The development of molecular water oxidation catalysts

被引:275
作者
Matheu, Roc [1 ,2 ]
Garrido-Barros, Pablo [1 ,2 ]
Gil-Sepulcre, Marcos [1 ]
Ertem, Mehmed Z. [3 ]
Sala, Xavier [4 ]
Gimbert-Surinach, Carolina [1 ]
Llobet, Antoni [1 ,4 ]
机构
[1] BIST, Inst Chem Res Catalonia ICIQ, Tarragona, Spain
[2] Univ Rovira & Virgili, Dept Quim Fis & Inorgan, Marcel Li Domingo S-N, Tarragona, Spain
[3] Brookhaven Natl Lab, Chem Div, Energy & Photon Sci Directorate, Upton, NY 11973 USA
[4] Univ Autonoma Barcelona, Dept Quim, Barcelona, Spain
关键词
HIGHLY EFFICIENT; PHOTOSYSTEM-II; BOND FORMATION; ARTIFICIAL PHOTOSYNTHESIS; IRIDIUM COMPLEXES; NEUTRAL PH; OXYGEN; COBALT; LIGHT; SITE;
D O I
10.1038/s41570-019-0096-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There is an urgent need to transition from fossil fuels to solar fuels-not only to lower CO2 emissions that cause global warming but also to ration fossil resources. Splitting H2O with sunlight emerges as a clean and sustainable energy conversion scheme that can afford practical technologies in the short-to-mid-term. A crucial component in such a device is a water oxidation catalyst (WOC). These artificial catalysts have been developed mainly over the past two decades, which is in contrast to nature's WOCs, which have featured in its photosynthetic apparatus for more than a billion years. Recent times have seen the development of increasingly active molecular WOCs, the study of which affords an understanding of catalytic mechanisms and decomposition pathways. This Perspective offers a historical description of the landmark molecular WOCs, particularly ruthenium systems, that have guided research to our present degree of understanding.
引用
收藏
页码:331 / 341
页数:11
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