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Dissolution of the Solid Electrolyte Interphase and Its Effects on Lithium Metal Anode Cyclability.
Sayavong, Philaphon; Zhang, Wenbo; Oyakhire, Solomon T; Boyle, David T; Chen, Yuelang; Kim, Sang Cheol; Vilá, Rafael A; Holmes, Sarah E; Kim, Mun Sek; Bent, Stacey F; Bao, Zhenan; Cui, Yi.
Afiliação
  • Sayavong P; Department of Chemistry, Stanford University, Stanford, California 94305-6104, United States.
  • Zhang W; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305-6104, United States.
  • Oyakhire ST; Department of Chemical Engineering, Stanford University, Stanford, California 94305-6104, United States.
  • Boyle DT; Department of Chemistry, Stanford University, Stanford, California 94305-6104, United States.
  • Chen Y; Department of Chemistry, Stanford University, Stanford, California 94305-6104, United States.
  • Kim SC; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305-6104, United States.
  • Vilá RA; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305-6104, United States.
  • Holmes SE; Department of Chemistry, Stanford University, Stanford, California 94305-6104, United States.
  • Kim MS; Department of Chemical Engineering, Stanford University, Stanford, California 94305-6104, United States.
  • Bent SF; Department of Chemical Engineering, Stanford University, Stanford, California 94305-6104, United States.
  • Bao Z; Department of Chemical Engineering, Stanford University, Stanford, California 94305-6104, United States.
  • Cui Y; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305-6104, United States.
J Am Chem Soc ; 145(22): 12342-12350, 2023 Jun 07.
Article em En | MEDLINE | ID: mdl-37220230
At >95% Coulombic efficiencies, most of the capacity loss for Li metal anodes (LMAs) is through the formation and growth of the solid electrolyte interphase (SEI). However, the mechanism through which this happens remains unclear. One property of the SEI that directly affects its formation and growth is the SEI's solubility in the electrolyte. Here, we systematically quantify and compare the solubility of SEIs derived from ether-based electrolytes optimized for LMAs using in-operando electrochemical quartz crystal microbalance (EQCM). A correlation among solubility, passivity, and cyclability established in this work reveals that SEI dissolution is a major contributor to the differences in passivity and electrochemical performance among battery electrolytes. Together with our EQCM, X-ray photoelectron spectroscopy (XPS), and nuclear magnetic resonance (NMR) spectroscopy results, we show that solubility depends on not only the SEI's composition but also the properties of the electrolyte. This provides a crucial piece of information that could help minimize capacity loss due to SEI formation and growth during battery cycling and aging.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos