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Non-Solvating and Low-Dielectricity Cosolvent for Anion-Derived Solid Electrolyte Interphases in Lithium Metal Batteries.
Ding, Jun-Fan; Xu, Rui; Yao, Nan; Chen, Xiang; Xiao, Ye; Yao, Yu-Xing; Yan, Chong; Xie, Jin; Huang, Jia-Qi.
Afiliação
  • Ding JF; School of Materials Science and Engineering, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Xu R; Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Yao N; School of Materials Science and Engineering, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Chen X; Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Xiao Y; Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
  • Yao YX; Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
  • Yan C; School of Materials Science and Engineering, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Xie J; Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, P. R. China.
  • Huang JQ; Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
Angew Chem Int Ed Engl ; 60(20): 11442-11447, 2021 May 10.
Article em En | MEDLINE | ID: mdl-33655631
Lithium (Li) metal anodes hold great promise for next-generation high-energy-density batteries, while the insufficient fundamental understanding of the complex solid electrolyte interphase (SEI) is the major obstacle for the full demonstration of their potential in working batteries. The characteristics of SEI highly depend on the inner solvation structure of lithium ions (Li+ ). Herein, we clarify the critical significance of cosolvent properties on both Li+ solvation structure and the SEI formation on working Li metal anodes. Non-solvating and low-dielectricity (NL) cosolvents intrinsically enhance the interaction between anion and Li+ by affording a low dielectric environment. The abundant positively charged anion-cation aggregates generated as the introduction of NL cosolvents are preferentially brought to the negatively charged Li anode surface, inducing an anion-derived inorganic-rich SEI. A solvent diagram is further built to illustrate that a solvent with both proper relative binding energy toward Li+ and dielectric constant is suitable as NL cosolvent.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article