Applied Catalysis2022,Vol.3078.DOI:10.1016/j.apcatb.2022.121171

Dual-active sites design of Sn-x-Sb-y-O-GO nanosheets for enhancing electrochemical CO2 reduction via Sb-accelerating water activation

He, Haichuan Wu, Jian Yu, Xiao Xia, Dan Wang, Yan Chen, Fei Wang, Liqiang Wu, Linlin Huang, Jianhan Zhao, Ning Deng, Liu Liu, You-Nian
Applied Catalysis2022,Vol.3078.DOI:10.1016/j.apcatb.2022.121171

Dual-active sites design of Sn-x-Sb-y-O-GO nanosheets for enhancing electrochemical CO2 reduction via Sb-accelerating water activation

He, Haichuan 1Wu, Jian 1Yu, Xiao 1Xia, Dan 1Wang, Yan 1Chen, Fei 1Wang, Liqiang 2Wu, Linlin 1Huang, Jianhan 1Zhao, Ning 3Deng, Liu 1Liu, You-Nian1
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作者信息

  • 1. Cent South Univ
  • 2. Zhengzhou Univ
  • 3. Chinese Acad Sci
  • 折叠

Abstract

Electrochemical CO2 reduction reaction (eCO(2)RR) is a promising approach for the sustainable development of energy and environment, yet the control over selectivity of eCO(2)RR is challenging and entails intelligent active site design. Herein, we firstly propose dual-active sites design of Sn-x-Sb-y-O-GO nanosheets (NSs) for controlling the reaction pathways. The Sn-x-Sb-y-O-GO NSs catalyst possesses large-size ultrathin structure and controllable Sn/Sb ratio, strengthening the interaction at the active site with OCHO* intermediate. The optimized Sn-7-Sb-3-O-GO NSs exhibit a HCOOH selectivity of 96.5% and partial current density of -21.6 mA cm(-2). The experiments and theory calculations show that the introduction of Sb secondary active site can accelerate water activation for forming unique *H species and the binding strength of OCHO* key intermediates, thereby enhancing the HCOOH selectivity in eCO(2)RR. This work lends credence to the novel metal-metal dual-active sites design strategy for eCO(2)RR sustainable energy conversion.

Key words

Dual-active site/Carbon dioxide reduction/Sn-/Sb-based electrocatalyst/Formic acid/CARBON-DIOXIDE ELECTROREDUCTION/EFFICIENT/ELECTROCATALYST/CONVERSION/NANOWIRES

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出版年

2022
Applied Catalysis

Applied Catalysis

ISSN:0926-3373
被引量7
参考文献量48
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