Solar water splitting in a molecular photoelectrochemical cell

被引:200
作者
Alibabaei, Leila [1 ]
Brennaman, M. Kyle [1 ]
Norris, Michael R. [1 ]
Kalanyan, Berc [2 ]
Song, Wenjing [1 ]
Losego, Mark D. [2 ]
Concepcion, Javier J. [1 ]
Binstead, Robert A. [1 ]
Parsons, Gregory N. [2 ]
Meyer, Thomas J. [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
关键词
ELECTRON-TRANSFER; IRIDIUM COMPLEXES; SINGLE-SITE; OXIDATION; EFFICIENCY; CATALYST; FUELS; TIO2;
D O I
10.1073/pnas.1319628110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Artificial photosynthesis and the production of solar fuels could be a key element in a future renewable energy economy providing a solution to the energy storage problem in solar energy conversion. We describe a hybrid strategy for solar water splitting based on a dye sensitized photoelectrosynthesis cell. It uses a derivatized, core-shell nanostructured photoanode with the core a high surface area conductive metal oxide film--indium tin oxide or antimony tin oxide-coated with a thin outer shell of TiO2 formed by atomic layer deposition. A "chromophore-catalyst assembly" 1, [(PO3H2)(2)bpy)(2)Ru(4-Mebpy-4-bimpy)Rub(tpy)(OH2)](4+), which combines both light absorber and water oxidation catalyst in a single molecule, was attached to the TiO2 shell. Visible photolysis of the resulting core-shell assembly structure with a Pt cathode resulted in water splitting into hydrogen and oxygen with an absorbed photon conversion efficiency of 4.4% at peak photocurrent.
引用
收藏
页码:20008 / 20013
页数:6
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