanning unit 131, the horizontal selection unit 133, the column scanning unit 134, and the like based on the various timing signals generated by the timing generator. Peripheral circuit drive control.
- FIG. 13 shows a schematic configuration of an electronic device 2 (camera) as an example.
- the electronic device 2 is, for example, a video camera capable of taking a still image or a moving image, and includes a solid-state imaging device 1, an optical system (optical lens) 310, a shutter device 311, the solid-state imaging device 1 and the shutter device 311.
- a driving unit 313 for driving and a signal processing unit 312 are included.
- the optical system 310 guides image light (incident light) from a subject to the pixel unit 1 a of the solid-state imaging device 1.
- the optical system 310 may be composed of a plurality of optical lenses.
- the shutter device 311 controls the light irradiation period and the light shielding period for the solid-state imaging device 1.
- the drive unit 313 controls the transfer operation of the solid-state imaging device 1 and the shutter operation of the shutter device 311.
- the signal processing unit 312 performs various types of signal processing on the signal output from the solid-state imaging device 1.
- the video signal Dout after the signal processing is stored in a storage medium such as a memory, or is output to a monitor or the like.
- Example> Various samples according to the embodiments of the present disclosure were prepared below, and changes in absorption spectra before and after heating, changes in external quantum efficiency and response time due to heating were evaluated.
- Subphthalocyanine derivative A was synthesized based on the following scheme (A). First, subphthalocyanine chloride was dissolved in dry toluene, and perfluorophenyl magnesium bromide was added under an argon atmosphere. After this toluene solution was stirred and reacted at 40 ° C., the resulting mixture was purified by column chromatography to obtain subphthalocyanine derivative A.
- Subphthalocyanine derivative B was synthesized based on the following scheme (B). First, fluorinated subphthalocyanine chloride was dissolved in dry toluene, and perfluorophenylmagnesium bromide was added under an argon atmosphere. After this toluene solution was stirred and reacted at 40 ° C., the resulting mixture was purified by column chromatography to obtain subphthalocyanine derivative B.
- sample preparation First, an organic thin film A was formed on a quartz substrate using a subphthalocyanine derivative A as a deposition source in a vacuum deposition apparatus. Subsequently, an ITO film was formed on the organic thin film A, and a sample 1-1 for evaluating a spectral shape change during heating was produced. Sample 2-1 was prepared using the same method except that subphthalocyanine derivative B was used in place of subphthalocyanine derivative A as the evaporation source. Further, regarding the subphthalocyanine derivative B, a sample 2-2 for evaluating the external quantum efficiency in which an organic thin film B made of the subphthalocyanine derivative B is formed and an ITO film as a lower electrode and an AlSiCu film as an upper electrode is formed was prepared. .
- subphthalocyanine derivatives C and D in which a substituent R (perfluorophenyl group) is bonded to B shown in the following formulas (C) and (D) via oxygen (O) as a linker are shown.
- Samples 3-1 and 4-1 for evaluating the spectral shape change during heating and sample 4-2 for evaluating the external quantum efficiency were respectively used.
- FIGS. 13 to 16 show absorption spectra for each heating time of Sample 1-1 (FIG. 13), Sample 2-1 (FIG. 14), Sample 3-1 (FIG. 15), and Sample 4-1 (FIG. 16). Is a summary.
- the rate of change in external quantum efficiency due to heating was measured using a light source, a filter, and a semiconductor parameter analyzer. Specifically, the light intensity when the light amount applied to the samples 2-2 and 4-2 from the light source through the filter is 0 to 5 ⁇ W / cm 2 and the voltage applied between the electrodes is 1 V. The external quantum efficiency was calculated from the current value and the dark current value.
- FIG. 17 is obtained by dividing the value before and after heating and plotting the rate of change with the value before heating being 1.
- FIG. 18 is a plot of the response time at each heating time.
- a subphthalocyanine derivative constituting, for example, a photoelectric conversion layer of a photoelectric conversion element, a subphthalocyanine in which a substituent R is directly bonded to an atom M having a bond angle in a direction perpendicular to the conjugate plane of the present disclosure. It has been found that the use of a derivative improves the heat resistance and suppresses the deterioration of device characteristics due to heating.
- the present disclosure is not limited to the above-described embodiments and the like, and various modifications are possible.
- the photoelectric conversion element solid-state imaging device
- the organic photoelectric conversion unit 11G that detects green light and the inorganic photoelectric conversion units 11B and 11R that detect blue light and red light are stacked.
- the present disclosure is not limited to such a structure. That is, red light or blue light may be detected in the organic photoelectric conversion unit, or green light may be detected in the inorganic photoelectric conversion unit.
- the number and ratio of these organic photoelectric conversion units and inorganic photoelectric conversion units are not limited, and two or more organic photoelectric conversion units may be provided.
- a signal may be obtained.
- a red photoelectric conversion unit 40R, a green photoelectric conversion unit 40G, and a blue photoelectric conversion unit 40B each having organic photoelectric conversion layers 42R, 42G, and 42B are stacked in this order. Also good.
- the red photoelectric conversion unit 40R, the green photoelectric conversion unit 40G, and the blue photoelectric conversion unit 40B are stacked on the silicon substrate 61 via the insulating layer 62, and on the blue photoelectric conversion unit 40B, An on-chip lens 32 is provided via the protective layer 33 and the planarizing layer 31.
- a red power storage layer 310R, a green power storage layer 310G, and a blue power storage layer 310B are provided in the silicon substrate 61.
- the light incident on the on-chip lens 32 is photoelectrically converted by the red photoelectric conversion unit 40R, the green photoelectric conversion unit 40G, and the blue photoelectric conversion unit 40B, from the red photoelectric conversion unit 40R to the red power storage layer 310R, and from the green photoelectric conversion unit 40G.
- Signal charges are respectively sent from the blue photoelectric conversion unit 340B to the blue power storage layer 310B to the green power storage layer 310G.
- the organic photoelectric conversion part and the inorganic photoelectric conversion part are not limited to the structure in which the organic photoelectric conversion part and the inorganic photoelectric conversion part are stacked in the vertical direction, but may be arranged in parallel along the substrate surface.
- the configuration of the back-illuminated solid-state imaging device is illustrated, but the present disclosure can also be applied to a front-illuminated solid-state imaging device.
- the solid-state imaging device (photoelectric conversion element) of the present disclosure does not have to include all the components described in the above embodiments, and may include other layers.
- the present disclosure may be configured as follows.
- the first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane.
- a photoelectric conversion layer containing a conjugated compound having an atom The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom
- a photoelectric conversion element having a molecular structure in which a bond angle of the second atom that forms a bond with is fixed.
- the second atom is any one of carbon (C), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si).
- the substituent R is a linear, branched, or cyclic alkyl group having 1 to 80 carbon atoms, a perfluoroalkyl group, an aromatic compound, a heterocyclic compound, or a conjugated compound in which an aromatic compound and a heterocyclic compound are condensed.
- the straight chain, branched or cyclic alkyl group having 1 to 80 carbon atoms, perfluoroalkyl group, aromatic compound is phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene.
- the heterocyclic compounds include aniline, pyrrole, triallylamine, imidazole, triazole, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and these
- the photoelectric conversion device according to [4] which is a derivative.
- Conjugated compounds in which the aromatic compound and the heterocyclic compound are condensed include phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene, aniline, pyrrole, triallylamine, imidazole, and triazole.
- R1 to R12 are each independently a hydrogen atom, halogen atom, linear, branched, or cyclic alkyl group, aryl group, partial fluoroalkyl group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group.
- R 1 to R 12 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon Z1 to Z3 are each independently a nitrogen atom or CR13, and each R13 is independently a hydrogen atom, a halogen atom, a linear, branched or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- R14 to R29 are each independently a hydrogen atom, halogen atom, linear, branched, or cyclic alkyl group, aryl group, partial fluoroalkyl group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group.
- any adjacent R14 to R29 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon.
- Z4 to Z7 are each independently a nitrogen atom or CR30, and each R30 is independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- perfluoroalkyl group silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, (Acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group, acyl group, sulfonyl group, cyano group, and nitro group.
- M2 is boron or a divalent or trivalent metal.
- R31 to R36 are each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, a partial fluoroalkyl group, a perfluoroalkyl group, a silylalkyl group, a silylalkoxy group, an arylsilyl group.
- R 31 to R 36 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon.
- Z8 to Z10 are each independently a nitrogen atom or CR37, and R37 is each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- perfluoroalkyl group silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, (Acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group, acyl group, sulfonyl group, cyano group, and nitro group.
- M3 is boron or a divalent or trivalent metal.
- R38 to R45 are each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, a partial fluoroalkyl group, a perfluoroalkyl group, a silylalkyl group, a silylalkoxy group, an arylsilyl group.
- any adjacent R38 to R45 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring.
- a fused aromatic ring contains one or more atoms other than carbon.
- Z11 to Z14 are each independently a nitrogen atom or CR46, and each R46 is independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group.
- perfluoroalkyl group silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, (Acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group, acyl group, sulfonyl group, cyano group, and nitro group.
- Each pixel includes one or more organic photoelectric conversion units, The organic photoelectric conversion unit is A first electrode and a second electrode disposed opposite to each other; The first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane.
- a photoelectric conversion layer containing a conjugated compound having an atom The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom
- a solid-state imaging device having a molecular structure in which a bond angle of the second atom forming a bond with the second atom is fixed.
- the inorganic photoelectric conversion unit is embedded in a semiconductor substrate, The organic photoelectric conversion unit according to [13], wherein the organic photoelectric conversion unit is formed on a first surface side of the semiconductor substrate. [15] The organic photoelectric conversion unit performs green light photoelectric conversion, The solid-state imaging according to [13] or [14], wherein an inorganic photoelectric conversion unit that performs photoelectric conversion of blue light and an inorganic photoelectric conversion unit that performs photoelectric conversion of red light are stacked in the semiconductor substrate. apparatus.
Abstract
A photoelectric conversion element according to an embodiment of the present disclosure is provided with: a first electrode and a second electrode that are disposed opposing each other; and a photoelectric conversion layer which is disposed between the first electrode and the second electrode and which includes a conjugate system compound having a conjugate plane, the conjugate system compound being included in the conjugate plane and having a first atom with a substitution group R directly bonded thereto in a substantially perpendicular direction with respect to the conjugate plane, wherein the substitution group R includes a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and has a molecular structure in which the second atom, forming a bond with the first atom and the third atom, has a fixed bond angle.
Description
本開示は、例えば、有機半導体を用いた光電変換素子およびこれを備えた固体撮像装置に関する。
The present disclosure relates to, for example, a photoelectric conversion element using an organic semiconductor and a solid-state imaging device including the photoelectric conversion element.
近年、高感度で高解像度な画像を生成可能なＣＣＤ（Charge Coupled Device）イメージセンサ、あるいはＣＭＯＳ（Complementary Metal Oxide Semiconductor）イメージセンサ等の固体撮像装置が開発されている。
In recent years, solid-state imaging devices such as CCD (Charge Coupled Device) image sensors or CMOS (Complementary Metal Oxide Semiconductor) image sensors capable of generating high-sensitivity and high-resolution images have been developed.
固体撮像装置の感度は、固体撮像装置を構成する光電変換素子の外部量子効率（External Quantum Efficiency：ＥＱＥ）および分光形状を改善することによって向上させることができる。例えば特許文献１では、ブロッキング層や電荷輸送層をサブフタロシアニン化合物で構成することで外部量子効率が改善された有機感光性デバイスが開示されている。
The sensitivity of the solid-state imaging device can be improved by improving the external quantum efficiency (Equation: EQE) and spectral shape of the photoelectric conversion elements constituting the solid-state imaging device. For example, Patent Document 1 discloses an organic photosensitive device in which external quantum efficiency is improved by constituting a blocking layer and a charge transport layer with a subphthalocyanine compound.
しかしながら、例えば光電変換層を引用文献１に記載のサブフタロシアニン化合物で構成した光電変換素子では、その実装工程における加熱処理等において性能の低下や、変形あるいは破壊等が生じるという問題があった。
However, for example, in the photoelectric conversion element in which the photoelectric conversion layer is composed of the subphthalocyanine compound described in the cited document 1, there is a problem in that performance is deteriorated, deformation, or destruction occurs in the heat treatment in the mounting process.
従って、耐熱性を向上させることが可能な光電変換素子および固体撮像装置を提供することが望ましい。
Therefore, it is desirable to provide a photoelectric conversion element and a solid-state imaging device that can improve heat resistance.
本開示の一実施形態の光電変換素子は、対向配置された第１電極および第２電極と、第１電極と第２電極との間に設けられ、共役面を有し、共役面に含まれると共に、共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを備えたものであり、置換基Ｒは、第１の原子に直接結合する第２の原子と、第２の原子と直接結合する第３の原子とを有し、第１の原子および第３の原子と結合を形成する第２の原子の結合角が固定された分子構造を有する。
A photoelectric conversion element according to an embodiment of the present disclosure is provided between a first electrode and a second electrode arranged to face each other, and between the first electrode and the second electrode, and has a conjugate plane and is included in the conjugate plane. And a photoelectric conversion layer including a conjugated compound having a first atom in which the substituent R is directly bonded in a direction substantially perpendicular to the conjugate plane. The substituent R is attached to the first atom. The bond angle of the second atom that has the second atom directly bonded and the third atom directly bonded to the second atom and forms a bond with the first atom and the third atom is fixed. Have a molecular structure.
本開示の一実施形態の固体撮像装置は、各画素が１または複数の有機光電変換部を含み、有機光電変換部として上記本開示の一実施形態の固体撮像素子を有するものである。
The solid-state imaging device according to an embodiment of the present disclosure includes each pixel including one or a plurality of organic photoelectric conversion units, and the solid-state imaging device according to the embodiment of the present disclosure as the organic photoelectric conversion unit.
本開示の一実施形態の光電変換素子および一実施形態の固体撮像装置では、対向配置された第１電極と第２電極との間の光電変換層を、共役面を有し、共役面に含まれると共に、共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを用いて形成するようにした。この共役系化合物の置換基Ｒは、第１の原子に直接結合する第２の原子と、第２の原子と直接結合する第３の原子とを有し、第１の原子および第３の原子と結合を形成する第２の原子の結合角が固定された分子構造を有するものである。これにより、置換基Ｒの回転自由度が低下し、共役系化合物のマイグレーションの発生を抑制することが可能となる。
In the photoelectric conversion element according to the embodiment of the present disclosure and the solid-state imaging device according to the embodiment, the photoelectric conversion layer between the first electrode and the second electrode that are arranged to face each other has a conjugate plane and is included in the conjugate plane. And a photoelectric conversion layer containing a conjugated compound having a first atom in which a substituent R is directly bonded in a direction substantially perpendicular to the conjugated surface. The substituent R of the conjugated compound has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom And a molecular structure in which the bond angle of the second atom forming the bond is fixed. Thereby, the rotational freedom degree of substituent R falls and it becomes possible to suppress generation | occurrence | production of the migration of a conjugated compound.
本開示の一実施形態の光電変換素子および一実施形態の固体撮像装置によれば、共役面に含まれると共に、共役面に対して略垂直方向い結合角を有する第１の原子に上記置換基Ｒが直接結合した共役系化合物を用いて光電変換層を形成するようにしたので、置換基Ｒの回転自由度が低下し、共役系化合物のマイグレーションの発生が抑制される。よって、光電変換層の耐熱性が向上し、高い耐熱性を有する光電変換素子およびこれを備えた固体撮像装置を提供することが可能となる。なお、ここに記載された効果は必ずしも限定されるものではなく、本開示中に記載されたいずれの効果であってもよい。
According to the photoelectric conversion element of one embodiment of the present disclosure and the solid-state imaging device of one embodiment, the substituent is added to the first atom that is included in the conjugate plane and has a bond angle substantially perpendicular to the conjugate plane. Since the photoelectric conversion layer is formed using a conjugated compound in which R is directly bonded, the degree of freedom of rotation of the substituent R is reduced, and the occurrence of migration of the conjugated compound is suppressed. Therefore, the heat resistance of the photoelectric conversion layer is improved, and a photoelectric conversion element having high heat resistance and a solid-state imaging device including the photoelectric conversion element can be provided. Note that the effects described here are not necessarily limited, and may be any effects described in the present disclosure.
以下、本開示における一実施形態について、図面を参照して詳細に説明する。なお、説明する順序は、下記の通りである。
１．実施の形態（有機光電変換層の材料として原子Ｍに置換基Ｒが直接結合した共役系化合物を用いた例）
１－１．基本構成
１－２．製造方法
１－３．作用・効果
２．適用例
３．実施例 Hereinafter, an embodiment of the present disclosure will be described in detail with reference to the drawings. The order of explanation is as follows.
1. Embodiment (Example using a conjugated compound in which a substituent R is directly bonded to an atom M as a material of an organic photoelectric conversion layer)
1-1. Basic configuration 1-2. Manufacturing method 1-3. Action / Effect Application Example 3 Example
１．実施の形態（有機光電変換層の材料として原子Ｍに置換基Ｒが直接結合した共役系化合物を用いた例）
１－１．基本構成
１－２．製造方法
１－３．作用・効果
２．適用例
３．実施例 Hereinafter, an embodiment of the present disclosure will be described in detail with reference to the drawings. The order of explanation is as follows.
1. Embodiment (Example using a conjugated compound in which a substituent R is directly bonded to an atom M as a material of an organic photoelectric conversion layer)
1-1. Basic configuration 1-2. Manufacturing method 1-3. Action / Effect Application Example 3 Example
＜１．実施の形態＞
図１は、本開示の一実施の形態の光電変換素子（光電変換素子１０）の断面構成を表したものである。光電変換素子１０は、例えば、ＣＣＤイメージセンサまたはＣＭＯＳイメージセンサ等の固体撮像装置（後述）において１つの画素を構成するものである。光電変換素子１０は、半導体基板１１の表面（受光面とは反対側の面Ｓ２）側に、画素トランジスタ（後述の転送トランジスタＴｒ１～３を含む）が形成されると共に、多層配線層（多層配線層５１）を有するものである。 <1. Embodiment>
FIG. 1 illustrates a cross-sectional configuration of a photoelectric conversion element (photoelectric conversion element 10) according to an embodiment of the present disclosure. Thephotoelectric conversion element 10 constitutes one pixel in a solid-state imaging device (described later) such as a CCD image sensor or a CMOS image sensor. In the photoelectric conversion element 10, a pixel transistor (including transfer transistors Tr1 to 3 described later) is formed on the surface (surface S2 opposite to the light receiving surface) of the semiconductor substrate 11, and a multilayer wiring layer (multilayer wiring) Layer 51).
図１は、本開示の一実施の形態の光電変換素子（光電変換素子１０）の断面構成を表したものである。光電変換素子１０は、例えば、ＣＣＤイメージセンサまたはＣＭＯＳイメージセンサ等の固体撮像装置（後述）において１つの画素を構成するものである。光電変換素子１０は、半導体基板１１の表面（受光面とは反対側の面Ｓ２）側に、画素トランジスタ（後述の転送トランジスタＴｒ１～３を含む）が形成されると共に、多層配線層（多層配線層５１）を有するものである。 <1. Embodiment>
FIG. 1 illustrates a cross-sectional configuration of a photoelectric conversion element (photoelectric conversion element 10) according to an embodiment of the present disclosure. The
本実施の形態の光電変換素子１０は、それぞれ異なる波長域の光を選択的に検出して光電変換を行う１つの有機光電変換部１１Ｇと、２つの無機光電変換部１１Ｂ，１１Ｒとが縦方向に積層された構造を有し、有機光電変換部１１Ｇは、共役面を有し、共役面に含まれると共に、共役面に対して略垂直方向に置換基Ｒが直接結合した原子Ｍ（第１の原子）を有する共役系化合物を用いて形成されたものである。
In the photoelectric conversion element 10 according to the present embodiment, one organic photoelectric conversion unit 11G that selectively detects light in different wavelength ranges and performs photoelectric conversion, and two inorganic photoelectric conversion units 11B and 11R are in the vertical direction. The organic photoelectric conversion unit 11G has a conjugate plane, is included in the conjugate plane, and has an atom M (the first M) in which the substituent R is directly bonded in a direction substantially perpendicular to the conjugate plane. Formed by using a conjugated compound having the above-mentioned atoms).
（１－１．基本構成）
光電変換素子１０は、１つの有機光電変換部１１Ｇと、２つの無機光電変換部１１Ｂ，１１Ｒとの積層構造を有しており、これにより、１つの素子で赤（Ｒ），緑（Ｇ），青（Ｂ）の各色信号を取得するようになっている。有機光電変換部１１Ｇは、半導体基板１１の裏面（面Ｓ１）上に形成され、無機光電変換部１１Ｂ，１１Ｒは、半導体基板１１内に埋め込み形成されている。以下、各部の構成について説明する。 (1-1. Basic configuration)
Thephotoelectric conversion element 10 has a laminated structure of one organic photoelectric conversion unit 11G and two inorganic photoelectric conversion units 11B and 11R. With this, red (R) and green (G) are obtained with one element. , Blue (B) color signals are acquired. The organic photoelectric conversion unit 11G is formed on the back surface (surface S1) of the semiconductor substrate 11, and the inorganic photoelectric conversion units 11B and 11R are embedded in the semiconductor substrate 11. Hereinafter, the configuration of each unit will be described.
光電変換素子１０は、１つの有機光電変換部１１Ｇと、２つの無機光電変換部１１Ｂ，１１Ｒとの積層構造を有しており、これにより、１つの素子で赤（Ｒ），緑（Ｇ），青（Ｂ）の各色信号を取得するようになっている。有機光電変換部１１Ｇは、半導体基板１１の裏面（面Ｓ１）上に形成され、無機光電変換部１１Ｂ，１１Ｒは、半導体基板１１内に埋め込み形成されている。以下、各部の構成について説明する。 (1-1. Basic configuration)
The
（有機光電変換部１１Ｇ）
有機光電変換部１１Ｇは、有機半導体を用いて、選択的な波長域の光（ここでは緑色光）を吸収して、電子－正孔対を発生させる有機光電変換素子である。有機光電変換部１１Ｇは、信号電荷を取り出すための一対の電極（下部電極１５ａ，上部電極１８）間に有機光電変換層１７を挟み込んだ構成を有している。下部電極１５ａおよび上部電極１８は、後述するように、配線層やコンタクトメタル層を介して、半導体基板１１内に埋設された導電性プラグ１２０ａ１，１２０ｂ１に電気的に接続されている。なお、本実施の形態の有機光電変換層１７が、本開示における「有機半導体層」の一具体例である。 (Organicphotoelectric conversion unit 11G)
The organicphotoelectric conversion unit 11G is an organic photoelectric conversion element that generates an electron-hole pair by absorbing light in a selective wavelength range (here, green light) using an organic semiconductor. The organic photoelectric conversion unit 11G has a configuration in which the organic photoelectric conversion layer 17 is sandwiched between a pair of electrodes (lower electrode 15a and upper electrode 18) for extracting signal charges. The lower electrode 15a and the upper electrode 18 are electrically connected to conductive plugs 120a1 and 120b1 embedded in the semiconductor substrate 11 through a wiring layer and a contact metal layer, as will be described later. The organic photoelectric conversion layer 17 of the present embodiment is a specific example of the “organic semiconductor layer” in the present disclosure.
有機光電変換部１１Ｇは、有機半導体を用いて、選択的な波長域の光（ここでは緑色光）を吸収して、電子－正孔対を発生させる有機光電変換素子である。有機光電変換部１１Ｇは、信号電荷を取り出すための一対の電極（下部電極１５ａ，上部電極１８）間に有機光電変換層１７を挟み込んだ構成を有している。下部電極１５ａおよび上部電極１８は、後述するように、配線層やコンタクトメタル層を介して、半導体基板１１内に埋設された導電性プラグ１２０ａ１，１２０ｂ１に電気的に接続されている。なお、本実施の形態の有機光電変換層１７が、本開示における「有機半導体層」の一具体例である。 (Organic
The organic
具体的には、有機光電変換部１１Ｇでは、半導体基板１１の面Ｓ１上に、層間絶縁膜１２，１４が形成され、層間絶縁膜１２には、後述する導電性プラグ１２０ａ１，１２０ｂ１のそれぞれと対向する領域に貫通孔が設けられ、各貫通孔に導電性プラグ１２０ａ２，１２０ｂ２が埋設されている。層間絶縁膜１４には、導電性プラグ１２０ａ２，１２０ｂ２のそれぞれと対向する領域に、配線層１３ａ，１３ｂが埋設されている。この層間絶縁膜１４上に、下部電極１５ａが設けられると共に、この下部電極１５ａと絶縁膜１６によって電気的に分離された配線層１５ｂが設けられている。これらのうち、下部電極１５ａ上に、有機光電変換層１７が形成され、有機光電変換層１７を覆うように上部電極１８が形成されている。詳細は後述するが、上部電極１８上には、その表面を覆うように保護層１９が形成されている。保護層１９の所定の領域にはコンタクトホールＨが設けられ、保護層１９上には、コンタクトホールＨを埋め込み、かつ配線層１５ｂの上面まで延在するコンタクトメタル層２０が形成されている。
Specifically, in the organic photoelectric conversion unit 11G, interlayer insulating films 12 and 14 are formed on the surface S1 of the semiconductor substrate 11, and the interlayer insulating film 12 is opposed to respective conductive plugs 120a1 and 120b1 described later. Through-holes are provided in the regions to be conducted, and conductive plugs 120a2 and 120b2 are embedded in the respective through-holes. In the interlayer insulating film 14, wiring layers 13a and 13b are embedded in regions facing the conductive plugs 120a2 and 120b2, respectively. A lower electrode 15 a is provided on the interlayer insulating film 14, and a wiring layer 15 b electrically separated by the lower electrode 15 a and the insulating film 16 is provided. Among these, the organic photoelectric conversion layer 17 is formed on the lower electrode 15 a, and the upper electrode 18 is formed so as to cover the organic photoelectric conversion layer 17. Although details will be described later, a protective layer 19 is formed on the upper electrode 18 so as to cover the surface thereof. A contact hole H is provided in a predetermined region of the protective layer 19, and a contact metal layer 20 that fills the contact hole H and extends to the upper surface of the wiring layer 15b is formed on the protective layer 19.
導電性プラグ１２０ａ２は、導電性プラグ１２０ａ１と共にコネクタとして機能すると共に、導電性プラグ１２０ａ１および配線層１３ａと共に、下部電極１５ａから後述する緑用蓄電層１１０Ｇへの電荷（電子）の伝送経路を形成するものである。導電性プラグ１２０ｂ２は、導電性プラグ１２０ｂ１と共にコネクタとして機能すると共に、導電性プラグ１２０ｂ１、配線層１３ｂ、配線層１５ｂおよびコンタクトメタル層２０と共に、上部電極１８からの電荷（正孔）の排出経路を形成するものである。導電性プラグ１２０ａ２，１２０ｂ２は、遮光膜としても機能させるために、例えば、チタン（Ｔｉ）、窒化チタン（ＴｉＮ）およびタングステン等の金属材料の積層膜により構成されることが望ましい。また、このような積層膜を用いることにより、導電性プラグ１２０ａ１，１２０ｂ１をｎ型またはｐ型の半導体層として形成した場合にも、シリコンとのコンタクトを確保することができるため望ましい。
The conductive plug 120a2 functions as a connector together with the conductive plug 120a1, and together with the conductive plug 120a1 and the wiring layer 13a, forms a charge (electron) transmission path from the lower electrode 15a to the green power storage layer 110G described later. Is. The conductive plug 120b2 functions as a connector together with the conductive plug 120b1, and together with the conductive plug 120b1, the wiring layer 13b, the wiring layer 15b, and the contact metal layer 20, provides a discharge path for charges (holes) from the upper electrode 18. To form. The conductive plugs 120a2 and 120b2 are desirably formed of a laminated film of a metal material such as titanium (Ti), titanium nitride (TiN) and tungsten in order to function as a light shielding film. In addition, the use of such a laminated film is desirable because contact with silicon can be ensured even when the conductive plugs 120a1 and 120b1 are formed as n-type or p-type semiconductor layers.
層間絶縁膜１２は、半導体基板１１（シリコン層１１０）との界面準位を低減させると共に、シリコン層１１０との界面からの暗電流の発生を抑制するために、界面準位の小さな絶縁膜から構成されることが望ましい。このような絶縁膜としては、例えば、酸化ハフニウム（ＨｆＯ2）膜と酸化シリコン（ＳｉＯ2）膜との積層膜を用いることができる。層間絶縁膜１４は、例えば、酸化シリコン、窒化シリコンおよび酸窒化シリコン（ＳｉＯＮ）等のうちの１種よりなる単層膜か、あるいはこれらのうちの２種以上よりなる積層膜により構成されている。
The interlayer insulating film 12 is made of an insulating film having a small interface state in order to reduce the interface state with the semiconductor substrate 11 (silicon layer 110) and to suppress the generation of dark current from the interface with the silicon layer 110. Desirably configured. As such an insulating film, for example, a stacked film of a hafnium oxide (HfO 2 ) film and a silicon oxide (SiO 2 ) film can be used. The interlayer insulating film 14 is composed of, for example, a single layer film made of one of silicon oxide, silicon nitride, silicon oxynitride (SiON), or the like, or a laminated film made of two or more of these. .
絶縁膜１６は、例えば、酸化シリコン、窒化シリコンおよび酸窒化シリコン（ＳｉＯＮ）等のうちの１種よりなる単層膜か、あるいはこれらのうちの２種以上よりなる積層膜により構成されている。絶縁膜１６は、例えば、その表面が平坦化されており、下部電極１５ａとほぼ段差のない形状およびパターンを有している。この絶縁膜１６は、光電変換素子１０が、固体撮像装置の画素として用いられる場合に、各画素の下部電極１５ａ間を電気的に分離する機能を有している。
The insulating film 16 is formed of, for example, a single layer film made of one of silicon oxide, silicon nitride, silicon oxynitride (SiON), or the like, or a laminated film made of two or more of these. For example, the surface of the insulating film 16 is flattened, and has a shape and a pattern substantially free of steps from the lower electrode 15a. The insulating film 16 has a function of electrically separating the lower electrodes 15a of each pixel when the photoelectric conversion element 10 is used as a pixel of a solid-state imaging device.
下部電極１５ａは、半導体基板１１内に形成された無機光電変換部１１Ｂ，１１Ｒの受光面と正対して、これらの受光面を覆う領域に設けられている。この下部電極１５ａは、光透過性を有する導電膜により構成され、例えば、ＩＴＯ（インジウム錫酸化物）により構成されている。但し、下部電極１５ａの構成材料としては、このＩＴＯの他にも、ドーパントを添加した酸化スズ（ＳｎＯ2）系材料、あるいはアルミニウム亜鉛酸化物（ＺｎＯ）にドーパントを添加してなる酸化亜鉛系材料を用いてもよい。酸化亜鉛系材料としては、例えば、ドーパントとしてアルミニウム（Ａｌ）を添加したアルミニウム亜鉛酸化物（ＡＺＯ）、ガリウム（Ｇａ）添加のガリウム亜鉛酸化物（ＧＺＯ）、インジウム（Ｉｎ）添加のインジウム亜鉛酸化物（ＩＺＯ）が挙げられる。また、この他にも、ＣｕＩ、ＩｎＳｂＯ4、ＺｎＭｇＯ、ＣｕＩｎＯ2、ＭｇＩＮ2Ｏ4、ＣｄＯ、ＺｎＳｎＯ3等が用いられてもよい。なお、本実施の形態では、下部電極１５ａから信号電荷（電子）の取り出しがなされるので、光電変換素子１０を画素として用いた後述の固体撮像装置では、この下部電極１５ａは画素毎に分離されて形成される。
The lower electrode 15a is provided in a region covering the light receiving surfaces facing the light receiving surfaces of the inorganic photoelectric conversion portions 11B and 11R formed in the semiconductor substrate 11. The lower electrode 15a is made of a light-transmitting conductive film, for example, ITO (Indium Tin Oxide). However, as a constituent material of the lower electrode 15a, besides this ITO, a tin oxide (SnO 2 ) -based material to which a dopant is added, or a zinc oxide-based material obtained by adding a dopant to aluminum zinc oxide (ZnO) May be used. Examples of the zinc oxide-based material include aluminum zinc oxide (AZO) to which aluminum (Al) is added as a dopant, gallium zinc oxide (GZO) to which gallium (Ga) is added, and indium zinc oxide to which indium (In) is added. (IZO). In addition, CuI, InSbO 4 , ZnMgO, CuInO 2 , MgIN 2 O 4 , CdO, ZnSnO 3, or the like may be used. In this embodiment, since signal charges (electrons) are taken out from the lower electrode 15a, the lower electrode 15a is separated for each pixel in a solid-state imaging device described later using the photoelectric conversion element 10 as a pixel. Formed.
有機光電変換層１７は、有機ｐ型半導体および有機ｎ型半導体のうちの一方または両方を含むと共に、選択的な波長域の光を光電変換する一方、他の波長域の光を透過させるものである。ここでは、有機光電変換層１７は、例えば４５０ｎｍ以上６５０ｎｍ以下の範囲において極大吸収波長を有する。
The organic photoelectric conversion layer 17 includes one or both of an organic p-type semiconductor and an organic n-type semiconductor, and photoelectrically converts light in a selective wavelength range while transmitting light in other wavelength ranges. is there. Here, the organic photoelectric conversion layer 17 has a maximum absorption wavelength in a range of 450 nm or more and 650 nm or less, for example.
本実施の形態では、有機光電変換層１７は、例えば図２に示したように、原子Ｍを含む共役面（共役面Ｐ）を有し、この原子Ｍが共役面Ｐに対して略垂直方向（所謂アキシャル位）に置換基Ｒを有する共役系化合物を用いて形成されている。置換基Ｒは、原子Ｍに直接結合している。置換基Ｒは、原子Ｍに直接結合する原子Ａ（第２の原子）と、この原子Ａと直接結合する原子Ｂ（第３の原子）とを有し、原子Ｍおよび原子Ｂと結合を形成する原子Ａの結合角、換言すると、原子Ｍと原子Ａとの結合および原子Ｂと原子Ａとの結合が形成する原子Ａの結合角が固定された分子構造を有するものである。この結合角は、置換基Ｒが形成する混成軌道によって決定される。このような置換基Ｒが原子Ｍに直接結合することにより、原子Ｍに対する置換基Ｒの回転自由度が低下し、共役系化合物の分子内におけるマイグレーションの発生が抑制される。
In the present embodiment, the organic photoelectric conversion layer 17 has a conjugate plane (conjugate plane P) including the atoms M as shown in FIG. 2, for example, and the atoms M are substantially perpendicular to the conjugate plane P. It is formed using a conjugated compound having a substituent R at a so-called axial position. The substituent R is directly bonded to the atom M. The substituent R has an atom A (second atom) directly bonded to the atom M and an atom B (third atom) directly bonded to the atom A, and forms a bond with the atom M and the atom B. The bond angle of the atom A, that is, the bond angle of the atom A formed by the bond between the atom M and the atom A and the bond between the atom B and the atom A is fixed. This bond angle is determined by the hybrid orbital formed by the substituent R. When such a substituent R is directly bonded to the atom M, the degree of freedom of rotation of the substituent R with respect to the atom M is reduced, and the occurrence of migration in the molecule of the conjugated compound is suppressed.
原子Ａとしては、例えば原子価が３価以上の原子であることが好ましく、例えば炭素（Ｃ）、窒素（Ｎ）および硫黄（Ｓ）のうちのいずれかであることが好ましい。例えば、２価の原子（例えば酸素（Ｏ））の場合には、酸素（Ｏ）を基点とした置換基Ｒの回転が可能となるからである。このため、具体的な置換基Ｒとしては、炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物、複素環化合物、芳香族化合物と複素環化合物が縮環した共役系化合物、アシル基、シアノ基およびニトロ基が挙げられる。
As the atom A, for example, an atom having a valence of 3 or more is preferable, and for example, any one of carbon (C), nitrogen (N), and sulfur (S) is preferable. For example, in the case of a divalent atom (for example, oxygen (O)), the rotation of the substituent R with oxygen (O) as a starting point becomes possible. For this reason, specific substituents R include linear, branched, or cyclic alkyl groups having 1 to 80 carbon atoms, perfluoroalkyl groups, aromatic compounds, heterocyclic compounds, aromatic compounds and heterocyclic compounds. Examples include condensed conjugated compounds, acyl groups, cyano groups, and nitro groups.
炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物の具体例としては、例えばフェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレンおよびこれらの誘導体が挙げられる。複素環化合物の具体例としては、例えばアニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体が挙げられる。芳香族化合物と複素環化合物が縮環した共役系化合物（含複素環共役系化合物）の具体例としては、例えばフェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレン、アニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体のいずれかが互いに縮環したものが挙げられる。この他、置換基Ｒとしては、原子Ｍと、Ｍに結合している原子と、さらに隣接する原子がなす角度が、分子が形成する混成軌道により固定されているような置換基、例えばトリメチルシリル基、トリアリールシリル基、スルホニル基、シアノ基およびニトロ基であってもよい。
Specific examples of linear, branched, or cyclic alkyl groups having 1 to 80 carbon atoms, perfluoroalkyl groups, and aromatic compounds include phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, and triphenylene. , Rubrene, fullerene and derivatives thereof. Specific examples of the heterocyclic compound include aniline, pyrrole, triallylamine, imidazole, triazole, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, And furan and derivatives thereof. Specific examples of a conjugated compound (heterocyclic conjugated compound) in which an aromatic compound and a heterocyclic compound are condensed include phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, Fullerene, aniline, pyrrole, triallylamine, imidazole, triazole, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and any of these derivatives Are mutually condensed rings. In addition, examples of the substituent R include a substituent in which an angle formed by an atom M, an atom bonded to M, and an adjacent atom is fixed by a hybrid orbital formed by the molecule, such as a trimethylsilyl group. , A triarylsilyl group, a sulfonyl group, a cyano group and a nitro group.
共役系化合物の具体例としては、例えば下記式（１）で表わされるサブフタロシアニン誘導体が挙げられる。
Specific examples of the conjugated compound include a subphthalocyanine derivative represented by the following formula (1).
また、共役系化合物として、下記式（２）で表わされるフタロシアニン誘導体が挙げられる。
Further, as the conjugated compound, a phthalocyanine derivative represented by the following formula (2) can be given.
また、共役系化合物として、下記式（３）で表わされるサブポルフィリン誘導体が挙げられる。
In addition, examples of the conjugated compound include a subporphyrin derivative represented by the following formula (3).
また、共役系化合物として、下記式（４）で表わされるポルフィリン誘導体が挙げられる。
In addition, examples of the conjugated compound include porphyrin derivatives represented by the following formula (4).
有機光電変換層１７の材料としては、上記共役系化合物の他に、例えばキナクリドンおよびその誘導体、フラーレンおよびその誘導体等を用いてもよい。例えば上記共役系化合物と共に、キナクリドン誘導体とを用いた場合には、共役系化合物は有機ｎ型半導体として機能し、キナクリドン誘導体は有機ｐ型半導体として機能する。
As a material for the organic photoelectric conversion layer 17, for example, quinacridone and derivatives thereof, fullerene and derivatives thereof, and the like may be used in addition to the conjugated compound. For example, when a quinacridone derivative is used together with the conjugated compound, the conjugated compound functions as an organic n-type semiconductor, and the quinacridone derivative functions as an organic p-type semiconductor.
有機光電変換層１７の下部電極１５ａとの間、および上部電極１８との間には、図示しない他の層が設けられていてもよい。例えば、下部電極１５ａ側から順に、下引き膜、正孔輸送層、電子ブロッキング膜、有機光電変換層１７、正孔ブロッキング膜、バッファ膜、電子輸送層および仕事関数調整膜が積層されていてもよい。
Other layers (not shown) may be provided between the lower electrode 15 a of the organic photoelectric conversion layer 17 and the upper electrode 18. For example, even if an undercoat film, a hole transport layer, an electron blocking film, an organic photoelectric conversion layer 17, a hole blocking film, a buffer film, an electron transport layer, and a work function adjusting film are stacked in this order from the lower electrode 15a side. Good.
上部電極１８は、下部電極１５ａと同様の光透過性を有する導電膜により構成されている。光電変換素子１０を画素として用いた固体撮像装置では、この上部電極１８が画素毎に分離されていてもよいし、各画素に共通の電極として形成されていてもよい。上部電極１８の厚みは、例えば、１０ｎｍ～２００ｎｍである。
The upper electrode 18 is composed of a conductive film having the same optical transparency as the lower electrode 15a. In the solid-state imaging device using the photoelectric conversion element 10 as a pixel, the upper electrode 18 may be separated for each pixel, or may be formed as a common electrode for each pixel. The thickness of the upper electrode 18 is, for example, 10 nm to 200 nm.
保護層１９は、光透過性を有する材料により構成され、例えば、酸化シリコン、窒化シリコンおよび酸窒化シリコン等のうちのいずれかよりなる単層膜、あるいはそれらのうちの２種以上よりなる積層膜である。この保護層１９の厚みは、例えば、１００ｎｍ～３００００ｎｍである。
The protective layer 19 is made of a light-transmitting material. For example, the protective layer 19 is a single-layer film made of any of silicon oxide, silicon nitride, silicon oxynitride, or the like, or a laminated film made of two or more of them. It is. The thickness of the protective layer 19 is, for example, 100 nm to 30000 nm.
コンタクトメタル層２０は、例えば、チタン、タングステン、窒化チタンおよびアルミニウム等のいずれか、あるいはそれらのうちの２種以上よりなる積層膜により構成されている。
The contact metal layer 20 is made of, for example, any one of titanium, tungsten, titanium nitride, aluminum and the like, or a laminated film made of two or more of them.
上部電極１８および保護層１９は、例えば、有機光電変換層１７を覆うように設けられている。図３は、有機光電変換層１７、保護層１９（上部電極１８）およびコンタクトホールＨの平面構成を表したものである。
The upper electrode 18 and the protective layer 19 are provided so as to cover the organic photoelectric conversion layer 17, for example. FIG. 3 shows a planar configuration of the organic photoelectric conversion layer 17, the protective layer 19 (upper electrode 18), and the contact hole H.
具体的には、保護層１９（上部電極１８も同様）の周縁部ｅ２は、有機光電変換層１７の周縁部ｅ１よりも外側に位置しており、保護層１９および上部電極１８は、有機光電変換層１７よりも外側に張り出して形成されている。詳細には、上部電極１８は、有機光電変換層１７の上面および側面を覆うと共に、絶縁膜１６上まで延在するように形成されている。保護層１９は、そのような上部電極１８の上面を覆って、上部電極１８と同等の平面形状で形成されている。コンタクトホールＨは、保護層１９のうちの有機光電変換層１７に非対向の領域（周縁部ｅ１よりも外側の領域）に設けられ、上部電極１８の表面の一部を露出させている。周縁部ｅ１，ｅ２間の距離は、特に限定されるものではないが、例えば、１μｍ～５００μｍである。なお、図３では、有機光電変換層１７の端辺に沿った１つの矩形状のコンタクトホールＨを設けているが、コンタクトホールＨの形状や個数はこれに限定されず、他の形状（例えば、円形、正方形等）であってもよいし、複数設けられていてもよい。
Specifically, the peripheral edge e2 of the protective layer 19 (the same applies to the upper electrode 18) is located outside the peripheral edge e1 of the organic photoelectric conversion layer 17, and the protective layer 19 and the upper electrode 18 are organic photoelectric photoelectric. It is formed to protrude outward from the conversion layer 17. Specifically, the upper electrode 18 is formed so as to cover the upper surface and side surfaces of the organic photoelectric conversion layer 17 and to extend onto the insulating film 16. The protective layer 19 is formed in a planar shape equivalent to the upper electrode 18 so as to cover the upper surface of the upper electrode 18. The contact hole H is provided in a region of the protective layer 19 that is not opposed to the organic photoelectric conversion layer 17 (region outside the peripheral edge e1), and exposes a part of the surface of the upper electrode 18. The distance between the peripheral portions e1 and e2 is not particularly limited, but is, for example, 1 μm to 500 μm. In FIG. 3, one rectangular contact hole H is provided along the edge of the organic photoelectric conversion layer 17. However, the shape and number of the contact holes H are not limited to this, and other shapes (for example, , Circular, square, etc.) or a plurality of them may be provided.
保護層１９およびコンタクトメタル層２０上には、全面を覆うように、平坦化膜２１が形成されている。平坦化膜２１上には、オンチップレンズ２２（マイクロレンズ）が設けられている。オンチップレンズ２２は、その上方から入射した光を、有機光電変換部１１Ｇ、無機光電変換部１１Ｂ，１１Ｒの各受光面へ集光させるものである。本実施の形態では、多層配線層５１が半導体基板１１の面Ｓ２側に形成されていることから、有機光電変換部１１Ｇ、無機光電変換部１１Ｂ，１１Ｒの各受光面を互いに近づけて配置することができ、オンチップレンズ２２のＦ値に依存して生じる各色間の感度のばらつきを低減することができる。
A planarizing film 21 is formed on the protective layer 19 and the contact metal layer 20 so as to cover the entire surface. On the planarization film 21, an on-chip lens 22 (microlens) is provided. The on-chip lens 22 focuses light incident from above on the light receiving surfaces of the organic photoelectric conversion unit 11G and the inorganic photoelectric conversion units 11B and 11R. In the present embodiment, since the multilayer wiring layer 51 is formed on the surface S2 side of the semiconductor substrate 11, the light receiving surfaces of the organic photoelectric conversion unit 11G and the inorganic photoelectric conversion units 11B and 11R are arranged close to each other. Thus, it is possible to reduce the variation in sensitivity between the colors depending on the F value of the on-chip lens 22.
なお、本実施の形態の光電変換素子１０では、下部電極１５ａから信号電荷（電子）を取り出すことから、これを画素として用いる固体撮像装置においては、上部電極１８を共通電極としてもよい。この場合には、上述したコンタクトホールＨ、コンタクトメタル層２０、配線層１５ｂ，１３ｂ、導電性プラグ１２０ｂ１，１２０ｂ２からなる伝送経路は、全画素に対して少なくとも１箇所に形成されればよい。
In the photoelectric conversion element 10 of the present embodiment, signal charges (electrons) are taken out from the lower electrode 15a. Therefore, in the solid-state imaging device using this as a pixel, the upper electrode 18 may be used as a common electrode. In this case, the transmission path including the contact hole H, the contact metal layer 20, the wiring layers 15b and 13b, and the conductive plugs 120b1 and 120b2 may be formed in at least one place for all the pixels.
半導体基板１１は、例えば、ｎ型のシリコン（Ｓｉ）層１１０の所定の領域に、無機光電変換部１１Ｂ，１１Ｒと緑用蓄電層１１０Ｇとが埋め込み形成されたものである。半導体基板１１には、また、有機光電変換部１１Ｇからの電荷（電子または正孔（正孔））の伝送経路となる導電性プラグ１２０ａ１，１２０ｂ１が埋設されている。本実施の形態では、この半導体基板１１の裏面（面Ｓ１）が受光面となっていえる。半導体基板１１の表面（面Ｓ２）側には、有機光電変換部１１Ｇ，無機光電変換部１１Ｂ，１１Ｒのそれぞれに対応する複数の画素トランジスタ（転送トランジスタＴｒ１～Ｔｒ３を含む）が形成されると共に、ロジック回路等からなる周辺回路が形成されている。
The semiconductor substrate 11 is, for example, formed by embedding inorganic photoelectric conversion portions 11B and 11R and a green power storage layer 110G in a predetermined region of an n-type silicon (Si) layer 110. The semiconductor substrate 11 is also embedded with conductive plugs 120a1 and 120b1 serving as a transmission path for charges (electrons or holes (holes)) from the organic photoelectric conversion unit 11G. In the present embodiment, the back surface (surface S1) of the semiconductor substrate 11 can be said to be a light receiving surface. On the surface (surface S2) side of the semiconductor substrate 11, a plurality of pixel transistors (including transfer transistors Tr1 to Tr3) corresponding to the organic photoelectric conversion unit 11G and the inorganic photoelectric conversion units 11B and 11R are formed. A peripheral circuit composed of a logic circuit or the like is formed.
画素トランジスタとしては、例えば、転送トランジスタ、リセットトランジスタ、増幅トランジスタおよび選択トランジスタが挙げられる。これらの画素トランジスタは、いずれも例えば、ＭＯＳトランジスタにより構成され、面Ｓ２側のｐ型半導体ウェル領域に形成されている。このような画素トランジスタを含む回路が、赤、緑、青の光電変換部毎に形成されている。各回路では、これらの画素トランジスタのうち、例えば、転送トランジスタ、リセットトランジスタおよび増幅トランジスタからなる、計３つのトランジスタを含む３トランジスタ構成を有していてもよいし、これに選択トランジスタを加えた４トランジスタ構成であってもよい。ここでは、これらの画素トランジスタのうち、転送トランジスタＴｒ１～Ｔｒ３についてのみ図示および説明を行っている。また、転送トランジスタ以外の他の画素トランジスタについては、光電変換部間あるいは画素間において共有することもできる。また、フローティングディフージョンを共有する、いわゆる画素共有構造を適用することもできる。
Examples of the pixel transistor include a transfer transistor, a reset transistor, an amplification transistor, and a selection transistor. Each of these pixel transistors is composed of, for example, a MOS transistor, and is formed in a p-type semiconductor well region on the surface S2. A circuit including such a pixel transistor is formed for each of the red, green, and blue photoelectric conversion units. Each circuit may have a three-transistor configuration including a total of three transistors including a transfer transistor, a reset transistor, and an amplifying transistor, among these pixel transistors. A transistor configuration may be used. Here, among these pixel transistors, only the transfer transistors Tr1 to Tr3 are shown and described. Further, pixel transistors other than the transfer transistor can be shared between photoelectric conversion units or between pixels. Further, a so-called pixel sharing structure that shares a floating diffusion can also be applied.
転送トランジスタＴｒ１～Ｔｒ３は、ゲート電極（ゲート電極ＴＧ１～ＴＧ３）と、フローティングディフージョン（ＦＤ１１３，１１４，１１６）とを含んで構成されている。転送トランジスタＴｒ１は、有機光電変換部１１Ｇにおいて発生し、緑用蓄電層１１０Ｇに蓄積された、緑色に対応する信号電荷（本実施の形態では電子）を、後述の垂直信号線Ｌsigへ転送するものである。転送トランジスタＴｒ２は、無機光電変換部１１Ｂにおいて発生し、蓄積された、青色に対応する信号電荷（本実施の形態では電子）を、後述の垂直信号線Ｌsigへ転送するものである。同様に、転送トランジスタＴｒ３は、無機光電変換部１１Ｒにおいて発生し、蓄積された、赤色に対応する信号電荷（本実施の形態では電子）を、後述の垂直信号線Ｌsigへ転送するものである。
The transfer transistors Tr1 to Tr3 are configured to include gate electrodes (gate electrodes TG1 to TG3) and floating diffusions ( FDs 113, 114, and 116). The transfer transistor Tr1 transfers the signal charge corresponding to green (electrons in the present embodiment) generated in the organic photoelectric conversion unit 11G and accumulated in the green power storage layer 110G to a vertical signal line Lsig described later. It is. The transfer transistor Tr2 transfers the signal charge (electrons in the present embodiment) corresponding to blue generated and accumulated in the inorganic photoelectric conversion unit 11B to a vertical signal line Lsig described later. Similarly, the transfer transistor Tr3 transfers signal charges (electrons in the present embodiment) corresponding to red color generated and accumulated in the inorganic photoelectric conversion unit 11R to a vertical signal line Lsig described later.
無機光電変換部１１Ｂ，１１Ｒはそれぞれ、ｐｎ接合を有するフォトダイオード（Photo Diode）であり、半導体基板１１内の光路上において、面Ｓ１側から無機光電変換部１１Ｂ，１１Ｒの順に形成されている。これらのうち、無機光電変換部１１Ｂは、青色光を選択的に検出して青色に対応する信号電荷を蓄積させるものであり、例えば、半導体基板１１の面Ｓ１に沿った選択的な領域から、多層配線層５１との界面近傍の領域にかけて延在して形成されている。無機光電変換部１１Ｒは、赤色光を選択的に検出して赤色に対応する信号電荷を蓄積させるものであり、例えば、無機光電変換部１１Ｂよりも下層（面Ｓ２側）の領域にわたって形成されている。なお、青（Ｂ）は、例えば、４５０ｎｍ～４９５ｎｍの波長域、赤（Ｒ）は、例えば、６２０ｎｍ～７５０ｎｍの波長域にそれぞれ対応する色であり、無機光電変換部１１Ｂ，１１Ｒはそれぞれ、各波長域のうちの一部または全部の波長域の光を検出可能となっていればよい。
The inorganic photoelectric conversion units 11B and 11R are photodiodes having pn junctions (Photo-Diodes), and are formed in the order of the inorganic photoelectric conversion units 11B and 11R from the surface S1 side on the optical path in the semiconductor substrate 11. Among these, the inorganic photoelectric conversion unit 11B selectively detects blue light and accumulates signal charges corresponding to blue. For example, from a selective region along the surface S1 of the semiconductor substrate 11, It is formed to extend over a region near the interface with the multilayer wiring layer 51. The inorganic photoelectric conversion unit 11R selectively detects red light and accumulates signal charges corresponding to red. For example, the inorganic photoelectric conversion unit 11R is formed over a lower layer (surface S2 side) than the inorganic photoelectric conversion unit 11B. Yes. For example, blue (B) is a color corresponding to a wavelength range of 450 nm to 495 nm, red (R) is a color corresponding to a wavelength range of 620 nm to 750 nm, for example, and the inorganic photoelectric conversion units 11B and 11R are respectively It is only necessary that light in a part or all of the wavelength range can be detected.
図４（Ａ）は、無機光電変換部１１Ｂ，１１Ｒの詳細構成例を表したものである。図４（Ｂ）は、図４（Ａ）の他の断面における構成に相当するものである。なお、本実施の形態では、光電変換によって生じる電子および正孔の対のうち、電子を信号電荷として読み出す場合（ｎ型半導体領域を光電変換層とする場合）について説明を行う。また、図中において、「ｐ」「ｎ」に上付きで記した「＋（プラス）」は、ｐ型またはｎ型の不純物濃度が高いことを表している。また、画素トランジスタのうち、転送トランジスタＴｒ２，Ｔｒ３のゲート電極ＴＧ２，ＴＧ３についても示している。
FIG. 4A shows a detailed configuration example of the inorganic photoelectric conversion units 11B and 11R. FIG. 4B corresponds to a structure in another cross section of FIG. Note that in this embodiment, a case where electrons are read out as signal charges out of a pair of electrons and holes generated by photoelectric conversion (when an n-type semiconductor region is used as a photoelectric conversion layer) will be described. In the figure, “+ (plus)” superscripted on “p” and “n” represents a high p-type or n-type impurity concentration. In addition, among the pixel transistors, the gate electrodes TG2 and TG3 of the transfer transistors Tr2 and Tr3 are also shown.
無機光電変換部１１Ｂは、例えば、正孔蓄積層となるｐ型半導体領域（以下、単にｐ型領域という、ｎ型の場合についても同様。）１１１ｐと、電子蓄積層となるｎ型光電変換層（ｎ型領域）１１１ｎとを含んで構成されている。ｐ型領域１１１ｐおよびｎ型光電変換層１１１ｎはそれぞれ、面Ｓ１近傍の選択的な領域に形成されると共に、その一部が屈曲し、面Ｓ２との界面に達するように延在形成されている。ｐ型領域１１１ｐは、面Ｓ１側において、図示しないｐ型半導体ウェル領域に接続されている。ｎ型光電変換層１１１ｎは、青色用の転送トランジスタＴｒ２のＦＤ１１３（ｎ型領域）に接続されている。なお、ｐ型領域１１１ｐおよびｎ型光電変換層１１１ｎの面Ｓ２側の各端部と面Ｓ２との界面近傍には、ｐ型領域１１３ｐ（正孔蓄積層）が形成されている。
The inorganic photoelectric conversion unit 11B includes, for example, a p-type semiconductor region (hereinafter simply referred to as a p-type region, also referred to as an n-type) 111p serving as a hole accumulation layer, and an n-type photoelectric conversion layer serving as an electron accumulation layer. (N-type region) 111n. Each of the p-type region 111p and the n-type photoelectric conversion layer 111n is formed in a selective region in the vicinity of the surface S1, and a part thereof is bent so as to extend to reach the interface with the surface S2. . The p-type region 111p is connected to a p-type semiconductor well region (not shown) on the surface S1 side. The n-type photoelectric conversion layer 111n is connected to the FD 113 (n-type region) of the blue transfer transistor Tr2. Note that a p-type region 113p (hole accumulation layer) is formed in the vicinity of the interface between each end of the p-type region 111p and the n-type photoelectric conversion layer 111n on the surface S2 side and the surface S2.
無機光電変換部１１Ｒは、例えば、ｐ型領域１１２ｐ１，１１２ｐ２（正孔蓄積層）間に、ｎ型光電変換層１１２ｎ（電子蓄積層）を挟み込んで形成されている（ｐ－ｎ－ｐの積層構造を有する）。ｎ型光電変換層１１２ｎは、その一部が屈曲し、面Ｓ２との界面に達するように延在形成されている。ｎ型光電変換層１１２ｎは、赤色用の転送トランジスタＴｒ３のＦＤ１１４（ｎ型領域）に接続されている。なお、少なくともｎ型光電変換層１１１ｎの面Ｓ２側の端部と面Ｓ２との界面近傍にはｐ型領域１１３ｐ（正孔蓄積層）が形成されている。
For example, the inorganic photoelectric conversion unit 11R is formed by sandwiching an n-type photoelectric conversion layer 112n (electron storage layer) between p-type regions 112p1 and 112p2 (hole storage layer) (stacking of pnp). Having structure). A part of the n-type photoelectric conversion layer 112n is bent and extended so as to reach the interface with the surface S2. The n-type photoelectric conversion layer 112n is connected to the FD 114 (n-type region) of the red transfer transistor Tr3. A p-type region 113p (hole accumulation layer) is formed at least near the interface between the end of the n-type photoelectric conversion layer 111n on the surface S2 side and the surface S2.
図５は、緑用蓄電層１１０Ｇの詳細構成例を表したものである。なお、ここでは、有機光電変換部１１Ｇによって生じる電子および正孔の対のうち、電子を信号電荷として、下部電極１５ａ側から読み出す場合について説明を行う。また、図５には、画素トランジスタのうち、転送トランジスタＴｒ１のゲート電極ＴＧ１についても示している。
FIG. 5 shows a detailed configuration example of the green power storage layer 110G. Here, a description will be given of a case where electrons out of the pair of electrons and holes generated by the organic photoelectric conversion unit 11G are read from the lower electrode 15a side as signal charges. FIG. 5 also shows the gate electrode TG1 of the transfer transistor Tr1 among the pixel transistors.
緑用蓄電層１１０Ｇは、電子蓄積層となるｎ型領域１１５ｎを含んで構成されている。ｎ型領域１１５ｎの一部は、導電性プラグ１２０ａ１に接続されており、下部電極１５ａ側から導電性プラグ１２０ａ１を介して伝送される電子を蓄積するようになっている。このｎ型領域１１５ｎは、また、緑色用の転送トランジスタＴｒ１のＦＤ１１６（ｎ型領域）に接続されている。なお、ｎ型領域１１５ｎと面Ｓ２との界面近傍には、ｐ型領域１１５ｐ（正孔蓄積層）が形成されている。
The green power storage layer 110G includes an n-type region 115n that serves as an electron storage layer. A part of the n-type region 115n is connected to the conductive plug 120a1, and accumulates electrons transmitted from the lower electrode 15a side through the conductive plug 120a1. The n-type region 115n is also connected to the FD 116 (n-type region) of the green transfer transistor Tr1. A p-type region 115p (hole accumulation layer) is formed in the vicinity of the interface between the n-type region 115n and the surface S2.
導電性プラグ１２０ａ１，１２０ｂ１は、後述の導電性プラグ１２０ａ２，１２０ｂ２と共に、有機光電変換部１１Ｇと半導体基板１１とのコネクタとして機能すると共に、有機光電変換部１１Ｇにおいて生じた電子または正孔の伝送経路となるものである。本実施の形態では、導電性プラグ１２０ａ１は、有機光電変換部１１Ｇの下部電極１５ａと導通しており、緑用蓄電層１１０Ｇと接続されている。導電性プラグ１２０ｂ１は、有機光電変換部１１Ｇの上部電極１８と導通しており、正孔を排出するための配線となっている。
The conductive plugs 120a1 and 120b1, together with conductive plugs 120a2 and 120b2 described later, function as a connector between the organic photoelectric conversion unit 11G and the semiconductor substrate 11, and a transmission path for electrons or holes generated in the organic photoelectric conversion unit 11G. It will be. In the present embodiment, the conductive plug 120a1 is electrically connected to the lower electrode 15a of the organic photoelectric conversion unit 11G and is connected to the green power storage layer 110G. The conductive plug 120b1 is electrically connected to the upper electrode 18 of the organic photoelectric conversion unit 11G, and serves as a wiring for discharging holes.
これらの導電性プラグ１２０ａ１，１２０ｂ１はそれぞれ、例えば、導電型の半導体層により構成され、半導体基板１１に埋め込み形成されたものである。この場合、導電性プラグ１２０ａ１はｎ型とし（電子の伝送経路となるため）、導電性プラグ１２０ｂ１は、ｐ型とする（正孔の伝送経路となるため）とよい。あるいは、導電性プラグ１２０ａ１，１２０ｂ１は、例えば、貫通ビアにタングステン等の導電膜材料が埋設されたものであってもよい。この場合、例えば、シリコンとの短絡を抑制するために、酸化シリコン（ＳｉＯ2）または窒化シリコン（ＳｉＮ）等の絶縁膜でビア側面が覆われていることが望ましい。
Each of these conductive plugs 120a1 and 120b1 is made of, for example, a conductive semiconductor layer and is embedded in the semiconductor substrate 11. In this case, the conductive plug 120a1 may be n-type (because it becomes an electron transmission path), and the conductive plug 120b1 may be p-type (because it becomes a hole transmission path). Alternatively, the conductive plugs 120a1 and 120b1 may be, for example, those in which a conductive film material such as tungsten is embedded in the through via. In this case, for example, in order to suppress a short circuit with silicon, it is desirable that the via side surface be covered with an insulating film such as silicon oxide (SiO 2 ) or silicon nitride (SiN).
半導体基板１１の面Ｓ２上には、多層配線層５１が形成されている。多層配線層５１では、複数の配線５１ａが層間絶縁膜５２を介して配設されている。このように、光電変換素子１０では、多層配線層５１が受光面とは反対側に形成されており、いわゆる裏面照射型の固体撮像装置を実現可能となっている。この多層配線層５１には、例えば、シリコンよりなる支持基板５３が貼り合わせられている。
A multilayer wiring layer 51 is formed on the surface S2 of the semiconductor substrate 11. In the multilayer wiring layer 51, a plurality of wirings 51 a are arranged via an interlayer insulating film 52. Thus, in the photoelectric conversion element 10, the multilayer wiring layer 51 is formed on the side opposite to the light receiving surface, and a so-called back-illuminated solid-state imaging device can be realized. For example, a support substrate 53 made of silicon is bonded to the multilayer wiring layer 51.
（１－２．製造方法）
光電変換素子１０は、例えば、次のようにして製造することができる。図６Ａ～図８Ｃは、光電変換素子１０の製造方法を工程順に表したものである。なお、図８Ａ～図８Ｃでは、光電変換素子１０の要部構成のみを示している。なお、以下に述べる光電変換素子１０の作製方法はあくまでも一例であって、本開示の実施形態に係る光電変換素子１０（および後述する光電変換素子３０）作製方法が下記の例に限定されるものではない。 (1-2. Manufacturing method)
Thephotoelectric conversion element 10 can be manufactured as follows, for example. 6A to 8C show a method for manufacturing the photoelectric conversion element 10 in the order of steps. 8A to 8C show only the main configuration of the photoelectric conversion element 10. Note that the manufacturing method of the photoelectric conversion element 10 described below is merely an example, and the manufacturing method of the photoelectric conversion element 10 (and the photoelectric conversion element 30 described later) according to the embodiment of the present disclosure is limited to the following example. is not.
光電変換素子１０は、例えば、次のようにして製造することができる。図６Ａ～図８Ｃは、光電変換素子１０の製造方法を工程順に表したものである。なお、図８Ａ～図８Ｃでは、光電変換素子１０の要部構成のみを示している。なお、以下に述べる光電変換素子１０の作製方法はあくまでも一例であって、本開示の実施形態に係る光電変換素子１０（および後述する光電変換素子３０）作製方法が下記の例に限定されるものではない。 (1-2. Manufacturing method)
The
まず、半導体基板１１を形成する。具体的には、シリコン基体１１０１上にシリコン酸化膜１１０２を介して、シリコン層１１０が形成された、いわゆるＳＯＩ基板を用意する。なお、シリコン層１１０のシリコン酸化膜１１０２側の面が半導体基板１１の裏面（面Ｓ１）となる。図６Ａ，図６Ｂでは、図１に示した構造と上下を逆転させた状態で図示している。続いて、図６Ａに示したように、シリコン層１１０に、導電性プラグ１２０ａ１，１２０ｂ１を形成する。この際、導電性プラグ１２０ａ１，１２０ｂ１は、例えば、シリコン層１１０に貫通ビアを形成した後、この貫通ビア内に、上述したような窒化シリコン等のバリアメタルと、タングステンを埋め込むことにより形成することができる。あるいは、例えば、シリコン層１１０へのイオン注入により導電型不純物半導体層を形成してもよい。この場合、導電性プラグ１２０ａ１をｎ型半導体層、導電性プラグ１２０ｂ１をｐ型半導体層として形成する。この後、シリコン層１１０内の深さの異なる領域に（互いに重畳するように）、例えば、図４Ａに示したようなｐ型領域およびｎ型領域をそれぞれ有する無機光電変換部１１Ｂ，１１Ｒを、イオン注入により形成する。また、導電性プラグ１２０ａ１に隣接する領域には、緑用蓄電層１１０Ｇをイオン注入により形成する。このようにして、半導体基板１１が形成される。
First, the semiconductor substrate 11 is formed. Specifically, a so-called SOI substrate in which a silicon layer 110 is formed on a silicon substrate 1101 with a silicon oxide film 1102 interposed therebetween is prepared. The surface of the silicon layer 110 on the silicon oxide film 1102 side is the back surface (surface S1) of the semiconductor substrate 11. 6A and 6B, the structure shown in FIG. 1 is shown upside down. Subsequently, as shown in FIG. 6A, conductive plugs 120 a 1 and 120 b 1 are formed in the silicon layer 110. At this time, the conductive plugs 120a1 and 120b1 are formed by, for example, forming a through via in the silicon layer 110 and then burying the barrier metal such as silicon nitride and tungsten as described above in the through via. Can do. Alternatively, for example, a conductive impurity semiconductor layer may be formed by ion implantation into the silicon layer 110. In this case, the conductive plug 120a1 is formed as an n-type semiconductor layer, and the conductive plug 120b1 is formed as a p-type semiconductor layer. Thereafter, inorganic photoelectric conversion units 11B and 11R each having a p-type region and an n-type region as shown in FIG. 4A, for example, in regions with different depths in the silicon layer 110 (so as to overlap each other) It is formed by ion implantation. In addition, in the region adjacent to the conductive plug 120a1, the green power storage layer 110G is formed by ion implantation. In this way, the semiconductor substrate 11 is formed.
次いで、半導体基板１１の面Ｓ２側に、転送トランジスタＴｒ１～Ｔｒ３を含む画素トランジスタと、ロジック回路等の周辺回路を形成したのち、図６Ｂに示したように、半導体基板１１の面Ｓ２上に、層間絶縁膜５２を介して複数層の配線５１ａを形成することにより、多層配線層５１を形成する。続いて、多層配線層５１上に、シリコンよりなる支持基板５３を貼り付けたのち、半導体基板１１の面Ｓ１側から、シリコン基体１１０１およびシリコン酸化膜１１０２を剥離し、半導体基板１１の面Ｓ１を露出させる。
Next, after forming pixel transistors including transfer transistors Tr1 to Tr3 and peripheral circuits such as logic circuits on the surface S2 side of the semiconductor substrate 11, as shown in FIG. 6B, on the surface S2 of the semiconductor substrate 11, A multilayer wiring layer 51 is formed by forming a plurality of layers of wirings 51 a via the interlayer insulating film 52. Subsequently, after a support substrate 53 made of silicon is pasted on the multilayer wiring layer 51, the silicon substrate 1101 and the silicon oxide film 1102 are peeled off from the surface S1 side of the semiconductor substrate 11, and the surface S1 of the semiconductor substrate 11 is removed. Expose.
次に、半導体基板１１の面Ｓ１上に、有機光電変換部１１Ｇを形成する。具体的には、まず、図７Ａに示したように、半導体基板１１の面Ｓ１上に、上述したような酸化ハフニウム膜と酸化シリコン膜との積層膜よりなる層間絶縁膜１２を形成する。例えば、ＡＬＤ（原子層堆積）法により酸化ハフニウム膜を成膜した後、例えば、プラズマＣＶＤ（Chemical Vapor Deposition：化学気相成長）法により酸化シリコン膜を成膜する。この後、層間絶縁膜１２の導電性プラグ１２０ａ１，１２０ｂ１に対向する位置に、コンタクトホールＨ１ａ，Ｈ１ｂを形成し、これらのコンタクトホールＨ１ａ，Ｈ１ｂをそれぞれ埋め込むように、上述した材料よりなる導電性プラグ１２０ａ２，１２０ｂ２を形成する。この際、導電性プラグ１２０ａ２，１２０ｂ２を、遮光したい領域まで張り出して（遮光したい領域を覆うように）形成してもよいし、導電性プラグ１２０ａ２，１２０ｂ２とは分離した領域に遮光層を形成してもよい。
Next, the organic photoelectric conversion unit 11G is formed on the surface S1 of the semiconductor substrate 11. Specifically, first, as shown in FIG. 7A, on the surface S1 of the semiconductor substrate 11, the interlayer insulating film 12 made of the laminated film of the hafnium oxide film and the silicon oxide film as described above is formed. For example, after forming a hafnium oxide film by an ALD (atomic layer deposition) method, a silicon oxide film is formed by, for example, a plasma CVD (Chemical Vapor Deposition) method. After that, contact holes H1a and H1b are formed at positions facing the conductive plugs 120a1 and 120b1 of the interlayer insulating film 12, and the conductive plugs made of the above-described materials so as to embed these contact holes H1a and H1b, respectively. 120a2 and 120b2 are formed. At this time, the conductive plugs 120a2 and 120b2 may be formed so as to extend to a region where light shielding is desired (so as to cover the region where light shielding is desired), or a light shielding layer may be formed in a region separated from the conductive plugs 120a2 and 120b2. May be.
続いて、図７Ｂに示したように、上述した材料よりなる層間絶縁膜１４を、例えば、プラズマＣＶＤ法により成膜する。なお、成膜後、例えば、ＣＭＰ（Chemical Mechanical Polishing：化学機械研磨）法により、層間絶縁膜１４の表面を平坦化することが望ましい。次いで、層間絶縁膜１４の導電性プラグ１２０ａ２，１２０ｂ２に対向する位置に、コンタクトホールをそれぞれ開口し、上述した材料を埋め込むことにより、配線層１３ａ，１３ｂを形成する。なお、この後、例えば、ＣＭＰ法等を用いて、層間絶縁膜１４上の余剰の配線層材料（タングステン等）を除去することが望ましい。次いで、層間絶縁膜１４上に下部電極１５ａを形成する。具体的には、まず、層間絶縁膜１４上の全面にわたって、例えば、スパッタ法により、上述した透明導電膜を成膜する。この後、フォトリソグラフィ法を用いて（フォトレジスト膜の露光、現像、ポストベーク等を行い）、例えば、ドライエッチングまたはウェットエッチングを用いて、選択的な部分を除去することにより、下部電極１５ａを形成する。この際、下部電極１５ａを、配線層１３ａに対向する領域に形成する。また、透明導電膜の加工の際には、配線層１３ｂに対向する領域にも透明導電膜を残存させることにより、正孔の伝送経路の一部を構成する配線層１５ｂを、下部電極１５ａと共に形成する。
Subsequently, as shown in FIG. 7B, the interlayer insulating film 14 made of the above-described material is formed by, for example, a plasma CVD method. Note that, after the film formation, it is desirable to planarize the surface of the interlayer insulating film 14 by, for example, a CMP (Chemical Mechanical Polishing) method. Subsequently, contact holes are respectively opened at positions of the interlayer insulating film 14 facing the conductive plugs 120a2 and 120b2, and the wiring layers 13a and 13b are formed by embedding the above-described materials. After that, it is desirable to remove excess wiring layer material (tungsten or the like) on the interlayer insulating film 14 by using, for example, a CMP method. Next, a lower electrode 15 a is formed on the interlayer insulating film 14. Specifically, first, the above-described transparent conductive film is formed over the entire surface of the interlayer insulating film 14 by, eg, sputtering. Thereafter, the lower electrode 15a is removed by removing a selective portion using, for example, dry etching or wet etching using a photolithography method (exposure, development, post-bake, etc. of the photoresist film). Form. At this time, the lower electrode 15a is formed in a region facing the wiring layer 13a. Further, when the transparent conductive film is processed, the transparent conductive film is also left in the region facing the wiring layer 13b, so that the wiring layer 15b constituting a part of the hole transmission path is formed together with the lower electrode 15a. Form.
続いて、絶縁膜１６を形成する。この際、まず半導体基板１１上の全面にわたって、層間絶縁膜１４、下部電極１５ａおよび配線層１５ｂを覆うように、上述した材料よりなる絶縁膜１６を、例えば、プラズマＣＶＤ法により成膜する。この後、図８Ａに示したように、成膜した絶縁膜１６を、例えば、ＣＭＰ法により研磨することにより、下部電極１５ａおよび配線層１５ｂを絶縁膜１６から露出させると共に、下部電極１５ａおよび絶縁膜１６間の段差を緩和する（望ましくは、平坦化する）。
Subsequently, an insulating film 16 is formed. At this time, first, the insulating film 16 made of the above-described material is formed by, for example, a plasma CVD method so as to cover the entire surface of the semiconductor substrate 11 so as to cover the interlayer insulating film 14, the lower electrode 15a, and the wiring layer 15b. Thereafter, as shown in FIG. 8A, the formed insulating film 16 is polished by, for example, a CMP method so that the lower electrode 15a and the wiring layer 15b are exposed from the insulating film 16, and the lower electrode 15a and the insulating film 16 are insulated. Steps between the films 16 are alleviated (preferably planarized).
次に、図８Ｂに示したように、下部電極１５ａ上に有機光電変換層１７を形成する。この際、例えば上述したサブフタロシアニン誘導体およびキナクリドン誘導体を、例えば、真空蒸着法によりパターン形成する。なお、上述のように、有機光電変換層１７の上層または下層に、他の有機層（電子ブロッキング膜等）を形成する際には、真空工程において連続的に（真空一貫プロセスで）形成することが望ましい。また、有機光電変換層１７の成膜方法としては、必ずしも上記のような真空蒸着法を用いた手法に限られず、他の手法、例えば、プリント技術等を用いても構わない。
Next, as shown in FIG. 8B, the organic photoelectric conversion layer 17 is formed on the lower electrode 15a. At this time, for example, the above-described subphthalocyanine derivative and quinacridone derivative are patterned by, for example, vacuum deposition. As described above, when another organic layer (such as an electron blocking film) is formed on the upper layer or the lower layer of the organic photoelectric conversion layer 17, it is formed continuously in a vacuum process (by a consistent vacuum process). Is desirable. Further, the method for forming the organic photoelectric conversion layer 17 is not necessarily limited to the method using the vacuum deposition method as described above, and other methods such as a printing technique may be used.
続いて、図８Ｃに示したように、上部電極１８および保護層１９を形成する。まず、上述した透明導電膜よりなる上部電極１８を基板全面にわたって、例えば、真空蒸着法またはスパッタ法により、有機光電変換層１７の上面および側面を覆うように成膜する。なお、有機光電変換層１７は、水分、酸素、水素等の影響を受けて特性が変動し易いため、上部電極１８は、有機光電変換層１７と真空一貫プロセスにより成膜することが望ましい。この後（上部電極１８をパターニングする前に）、上部電極１８の上面を覆うように、上述した材料よりなる保護層１９を、例えば、プラズマＣＶＤ法により成膜する。次いで、上部電極１８上に保護層１９を形成した後、上部電極１８を加工する。
Subsequently, as shown in FIG. 8C, the upper electrode 18 and the protective layer 19 are formed. First, the upper electrode 18 made of the above-described transparent conductive film is formed over the entire surface of the substrate so as to cover the upper surface and side surfaces of the organic photoelectric conversion layer 17 by, for example, vacuum deposition or sputtering. Note that the characteristics of the organic photoelectric conversion layer 17 are likely to fluctuate due to the influence of moisture, oxygen, hydrogen, etc., and therefore it is desirable that the upper electrode 18 be formed with the organic photoelectric conversion layer 17 by a consistent vacuum process. Thereafter (before patterning the upper electrode 18), the protective layer 19 made of the above-described material is formed by, for example, a plasma CVD method so as to cover the upper surface of the upper electrode 18. Next, after forming the protective layer 19 on the upper electrode 18, the upper electrode 18 is processed.
この後、フォトリソグラフィ法を用いたエッチングにより、上部電極１８および保護層１９の選択的な部分を一括除去する。続いて、保護層１９に、コンタクトホールＨを、例えば、フォトリソグラフィ法を用いたエッチングにより形成する。この際、コンタクトホールＨは、有機光電変換層１７と非対向の領域に形成することが望ましい。このコンタクトホールＨの形成後においても、上記と同様、フォトレジストを剥離して、薬液を用いた洗浄を行うため、コンタクトホールＨに対向する領域では、上部電極１８が保護層１９から露出することになる。このため、上述したようなピンホールの発生を考慮すると、有機光電変換層１７の形成領域を避けて、コンタクトホールＨが設けられることが望ましい。続いて、上述した材料よりなるコンタクトメタル層２０を、例えば、スパッタ法等を用いて形成する。この際、コンタクトメタル層２０は、保護層１９上に、コンタクトホールＨを埋め込み、かつ配線層１５ｂの上面まで延在するように形成する。最後に、半導体基板１１上の全面にわたって、平坦化膜２１を形成した後、この平坦化膜２１上にオンチップレンズ２２を形成することにより、図１に示した光電変換素子１０を完成する。
Thereafter, selective portions of the upper electrode 18 and the protective layer 19 are collectively removed by etching using a photolithography method. Subsequently, a contact hole H is formed in the protective layer 19 by, for example, etching using a photolithography method. At this time, the contact hole H is desirably formed in a region not facing the organic photoelectric conversion layer 17. Even after the contact hole H is formed, the photoresist is peeled off and cleaning with a chemical solution is performed in the same manner as described above, so that the upper electrode 18 is exposed from the protective layer 19 in the region facing the contact hole H. become. For this reason, in consideration of the occurrence of pinholes as described above, it is desirable to provide the contact hole H while avoiding the formation region of the organic photoelectric conversion layer 17. Subsequently, the contact metal layer 20 made of the above-described material is formed using, for example, a sputtering method. At this time, the contact metal layer 20 is formed on the protective layer 19 so as to bury the contact hole H and extend to the upper surface of the wiring layer 15b. Finally, after the planarization film 21 is formed over the entire surface of the semiconductor substrate 11, the on-chip lens 22 is formed on the planarization film 21, thereby completing the photoelectric conversion element 10 shown in FIG.
上記のような光電変換素子１０では、例えば、固体撮像装置の画素として、次のようにして信号電荷が取得される。即ち、図９に示したように、光電変換素子１０に、オンチップレンズ２２（図９には図示せず）を介して光Ｌが入射すると、光Ｌは、有機光電変換部１１Ｇ、無機光電変換部１１Ｂ，１１Ｒの順に通過し、その通過過程において赤、緑、青の色光毎に光電変換される。図１０に、入射光に基づく信号電荷（電子）取得の流れを模式的に示す。以下、各光電変換部における具体的な信号取得動作について説明する。
In the photoelectric conversion element 10 as described above, for example, signal charges are acquired as pixels of a solid-state imaging device as follows. That is, as shown in FIG. 9, when the light L is incident on the photoelectric conversion element 10 via the on-chip lens 22 (not shown in FIG. 9), the light L is converted into the organic photoelectric conversion unit 11G, the inorganic photoelectric conversion element. The conversion units 11B and 11R pass in order, and photoelectric conversion is performed for each of the red, green, and blue color lights in the passing process. FIG. 10 schematically shows a flow of signal charge (electron) acquisition based on incident light. Hereinafter, a specific signal acquisition operation in each photoelectric conversion unit will be described.
（有機光電変換部１１Ｇによる緑色信号の取得）
光電変換素子１０へ入射した光Ｌのうち、まず、緑色光Ｌｇが、有機光電変換部１１Ｇにおいて選択的に検出（吸収）され、光電変換される。これにより、発生した電子－正孔対のうちの電子Ｅｇが下部電極１５ａ側から取り出された後、伝送経路Ａ（配線層１３ａおよび導電性プラグ１２０ａ１，１２０ａ２）を介して緑用蓄電層１１０Ｇへ蓄積される。蓄積された電子Ｅｇは、読み出し動作の際にＦＤ１１６へ転送される。なお、正孔Ｈｇは、上部電極１８側から伝送経路Ｂ（コンタクトメタル層２０、配線層１３ｂ，１５ｂおよび導電性プラグ１２０ｂ１，１２０ｂ２）を介して排出される。 (Acquisition of green signal by organicphotoelectric conversion unit 11G)
Of the light L incident on thephotoelectric conversion element 10, first, the green light Lg is selectively detected (absorbed) by the organic photoelectric conversion unit 11G and subjected to photoelectric conversion. As a result, electrons Eg out of the generated electron-hole pairs are taken out from the lower electrode 15a side, and then transferred to the green power storage layer 110G via the transmission path A (the wiring layer 13a and the conductive plugs 120a1 and 120a2). Accumulated. The accumulated electron Eg is transferred to the FD 116 during a read operation. The holes Hg are discharged from the upper electrode 18 side through the transmission path B (contact metal layer 20, wiring layers 13b and 15b, and conductive plugs 120b1 and 120b2).
光電変換素子１０へ入射した光Ｌのうち、まず、緑色光Ｌｇが、有機光電変換部１１Ｇにおいて選択的に検出（吸収）され、光電変換される。これにより、発生した電子－正孔対のうちの電子Ｅｇが下部電極１５ａ側から取り出された後、伝送経路Ａ（配線層１３ａおよび導電性プラグ１２０ａ１，１２０ａ２）を介して緑用蓄電層１１０Ｇへ蓄積される。蓄積された電子Ｅｇは、読み出し動作の際にＦＤ１１６へ転送される。なお、正孔Ｈｇは、上部電極１８側から伝送経路Ｂ（コンタクトメタル層２０、配線層１３ｂ，１５ｂおよび導電性プラグ１２０ｂ１，１２０ｂ２）を介して排出される。 (Acquisition of green signal by organic
Of the light L incident on the
具体的には、次のようにして信号電荷を蓄積する。即ち、本実施の形態では、下部電極１５ａに、例えば、所定の負の電位ＶＬ（＜０Ｖ）が印加され、上部電極１８には、電位ＶＬよりも低い電位ＶＵ（＜ＶＬ）が印加される。なお、電位ＶＬは、例えば、多層配線層５１内の配線５１ａから、伝送経路Ａを通じて、下部電極１５ａへ与えられる。電位ＶＬは、例えば、多層配線層５１内の配線５１ａから、伝送経路Ｂを通じて、上部電極１８へ与えられる。これにより、電荷蓄積状態（図示しないリセットトランジスタおよび転送トランジスタＴｒ１のオフ状態）では、有機光電変換層１７で発生した電子－正孔対のうち、電子が、相対的に高電位となっている下部電極１５ａ側へ導かれる（正孔は上部電極１８側へ導かれる）。このようにして、下部電極１５ａから電子Ｅｇが取り出され、伝送経路Ａを介して緑用蓄電層１１０Ｇ（詳細には、ｎ型領域１１５ｎ）に蓄積される。また、この電子Ｅｇの蓄積により、緑用蓄電層１１０Ｇと導通する下部電極１５ａの電位ＶＬも変動する。この電位ＶＬの変化量が信号電位（ここでは、緑色信号の電位）に相当する。
Specifically, signal charges are accumulated as follows. That is, in the present embodiment, for example, a predetermined negative potential VL (<0 V) is applied to the lower electrode 15a, and a potential VU (<VL) lower than the potential VL is applied to the upper electrode 18. . The potential VL is applied to the lower electrode 15a from the wiring 51a in the multilayer wiring layer 51 through the transmission path A, for example. The potential VL is applied to the upper electrode 18 from the wiring 51a in the multilayer wiring layer 51 through the transmission path B, for example. Thereby, in the charge accumulation state (the unillustrated reset transistor and transfer transistor Tr1 are in the off state), the electrons out of the electron-hole pairs generated in the organic photoelectric conversion layer 17 have a relatively high potential. It is led to the electrode 15a side (holes are led to the upper electrode 18 side). In this way, the electrons Eg are extracted from the lower electrode 15a and accumulated in the green power storage layer 110G (specifically, the n-type region 115n) via the transmission path A. Further, due to the accumulation of the electrons Eg, the potential VL of the lower electrode 15a connected to the green power storage layer 110G also varies. The amount of change in the potential VL corresponds to the signal potential (here, the potential of the green signal).
そして、読み出し動作の際には、転送トランジスタＴｒ１がオン状態となり、緑用蓄電層１１０Ｇに蓄積された電子Ｅｇが、ＦＤ１１６に転送される。これにより、緑色光Ｌｇの受光量に基づく緑色信号が、図示しない他の画素トランジスタを通じて後述の垂直信号線Ｌsigに読み出される。この後、図示しないリセットトランジスタおよび転送トランジスタＴｒ１がオン状態となり、ｎ型領域であるＦＤ１１６と、緑用蓄電層１１０Ｇの蓄電領域（ｎ型領域１１５ｎ）とが、例えば、電源電圧ＶＤＤにリセットされる。
In the read operation, the transfer transistor Tr1 is turned on, and the electron Eg stored in the green power storage layer 110G is transferred to the FD. As a result, a green signal based on the amount of received light of the green light Lg is read out to a vertical signal line Lsig described later through another pixel transistor (not shown). Thereafter, the reset transistor and transfer transistor Tr1 (not shown) are turned on, and the FD 116, which is the n-type region, and the power storage region (n-type region 115n) of the green power storage layer 110G are reset to the power supply voltage VDD, for example. .
（無機光電変換部１１Ｂ，１１Ｒによる青色信号，赤色信号の取得）
続いて、有機光電変換部１１Ｇを透過した光のうち、青色光は無機光電変換部１１Ｂ、赤色光は無機光電変換部１１Ｒにおいて、それぞれ順に吸収され、光電変換される。無機光電変換部１１Ｂでは、入射した青色光に対応した電子Ｅｂがｎ型領域（ｎ型光電変換層１１１ｎ）に蓄積され、蓄積された電子Ｅｄは、読み出し動作の際にＦＤ１１３へと転送される。なお、正孔は、図示しないｐ型領域に蓄積される。同様に、無機光電変換部１１Ｒでは、入射した赤色光に対応した電子Ｅｒがｎ型領域（ｎ型光電変換層１１２ｎ）に蓄積され、蓄積された電子Ｅｒは、読み出し動作の際にＦＤ１１４へと転送される。なお、正孔は、図示しないｐ型領域に蓄積される。 (Acquisition of blue and red signals by the inorganic photoelectric conversion units 11B and 11R)
Subsequently, among the light transmitted through the organicphotoelectric conversion unit 11G, blue light is absorbed and photoelectrically converted in order by the inorganic photoelectric conversion unit 11B and red light by the inorganic photoelectric conversion unit 11R. In the inorganic photoelectric conversion unit 11B, the electrons Eb corresponding to the incident blue light are accumulated in the n-type region (n-type photoelectric conversion layer 111n), and the accumulated electrons Ed are transferred to the FD 113 during the read operation. . Holes are accumulated in a p-type region (not shown). Similarly, in the inorganic photoelectric conversion unit 11R, electrons Er corresponding to the incident red light are accumulated in the n-type region (n-type photoelectric conversion layer 112n), and the accumulated electrons Er are transferred to the FD 114 during the read operation. Transferred. Holes are accumulated in a p-type region (not shown).
続いて、有機光電変換部１１Ｇを透過した光のうち、青色光は無機光電変換部１１Ｂ、赤色光は無機光電変換部１１Ｒにおいて、それぞれ順に吸収され、光電変換される。無機光電変換部１１Ｂでは、入射した青色光に対応した電子Ｅｂがｎ型領域（ｎ型光電変換層１１１ｎ）に蓄積され、蓄積された電子Ｅｄは、読み出し動作の際にＦＤ１１３へと転送される。なお、正孔は、図示しないｐ型領域に蓄積される。同様に、無機光電変換部１１Ｒでは、入射した赤色光に対応した電子Ｅｒがｎ型領域（ｎ型光電変換層１１２ｎ）に蓄積され、蓄積された電子Ｅｒは、読み出し動作の際にＦＤ１１４へと転送される。なお、正孔は、図示しないｐ型領域に蓄積される。 (Acquisition of blue and red signals by the inorganic
Subsequently, among the light transmitted through the organic
電荷蓄積状態では、上述のように、有機光電変換部１１Ｇの下部電極１５ａに負の電位ＶＬが印加されることから、無機光電変換部１１Ｂの正孔蓄積層であるｐ型領域（図３のｐ型領域１１１ｐ）の正孔濃度が増える傾向になる。このため、ｐ型領域１１１ｐと層間絶縁膜１２との界面における暗電流の発生を抑制することができる。
In the charge accumulation state, as described above, since the negative potential VL is applied to the lower electrode 15a of the organic photoelectric conversion unit 11G, the p-type region (a hole accumulation layer of the inorganic photoelectric conversion unit 11B (see FIG. 3)). The hole concentration of the p-type region 111p) tends to increase. For this reason, generation of dark current at the interface between the p-type region 111p and the interlayer insulating film 12 can be suppressed.
読み出し動作の際には、上記有機光電変換部１１Ｇと同様、転送トランジスタＴｒ２，Ｔｒ３がオン状態となり、ｎ型光電変換層１１１ｎ，１１２ｎにそれぞれ蓄積された電子Ｅｂ，Ｅｒが、ＦＤ１１３，１１４に転送される。これにより、青色光Ｌｂの受光量に基づく青色信号と、赤色光Ｌｒの受光量に基づく赤色信号とがそれぞれ、図示しない他の画素トランジスタを通じて後述の垂直信号線Ｌsigに読み出される。この後、図示しないリセットトランジスタおよび転送トランジスタＴｒ２，Ｔｒ３がオン状態となり、ｎ型領域であるＦＤ１１３，１１４が、例えば、電源電圧ＶＤＤにリセットされる。
In the read operation, similarly to the organic photoelectric conversion unit 11G, the transfer transistors Tr2 and Tr3 are turned on, and the electrons Eb and Er accumulated in the n-type photoelectric conversion layers 111n and 112n are transferred to the FDs 113 and 114, respectively. Is done. As a result, a blue signal based on the amount of received light of the blue light Lb and a red signal based on the amount of received light of the red light Lr are read out to a vertical signal line Lsig described later through another pixel transistor (not shown). Thereafter, the reset transistor (not shown) and the transfer transistors Tr2 and Tr3 are turned on, and the FDs 113 and 114, which are n-type regions, are reset to, for example, the power supply voltage VDD.
このように、縦方向に有機光電変換部１１Ｇを、無機光電変換部１１Ｂ，１１Ｒを積層することにより、カラーフィルタを設けることなく、赤、緑、青の色光を分離して検出すし、各色の信号電荷を得ることができる。これにより、カラーフィルタの色光吸収に起因する光損失（感度低下）や、画素補間処理に伴う偽色の発生を抑制することができる。
Thus, by stacking the organic photoelectric conversion unit 11G in the vertical direction and the inorganic photoelectric conversion units 11B and 11R, the red, green and blue color lights are separated and detected without providing a color filter. A signal charge can be obtained. Thereby, it is possible to suppress light loss (sensitivity reduction) due to color light absorption of the color filter and generation of false color associated with pixel interpolation processing.
（１－３．作用・効果）
光電変換層の材料として下記式（５）に示したような一般的なサブフタロシアニンあるいはその誘導体を用いたて形成した光電変換素子は、外部量子効率や分光特性に優れるものの耐熱性が低いという問題があった。例えばリフロー方式の半田付け等の加熱処理等によって色味の変化や電気特性等のデバイス特性の低下、あるいは変形や破壊が生じる。 (1-3. Action and effect)
The photoelectric conversion element formed by using a general subphthalocyanine or its derivative as shown in the following formula (5) as a material of the photoelectric conversion layer has a problem that it has excellent external quantum efficiency and spectral characteristics but has low heat resistance. was there. For example, heat treatment such as reflow soldering causes a change in color, a decrease in device characteristics such as electrical characteristics, or deformation or destruction.
光電変換層の材料として下記式（５）に示したような一般的なサブフタロシアニンあるいはその誘導体を用いたて形成した光電変換素子は、外部量子効率や分光特性に優れるものの耐熱性が低いという問題があった。例えばリフロー方式の半田付け等の加熱処理等によって色味の変化や電気特性等のデバイス特性の低下、あるいは変形や破壊が生じる。 (1-3. Action and effect)
The photoelectric conversion element formed by using a general subphthalocyanine or its derivative as shown in the following formula (5) as a material of the photoelectric conversion layer has a problem that it has excellent external quantum efficiency and spectral characteristics but has low heat resistance. was there. For example, heat treatment such as reflow soldering causes a change in color, a decrease in device characteristics such as electrical characteristics, or deformation or destruction.
この耐熱性の低さは、サブフタロシアニンの共役面に対して垂直方向に結合角を有するホウ素（Ｂ）に結合したリンカーＸによる置換基Ｒ’の回転自由度の高さによると考えられる。この置換基Ｒ’は、リンカーＸを介してホウ素（Ｂ）に結合している。リンカーＸとしては、一般に、例えば酸素（Ｏ）が挙げられ、これらは２価の原子であるため結合角が固定されず、リンカーＸに結合している置換基Ｒ’は比較的自由に回転することが可能となる。このため、光電変換層中の式（５）に示したようなサブフタロシアニンあるいはその誘導体は、上述した半田付けや高温環境下による加温によって分子内でマイグレーションが生じ、光電変換層内におけるサブフタロシアニン分子の凝集や配向性に変化が生じる。これによって、デバイス特性の変化や低下、あるいは変形や破壊が生じると考えられる。
This low heat resistance is considered to be due to the high degree of freedom of rotation of the substituent R ′ by the linker X bonded to boron (B) having a bond angle in a direction perpendicular to the conjugate plane of the subphthalocyanine. This substituent R ′ is bonded to boron (B) via the linker X. The linker X generally includes, for example, oxygen (O). Since these are divalent atoms, the bond angle is not fixed, and the substituent R ′ bonded to the linker X rotates relatively freely. It becomes possible. For this reason, the subphthalocyanine or its derivative as shown in the formula (5) in the photoelectric conversion layer undergoes migration within the molecule by the above-described soldering or heating under a high temperature environment, and the subphthalocyanine in the photoelectric conversion layer Changes occur in the aggregation and orientation of molecules. As a result, it is considered that the device characteristics change or decrease, or deform or break.
これに対して本実施の形態では、共役面Ｐに対して垂直方向に結合角を有する原子Ｍ（例えばホウ素（Ｂ））に、置換基Ｒが直接結合したサブフタロシアニン誘導体、また、サブフタロシアニン誘導体と同様に、共役面Ｐに対して垂直方向に結合角を有する原子Ｍを有する共役系化合物を用いて有機光電変換層１７を形成するようにした。置換基Ｒは、原子Ｍと原子Ａとの結合および原子Ｂと原子Ａとの結合が形成する原子Ａの結合角が固定された分子構造を有するものである。サブフタロシアニン誘導体以外の共役系化合物としては、フタロシアニン誘導体、サブポルフィリン誘導体およびポルフィリン誘導体が挙げられる。これにより、サブフタロシアニン誘導体およびその他の共役系化合物の共役面Ｐに対して垂直方向に結合角を有する原子Ｍに結合した置換基Ｒの回転自由度が低下し、温度上昇によるマイグレーションの発生を抑制することが可能となる。
In contrast, in the present embodiment, a subphthalocyanine derivative in which a substituent R is directly bonded to an atom M (for example, boron (B)) having a bond angle in a direction perpendicular to the conjugate plane P, or a subphthalocyanine derivative. Similarly to the above, the organic photoelectric conversion layer 17 is formed using a conjugated compound having an atom M having a bond angle in a direction perpendicular to the conjugated plane P. The substituent R has a molecular structure in which the bond angle of the atom A formed by the bond between the atom M and the atom A and the bond between the atom B and the atom A is fixed. Examples of conjugated compounds other than subphthalocyanine derivatives include phthalocyanine derivatives, subporphyrin derivatives, and porphyrin derivatives. This reduces the rotational freedom of the substituent R bonded to the atom M having a bond angle perpendicular to the conjugate plane P of the subphthalocyanine derivative and other conjugated compounds, and suppresses the occurrence of migration due to temperature rise. It becomes possible to do.
以上、本実施の形態の光電変換素子１０では、有機光電変換層１７を共役面Ｐに対して垂直方向に結合角を有する原子Ｍに、回転自由度が低い置換基を有する共役系化合物を用いて有機光電変換層１７を形成するようにした。これにより、半田付け等の加熱処理や高温条件下による温度上昇によるマイグレーションの発生が抑制される。よって、光電変換素子の耐熱性を向上させることが可能となる。
As described above, in the photoelectric conversion element 10 according to the present embodiment, the organic photoelectric conversion layer 17 is a conjugated compound having a substituent having a low degree of rotational freedom for the atom M having a bond angle in the direction perpendicular to the conjugate plane P. Thus, the organic photoelectric conversion layer 17 was formed. Thereby, generation | occurrence | production of the migration by heat processing, such as soldering, and the temperature rise by high temperature conditions is suppressed. Therefore, it is possible to improve the heat resistance of the photoelectric conversion element.
＜２．適用例＞
（適用例１）
図１２は、上記実施の形態において説明した光電変換素子１０（あるいは、光電変換素子３０）を各画素に用いた固体撮像装置（固体撮像装置１）の全体構成を表したものである。この固体撮像装置１は、ＣＭＯＳイメージセンサであり、半導体基板１１上に、撮像エリアとしての画素部１ａを有すると共に、この画素部１ａの周辺領域に、例えば、行走査部１３１、水平選択部１３３、列走査部１３４およびシステム制御部１３２からなる周辺回路部１３０を有している。 <2. Application example>
(Application example 1)
FIG. 12 illustrates an overall configuration of a solid-state imaging device (solid-state imaging device 1) using the photoelectric conversion element 10 (or the photoelectric conversion element 30) described in the above embodiment for each pixel. The solid-state imaging device 1 is a CMOS image sensor, and has a pixel unit 1a as an imaging area on a semiconductor substrate 11, and, for example, a row scanning unit 131 and a horizontal selection unit 133 in a peripheral region of the pixel unit 1a. The peripheral circuit unit 130 includes a column scanning unit 134 and a system control unit 132.
（適用例１）
図１２は、上記実施の形態において説明した光電変換素子１０（あるいは、光電変換素子３０）を各画素に用いた固体撮像装置（固体撮像装置１）の全体構成を表したものである。この固体撮像装置１は、ＣＭＯＳイメージセンサであり、半導体基板１１上に、撮像エリアとしての画素部１ａを有すると共に、この画素部１ａの周辺領域に、例えば、行走査部１３１、水平選択部１３３、列走査部１３４およびシステム制御部１３２からなる周辺回路部１３０を有している。 <2. Application example>
(Application example 1)
FIG. 12 illustrates an overall configuration of a solid-state imaging device (solid-state imaging device 1) using the photoelectric conversion element 10 (or the photoelectric conversion element 30) described in the above embodiment for each pixel. The solid-
画素部１ａは、例えば、行列状に２次元配置された複数の単位画素Ｐ（光電変換素子１０に相当）を有している。この単位画素Ｐには、例えば、画素行ごとに画素駆動線Ｌread（具体的には行選択線およびリセット制御線）が配線され、画素列ごとに垂直信号線Ｌsigが配線されている。画素駆動線Ｌreadは、画素からの信号読み出しのための駆動信号を伝送するものである。画素駆動線Ｌreadの一端は、行走査部１３１の各行に対応した出力端に接続されている。
The pixel unit 1a has, for example, a plurality of unit pixels P (corresponding to the photoelectric conversion element 10) arranged two-dimensionally in a matrix. In the unit pixel P, for example, a pixel drive line Lread (specifically, a row selection line and a reset control line) is wired for each pixel row, and a vertical signal line Lsig is wired for each pixel column. The pixel drive line Lread transmits a drive signal for reading a signal from the pixel. One end of the pixel drive line Lread is connected to an output end corresponding to each row of the row scanning unit 131.
行走査部１３１は、シフトレジスタやアドレスデコーダ等によって構成され、画素部１ａの各単位画素Ｐを、例えば、行単位で駆動する画素駆動部である。行走査部１３１によって選択走査された画素行の各単位画素Ｐから出力される信号は、垂直信号線Ｌsigの各々を通して水平選択部１３３に供給される。水平選択部１３３は、垂直信号線Ｌsigごとに設けられたアンプや水平選択スイッチ等によって構成されている。
The row scanning unit 131 is configured by a shift register, an address decoder, or the like, and is a pixel driving unit that drives each unit pixel P of the pixel unit 1a, for example, in units of rows. A signal output from each unit pixel P of the pixel row that is selectively scanned by the row scanning unit 131 is supplied to the horizontal selection unit 133 through each of the vertical signal lines Lsig. The horizontal selection unit 133 is configured by an amplifier, a horizontal selection switch, and the like provided for each vertical signal line Lsig.
列走査部１３４は、シフトレジスタやアドレスデコーダ等によって構成され、水平選択部１３３の各水平選択スイッチを走査しつつ順番に駆動するものである。この列走査部１３４による選択走査により、垂直信号線Ｌsigの各々を通して伝送される各画素の信号が順番に水平信号線１３５に出力され、当該水平信号線１３５を通して半導体基板１１の外部へ伝送される。
The column scanning unit 134 includes a shift register, an address decoder, and the like, and drives the horizontal selection switches in the horizontal selection unit 133 in order while scanning. By the selective scanning by the column scanning unit 134, the signal of each pixel transmitted through each of the vertical signal lines Lsig is sequentially output to the horizontal signal line 135 and transmitted to the outside of the semiconductor substrate 11 through the horizontal signal line 135. .
行走査部１３１、水平選択部１３３、列走査部１３４および水平信号線１３５からなる回路部分は、半導体基板１１上に直に形成されていてもよいし、あるいは外部制御ＩＣに配設されたものであってもよい。また、それらの回路部分は、ケーブル等により接続された他の基板に形成されていてもよい。
The circuit portion including the row scanning unit 131, the horizontal selection unit 133, the column scanning unit 134, and the horizontal signal line 135 may be formed directly on the semiconductor substrate 11, or provided in the external control IC. It may be. In addition, these circuit portions may be formed on another substrate connected by a cable or the like.
システム制御部１３２は、半導体基板１１の外部から与えられるクロックや、動作モードを指令するデータ等を受け取り、また、固体撮像装置１の内部情報等のデータを出力するものである。システム制御部１３２はさらに、各種のタイミング信号を生成するタイミングジェネレータを有し、当該タイミングジェネレータで生成された各種のタイミング信号を基に行走査部１３１、水平選択部１３３および列走査部１３４等の周辺回路の駆動制御を行う。
The system control unit 132 receives a clock given from the outside of the semiconductor substrate 11, data for instructing an operation mode, and the like, and outputs data such as internal information of the solid-state imaging device 1. The system control unit 132 further includes a timing generator that generates various timing signals, and the row scanning unit 131, the horizontal selection unit 133, the column scanning unit 134, and the like based on the various timing signals generated by the timing generator. Peripheral circuit drive control.
（適用例２）
上述の固体撮像装置１は、例えば、デジタルスチルカメラやビデオカメラ等のカメラシステムや、撮像機能を有する携帯電話等、撮像機能を備えたあらゆるタイプの電子機器に適用することができる。図１３に、その一例として、電子機器２（カメラ）の概略構成を示す。この電子機器２は、例えば、静止画または動画を撮影可能なビデオカメラであり、固体撮像装置１と、光学系（光学レンズ）３１０と、シャッタ装置３１１と、固体撮像装置１およびシャッタ装置３１１を駆動する駆動部３１３と、信号処理部３１２とを有する。 (Application example 2)
The above-described solid-state imaging device 1 can be applied to any type of electronic apparatus having an imaging function, such as a camera system such as a digital still camera or a video camera, or a mobile phone having an imaging function. FIG. 13 shows a schematic configuration of an electronic device 2 (camera) as an example. The electronic device 2 is, for example, a video camera capable of taking a still image or a moving image, and includes a solid-state imaging device 1, an optical system (optical lens) 310, a shutter device 311, the solid-state imaging device 1 and the shutter device 311. A driving unit 313 for driving and a signal processing unit 312 are included.
上述の固体撮像装置１は、例えば、デジタルスチルカメラやビデオカメラ等のカメラシステムや、撮像機能を有する携帯電話等、撮像機能を備えたあらゆるタイプの電子機器に適用することができる。図１３に、その一例として、電子機器２（カメラ）の概略構成を示す。この電子機器２は、例えば、静止画または動画を撮影可能なビデオカメラであり、固体撮像装置１と、光学系（光学レンズ）３１０と、シャッタ装置３１１と、固体撮像装置１およびシャッタ装置３１１を駆動する駆動部３１３と、信号処理部３１２とを有する。 (Application example 2)
The above-described solid-
光学系３１０は、被写体からの像光（入射光）を固体撮像装置１の画素部１ａへ導くものである。この光学系３１０は、複数の光学レンズから構成されていてもよい。シャッタ装置３１１は、固体撮像装置１への光照射期間および遮光期間を制御するものである。駆動部３１３は、固体撮像装置１の転送動作およびシャッタ装置３１１のシャッタ動作を制御するものである。信号処理部３１２は、固体撮像装置１から出力された信号に対し、各種の信号処理を行うものである。信号処理後の映像信号Ｄoutは、メモリ等の記憶媒体に記憶されるか、あるいは、モニタ等に出力される。
The optical system 310 guides image light (incident light) from a subject to the pixel unit 1 a of the solid-state imaging device 1. The optical system 310 may be composed of a plurality of optical lenses. The shutter device 311 controls the light irradiation period and the light shielding period for the solid-state imaging device 1. The drive unit 313 controls the transfer operation of the solid-state imaging device 1 and the shutter operation of the shutter device 311. The signal processing unit 312 performs various types of signal processing on the signal output from the solid-state imaging device 1. The video signal Dout after the signal processing is stored in a storage medium such as a memory, or is output to a monitor or the like.
＜３．実施例＞
以下に本開示の実施の形態に係る各種サンプルを作製し、加熱前後の吸収スペクトルの変化、加熱による外部量子効率および応答時間の変化について評価した。 <3. Example>
Various samples according to the embodiments of the present disclosure were prepared below, and changes in absorption spectra before and after heating, changes in external quantum efficiency and response time due to heating were evaluated.
以下に本開示の実施の形態に係る各種サンプルを作製し、加熱前後の吸収スペクトルの変化、加熱による外部量子効率および応答時間の変化について評価した。 <3. Example>
Various samples according to the embodiments of the present disclosure were prepared below, and changes in absorption spectra before and after heating, changes in external quantum efficiency and response time due to heating were evaluated.
（サブフタロシアニン誘導体Ａの合成）
下記スキーム（Ａ）に基づいてサブフタロシアニン誘導体Ａを合成した。まず、乾燥トルエンにサブフタロシアニンクロライドを溶解し、アルゴン雰囲気下においてパーフルオロフェニルマグネシウムブロマイドを添加した。このトルエン溶液を４０℃にて攪拌して反応させたのち、得られた混合物をカラムクロマトグラフィーにて精製し、サブフタロシアニン誘導体Ａを得た。 (Synthesis of subphthalocyanine derivative A)
Subphthalocyanine derivative A was synthesized based on the following scheme (A). First, subphthalocyanine chloride was dissolved in dry toluene, and perfluorophenyl magnesium bromide was added under an argon atmosphere. After this toluene solution was stirred and reacted at 40 ° C., the resulting mixture was purified by column chromatography to obtain subphthalocyanine derivative A.
下記スキーム（Ａ）に基づいてサブフタロシアニン誘導体Ａを合成した。まず、乾燥トルエンにサブフタロシアニンクロライドを溶解し、アルゴン雰囲気下においてパーフルオロフェニルマグネシウムブロマイドを添加した。このトルエン溶液を４０℃にて攪拌して反応させたのち、得られた混合物をカラムクロマトグラフィーにて精製し、サブフタロシアニン誘導体Ａを得た。 (Synthesis of subphthalocyanine derivative A)
Subphthalocyanine derivative A was synthesized based on the following scheme (A). First, subphthalocyanine chloride was dissolved in dry toluene, and perfluorophenyl magnesium bromide was added under an argon atmosphere. After this toluene solution was stirred and reacted at 40 ° C., the resulting mixture was purified by column chromatography to obtain subphthalocyanine derivative A.
（サブフタロシアニン誘導体Ｂの合成）
下記スキーム（Ｂ）に基づいてサブフタロシアニン誘導体Ｂを合成した。まず、乾燥トルエンにフッ素化サブフタロシアニンクロライドを溶解し、アルゴン雰囲気下においてパーフルオロフェニルマグネシウムブロマイドを添加した。このトルエン溶液を４０℃にて攪拌して反応させたのち、得られた混合物をカラムクロマトグラフィーにて精製し、サブフタロシアニン誘導体Ｂを得た。 (Synthesis of subphthalocyanine derivative B)
Subphthalocyanine derivative B was synthesized based on the following scheme (B). First, fluorinated subphthalocyanine chloride was dissolved in dry toluene, and perfluorophenylmagnesium bromide was added under an argon atmosphere. After this toluene solution was stirred and reacted at 40 ° C., the resulting mixture was purified by column chromatography to obtain subphthalocyanine derivative B.
下記スキーム（Ｂ）に基づいてサブフタロシアニン誘導体Ｂを合成した。まず、乾燥トルエンにフッ素化サブフタロシアニンクロライドを溶解し、アルゴン雰囲気下においてパーフルオロフェニルマグネシウムブロマイドを添加した。このトルエン溶液を４０℃にて攪拌して反応させたのち、得られた混合物をカラムクロマトグラフィーにて精製し、サブフタロシアニン誘導体Ｂを得た。 (Synthesis of subphthalocyanine derivative B)
Subphthalocyanine derivative B was synthesized based on the following scheme (B). First, fluorinated subphthalocyanine chloride was dissolved in dry toluene, and perfluorophenylmagnesium bromide was added under an argon atmosphere. After this toluene solution was stirred and reacted at 40 ° C., the resulting mixture was purified by column chromatography to obtain subphthalocyanine derivative B.
（サンプルの作製）
まず、真空蒸着装置内にてサブフタロシアニン誘導体Ａを蒸着源として石英基板上に有機薄膜Ａを成膜した。続いて、有機薄膜Ａ上にＩＴＯ膜を成膜し、加熱時における分光形状変化を評価するサンプル１－１を作製した。また、蒸着源としてサブフタロシアニン誘導体Ａの代わりにサブフタロシアニン誘導体Ｂを用いた以外、同様の方法を用いてサンプル２－１を作成した。更に、サブフタロシアニン誘導体Ｂに関しては、サブフタロシアニン誘導体Ｂからなる有機薄膜Ｂを間に、下部電極としてＩＴＯ膜を、上部電極としてＡｌＳｉＣｕ膜を形成した外部量子効率を評価するサンプル２－２を作製した。 (Sample preparation)
First, an organic thin film A was formed on a quartz substrate using a subphthalocyanine derivative A as a deposition source in a vacuum deposition apparatus. Subsequently, an ITO film was formed on the organic thin film A, and a sample 1-1 for evaluating a spectral shape change during heating was produced. Sample 2-1 was prepared using the same method except that subphthalocyanine derivative B was used in place of subphthalocyanine derivative A as the evaporation source. Further, regarding the subphthalocyanine derivative B, a sample 2-2 for evaluating the external quantum efficiency in which an organic thin film B made of the subphthalocyanine derivative B is formed and an ITO film as a lower electrode and an AlSiCu film as an upper electrode is formed was prepared. .
まず、真空蒸着装置内にてサブフタロシアニン誘導体Ａを蒸着源として石英基板上に有機薄膜Ａを成膜した。続いて、有機薄膜Ａ上にＩＴＯ膜を成膜し、加熱時における分光形状変化を評価するサンプル１－１を作製した。また、蒸着源としてサブフタロシアニン誘導体Ａの代わりにサブフタロシアニン誘導体Ｂを用いた以外、同様の方法を用いてサンプル２－１を作成した。更に、サブフタロシアニン誘導体Ｂに関しては、サブフタロシアニン誘導体Ｂからなる有機薄膜Ｂを間に、下部電極としてＩＴＯ膜を、上部電極としてＡｌＳｉＣｕ膜を形成した外部量子効率を評価するサンプル２－２を作製した。 (Sample preparation)
First, an organic thin film A was formed on a quartz substrate using a subphthalocyanine derivative A as a deposition source in a vacuum deposition apparatus. Subsequently, an ITO film was formed on the organic thin film A, and a sample 1-1 for evaluating a spectral shape change during heating was produced. Sample 2-1 was prepared using the same method except that subphthalocyanine derivative B was used in place of subphthalocyanine derivative A as the evaporation source. Further, regarding the subphthalocyanine derivative B, a sample 2-2 for evaluating the external quantum efficiency in which an organic thin film B made of the subphthalocyanine derivative B is formed and an ITO film as a lower electrode and an AlSiCu film as an upper electrode is formed was prepared. .
また、比較例として、下記式（Ｃ）および式（Ｄ）に示したＢにリンカーである酸素（Ｏ）を介して置換基Ｒ（パーフルオロフェニル基）が結合したサブフタロシアニン誘導体Ｃ，Ｄをそれぞれ用いて加熱時における分光形状変化を評価するサンプル３－１，４－１および外部量子効率を評価するサンプル４－２を作製した。
As a comparative example, subphthalocyanine derivatives C and D in which a substituent R (perfluorophenyl group) is bonded to B shown in the following formulas (C) and (D) via oxygen (O) as a linker are shown. Samples 3-1 and 4-1 for evaluating the spectral shape change during heating and sample 4-2 for evaluating the external quantum efficiency were respectively used.
上記サンプル１－１，２－１，３－１，４－１をそれぞれ１６０℃に加熱し、加熱時間０分，５分，６０分，２１０分ごとに紫外可視分光高度計を用いて吸収スペクトルを測定し、加熱による分光形状の変化を評価した。図１３～図１６は、サンプル１－１（図１３）、サンプル２－１（図１４）、サンプル３－１（図１５）およびサンプル４－１（図１６）の各加熱時間ごとの吸収スペクトルをまとめたものである。
Samples 1-1, 2-1, 3-1 and 4-1 were heated to 160 ° C., and absorption spectra were measured using an ultraviolet-visible spectrophotometer every heating time of 0 minutes, 5 minutes, 60 minutes and 210 minutes. Measurements were made to evaluate changes in spectral shape due to heating. FIGS. 13 to 16 show absorption spectra for each heating time of Sample 1-1 (FIG. 13), Sample 2-1 (FIG. 14), Sample 3-1 (FIG. 15), and Sample 4-1 (FIG. 16). Is a summary.
図１３～図１６から、本開示のサブフタロシアニン誘導体を用いたサンプル１－１，２－１では、加熱による吸光度α、極大吸収波長および分光形状の変化は小さいことがわかった。これに対して、酸素（Ｏ）を介して置換基Ｒが結合したサブフタロシアニン誘導体を用いたサンプル３－１，４－１では、加熱時間が長くなるにつれて吸光度α、極大吸収波長および分光形状が大きく変化することがわかった。よって、共役面に対して垂直方向に結合角を有する原子Ｍに、直接置換基Ｒを結合させたサブフタロシアニン誘導体は、熱安定性が向上することがわかった。
13 to 16, it was found that in samples 1-1 and 2-1 using the subphthalocyanine derivative of the present disclosure, changes in absorbance α, maximum absorption wavelength, and spectral shape due to heating were small. On the other hand, in samples 3-1 and 4-1 using the subphthalocyanine derivative to which the substituent R is bonded via oxygen (O), the absorbance α, the maximum absorption wavelength, and the spectral shape increase as the heating time increases. It turns out that it changes greatly. Therefore, it has been found that the thermal stability of the subphthalocyanine derivative in which the substituent R is directly bonded to the atom M having a bond angle in a direction perpendicular to the conjugate plane is improved.
次に、サンプル２－２およびサンプル４－２について、光源、フィルタ、半導体パラメータアナライザを用いて加熱による外部量子効率の変化率を測定した。具体的には、フィルタを介して光源からサンプル２－２およびサンプル４－２に照射される光の光量を０～５μＷ／ｃｍ2とし、電極間に印加される電圧を１Ｖとした場合の明電流値および暗電流値から外部量子効率を算出した。図１７は、加熱前後の値を割り算し、加熱前の値を１としてその変化率をプロットしたものである。
Next, for Sample 2-2 and Sample 4-2, the rate of change in external quantum efficiency due to heating was measured using a light source, a filter, and a semiconductor parameter analyzer. Specifically, the light intensity when the light amount applied to the samples 2-2 and 4-2 from the light source through the filter is 0 to 5 μW / cm 2 and the voltage applied between the electrodes is 1 V. The external quantum efficiency was calculated from the current value and the dark current value. FIG. 17 is obtained by dividing the value before and after heating and plotting the rate of change with the value before heating being 1.
図１７から、サブフタロシアニン誘導体Ｄを用いたサンプル４－２では、加熱後の外部量子効率が６割近くまで減少したのに対し、サブフタロシアニン誘導体Ｂを用いたサンプル２－１では、その外部量子効率は加熱後も９割程度保たれることがわかった。これにより、本開示のサブフタロシアニン誘導体を用いた光電変換素子は、加熱による外部量子効率の低下が抑制されることがわかった。
From FIG. 17, in sample 4-2 using subphthalocyanine derivative D, the external quantum efficiency after heating decreased to nearly 60%, whereas in sample 2-1 using subphthalocyanine derivative B, the external quantum efficiency was reduced. It was found that the efficiency was maintained about 90% after heating. Thereby, it turned out that the photoelectric conversion element using the subphthalocyanine derivative of this indication is suppressed from the fall of external quantum efficiency by heating.
更に、サンプル２－２およびサンプル４－２について、光オフ時の応答時間を、オン時に観測される電流が３％にまで減衰するのに要する時間として加熱による応答時間の変化を評価した。図１８は、各加熱時間における応答時間をプロットしたものである。
Furthermore, with respect to Sample 2-2 and Sample 4-2, the response time change due to heating was evaluated as the response time when the light was turned off as the time required for the current observed when turned on to decay to 3%. FIG. 18 is a plot of the response time at each heating time.
図１８から、サブフタロシアニン誘導体Ｄを用いたサンプル４－２では、加熱後の応答時間が２０倍程度に跳ね上がったのに対し、サブフタロシアニン誘導体Ｂを用いたサンプル２－１では、３倍程度に抑えられたことがわかった。これにより、本開示のサブフタロシアニン誘導体を用いた光電変換素子は、加熱による応答性の低下が抑制されることがわかった。
From FIG. 18, in sample 4-2 using subphthalocyanine derivative D, the response time after heating jumped about 20 times, whereas in sample 2-1 using subphthalocyanine derivative B, it was about 3 times. I found out that it was suppressed. Thereby, it turned out that the photoelectric conversion element using the subphthalocyanine derivative | guide_body of this indication suppresses the fall of the responsiveness by heating.
以上のことから、光電変換素子の例えば光電変換層を構成するサブフタロシアニン誘導体として、本開示の共役面に対して垂直方向に結合角を有する原子Ｍに、直接置換基Ｒを結合させたサブフタロシアニン誘導体を用いることにより、耐熱性が向上され、加熱によるデバイス特性の低下を抑制することが可能となることがわかった。
From the above, as a subphthalocyanine derivative constituting, for example, a photoelectric conversion layer of a photoelectric conversion element, a subphthalocyanine in which a substituent R is directly bonded to an atom M having a bond angle in a direction perpendicular to the conjugate plane of the present disclosure. It has been found that the use of a derivative improves the heat resistance and suppresses the deterioration of device characteristics due to heating.
以上、実施の形態および適用例ならびに実施例を挙げて説明したが、本開示内容は上記実施の形態等に限定されるものではなく、種々変形が可能である。例えば、上記実施の形態では、光電変換素子（固体撮像装置）として、緑色光を検出する有機光電変換部１１Ｇと、青色光，赤色光をそれぞれ検出する無機光電変換部１１Ｂ，１１Ｒとを積層させた構成としたが、本開示内容はこのような構造に限定されるものではない。即ち、有機光電変換部において赤色光あるいは青色光を検出するようにしてもよいし、無機光電変換部において緑色光を検出するようにしてもよい。
The embodiments, application examples, and examples have been described above, but the present disclosure is not limited to the above-described embodiments and the like, and various modifications are possible. For example, in the above embodiment, as the photoelectric conversion element (solid-state imaging device), the organic photoelectric conversion unit 11G that detects green light and the inorganic photoelectric conversion units 11B and 11R that detect blue light and red light are stacked. However, the present disclosure is not limited to such a structure. That is, red light or blue light may be detected in the organic photoelectric conversion unit, or green light may be detected in the inorganic photoelectric conversion unit.
また、これらの有機光電変換部および無機光電変換部の数やその比率も限定されるものではなく、２以上の有機光電変換部を設けてもよいし、有機光電変換部だけで複数色の色信号が得られるようにしてもよい。例えば図１９に示した光電変換素子３０のように、それぞれ有機光電変換層４２Ｒ，４２Ｇ，４２Ｂを有する赤色光電変換部４０Ｒ、緑色光電変換部４０Ｇおよび青色光電変換部４０Ｂをこの順に積層され構成としてもよい。この光電変換素子３０では、赤色光電変換部４０Ｒ、緑色光電変換部４０Ｇおよび青色光電変換部４０Ｂはシリコン基板６１上に絶縁層６２を介して積層されており、青色光電変換部４０Ｂ上には、保護層３３および平坦化層３１を介してオンチップレンズ３２が設けられている。シリコン基板６１内には、赤色蓄電層３１０Ｒ、緑色蓄電層３１０Ｇおよび青色蓄電層３１０Ｂが設けられている。オンチップレンズ３２に入射した光は、赤色光電変換部４０Ｒ、緑色光電変換部４０Ｇおよび青色光電変換部４０Ｂで光電変換され、赤色光電変換部４０Ｒから赤色蓄電層３１０Ｒへ、緑色光電変換部４０Ｇから緑色蓄電層３１０Ｇへ、青色光電変換部３４０Ｂから青色蓄電層３１０Ｂへそれぞれ信号電荷が送られるようになっている。更に、有機光電変換部および無機光電変換部を縦方向に積層させる構造に限らず、基板面に沿って並列させてもよい。
Further, the number and ratio of these organic photoelectric conversion units and inorganic photoelectric conversion units are not limited, and two or more organic photoelectric conversion units may be provided. A signal may be obtained. For example, as in the photoelectric conversion element 30 shown in FIG. 19, a red photoelectric conversion unit 40R, a green photoelectric conversion unit 40G, and a blue photoelectric conversion unit 40B each having organic photoelectric conversion layers 42R, 42G, and 42B are stacked in this order. Also good. In this photoelectric conversion element 30, the red photoelectric conversion unit 40R, the green photoelectric conversion unit 40G, and the blue photoelectric conversion unit 40B are stacked on the silicon substrate 61 via the insulating layer 62, and on the blue photoelectric conversion unit 40B, An on-chip lens 32 is provided via the protective layer 33 and the planarizing layer 31. In the silicon substrate 61, a red power storage layer 310R, a green power storage layer 310G, and a blue power storage layer 310B are provided. The light incident on the on-chip lens 32 is photoelectrically converted by the red photoelectric conversion unit 40R, the green photoelectric conversion unit 40G, and the blue photoelectric conversion unit 40B, from the red photoelectric conversion unit 40R to the red power storage layer 310R, and from the green photoelectric conversion unit 40G. Signal charges are respectively sent from the blue photoelectric conversion unit 340B to the blue power storage layer 310B to the green power storage layer 310G. Furthermore, the organic photoelectric conversion part and the inorganic photoelectric conversion part are not limited to the structure in which the organic photoelectric conversion part and the inorganic photoelectric conversion part are stacked in the vertical direction, but may be arranged in parallel along the substrate surface.
更にまた、上記実施の形態では、裏面照射型の固体撮像装置の構成を例示したが、本開示内容は表面照射型の固体撮像装置にも適用可能である。また、本開示の固体撮像装置（光電変換素子）では、上記実施の形態で説明した各構成要素を全て備えている必要はなく、また逆に他の層を備えていてもよい。
Furthermore, in the above-described embodiment, the configuration of the back-illuminated solid-state imaging device is illustrated, but the present disclosure can also be applied to a front-illuminated solid-state imaging device. Further, the solid-state imaging device (photoelectric conversion element) of the present disclosure does not have to include all the components described in the above embodiments, and may include other layers.
なお、本明細書中に記載された効果はあくまで例示であって限定されるものではなく、また、他の効果があってもよい。
In addition, the effect described in this specification is an illustration to the last, and is not limited, Moreover, there may exist another effect.
なお、本開示は、以下のような構成であってもよい。
［１］
対向配置された第１電極および第２電極と、
前記第１電極と前記第２電極との間に設けられ、共役面を有し、前記共役面に含まれると共に、前記共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを備え、
前記置換基Ｒは、前記第１の原子に直接結合する第２の原子と、前記第２の原子と直接結合する第３の原子とを有し、前記第１の原子および前記第３の原子と結合を形成する前記第２の原子の結合角が固定された分子構造を有する
光電変換素子。
［２］
前記結合角は、前記置換基Ｒが形成する混成軌道によって固定されている
前記［１］に記載の光電変換素子。
［３］
前記第２の原子は、炭素（Ｃ）、窒素（Ｎ）、硫黄（Ｓ）、リン（Ｐ）およびシリコン（Ｓｉ）のうちのいずれかである
前記［１］または［２］に記載の光電変換素子。
［４］
前記置換基Ｒは、炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物、複素環化合物、芳香族化合物と複素環化合物が縮環した共役系化合物、トリメチルシリル基、トリアリールシリル基、スルホニル基、シアノ基およびニトロ基のうちのいずれかである
前記［１］乃至［３］のうちのいずれかに記載の光電変換素子。
［５］
前記炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物は、フェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレンおよびこれらの誘導体である
前記［４］に記載の光電変換素子。
［６］
前記複素環化合物は、アニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体である
前記［４］に記載の光電変換素子。
［７］
前記芳香族化合物と複素環化合物が縮環した共役系化合物は、フェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレン、アニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体のいずれかが互いに縮環したものである
前記［４］に記載の光電変換素子。
［８］
前記共役系化合物は、下記式（１）で表わされるサブフタロシアニン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
（Ｒ１～Ｒ１２は、各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。隣り合う任意のＲ１～Ｒ１２は、互いに結合して縮合脂肪族環または縮合芳香環を形成していてもよい。前記縮合脂肪族環または縮合芳香環は、炭素以外の1または複数の原子を含んでいてもよい。Ｚ１～Ｚ３は、各々独立して窒素原子、ＣＲ１３であり、Ｒ１３は各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。Ｍ１はホウ素または２価あるいは３価の金属である。）
［９］
前記共役系化合物は、下記式（２）で表わされるフタロシアニン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
（Ｒ１４～Ｒ２９は、各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。隣り合う任意のＲ１４～Ｒ２９は、互いに結合して縮合脂肪族環または縮合芳香環を形成していてもよい。前記縮合脂肪族環または縮合芳香環は、炭素以外の1または複数の原子を含んでいてもよい。Ｚ４～Ｚ７は、各々独立して窒素原子、ＣＲ３０であり、Ｒ３０は各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。Ｍ２はホウ素または２価あるいは３価の金属である。）
［１０］
前記共役系化合物は、下記式（３）で表わされるサブポルフィリン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
（Ｒ３１～Ｒ３６は、各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。隣り合う任意のＲ３１～Ｒ３６は、互いに結合して縮合脂肪族環または縮合芳香環を形成していてもよい。前記縮合脂肪族環または縮合芳香環は、炭素以外の1または複数の原子を含んでいてもよい。Ｚ８～Ｚ１０は、各々独立して窒素原子、ＣＲ３７であり、Ｒ３７は各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。Ｍ３はホウ素または２価あるいは３価の金属である。）
［１１］
前記共役系化合物は、下記式（４）で表わされるポルフィリン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
（Ｒ３８～Ｒ４５は、各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。隣り合う任意のＲ３８～Ｒ４５は、互いに結合して縮合脂肪族環または縮合芳香環を形成していてもよい。前記縮合脂肪族環または縮合芳香環は、炭素以外の1または複数の原子を含んでいてもよい。Ｚ１１～Ｚ１４は、各々独立して窒素原子、ＣＲ４６であり、Ｒ４６は各々独立して、水素原子、ハロゲン原子、直鎖，分岐，または環状アルキル基、アリール基、パーシャルフルオロアルキル基、パーフルオロアルキル基、シリルアルキル基、シリルアルコキシ基、アリールシリル基、チオアルキル基、チオアリール基、アリールスルホニル基、アルキルスルホニル基、アミノ基、アルキルアミノ基、アリールアミノ基、ヒドロキシ基、アルコキシ基、アシルアミノ基、アシルオキシ基、カルボキシ基、カルボキソアミド基、カルボアルコキシ基、アシル基、スルホニル基、シアノ基およびニトロ基である。Ｍ４はホウ素または２価あるいは３価の金属である。）
［１２］
各画素が１または複数の有機光電変換部を含み、
前記有機光電変換部は、
対向配置された第１電極および第２電極と、
前記第１電極と前記第２電極との間に設けられ、共役面を有し、前記共役面に含まれると共に、前記共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを備え、
前記置換基Ｒは、前記第１の原子に直接結合する第２の原子と、前記第２の原子と直接結合する第３の原子とを有し、前記第１の原子および前記第３の原子と結合を形成する前記第２の原子の結合角が固定された分子構造を有する
固体撮像装置。
［１３］
各画素では、１または複数の前記有機光電変換部と、前記有機光電変換部とは異なる波長域の光電変換を行う１または複数の無機光電変換部とが積層されている、前記［１２］に記載の固体撮像装置。
［１４］
前記無機光電変換部は、半導体基板内に埋め込まれ、
前記有機光電変換部は、前記半導体基板の第１面側に形成されている、前記［１３］に記載の固体撮像装置。
［１５］
前記有機光電変換部が緑色光の光電変換を行い、
前記半導体基板内に、青色光の光電変換を行う無機光電変換部と、赤色光の光電変換を行う無機光電変換部とが積層されている、前記［１３］または［１４］に記載の固体撮像装置。 The present disclosure may be configured as follows.
[1]
A first electrode and a second electrode disposed opposite to each other;
The first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane. A photoelectric conversion layer containing a conjugated compound having an atom,
The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom A photoelectric conversion element having a molecular structure in which a bond angle of the second atom that forms a bond with is fixed.
[2]
The photoelectric conversion element according to [1], wherein the bond angle is fixed by a hybrid orbit formed by the substituent R.
[3]
The second atom is any one of carbon (C), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si). The photoelectric device according to [1] or [2]. Conversion element.
[4]
The substituent R is a linear, branched, or cyclic alkyl group having 1 to 80 carbon atoms, a perfluoroalkyl group, an aromatic compound, a heterocyclic compound, or a conjugated compound in which an aromatic compound and a heterocyclic compound are condensed. , A trimethylsilyl group, a triarylsilyl group, a sulfonyl group, a cyano group, or a nitro group. The photoelectric conversion device according to any one of [1] to [3].
[5]
The straight chain, branched or cyclic alkyl group having 1 to 80 carbon atoms, perfluoroalkyl group, aromatic compound is phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene. The photoelectric conversion device according to [4], which is a derivative thereof.
[6]
The heterocyclic compounds include aniline, pyrrole, triallylamine, imidazole, triazole, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and these The photoelectric conversion device according to [4], which is a derivative.
[7]
Conjugated compounds in which the aromatic compound and the heterocyclic compound are condensed include phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene, aniline, pyrrole, triallylamine, imidazole, and triazole. , Thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and their derivatives are condensed with each other [4] The photoelectric conversion element as described in 2.
[8]
The photoelectric conversion element according to any one of [1] to [7], wherein the conjugated compound is a subphthalocyanine derivative represented by the following formula (1).
(R1 to R12 are each independently a hydrogen atom, halogen atom, linear, branched, or cyclic alkyl group, aryl group, partial fluoroalkyl group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group. Group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group And any adjacent R 1 to R 12 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring. A fused aromatic ring contains one or more atoms other than carbon Z1 to Z3 are each independently a nitrogen atom or CR13, and each R13 is independently a hydrogen atom, a halogen atom, a linear, branched or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group. Perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, acylamino A group, an acyloxy group, a carboxy group, a carboxamide group, a carboalkoxy group, an acyl group, a sulfonyl group, a cyano group, and a nitro group, and M1 is boron or a divalent or trivalent metal.)
[9]
The photoelectric conversion device according to any one of [1] to [7], wherein the conjugated compound is a phthalocyanine derivative represented by the following formula (2).
(R14 to R29 are each independently a hydrogen atom, halogen atom, linear, branched, or cyclic alkyl group, aryl group, partial fluoroalkyl group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group. Group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group And any adjacent R14 to R29 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring. A fused aromatic ring contains one or more atoms other than carbon. Z4 to Z7 are each independently a nitrogen atom or CR30, and each R30 is independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group. Group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, (Acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group, acyl group, sulfonyl group, cyano group, and nitro group. M2 is boron or a divalent or trivalent metal.)
[10]
The photoelectric conversion element according to any one of [1] to [7], wherein the conjugated compound is a subporphyrin derivative represented by the following formula (3).
(R31 to R36 are each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, a partial fluoroalkyl group, a perfluoroalkyl group, a silylalkyl group, a silylalkoxy group, an arylsilyl group. Group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group And any adjacent R 31 to R 36 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring. A fused aromatic ring contains one or more atoms other than carbon. Z8 to Z10 are each independently a nitrogen atom or CR37, and R37 is each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group. Group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, (Acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group, acyl group, sulfonyl group, cyano group, and nitro group. M3 is boron or a divalent or trivalent metal.)
[11]
The photoelectric conversion element according to any one of [1] to [7], wherein the conjugated compound is a porphyrin derivative represented by the following formula (4).
(R38 to R45 are each independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, a partial fluoroalkyl group, a perfluoroalkyl group, a silylalkyl group, a silylalkoxy group, an arylsilyl group. Group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group And any adjacent R38 to R45 may be bonded to each other to form a condensed aliphatic ring or a condensed aromatic ring. A fused aromatic ring contains one or more atoms other than carbon. Z11 to Z14 are each independently a nitrogen atom or CR46, and each R46 is independently a hydrogen atom, a halogen atom, a linear, branched, or cyclic alkyl group, an aryl group, or a partial fluoroalkyl group. Group, perfluoroalkyl group, silylalkyl group, silylalkoxy group, arylsilyl group, thioalkyl group, thioaryl group, arylsulfonyl group, alkylsulfonyl group, amino group, alkylamino group, arylamino group, hydroxy group, alkoxy group, (Acylamino group, acyloxy group, carboxy group, carboxamide group, carboalkoxy group, acyl group, sulfonyl group, cyano group, and nitro group. M4 is boron or a divalent or trivalent metal.)
[12]
Each pixel includes one or more organic photoelectric conversion units,
The organic photoelectric conversion unit is
A first electrode and a second electrode disposed opposite to each other;
The first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane. A photoelectric conversion layer containing a conjugated compound having an atom,
The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom A solid-state imaging device having a molecular structure in which a bond angle of the second atom forming a bond with the second atom is fixed.
[13]
In each pixel, the one or more organic photoelectric conversion units and one or more inorganic photoelectric conversion units that perform photoelectric conversion in a wavelength region different from the organic photoelectric conversion unit are stacked. The solid-state imaging device described.
[14]
The inorganic photoelectric conversion unit is embedded in a semiconductor substrate,
The organic photoelectric conversion unit according to [13], wherein the organic photoelectric conversion unit is formed on a first surface side of the semiconductor substrate.
[15]
The organic photoelectric conversion unit performs green light photoelectric conversion,
The solid-state imaging according to [13] or [14], wherein an inorganic photoelectric conversion unit that performs photoelectric conversion of blue light and an inorganic photoelectric conversion unit that performs photoelectric conversion of red light are stacked in the semiconductor substrate. apparatus.
［１］
対向配置された第１電極および第２電極と、
前記第１電極と前記第２電極との間に設けられ、共役面を有し、前記共役面に含まれると共に、前記共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを備え、
前記置換基Ｒは、前記第１の原子に直接結合する第２の原子と、前記第２の原子と直接結合する第３の原子とを有し、前記第１の原子および前記第３の原子と結合を形成する前記第２の原子の結合角が固定された分子構造を有する
光電変換素子。
［２］
前記結合角は、前記置換基Ｒが形成する混成軌道によって固定されている
前記［１］に記載の光電変換素子。
［３］
前記第２の原子は、炭素（Ｃ）、窒素（Ｎ）、硫黄（Ｓ）、リン（Ｐ）およびシリコン（Ｓｉ）のうちのいずれかである
前記［１］または［２］に記載の光電変換素子。
［４］
前記置換基Ｒは、炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物、複素環化合物、芳香族化合物と複素環化合物が縮環した共役系化合物、トリメチルシリル基、トリアリールシリル基、スルホニル基、シアノ基およびニトロ基のうちのいずれかである
前記［１］乃至［３］のうちのいずれかに記載の光電変換素子。
［５］
前記炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物は、フェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレンおよびこれらの誘導体である
前記［４］に記載の光電変換素子。
［６］
前記複素環化合物は、アニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体である
前記［４］に記載の光電変換素子。
［７］
前記芳香族化合物と複素環化合物が縮環した共役系化合物は、フェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレン、アニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体のいずれかが互いに縮環したものである
前記［４］に記載の光電変換素子。
［８］
前記共役系化合物は、下記式（１）で表わされるサブフタロシアニン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
［９］
前記共役系化合物は、下記式（２）で表わされるフタロシアニン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
［１０］
前記共役系化合物は、下記式（３）で表わされるサブポルフィリン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
［１１］
前記共役系化合物は、下記式（４）で表わされるポルフィリン誘導体である
前記［１］乃至［７］のうちのいずれかに記載の光電変換素子。
［１２］
各画素が１または複数の有機光電変換部を含み、
前記有機光電変換部は、
対向配置された第１電極および第２電極と、
前記第１電極と前記第２電極との間に設けられ、共役面を有し、前記共役面に含まれると共に、前記共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを備え、
前記置換基Ｒは、前記第１の原子に直接結合する第２の原子と、前記第２の原子と直接結合する第３の原子とを有し、前記第１の原子および前記第３の原子と結合を形成する前記第２の原子の結合角が固定された分子構造を有する
固体撮像装置。
［１３］
各画素では、１または複数の前記有機光電変換部と、前記有機光電変換部とは異なる波長域の光電変換を行う１または複数の無機光電変換部とが積層されている、前記［１２］に記載の固体撮像装置。
［１４］
前記無機光電変換部は、半導体基板内に埋め込まれ、
前記有機光電変換部は、前記半導体基板の第１面側に形成されている、前記［１３］に記載の固体撮像装置。
［１５］
前記有機光電変換部が緑色光の光電変換を行い、
前記半導体基板内に、青色光の光電変換を行う無機光電変換部と、赤色光の光電変換を行う無機光電変換部とが積層されている、前記［１３］または［１４］に記載の固体撮像装置。 The present disclosure may be configured as follows.
[1]
A first electrode and a second electrode disposed opposite to each other;
The first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane. A photoelectric conversion layer containing a conjugated compound having an atom,
The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom A photoelectric conversion element having a molecular structure in which a bond angle of the second atom that forms a bond with is fixed.
[2]
The photoelectric conversion element according to [1], wherein the bond angle is fixed by a hybrid orbit formed by the substituent R.
[3]
The second atom is any one of carbon (C), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si). The photoelectric device according to [1] or [2]. Conversion element.
[4]
The substituent R is a linear, branched, or cyclic alkyl group having 1 to 80 carbon atoms, a perfluoroalkyl group, an aromatic compound, a heterocyclic compound, or a conjugated compound in which an aromatic compound and a heterocyclic compound are condensed. , A trimethylsilyl group, a triarylsilyl group, a sulfonyl group, a cyano group, or a nitro group. The photoelectric conversion device according to any one of [1] to [3].
[5]
The straight chain, branched or cyclic alkyl group having 1 to 80 carbon atoms, perfluoroalkyl group, aromatic compound is phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene. The photoelectric conversion device according to [4], which is a derivative thereof.
[6]
The heterocyclic compounds include aniline, pyrrole, triallylamine, imidazole, triazole, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and these The photoelectric conversion device according to [4], which is a derivative.
[7]
Conjugated compounds in which the aromatic compound and the heterocyclic compound are condensed include phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene, aniline, pyrrole, triallylamine, imidazole, and triazole. , Thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and their derivatives are condensed with each other [4] The photoelectric conversion element as described in 2.
[8]
The photoelectric conversion element according to any one of [1] to [7], wherein the conjugated compound is a subphthalocyanine derivative represented by the following formula (1).
[9]
The photoelectric conversion device according to any one of [1] to [7], wherein the conjugated compound is a phthalocyanine derivative represented by the following formula (2).
[10]
The photoelectric conversion element according to any one of [1] to [7], wherein the conjugated compound is a subporphyrin derivative represented by the following formula (3).
[11]
The photoelectric conversion element according to any one of [1] to [7], wherein the conjugated compound is a porphyrin derivative represented by the following formula (4).
[12]
Each pixel includes one or more organic photoelectric conversion units,
The organic photoelectric conversion unit is
A first electrode and a second electrode disposed opposite to each other;
The first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane. A photoelectric conversion layer containing a conjugated compound having an atom,
The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom A solid-state imaging device having a molecular structure in which a bond angle of the second atom forming a bond with the second atom is fixed.
[13]
In each pixel, the one or more organic photoelectric conversion units and one or more inorganic photoelectric conversion units that perform photoelectric conversion in a wavelength region different from the organic photoelectric conversion unit are stacked. The solid-state imaging device described.
[14]
The inorganic photoelectric conversion unit is embedded in a semiconductor substrate,
The organic photoelectric conversion unit according to [13], wherein the organic photoelectric conversion unit is formed on a first surface side of the semiconductor substrate.
[15]
The organic photoelectric conversion unit performs green light photoelectric conversion,
The solid-state imaging according to [13] or [14], wherein an inorganic photoelectric conversion unit that performs photoelectric conversion of blue light and an inorganic photoelectric conversion unit that performs photoelectric conversion of red light are stacked in the semiconductor substrate. apparatus.
本出願は、日本国特許庁において２０１５年１１月１８日に出願された日本特許出願番号２０１５－２２５７７８号を基礎として優先権を主張するものであり、この出願の全ての内容を参照によって本出願に援用する。
This application claims priority on the basis of Japanese Patent Application No. 2015-225778 filed on November 18, 2015 at the Japan Patent Office. The entire contents of this application are hereby incorporated by reference. Incorporated into.
当業者であれば、設計上の要件や他の要因に応じて、種々の修正、コンビネーション、サブコンビネーション、および変更を想到し得るが、それらは添付の請求の範囲やその均等物の範囲に含まれるものであることが理解される。
Those skilled in the art will envision various modifications, combinations, subcombinations, and changes, depending on design requirements and other factors, which are within the scope of the appended claims and their equivalents. It is understood that
Claims (15)
- 対向配置された第１電極および第２電極と、
前記第１電極と前記第２電極との間に設けられ、共役面を有し、前記共役面に含まれると共に、前記共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを備え、
前記置換基Ｒは、前記第１の原子に直接結合する第２の原子と、前記第２の原子と直接結合する第３の原子とを有し、前記第１の原子および前記第３の原子と結合を形成する前記第２の原子の結合角が固定された分子構造を有する
光電変換素子。 A first electrode and a second electrode disposed opposite to each other;
The first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane. A photoelectric conversion layer containing a conjugated compound having an atom,
The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom A photoelectric conversion element having a molecular structure in which a bond angle of the second atom that forms a bond with is fixed. - 前記結合角は、前記置換基Ｒが形成する混成軌道によって固定されている
請求項１に記載の光電変換素子。 The photoelectric conversion element according to claim 1, wherein the bond angle is fixed by a hybrid orbit formed by the substituent R. - 前記第２の原子は、炭素（Ｃ）、窒素（Ｎ）、硫黄（Ｓ）、リン（Ｐ）およびシリコン（Ｓｉ）のうちのいずれかである
請求項１に記載の光電変換素子。 The photoelectric conversion element according to claim 1, wherein the second atom is any one of carbon (C), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si). - 前記置換基Ｒは、炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物、複素環化合物、芳香族化合物と複素環化合物が縮環した共役系化合物、トリメチルシリル基、トリアリールシリル基、スルホニル基、シアノ基およびニトロ基のうちのいずれかである
請求項１に記載の光電変換素子。 The substituent R is a linear, branched, or cyclic alkyl group having 1 to 80 carbon atoms, a perfluoroalkyl group, an aromatic compound, a heterocyclic compound, or a conjugated compound in which an aromatic compound and a heterocyclic compound are condensed. The photoelectric conversion element according to claim 1, wherein the photoelectric conversion element is any one of a trimethylsilyl group, a triarylsilyl group, a sulfonyl group, a cyano group, and a nitro group. - 前記炭素数１以上８０以下の直鎖，分岐，または環状アルキル基、パーフルオロアルキル基、芳香族化合物は、フェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレンおよびこれらの誘導体である
請求項４に記載の光電変換素子。 The straight chain, branched or cyclic alkyl group having 1 to 80 carbon atoms, perfluoroalkyl group, aromatic compound is phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene. The photoelectric conversion element according to claim 4, which is a derivative thereof. - 前記複素環化合物は、アニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体である
請求項４に記載の光電変換素子。 The heterocyclic compounds include aniline, pyrrole, triallylamine, imidazole, triazole, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and these The photoelectric conversion element according to claim 4, which is a derivative. - 前記芳香族化合物と複素環化合物が縮環した共役系化合物は、フェニル、フェニレンビニレン、フルオレン、ピレン、ペリレン、ペンタセン、ナフタレン、ピセン、トリフェニレン、ルブレン、フラーレン、アニリン、ピロール、トリアリルアミン、イミダゾール、トリアゾール、チアジアゾール、カルバゾール、アクリドン、キナクリドン、ナフタレンジイミド、ペリレンジイミド、チオフェン、ベンゾチオフェン、ジベンゾチオフェン、ナフトチオフェン、テトラチアフルバレン、フランおよびこれらの誘導体のいずれかが互いに縮環したものである
請求項４に記載の光電変換素子。 Conjugated compounds in which the aromatic compound and the heterocyclic compound are condensed include phenyl, phenylene vinylene, fluorene, pyrene, perylene, pentacene, naphthalene, picene, triphenylene, rubrene, fullerene, aniline, pyrrole, triallylamine, imidazole, and triazole. Any one of, thiadiazole, carbazole, acridone, quinacridone, naphthalene diimide, perylene diimide, thiophene, benzothiophene, dibenzothiophene, naphthothiophene, tetrathiafulvalene, furan and derivatives thereof are fused to each other. The photoelectric conversion element as described. - 前記共役系化合物は、下記式（１）で表わされるサブフタロシアニン誘導体である
請求項１に記載の光電変換素子。
- 前記共役系化合物は、下記式（２）で表わされるフタロシアニン誘導体である
請求項１に記載の光電変換素子。
- 前記共役系化合物は、下記式（３）で表わされるサブポルフィリン誘導体である
請求項１に記載の光電変換素子。
- 前記共役系化合物は、下記式（４）で表わされるポルフィリン誘導体である
請求項１に記載の光電変換素子。
- 各画素が１または複数の有機光電変換部を含み、
前記有機光電変換部は、
対向配置された第１電極および第２電極と、
前記第１電極と前記第２電極との間に設けられ、共役面を有し、前記共役面に含まれると共に、前記共役面に対して略垂直方向に置換基Ｒが直接結合した第１の原子を有する共役系化合物を含む光電変換層とを備え、
前記置換基Ｒは、前記第１の原子に直接結合する第２の原子と、前記第２の原子と直接結合する第３の原子とを有し、前記第１の原子および前記第３の原子と結合を形成する前記第２の原子の結合角が固定された分子構造を有する
固体撮像装置。 Each pixel includes one or more organic photoelectric conversion units,
The organic photoelectric conversion unit is
A first electrode and a second electrode disposed opposite to each other;
The first electrode is provided between the first electrode and the second electrode, has a conjugate plane, is included in the conjugate plane, and has a substituent R directly bonded in a direction substantially perpendicular to the conjugate plane. A photoelectric conversion layer containing a conjugated compound having an atom,
The substituent R has a second atom directly bonded to the first atom and a third atom directly bonded to the second atom, and the first atom and the third atom A solid-state imaging device having a molecular structure in which a bond angle of the second atom forming a bond with the second atom is fixed. - 各画素では、１または複数の前記有機光電変換部と、前記有機光電変換部とは異なる波長域の光電変換を行う１または複数の無機光電変換部とが積層されている、請求項１２に記載の固体撮像装置。 13. Each pixel includes one or more organic photoelectric conversion units and one or more inorganic photoelectric conversion units that perform photoelectric conversion in a wavelength region different from that of the organic photoelectric conversion unit. Solid-state imaging device.
- 前記無機光電変換部は、半導体基板内に埋め込まれ、
前記有機光電変換部は、前記半導体基板の第１面側に形成されている、請求項１３に記載の固体撮像装置。 The inorganic photoelectric conversion unit is embedded in a semiconductor substrate,
The solid-state imaging device according to claim 13, wherein the organic photoelectric conversion unit is formed on a first surface side of the semiconductor substrate. - 前記有機光電変換部が緑色光の光電変換を行い、
前記半導体基板内に、青色光の光電変換を行う無機光電変換部と、赤色光の光電変換を行う無機光電変換部とが積層されている、請求項１４に記載の固体撮像装置。 The organic photoelectric conversion unit performs green light photoelectric conversion,
The solid-state imaging device according to claim 14, wherein an inorganic photoelectric conversion unit that performs blue light photoelectric conversion and an inorganic photoelectric conversion unit that performs red light photoelectric conversion are stacked in the semiconductor substrate.
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