Surface passivation for highly active, selective, stable, and scalable CO2 electroreduction

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作者
Jiexin Zhu
Jiantao Li
Ruihu Lu
Ruohan Yu
Shiyong Zhao
Chengbo Li
Lei Lv
Lixue Xia
Xingbao Chen
Wenwei Cai
Jiashen Meng
Wei Zhang
Xuelei Pan
Xufeng Hong
Yuhang Dai
Yu Mao
Jiong Li
Liang Zhou
Guanjie He
Quanquan Pang
Yan Zhao
Chuan Xia
Ziyun Wang
Liming Dai
Liqiang Mai
机构
[1] Wuhan University of Technology,State Key Laboratory of Advanced Technology for Materials Synthesis and Processing
[2] University College London,Electrochemical Innovation Lab, Department of Chemical Engineering
[3] The University of Auckland,School of Chemical Sciences
[4] University of New South Wales,Australian Carbon Materials Centre (A
[5] University of Electronic Science and Technology of China,CMC), School of Chemical Engineering
[6] Wuhan University of Technology,School of Materials and Energy
[7] School of Materials Science and Engineering,International School of Materials Science and Engineering
[8] Peking University,Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials
[9] Chinese Academy of Sciences,Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute
[10] Wuhan University of Technology (Xiangyang Demonstration Zone),Hubei Longzhong Laboratory
来源
Nature Communications | / 14卷
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摘要
Electrochemical conversion of CO2 to formic acid using Bismuth catalysts is one the most promising pathways for industrialization. However, it is still difficult to achieve high formic acid production at wide voltage intervals and industrial current densities because the Bi catalysts are often poisoned by oxygenated species. Herein, we report a Bi3S2 nanowire-ascorbic acid hybrid catalyst that simultaneously improves formic acid selectivity, activity, and stability at high applied voltages. Specifically, a more than 95% faraday efficiency was achieved for the formate formation over a wide potential range above 1.0 V and at ampere-level current densities. The observed excellent catalytic performance was attributable to a unique reconstruction mechanism to form more defective sites while the ascorbic acid layer further stabilized the defective sites by trapping the poisoning hydroxyl groups. When used in an all-solid-state reactor system, the newly developed catalyst achieved efficient production of pure formic acid over 120 hours at 50 mA cm–2 (200 mA cell current).
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