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钴配合物的电催化析氧反应

Electrocatalytic oxygen evolution with a cobalt complex.

作者信息

Shi Hua-Tian, Li Xiu-Xiu, Wu Fang-Hui, Yu Wei-Bin

机构信息

Analysis and Testing Central Facility, Engineering Research Institute, Anhui University of Technology, Maanshan 243002, P. R. China.

出版信息

Dalton Trans. 2017 Nov 28;46(46):16321-16326. doi: 10.1039/c7dt03653a.

DOI:10.1039/c7dt03653a
PMID:29143044
Abstract

The development of an earth-abundant, first-row water oxidation catalyst that operates at a high TOF and a low overpotential remains a fundamental chemical challenge. Cobalt complexes are important members of water oxidation catalysts. Herein, we report a cobalt-based robust homogeneous water oxidation catalyst, which can electrocatalyze water oxidation at a high pH and a low overpotential (η = 520 mV) in phosphate buffer. This homogeneous system exhibits a high turnover frequency (about 5 s) of catalyzing water oxidation to produce oxygen at η = 720 mV. We speculate the mechanism of the reaction that O-O bond formation prefers a HO-OH coupling in catalytic water oxidation.

摘要

开发一种储量丰富的第一排元素水氧化催化剂,使其在高周转频率(TOF)和低过电位下运行,仍然是一项基本的化学挑战。钴配合物是水氧化催化剂的重要成员。在此,我们报道了一种基于钴的稳健均相水氧化催化剂,它可以在磷酸盐缓冲液中,于高pH值和低过电位(η = 520 mV)下电催化水氧化。该均相体系在η = 720 mV时表现出催化水氧化产生氧气的高周转频率(约5 s⁻¹)。我们推测了该反应的机理,即在催化水氧化过程中,O - O键的形成更倾向于HO - OH偶联。

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