4.8 Article

Alloyed Palladium Silver Nanowires Enabling Ultrastable Carbon Dioxide Reduction to Formate

期刊

ADVANCED MATERIALS
卷 33, 期 4, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202005821

关键词

CO poisoning; electrochemical CO2 reduction; formate; palladium-silver nanowires

资金

  1. Ministry of Science and Technology of China [2017YFA0204800, 2017YFA0700104]
  2. National Natural Science Foundation of China [21902114, 51825102, 21771156]
  3. Tianjin Science Fund for Distinguished Young Scholars [19JCJQJC61800]
  4. Early Career Scheme (ECS) fund from the Research Grant Council (RGC) in Hong Kong [PolyU 253026/16P]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions
  6. Collaborative Innovation Center of Suzhou Nano Science and Technology

向作者/读者索取更多资源

Alloying palladium with silver significantly enhances electrocatalytic stability, leading to outstanding performance in selective formate production. The enhanced CO tolerance and selective stabilization of key reaction intermediates on the alloy nanowires contribute to the impressive long-term stability observed.
Palladium can enable the electrochemical CO2 reduction to formate with nearly zero overpotential and good selectivity. However, it usually has very limited stability owing to CO poisoning from the side reaction intermediate. Herein, it is demonstrated that alloying palladium with silver is a viable strategy to significantly enhance the electrocatalytic stability. Palladium-silver alloy nanowires are prepared in aqueous solution with tunable chemical compositions, large aspect ratio, and roughened surfaces. Thanks to the unique synergy between palladium and silver, these nanowires exhibit outstanding electrocatalytic performances for selective formate production. Most remarkably, impressive long-term stability is measured even at <-0.4 V versus reversible hydrogen electrode where people previously believed that formate cannot be stably formed on palladium. Such stability results from the enhanced CO tolerance and selective stabilization of key reaction intermediates on alloy nanowires as supported by detailed electrochemical characterizations and theoretical computations.

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