A highly active nickel electrocatalyst shows excellent selectivity for CO2 reduction in acidic media

被引:77
作者
Neri, Gaia [1 ]
Aldous, Iain M. [1 ]
Walsh, James J. [1 ]
Hardwick, Laurence J. [1 ]
Cowan, Alexander J. [1 ]
机构
[1] Univ Liverpool, Dept Chem, Stephenson Inst Renewable Energy, Liverpool L69 3BX, Merseyside, England
基金
英国工程与自然科学研究理事会;
关键词
CO2-TO-CO ELECTROCHEMICAL CONVERSION; IRIDIUM PINCER CATALYST; LOCAL PROTON SOURCE; CARBON-DIOXIDE; CYCLIC VOLTAMMETRY; GLASSY-CARBON; WATER; ELECTROREDUCTION; ELECTRODES; COMPLEXES;
D O I
10.1039/c5sc03225c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of selective electrocatalysts for CO2 reduction in water offers a sustainable route to carbon based fuels and feedstocks. However, molecular catalysts are typically studied in non-aqueous solvents, in part to avoid competitive H-2 evolution. [Ni(cyclam)](2+) (1) is one of the few known electrocatalysts that operate in water and 30 years after its report its activity remains a rarely surpassed benchmark. Here we report that [Ni(cyclam-CO2H)](2+) (cyclam-CO2H = 1,4,8,11-tetraazacyclotetradecane-6-carboxylic acid (2)) shows greatly enhanced activity versus 1 for CO production. At pHs < pK(a) of the pendant carboxylic acid a large increase in catalytic activity occurs. Remarkably, despite the high proton concentration (pH 2), 2 maintains selectivity for CO2 reduction and is believed to be unique in operating selectively in such acidic aqueous solutions.
引用
收藏
页码:1521 / 1526
页数:6
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