Industrial-Current-Density CO2-to-C2+ Electroreduction by Anti-swelling Anion-Exchange Ionomer-Modified Oxide-Derived Cu Nanosheets

被引:142
|
作者
Zhao, Yuan [1 ]
Zu, Xiaolong [1 ]
Chen, Runhua [1 ]
Li, Xiaodong [1 ]
Jiang, Yawen [1 ]
Wang, Zhiqiang [1 ]
Wang, Shumin [1 ]
Wu, Yang [1 ]
Sun, Yongfu [1 ,2 ]
Xie, Yi [1 ,2 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Hefei 230026, Peoples R China
[2] Hefei Comprehens Natl Sci Ctr, Inst Energy, Hefei 230031, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CARBON-DIOXIDE; CO2; REDUCTION; ELECTROCHEMICAL REDUCTION; DIFFUSION; ELECTRODE; CATALYST; POLYMERIZATION; SELECTIVITY; CONVERSION; PRODUCTS;
D O I
10.1021/jacs.2c02594
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO2 electroreduction to high-energy-density C2+ products is highly attractive, whereas the C2+ selectivity under industrial current densities is still unsatisfying. Here, an anti-swelling anion exchange ionomer (AEI) was first proposed to optimize the local environment for promoting industrial-current-density CO2-to-C2+ electroreduction. Taking the anti-swelling AEI-modified oxide-derived Cu nanosheets as an example, in situ Raman spectroscopy and contact angle measurements revealed that the OH--accumulated-N(CH3)(3)(+) groups and anti-swelling backbone of AEI could synergistically regulate the local pH level and water content. In situ Fourier-transform infrared spectroscopy and theoretical calculations demonstrated that the higher local pH value could lower the energy barrier for the rate-limiting COCO* hydrogenated to COCOH* from 0.08 to 0.04 eV, thereby boosting the generation of C2+ products. Owing to the anti-swelling backbone, the optimized water content of 3.5% could suppress the competing H-2 evolution and hence facilitate the proton-electron transfer step for C2+ production. As a result, the anti-swelling AEI-modified oxide-derived Cu nanosheets achieved a C2+ Faradaic efficiency of 85.1% at a current density up to 800 mA cm(-2) with a half-cell power conversion efficiency exceeding 50%, outperforming most reported powder catalysts.
引用
收藏
页码:10446 / 10454
页数:9
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