Molecular water-oxidation catalysts for photoelectrochemical cells

被引:114
作者
Brimblecombe, Robin [1 ,2 ,3 ]
Dismukes, G. Charles [2 ,3 ]
Swiegers, Gerhard F. [4 ]
Spiccia, Leone [1 ]
机构
[1] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[2] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
[3] Princeton Univ, Princeton Environm Inst, Princeton, NJ 08544 USA
[4] Univ Wollongong, Intelligent Polymer Res Inst, Wollongong, NSW 2522, Australia
基金
美国国家卫生研究院; 澳大利亚研究理事会;
关键词
OXYGEN-EVOLVING COMPLEX; O BOND FORMATION; HYDROGEN-PRODUCTION; PHOTOSYSTEM-II; FUNCTIONAL-MODEL; EVOLUTION; LIGHT; SENSITIZERS; PERFORMANCE; NANOPARTICLES;
D O I
10.1039/b912669d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Photoelectrochemical cells that efficiently split water into oxygen and hydrogen, "the fuel of the future", need to combine robust water oxidation catalysts at the anode (2H(2)O -> O-2 + 4H(+) + 4e(-)) with hydrogen reduction catalysts at the cathode (2H(+) + 2e(-) -> H-2). Both sets of catalysts will, ideally, operate at low overpotentials and employ light-driven or light-assisted processes. In this Perspective article, we focus on significant efforts to develop solid state materials and molecular coordination complexes as catalyst for water oxidation. We briefly review the field with emphasis on the various molecular catalysts that have been developed and then examine the activity of molecular catalysts in water oxidation following their attachment to conducting electrodes. For such molecular species to be useful in a solar water-splitting device it is preferable that they are securely and durably affixed to an electrode surface. We also consider recent developments aimed at combining the action of molecular catalysts with light absorption so that light driven water oxidation may be achieved.
引用
收藏
页码:9374 / 9384
页数:11
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