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Proximity Matters: Interfacial Solvation Dictates Solid Electrolyte Interphase Composition.
Oyakhire, Solomon T; Liao, Sheng-Lun; Shuchi, Sanzeeda Baig; Kim, Mun Sek; Kim, Sang Cheol; Yu, Zhiao; Vilá, Rafael A; Rudnicki, Paul E; Cui, Yi; Bent, Stacey F.
Afiliación
  • Oyakhire ST; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Liao SL; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Shuchi SB; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Kim MS; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Kim SC; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Yu Z; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Vilá RA; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Rudnicki PE; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Cui Y; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Bent SF; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
Nano Lett ; 23(16): 7524-7531, 2023 Aug 23.
Article en En | MEDLINE | ID: mdl-37565722
ABSTRACT
The composition of the solid electrolyte interphase (SEI) plays an important role in controlling Li-electrolyte reactions, but the underlying cause of SEI composition differences between electrolytes remains unclear. Many studies correlate SEI composition with the bulk solvation of Li ions in the electrolyte, but this correlation does not fully capture the interfacial phenomenon of SEI formation. Here, we provide a direct connection between SEI composition and Li-ion solvation by forming SEIs using polar substrates that modify interfacial solvation structures. We circumvent the deposition of Li metal by forming the SEI above Li+/Li redox potential. Using theory, we show that an increase in the probability density of anions near a polar substrate increases anion incorporation within the SEI, providing a direct correlation between interfacial solvation and SEI composition. Finally, we use this concept to form stable anion-rich SEIs, resulting in high performance lithium metal batteries.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nano Lett Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Nano Lett Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos