Alloying strategies for tuning product selectivity during electrochemical CO2 reduction over Cu

被引:17
|
作者
Mosali, Venkata Sai Sriram [1 ]
Bond, Alan M. [1 ,2 ]
Zhang, Jie [1 ,2 ]
机构
[1] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[2] Monash Univ, ARC Ctr Excellence Electromat Sci, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
MESOPOROUS SNO2 NANOSHEETS; HYDROGEN-STORING MATERIALS; GAS-DIFFUSION ELECTRODES; CARBON-DIOXIDE REDUCTION; ELECTROCATALYTIC REDUCTION; OXIDATION-STATE; AQUEOUS CO2; RATIONAL DESIGN; HIGH-EFFICIENCY; ENHANCED SELECTIVITY;
D O I
10.1039/d2nr03539a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Excessive reliance on fossil fuels has led to the release and accumulation of large quantities of CO2 into the atmosphere which has raised serious concerns related to environmental pollution and global warming. One way to mitigate this problem is to electrochemically recycle CO2 to value-added chemicals or fuels using electricity from renewable energy sources. Cu is the only metallic electrocatalyst that has been shown to produce a wide range of industrially important chemicals at appreciable rates. However, low product selectivity is a fundamental issue limiting commercial applications of electrochemical CO2 reduction over Cu catalysts. Combining copper with other metals that actively contribute to the electrochemical CO2 reduction reaction process can selectively facilitate generation of desirable products. Alloying Cu can alter surface binding strength through electronic and geometric effects, enhancing the availability of surface confined carbon species, and stabilising key reduction intermediates. As a result, significant research has been undertaken to design and fabricate copper-based alloy catalysts with structures that can enhance the selectivity of targeted products. In this article, progress with use of alloying strategies for development of Cu-alloy catalysts are reviewed. Challenges in achieving high selectivity and possible future directions for development of new copper-based alloy catalysts are considered.
引用
收藏
页码:15560 / 15585
页数:26
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