| Literature DB >> 20223949 |
Qiushi Yin1, Jeffrey Miles Tan, Claire Besson, Yurii V Geletii, Djamaladdin G Musaev, Aleksey E Kuznetsov, Zhen Luo, Ken I Hardcastle, Craig L Hill.
Abstract
Traditional homogeneous water oxidation catalysts are plagued by instability under the reaction conditions. We report that the complex [Co4(H2O)2(PW9O34)2]10-, comprising a Co4O4 core stabilized by oxidatively resistant polytungstate ligands, is a hydrolytically and oxidatively stable homogeneous water oxidation catalyst that self-assembles in water from salts of earth-abundant elements (Co, W, and P). With [Ru(bpy)3]3+ (bpy is 2,2'-bipyridine) as the oxidant, we observe catalytic turnover frequencies for O2 production > or = 5 s(-1) at pH = 8. The rate's pH sensitivity reflects the pH dependence of the four-electron O2-H2O couple. Extensive spectroscopic, electrochemical, and inhibition studies firmly indicate that [Co4(H2O)2(PW9O34)2]10- is stable under catalytic turnover conditions: Neither hydrated cobalt ions nor cobalt hydroxide/oxide particles form in situ.Entities:
Year: 2010 PMID: 20223949 DOI: 10.1126/science.1185372
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728