Your browser doesn't support javascript.
loading
Molten-Salt Electrochemical-Assisted Synthesis of the CeO2-OV@GC Composite-Supported Pt Clusters with a Pt-O-Ce Structure for the Oxygen Reduction Reaction.
Fan, Chenming; Dou, Shixue; Zhan, Xiaoqiang; Li, Shenggang; Wang, Qiang; Li, Bing.
Afiliación
  • Fan C; School of Mechanical and Power Engineering, East China University of Science and Technology, Shanghai 200237, People's Republic of China.
  • Dou S; Institute of Energy Materials Science, University of Shanghai for Science and Technology, Shanghai 200093, People's Republic of China.
  • Zhan X; Institute of Micro/Nano Materials and Devices, Ningbo University of Technology, Ningbo 315211, People's Republic of China.
  • Li S; CAS Key Laboratory of Lowcarbon Science and Technology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, People's Republic of China.
  • Wang Q; 2020 X-Lab, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, Shanghai 200050, People's Republic of China.
  • Li B; School of Mechanical and Power Engineering, East China University of Science and Technology, Shanghai 200237, People's Republic of China.
Nano Lett ; 24(23): 6957-6964, 2024 Jun 12.
Article en En | MEDLINE | ID: mdl-38805355
ABSTRACT
Highly active and robust Pt-based electrocatalysts for an oxygen reduction reaction (ORR) are of crucial significance for the development of proton exchange membrane fuel cells (PEMFCs). Herein, the high-loading and well-dispersive Pt clusters on graphitic carbon-supported CeO2 with abundant oxygen vacancies (PtAC/CeO2-OV@GC) were successfully fabricated by a molten-salt electrochemical-assisted method. The bonding of Pt with the highly electronegative O induces charge redistribution through the Pt-O-Ce structure, thus reducing the adsorption energies of oxygen-containing species. Such a PtAC/CeO2-OV@GC electrocatalyst exhibits a greatly enhanced ORR performance with a mass activity of 0.41 ± 0.02 A·mg-1Pt at 0.9 V versus a reversible hydrogen electrode, which is 2.7 times the value of a commercial Pt/C catalyst and shows negligible activity decay after 20000 cycles of accelerated degradation tests. It is anticipated that this work will provide enlightening guidance on the controllable synthesis and rational design of high-performance Pt-based electrocatalysts for PEMFCs.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Nano Lett Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Nano Lett Año: 2024 Tipo del documento: Article