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Paper | Open Access

In-situ structural evolution of Bi2O3 nanoparticle catalysts for CO2 electroreduction

Hongbo Wang1Chongyang Tang1Bo Sun1Jiangchao Liu1Yan Xia1Wenqing Li1Changzhong Jiang1Dong He1 ( )Xiangheng Xiao1,2 ( )
Department of Physics, Hubei Nuclear Solid Physics Key Laboratory, Wuhan University, Wuhan 430072, People’s Republic of China
Hubei Yangtze Memory Laboratories, Wuhan 430205, People’s Republic of China
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Abstract

Under the complex external reaction conditions, uncovering the true structural evolution of the catalyst is of profound significance for the establishment of relevant structure–activity relationships and the rational design of electrocatalysts. Here, the surface reconstruction of the catalyst was characterized by ex-situ methods and in-situ Raman spectroscopy in CO2 electroreduction. The final results showed that the Bi2O3 nanoparticles were transformed into Bi/Bi2O3 two-dimensional thin-layer nanosheets (NSs). It is considered to be the active phase in the electrocatalytic process. The Bi/Bi2O3 NSs showed good catalytic performance with a Faraday efficiency (FE) of 94.8% for formate and a current density of 26 mA cm−2 at −1.01 V. While the catalyst maintained a 90% FE in a wide potential range (−0.91 V to −1.21 V) and long-term stability (24 h). Theoretical calculations support the theory that the excellent performance originates from the enhanced bonding state of surface Bi-Bi, which stabilized the adsorption of the key intermediate OCHO* and thus promoted the production of formate.

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International Journal of Extreme Manufacturing
Pages 035002-035002

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Cite this article:
Wang H, Tang C, Sun B, et al. In-situ structural evolution of Bi2O3 nanoparticle catalysts for CO2 electroreduction. International Journal of Extreme Manufacturing, 2022, 4(3): 035002. https://doi.org/10.1088/2631-7990/ac7a6e

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Received: 17 January 2022
Revised: 12 April 2022
Accepted: 20 June 2022
Published: 01 July 2022
© 2022 The Author(s).

Original content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence. Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.