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Metal doping promotes the efficient electrochemical reduction of CO2 to CO in CuO nanosheets.

Authors :
Song, Tao
Liu, Hai
Liu, Errui
Wang, Fei
Cui, Li
Zhang, Xiaoli
Liu, Tianxia
Source :
Inorganic Chemistry Communications. Sep2023, Vol. 155, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

[Display omitted] • CuO catalyst was prepared by a simple hydrothermal method. • CuO/Bi,CuO/In and CuO/Sn catalysts were prepared. • The effect of introducing a second metal into CuO on the performance of CO 2 RR was explored. • The activity of CO 2 RR was enhanced by doping Bi, In and Sn in CuO. • The doping of Sn in CuO significantly promotes the selectivity and activity of CO 2 RR as CO. Electrocatalytic reduction of carbon dioxide to carbon monoxide is an effective strategy to solve renewable energy storage and carbon neutral-energy cycle, but the ability of selective reduction to carbon monoxide products still needs to be improved. This work reported a strategy to promote the electrochemical reduction of carbon dioxide to carbon monoxide in CuO nanosheets by metal doping. CuO, CuO/Bi, CuO/In, and CuO/Sn electrocatalysts were prepared by a simple hydrothermal method. According to the electrochemical test, the Faraday efficiencies of CuO, CuO/Bi, CuO/In and CuO/Sn catalysts were 21.29%, 37.25%, 87.88% and 92.44%, respectively, at the potential of −0.8 V vs. RHE. In addition, the electrocatalytic carbon dioxide reduction products of CuO/In and CuO/Sn catalysts are only hydrogen and carbon monoxide products, and the selectivity of carbon monoxide is almost 100%. The results showed that doping of Bi, In, and Sn in CuO significantly enhanced the activity and selectivity of electrocatalytic carbon dioxide reduction to carbon monoxide at low overpotential, while greatly inhibiting the occurrence of hydrogen evolution reaction. In addition, the stability of CuO/Sn catalyst was tested in 0.1 mol/L KHCO 3 electrolyte, and the current density remained unchanged within 6 h, indicating that the prepared catalyst has excellent stability. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13877003
Volume :
155
Database :
Academic Search Index
Journal :
Inorganic Chemistry Communications
Publication Type :
Academic Journal
Accession number :
169788671
Full Text :
https://doi.org/10.1016/j.inoche.2023.110976