Organic compound and photoelectric conversion element
US-2016260912-A1 · Sep 8, 2016 · US
US10062854B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10062854-B2 |
| Application number | US-201715596423-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 16, 2017 |
| Priority date | May 20, 2016 |
| Publication date | Aug 28, 2018 |
| Grant date | Aug 28, 2018 |
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To provide an organic material represented by General Formula (1) below: where, in General Formula (1), R 1 and R 2 are each independently an alkyl group having from 2 through 8 carbon atoms, R 3 and R 4 are each independently a straight-chain alkyl group having 1, 2, 4, 6, or 12 carbon atoms, or a hydrogen atom, and n is an integer of 1 or 2.
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What is claimed is: 1. An organic material represented by General Formula (1) below: where, in General Formula (1), R 1 and R 2 are each independently an alkyl group having from 2 through 8 carbon atoms, R 3 and R 4 are each independently a straight-chain alkyl group having 1, 2, 4, 6, or 12 carbon atoms, or a hydrogen atom, and n is an integer of 1 or 2. 2. The organic material according to claim 1 , wherein the organic material is represented by General Formula (2) below: where, in General Formula (2), R 1 and R 2 are each independently an alkyl group having from 2 through 8 carbon atoms, and R 3 and R 4 are each independently a straight-chain alkyl group having 1, 2, 4, 6, or 12 carbon atoms, or a hydrogen atom. 3. The organic material according to claim 1 , wherein the organic material is represented by General Formula (3) below: where, in General Formula (3), R 1 and R 2 are each independently an alkyl group having from 2 through 8 carbon atoms, and R 3 and R 4 are each independently a straight-chain alkyl group having 1, 2, 4, 6, or 12 carbon atoms, or a hydrogen atom. 4. A photoelectric conversion element comprising: a substrate; a first electrode; an electron-transporting layer; a photoelectric conversion layer; a hole-transporting layer; and a second electrode, where the first electrode, the electron-transporting layer, the photoelectric conversion layer, the hole-transporting layer, and the second electrode are disposed on the substrate, wherein the photoelectric conversion layer includes an organic material represented by General Formula (1) below, and an n-type semiconductor material, where, in General Formula (1), R 1 and R 2 are each independently an alkyl group having from 2 through 8 carbon atoms, R 3 and R 4 are each independently a straight-chain alkyl group having 1, 2, 4, 6, or 12 carbon atoms, or a hydrogen atom, and n is an integer of 1 or 2. 5. The photoelectric conversion element according to claim 4 , wherein the n-type semiconductor material included in the photoelectric conversion layer is a fullerene derivative, and wherein the fullerene derivative is a compound represented by General Formula (4) below: where, in General Formula (4), Y 1 and Y 2 are each independently a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, or an aralkyl group with the proviso that both Y 1 and Y 2 are not hydrogen atoms at the same time, Ar is an aryl group, and in General Formula (4), a site represented by: is a fullerene skeleton having 60 carbon atoms. 6. The photoelectric conversion element according to claim 4 , wherein the n-type semiconductor material included in the photoelectric conversion layer is a fullerene derivative, and wherein the fullerene derivative is a compound represented by General Formula (5) below: where, in General Formula (5), Z is a phenyl group, a 1-naphthyl group, or a 2-naphthyl group. 7. The photoelectric conversion element according to claim 4 , wherein the electron-transporting layer includes a first layer including metal oxide, and a second layer disposed between the first layer and the photoelectric conversion layer, the second layer including an amine compound represented by General Formula (6) below: where, in General Formula (6), R 5 and R 6 are each independently an alkyl group having from 1 through 4 carbon atoms, where R 5 and R 6 may be bonded to each other to form a ring, X is a bivalent aromatic group having is from 6 through 14 carbon atoms or an alkylene group having from 1 through 4 carbon atoms, and A is any one of substituents below: —COOH —P(═O)(OH) 2 —Si(OH) 3 .
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