Indium oxide induced electron-deficient indium hollow nanotubes for stable electroreduction of CO2 at industrial current densities

被引:14
作者
Chen, Zhipeng [1 ,2 ]
Zhang, Dongdong [1 ]
Zhao, Yusi [1 ]
Jia, Dedong [1 ]
Zhang, Hongna [1 ]
Liu, Licheng [2 ]
He, Xiaojun [1 ]
机构
[1] Anhui Univ Technol, Sch Chem & Chem Engn, Maanshan 243032, Peoples R China
[2] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Peoples R China
基金
中国国家自然科学基金;
关键词
Indium; CO2; electroreduction; Current density; MEA cell; Formate; GAS-DIFFUSION ELECTRODES; CARBON-DIOXIDE; REDUCTION; CONVERSION;
D O I
10.1016/j.cej.2023.142573
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Despite high selectivity for CO2 electroreduction to formate, the current density and stability over indium-based catalysts are far from the requirements of industrial applications. Herein, we report an aminated In-MOF-derived In/In2O3 hollow nanotube catalyst (In/In2O3 Ho-nt), which can maintain a stable In-0/In3+ heterostructure during the CO2 electrocatalysis. The stable In-0/In3+ species boosts the formate FE (Faradaic efficiency) to over 90% with a highest current density of similar to 650 mA cm(-2) in a wide potential range from 0.8 V to 1.2 V vs. RHE in flow cells. More impressively, In/In2O3 Ho-nt demonstrates a full-cell EE (energy efficiency) of 44.5% and a long-term stability of 70 h at a current density of 200 mA cm(-2) in membrane electrode assembly (MEA) cells by controlling the hydrophobicity of the catalyst interface. DFT calculations reveal that the charge redistribution between In3+ and In-0 sites endows In-0 sites with an electron-deficient environment, which enhances the adsorption capacity of CO2* intermediate and accelerates charge transfer kinetics, thus improving the activity of CO2 electroreduction to formate.
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页数:6
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