IP Library › Granted Patent US 8,247,680
Granted Patent B2
US 8,247,680 · App. 11/892,776 · Granted Aug 21, 2012

Light energy conversion material

Assignee: Kabushiki Kaisha Toyota Chuo Kenkyusho
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Quick Facts
Patent No.
US 8,247,680
App. No.
11/892,776
Granted
Aug 21, 2012
Kind
B2
Abstract

A light energy conversion material that includes a porous material including an electron donor in a skeleton thereof; and an electron acceptor disposed in at least one portion among a pore, the skeleton and the outer circumference of the porous material.

Claims (13)

1. A light energy conversion material, comprising:

a porous material including an electron donor in a skeleton thereof; and

an electron acceptor disposed in at least one portion among a pore, the skeleton and the outer circumference of the porous material,

wherein the porous material including the electron donor in the skeleton thereof is a silica porous material comprised of silicon atoms covalently bonded with an organic group,

wherein the organic group is the electron donor, and absorbs light energy and transfers electrons excited by the light energy to the electron acceptor, and

wherein the organic group is a molecule selected from the group consisting of 1,1-bi-2-naphthol, 1,3-di(N-carvazolyl)propane (DCzPr), 1,4-di(N-carvazolyl)butane (DCzBu), 1,4-diazabicyclo[2,2,2]octane, 2,3-dihydroxy-naphtol, 2,7-dihydroxy-naphthol, 2-naphthol, Cu(2,9-diphenyl-1,10-phenanthroline) 2+ , di(N-carvazolyl)methane (DCzMe), meso-2,4-di(N-carvazolyl)pentane (m-DCzPe), Mg(phthalocyanine) 4+ , N,N,N′,N′-tetramethyl-p-phenylenediamine, N,N,N′,N′-tetramethylbenzidine, N,N-diethylaniline, N,N-dimethylaniline, N-ethyl-carbazole (EtCz), Rh 2 (1,3-diisocyanopropane) 4 2+ , Ru(2,2′-bipyridine) 3 2+ , Tetrakis(dimethylamino)ethylene (TDAE), trans-1,2-di(N-carvazolyl)cyclobutane (DCzCBu), Zn(tetra(N-methylpyridinium)porphyrin) 4+ , a Zn porphyrin complex, Zn(tetraphenylporphyrin), Zn(octaethylporphyrin), a Zn phthalocyanine complex, indene, oxadiazole, quadricyclane, diazabicyclooctane, diphenylethylene, triethylamine, triphenylmethane, trimethoxybenzene, norbornadiene, hydrazone, phenothiazine and methoxynaphthalene.

2. The light energy conversion material according to claim 1 , wherein the electron acceptor is at least one kind selected from the group consisting of compounds represented by the following general formula (3):

Cr(2,2′-bipyridine) 3 2+ , Cr(2,21-bipyridine) 3 3+ , Cr(CN) 6 3− , Fe(CN) 6 4− , Fe 3+ , N,N-dimethylaniline, Pt 2 (P 2 O 5 ) 4 H 8 4− , methyl p-cyanobenzoate, p-dicyanobenzene, p-dinitrobenzene, p-benzoquinone, ReCl 8 2− , Rh 2 (1,3-diisocyanopropane) 4 2+ , Ru(2,2′-bipyridine) 3 2+ , trans-stilbene, UO 2 2+ , a Zn porphyrin complex, Zn(tetraphenylporphyrin), Zn(octaethylporphyrin), Zn phthalocyanine, acetophenone, anthracene, an osmium(II) complex, chloranil, cyanoanthracene, cyanonaphthalene, dimethylaniline, dicyanoanthracene, dicyanonaphthalene, dimethylbicyclohepta-2,5-diene-2,3-dicarboxylate, tetracyanoanthracene, tetracyanoethylene, triphenylpyrylium tetrafluoroborate, naphthalene, nitrobenzene, viologen, phenanthrene, fullerene C60, fullerene C60-μ-oxodimer(C120O), fullerene C70, benzophenone, methylviologen, methoxyacetophenone, oxygen and an aromatic vinyl polymer.

3. The light energy conversion material according to claim 1 , wherein the porous material has a periodic structure with an interval of 5 nm or less based on the regular arrangement of the organic groups.

4. The light energy conversion material according to claim 1 , wherein the porous material has the pore with a central pore diameter of 1 nm to 30 nm.

5. The light energy conversion material according to claim 1 , wherein the porous material has one or more peaks at a diffraction angle corresponding to a d value of 1 nm or more in an X-ray diffraction pattern.

6. The light energy conversion material according to claim 1 , wherein the electron acceptor is at least one kind selected from the group consisting of a quinone compound, an aromatic compound having a vinyl group, an aromatic compound having a cyano group, an aromatic compound having a nitro group, a nitrogen-containing aromatic compound, an organic compound having a dicyanomethylene group, a molecular metal complex containing an organic compound having a dicyanomethylene group as a ligand, an organic compound having a cyanoimino group, a molecular metal complex containing an organic compound having a cyanoimino group as a ligand, fullerene, a carbon nanotube, a metal complex having a nitrogen-containing organic ligand, a metal complex having a cyclic ligand, a metal complex salt, a metal ion and a metal oxide.

7. The light energy conversion material according to claim 1 , wherein the silica porous material has a skeleton structure of X—Si—O, X being the organic group that is covalently bound to the silicon atoms.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2007
From: INAGAKI, SHINJI; AOKI, MASAO; YAMANAKA, KEN-ICHI; NAKAJIMA, KIYOTAKA; OHASHI, MASATAKA
To: KABUSHIKI KAISHA TOYOTA CHUO KENKYUSHO
Reel/Frame 020000/0963 →
Priority Claims (2)
JP 2006-235638 · Aug 31, 2006 · national
JP 2007-189886 · Jul 20, 2007 · national
Continuity (1)
Related Publication 20080057420A1 · Mar 6, 2008