Metal-Organic Frameworks-derived Indium Clusters/Carbon Nanocomposites for Efficient CO2 Electroreduction

被引:9
作者
Gong Yu [1 ,2 ]
Pan Jing [1 ]
Zhang Lingling [1 ]
Wang Xiao [1 ,2 ]
Song Shuyan [1 ,2 ]
Zhang Hongjie [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[2] Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Peoples R China
[3] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Indium cluster; Indium oxide; Electrochemical reduction; CO2; electroreduction; ELECTROCHEMICAL REDUCTION; CATALYSTS; FORMATE; MIL-68(IN);
D O I
10.1007/s40242-022-2034-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical reduction of carbon dioxide into value-added products is a promising way to recycle the greenhouse gas, thus solving the crisis of global warming. Pressing challenges remain in regulating the catalytic selectivity. In this work, we demonstrated a metal-organic frameworks-assisted approach to synthesizing In species loaded on the surface of N doped carbon matrix. By controlling the particle sizes, the catalytic selectivity can be easily altered. The obtained In-c/NC possesses the outstanding capability for converting CO2 into CO. And 80.09% Faraday efficiency (FE) of CO can be achieved at 0.8 V vs. RHE. While the In2O3/C exhibits different catalytic behaviors, the main product is formic acid and the FE is more than 50% at 0.8 V vs. RHE. The selectivity reversal can be attributed to the strong interactions between In clusters and N atoms of carbon supports, which efficiently inhibits the formation of the by-product, formic acid. Our research has paved a new way to modulate catalytic selectivity by manipulating the fine structures of the catalysts.
引用
收藏
页码:1287 / 1291
页数:5
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