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Electrochemical Phase Evolution of Metal-Based Pre-Catalysts for High-Rate Polysulfide Conversion.
Zhao, Meng; Peng, Hong-Jie; Li, Bo-Quan; Chen, Xiao; Xie, Jin; Liu, Xinyan; Zhang, Qiang; Huang, Jia-Qi.
Afiliación
  • Zhao M; School of Materials Science & Engineering, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Peng HJ; Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Li BQ; Department of Chemical Engineering, Tsinghua University, Beijing, 100084, P. R. China.
  • Chen X; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
  • Xie J; School of Materials Science & Engineering, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Liu X; Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Zhang Q; Department of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
  • Huang JQ; Department of Chemical Engineering, Tsinghua University, Beijing, 100084, P. R. China.
Angew Chem Int Ed Engl ; 59(23): 9011-9017, 2020 Jun 02.
Article en En | MEDLINE | ID: mdl-32203631
ABSTRACT
In situ evolution of electrocatalysts is of paramount importance in defining catalytic reactions. Catalysts for aprotic electrochemistry such as lithium-sulfur (Li-S) batteries are the cornerstone to enhance intrinsically sluggish reaction kinetics but the true active phases are often controversial. Herein, we reveal the electrochemical phase evolution of metal-based pre-catalysts (Co4 N) in working Li-S batteries that renders highly active electrocatalysts (CoSx ). Electrochemical cycling induces the transformation from single-crystalline Co4 N to polycrystalline CoSx that are rich in active sites. This transformation propels all-phase polysulfide-involving reactions. Consequently, Co4 N enables stable operation of high-rate (10 C, 16.7 mA cm-2 ) and electrolyte-starved (4.7 µL mgS -1 ) Li-S batteries. The general concept of electrochemically induced sulfurization is verified by thermodynamic energetics for most of low-valence metal compounds.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article Pais de publicación: ALEMANHA / ALEMANIA / DE / DEUSTCHLAND / GERMANY

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article Pais de publicación: ALEMANHA / ALEMANIA / DE / DEUSTCHLAND / GERMANY