Experimental demonstrations of spontaneous, solar-driven photoelectrochemical water splitting

被引:479
作者
Ager, Joel W. [1 ,2 ]
Shaner, Matthew R. [3 ,4 ]
Walczak, Karl A. [1 ,2 ]
Sharp, Ian D. [1 ,5 ]
Ardo, Shane [6 ,7 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Joint Ctr Artificial Photosynth, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[3] CALTECH, Joint Ctr Artificial Photosynth, Pasadena, CA 91125 USA
[4] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[6] Univ Calif Irvine, Dept Chem, Irvine, CA 92717 USA
[7] Univ Calif Irvine, Dept Chem Engn & Mat Sci, Irvine, CA USA
关键词
HYDROGEN-PRODUCTION; PHOTOASSISTED ELECTROLYSIS; SEMICONDUCTOR ELECTRODES; CONVERSION EFFICIENCY; ELECTROCHEMICAL-CELL; RECENT PROGRESS; TRIPLE STACK; TANDEM CELL; ENERGY; PHOTOELECTROLYSIS;
D O I
10.1039/c5ee00457h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Laboratory demonstrations of spontaneous photoelectrochemical (PEC) solar water splitting cells are reviewed. Reported solar-to-hydrogen (STH) conversion efficiencies range from <1% to 18%. The demonstrations are categorized by the number of photovoltaic junctions employed (2 or 3), photovoltaic junction type (solid-solid or solid-liquid) and the ability of the systems to produce separated reaction product streams. Demonstrations employing two photovoltaic (PV) junctions have the highest reported efficiencies of 12.4% and 18%, which are for cells that, respectively, do and do not contain a semiconductor-liquid junction. These devices used PV components based on III-V semiconductors; recently, a number of demonstrations with >10% STH efficiency using potentially less costly materials have been reported. Device stability is a major challenge for the field, as evidenced by lifetimes of less than 24 hours in all but a few reports. No globally accepted protocol for evaluating and certifying STH efficiencies and lifetimes exists. It is our recommendation that a protocol similar to that used by the photovoltaic community be adopted so that future demonstrations of solar PEC water splitting can be compared on equal grounds.
引用
收藏
页码:2811 / 2824
页数:14
相关论文
共 109 条
[41]   An analysis of the optimal band gaps of light absorbers in integrated tandem photoelectrochemical water-splitting systems [J].
Hu, Shu ;
Xiang, Chengxiang ;
Haussener, Sophia ;
Berger, Alan D. ;
Lewis, Nathan S. .
ENERGY & ENVIRONMENTAL SCIENCE, 2013, 6 (10) :2984-2993
[42]   A monolithic device for solar water splitting based on series interconnected thin film absorbers reaching over 10% solar-to-hydrogen efficiency [J].
Jacobsson, T. Jesper ;
Fjallstrom, Viktor ;
Sahlberg, Martin ;
Edoff, Marika ;
Edvinsson, Tomas .
ENERGY & ENVIRONMENTAL SCIENCE, 2013, 6 (12) :3676-3683
[43]  
James B. D., 2009, GS10F009J DIR TECHN
[44]   SIGNIFICANT EFFICIENCY INCREASE IN SELF-DRIVEN PHOTOELECTROCHEMICAL CELL FOR WATER PHOTOELECTROLYSIS [J].
KAINTHLA, RC ;
ZELENAY, B ;
BOCKRIS, JO .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1987, 134 (04) :841-845
[45]  
Kayes B. M., 2011, 2011 37th IEEE Photovoltaic Specialists Conference (PVSC 2011), P000004, DOI 10.1109/PVSC.2011.6185831
[46]   ELECTRICITY FROM PHOTOSENSITIZATION OF TITANIUM [J].
KEENEY, J ;
WEINSTEIN, DH ;
HAAS, GM .
NATURE, 1975, 253 (5494) :719-720
[47]   Design and characterization of a robust photoelectrochemical device to generate hydrogen using solar water splitting [J].
Kelly, Nelson A. ;
Gibson, Thomas L. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2006, 31 (12) :1658-1673
[48]  
Kelzenberg MD, 2010, NAT MATER, V9, P239, DOI [10.1038/NMAT2635, 10.1038/nmat2635]
[49]   A monolithic photovoltaic-photoelectrochemical device for hydrogen production via water splitting [J].
Khaselev, O ;
Turner, JA .
SCIENCE, 1998, 280 (5362) :425-427
[50]   High-efficiency integrated multijunction photovoltaic/electrolysis systems for hydrogen production [J].
Khaselev, O ;
Bansal, A ;
Turner, JA .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2001, 26 (02) :127-132