Microsecond X-ray Absorption Spectroscopy Identification of CoI Intermediates in Cobaloxime-Catalyzed Hydrogen Evolution

被引:38
作者
Smolentsev, Grigory [1 ]
Cecconi, Bianca [2 ,3 ,4 ]
Guda, Alexander [5 ]
Chavarot-Kerlidou, Murielle [2 ]
van Bokhoven, Jeroen A. [1 ,6 ]
Nachtegaal, Maarten [1 ]
Artero, Vincent [2 ]
机构
[1] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[2] Univ Grenoble Alpes, CEA, CNRS, Lab Chem & Biol Met, Grenoble, France
[3] Univ Milano Bicocca, Dept Mat Sci, I-20125 Milan, Italy
[4] Univ Milano Bicocca, INSTM Unit, Milano Bicocca Solar Energy Res Ctr, I-20125 Milan, Italy
[5] Southern Fed Univ, Int Res Ctr Smart Mat, Rostov Na Donu 344090, Russia
[6] ETH, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会; 俄罗斯基础研究基金会;
关键词
photocatalysis; solar fuels; transient X-ray absorption; XANES; X-ray absorption spectroscopy; MOLECULAR-HYDROGEN; WATER; ACTIVATION; GENERATION; COMPLEXES; MECHANISM; SYSTEMS;
D O I
10.1002/chem.201502900
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rational development of efficient photocatalytic systems for hydrogen production requires understanding the catalytic mechanism and detailed information about the structure of intermediates in the catalytic cycle. We demonstrate how time-resolved X-ray absorption spectroscopy in the microsecond time range can be used to identify such intermediates and to determine their local geometric structure. This method was used to obtain the solution structure of the Co-I intermediate of cobaloxime, which is a non-noble metal catalyst for solar hydrogen production from water. Distances between cobalt and the nearest ligands including two solvent molecules and displacement of the cobalt atom out of plane formed by the planar ligands have been determined. Combining in situ X-ray absorption and UV/Vis data, we demonstrate how slight modification of the catalyst structure can lead to the formation of a catalytically inactive Co-I state under similar conditions. Possible deactivation mechanisms are discussed.
引用
收藏
页码:15158 / 15162
页数:5
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