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Urea-Functionalized Silver Catalyst toward Efficient and Robust CO2 Electrolysis with Relieved Reliance on Alkali Cations.
Garg, Sahil; Li, Mengran; Hussain, Tanveer; Idros, Mohamed Nazmi; Wu, Yuming; Zhao, Xiu Song; Wang, Geoff G X; Rufford, Thomas E.
Afiliação
  • Garg S; School of Chemical Engineering, the University of Queensland, St Lucia, 4072, Brisbane, Queensland, Australia.
  • Li M; Department of Physics, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.
  • Hussain T; School of Chemical Engineering, the University of Queensland, St Lucia, 4072, Brisbane, Queensland, Australia.
  • Idros MN; Department of Chemical Engineering, Faculty of Applied Sciences, Delft University of Technology, van der Maasweg 9, 2629 HZ Delft, The Netherlands.
  • Wu Y; School of Chemical Engineering, the University of Queensland, St Lucia, 4072, Brisbane, Queensland, Australia.
  • Zhao XS; School of Science and Technology, University of New England, Armidale, New South Wales 2351, Australia.
  • Wang GGX; School of Chemical Engineering, the University of Queensland, St Lucia, 4072, Brisbane, Queensland, Australia.
  • Rufford TE; School of Chemical Engineering, the University of Queensland, St Lucia, 4072, Brisbane, Queensland, Australia.
ACS Appl Mater Interfaces ; 14(31): 35504-35512, 2022 Aug 10.
Article em En | MEDLINE | ID: mdl-35912581
We report a new strategy to improve the reactivity and durability of a membrane electrode assembly (MEA)-type electrolyzer for CO2 electrolysis to CO by modifying the silver catalyst layer with urea. Our experimental and theoretical results show that mixing urea with the silver catalyst can promote electrochemical CO2 reduction (CO2R), relieve limitations of alkali cation transport from the anolyte, and mitigate salt precipitation in the gas diffusion electrode in long-term stability tests. In a 10 mM KHCO3 anolyte, the urea-modified Ag catalyst achieved CO selectivity 1.3 times better with energy efficiency 2.8-fold better than an untreated Ag catalyst, and operated stably at 100 mA cm-2 with a faradaic efficiency for CO above 85% for 200 h. Our work provides an alternative approach to fabricating catalyst interfaces in MEAs by modifying the catalyst structure and the local reaction environment for critical electrochemical applications such as CO2 electrolysis and fuel cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Ano de publicação: 2022 Tipo de documento: Article