Solar Fuels via Artificial Photosynthesis

被引:1773
作者
Gust, Devens [1 ]
Moore, Thomas A.
Moore, Ana L.
机构
[1] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
关键词
PHOTOINDUCED ELECTRON-TRANSFER; CHARGE SEPARATION; ENERGY-TRANSFER; ANTENNA; POTENTIALS; MIMICKING; DYNAMICS; MODEL; STATE;
D O I
10.1021/ar900209b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Because sunlight is diffuse and intermittent, substantial use of solar energy to meet humanity's needs will probably require energy storage in dense, transportable media via chemical bonds. Practical, cost effective technologies for conversion of sunlight directly into useful fuels do not currently exist, and will require new basic science. Photosynthesis provides a blueprint for solar energy storage in fuels. Indeed, all of the fossil-fuel-based energy consumed today derives from sunlight harvested by photosynthetic organisms. Artificial photosynthesis research applies the fundamental scientific principles of the natural process to the design of solar energy conversion systems. These constructs use different materials, and researchers tune them to produce energy efficiently and in forms useful to humans. Fuel production via natural or artificial photosynthesis requires three main components. First antenna/reaction center complexes absorb sunlight and convert the excitation energy to electrochemical energy (redox equivalents). Then, a water oxidation complex uses this redox potential to catalyze conversion of water to hydrogen ions, electrons stored as reducing equivalents, and oxygen. A second catalytic system uses the reducing equivalents to make fuels such as carbohydrates, lipids, or hydrogen gas. In this Account we review a few general approaches to artificial photosynthetic fuel production that may be useful for eventually overcoming the energy problem. A variety of research groups have prepared artificial reaction center molecules. These systems contain a chromophore, such as a porphyrin, covalently linked to one or more electron acceptors, such as fullerenes or quinones, and secondary electron donors. Following the excitation of the chromophore, photoinduced electron transfer generates a primary charge-separated state. Electron transfer chains spatially separate the redox: equivalents and reduce electronic coupling, slowing recombination of the charge-separated state to the point that catalysts can use the stored energy for fuel production. Antenna systems, employing a variety of chromophores that absorb light throughout the visible spectrum, have been coupled to artificial reaction centers and have incorporated control and photoprotective processes borrowed from photosynthesis. Thus far, researchers have not discovered practical solar-driven catalysts for water oxidation and fuel production that are robust and use earth-abundant elements, but they have developed artificial systems that use sunlight to produce fuel in the laboratory. For example, artificial reaction centers, where electrons are injected from a dye molecule into the conduction band of nanoparticulate titanium dioxide on a transparent electrode, coupled to catalysts, such as platinum or hydrogenase enzymes, can produce hydrogen gas. Oxidizing equivalents from such reaction centers can be coupled to iridium oxide nanoparticles, which can oxidize water. This System uses sunlight to split water to oxygen and hydrogen fuel, but efficiencies are low and an external electrical potential is required. Although attempts at artificial photosynthesis fall short of the efficiencies necessary for practical application, they illustrate that solar fuel production inspired by natural photosynthesis is achievable in the laboratory. More research will be needed to identify the most promising artificial photosynthetic systems and realize their potential.
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页码:1890 / 1898
页数:9
相关论文
共 40 条
[1]   A simple artificial light-harvesting dyad as a model for excess energy dissipation in oxygenic photosynthesis [J].
Berera, R ;
Herrero, C ;
van Stokkum, IHM ;
Vengris, M ;
Kodis, G ;
Palacios, RE ;
van Amerongen, H ;
van Grondelle, R ;
Gust, D ;
Moore, TA ;
Moore, AL ;
Kennis, JTM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (14) :5343-5348
[2]   Synthetic routes to multiporphyrin arrays [J].
Burrell, AK ;
Officer, DL ;
Plieger, PG ;
Reid, DCW .
CHEMICAL REVIEWS, 2001, 101 (09) :2751-2796
[3]   OXIDATION OF NADH INVOLVING RATE-LIMITING ONE-ELECTRON TRANSFER [J].
CARLSON, BW ;
MILLER, LL ;
NETA, P ;
GRODKOWSKI, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (23) :7233-7239
[4]   A LIGHT-HARVESTING ARRAY OF SYNTHETIC PORPHYRINS [J].
DAVILA, J ;
HARRIMAN, A ;
MILGROM, LR .
CHEMICAL PHYSICS LETTERS, 1987, 136 (05) :427-430
[5]   Enzyme-based photoelectrochemical biofuel cell [J].
de la Garza, L ;
Jeong, G ;
Liddell, PA ;
Sotomura, T ;
Moore, TA ;
Moore, AL ;
Gust, D .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (37) :10252-10260
[6]   Light-induced charge separation in ruthenium based triads -: New variations on an old theme [J].
Falkenstrom, Magnus ;
Johansson, Olof ;
Hammarstrom, Leif .
INORGANICA CHIMICA ACTA, 2007, 360 (03) :741-750
[7]   Photoinduced processes in dyads made of a porphyrin unit and a ruthenium complex [J].
Flamigni, L ;
Armaroli, N ;
Barigelletti, F ;
Balzani, V ;
Collin, JP ;
Dalbavie, JO ;
Heitz, V ;
Sauvage, JP .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (31) :5936-5943
[8]  
Forster T., 1959, Disc. Faraday Soc, V27, P7, DOI [DOI 10.1039/DF9592700007, 10.1039/DF9592700007]
[9]  
Fukuzumi S., 2001, ELECT TRANSFER CHEM, V2, P927
[10]   Fullerene-porphyrin architectures; photosynthetic antenna and reaction center models [J].
Guldi, DM .
CHEMICAL SOCIETY REVIEWS, 2002, 31 (01) :22-36