Engineering Electronic Structure of Stannous Sulfide by Amino-Functionalized Carbon: Toward Efficient Electrocatalytic Reduction of CO2 to Formate

被引:86
作者
Chen, Zhipeng [1 ]
Zhang, Xinxin [1 ,2 ]
Jiao, Mingyang [1 ]
Mou, Kaiwen [1 ,2 ]
Zhang, Xiangping [3 ]
Liu, Licheng [1 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, Qingdao 266101, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Inst Proc Engn Chinese, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
adsorption energy; CO2; reduction; electrocatalysis; electronic structure; formate; SELECTIVE ELECTROCHEMICAL REDUCTION; ENHANCED ACTIVITY; ELECTROREDUCTION; CATALYSTS; SITES; NANOWIRES; DIOXIDE; DENSITY;
D O I
10.1002/aenm.201903664
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
Engineering electronic structure to enhance the binding energies of reaction intermediates in order to achieve a high partial current density can lead to increased yield of target products. Herein, amino-functionalized carbon is used to regulate the electronic structure of tin-based catalysts to enhance activity of CO2 electroreduction. The hollow nanotubes composed of SnS (stannous sulfide) nanosheets are modified with amino-functionalized carbon layers, achieving a highest formate Faraday efficiency of 92.6% and a remarkable formate partial current density of 41.1 mA cm(-2) (a total current density of 52.1 mA cm(-2)) at a moderate overpotential of 0.9 V versus reversible hydrogen electrode, as well as a good stability. Density functional theory calculations demonstrate that the superior activity is attributed to the synergistic effect among SnS and Aminated-C in increasing the adsorption energies of the key intermediates and accelerating the charge transfer rate.
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页数:8
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