Single Electron Transfer Steps in Water Oxidation Catalysis. Redefining the Mechanistic Scenario

被引:67
作者
Funes-Ardoiz, Ignacio [1 ]
Garrido-Barros, Pablo [1 ,2 ]
Llobet, Antoni [1 ,3 ]
Maseras, Feliu [1 ,3 ]
机构
[1] Barcelona Inst Sci & Technol, Inst Chem Res Catalonia ICIQ, Avgda Paisos Catalans 16, Tarragona 43007, Spain
[2] Univ Rovira & Virgili, Dept Quim Fis & Inorgan, Campus Sescelades,C Marcelli Domingo S-N, E-43007 Tarragona, Spain
[3] Univ Autonoma Barcelona, Dept Quim, Bellaterra 08193, Spain
关键词
water oxidation; water splitting; first row transition metal complexes; DFT; mechanism; QUANTUM-CHEMICAL CHARACTERIZATION; ASTERISK IRIDIUM COMPLEXES; BASIS-SETS; ARTIFICIAL PHOTOSYNTHESIS; MANGANESE; EFFICIENT; CU; PERSPECTIVE; ACTIVATION; CHEMISTRY;
D O I
10.1021/acscatal.6b03253
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The systematic computational study of the mechanism for water oxidation in four different complexes confirms the existence of an alternative mechanism for the O-O bond formation step to those previously reported: the single electron transfer-water nucleophilic attack (SET-WNA). The calculated mechanism relies on two SET steps and features the existence of an intermediate with a (HO center dot center dot center dot OH)(-) moiety in the vicinity of the metal center. It is operative in at least three representative copper based complexes and is the only option that explains the experimentally observed efficiency in two of them. The proposal of this reaction pathway redefines the mechanistic scenario and, importantly, generates a promising avenue for designing more efficient water oxidation catalysts based on first row transition metals.
引用
收藏
页码:1712 / 1719
页数:8
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