High Formate Selectivity and Deactivation Mechanism of CuS Nanoparticles in CO2 Electrocatalytic Reduction Reaction

Author:

Wang Min1,Li Xiaoyao1,Ma Xia1,Wang Jie1,Jin Xixiong1,Zhang Lingxia123ORCID,Shi Jianlin12

Affiliation:

1. Institution Shanghai Institute of Ceramics Chinese Academy of Sciences 1295 Ding-xi Road Shanghai 200050 P.R. China

2. Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences No. 19 A Yuquan Road Beijing 100049 P.R. China

3. School of Chemistry and Materials Science Hangzhou Institute for Advanced Study University of Chinese Academy of Sciences 1 Sub-lane Xiangshan Hangzhou 310024 P.R. China

Abstract

AbstractCO2 electroreduction into liquid fuels is of broad interest and benefits reducing the energy crisis and environment burdens. CuS has been reported to be a desirable candidate for CO2 electroreduction into formate; however, its formate selectivity and stability are still far from the demands of practical application. Herein, we report CuS nanoparticles exhibiting good Faradaic efficiency of formate (about 98 %) in CO2 electroreduction and its deactivation mechanism during the reaction. The deactivation of CuS was found to be associated with the reconstruction and S loss of CuS, which deteriorates the Faradaic efficiency of formate. Combined with ionic and gas analyses, the S atom in CuS was lost in the form of H2S, SO2, and SO42−, followed by the reconstruction of CuS into copper oxides. Such a catalyst reconstruction facilitates electroreductions of CO2 and H2O, respectively, into CO and H2, etc., resulting in the degradation of catalytical performance of CO2 electroreduction into formate. This work reveals the important role of S loss and reconstruction of metal sulfide catalysts during the electroreduction reaction, which may benefit the further development of CuS‐based electro‐catalyst for CO2 electroreduction.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Energy,General Materials Science,General Chemical Engineering,Environmental Chemistry

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