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Potentiometric Measurement to Probe Solvation Energy and Its Correlation to Lithium Battery Cyclability.
Kim, Sang Cheol; Kong, Xian; Vilá, Rafael A; Huang, William; Chen, Yuelang; Boyle, David T; Yu, Zhiao; Wang, Hansen; Bao, Zhenan; Qin, Jian; Cui, Yi.
Afiliación
  • Kim SC; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Kong X; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Vilá RA; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Huang W; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Chen Y; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Boyle DT; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Yu Z; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Wang H; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Bao Z; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Qin J; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Cui Y; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
J Am Chem Soc ; 143(27): 10301-10308, 2021 Jul 14.
Article en En | MEDLINE | ID: mdl-34184873
ABSTRACT
The electrolyte plays a critical role in lithium-ion batteries, as it impacts almost every facet of a battery's performance. However, our understanding of the electrolyte, especially solvation of Li+, lags behind its significance. In this work, we introduce a potentiometric technique to probe the relative solvation energy of Li+ in battery electrolytes. By measuring open circuit potential in a cell with symmetric electrodes and asymmetric electrolytes, we quantitatively characterize the effects of concentration, anions, and solvents on solvation energy across varied electrolytes. Using the technique, we establish a correlation between cell potential (Ecell) and cyclability of high-performance electrolytes for lithium metal anodes, where we find that solvents with more negative cell potentials and positive solvation energies-those weakly binding to Li+-lead to improved cycling stability. Cryogenic electron microscopy reveals that weaker solvation leads to an anion-derived solid-electrolyte interphase that stabilizes cycling. Using the potentiometric measurement for characterizing electrolytes, we establish a correlation that can guide the engineering of effective electrolytes for the lithium metal anode.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
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