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Revealing the Multifunctions of Li3N in the Suspension Electrolyte for Lithium Metal Batteries.
Kim, Mun Sek; Zhang, Zewen; Wang, Jingyang; Oyakhire, Solomon T; Kim, Sang Cheol; Yu, Zhiao; Chen, Yuelang; Boyle, David T; Ye, Yusheng; Huang, Zhuojun; Zhang, Wenbo; Xu, Rong; Sayavong, Philaphon; Bent, Stacey F; Qin, Jian; Bao, Zhenan; Cui, Yi.
Affiliation
  • Kim MS; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Zhang Z; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Wang J; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Oyakhire ST; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Kim SC; Materials Sciences Division, Lawrence Berkeley Laboratory, Berkeley, California 94720, United States.
  • Yu Z; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Chen Y; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Boyle DT; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Ye Y; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Huang Z; Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
  • Zhang W; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Xu R; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Sayavong P; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Bent SF; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
  • Qin J; 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.
  • Cui Y; Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
ACS Nano ; 17(3): 3168-3180, 2023 Feb 14.
Article in En | MEDLINE | ID: mdl-36700841
ABSTRACT
Inorganic-rich solid-electrolyte interphases (SEIs) on Li metal anodes improve the electrochemical performance of Li metal batteries (LMBs). Therefore, a fundamental understanding of the roles played by essential inorganic compounds in SEIs is critical to realizing and developing high-performance LMBs. Among the prevalent SEI inorganic compounds observed for Li metal anodes, Li3N is often found in the SEIs of high-performance LMBs. Herein, we elucidate new features of Li3N by utilizing a suspension electrolyte design that contributes to the improved electrochemical performance of the Li metal anode. Through empirical and computational studies, we show that Li3N guides Li electrodeposition along its surface, creates a weakly solvating environment by decreasing Li+-solvent coordination, induces organic-poor SEI on the Li metal anode, and facilitates Li+ transport in the electrolyte. Importantly, recognizing specific roles of SEI inorganics for Li metal anodes can serve as one of the rational guidelines to design and optimize SEIs through electrolyte engineering for LMBs.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ACS Nano Year: 2023 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ACS Nano Year: 2023 Document type: Article Affiliation country: United States
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