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An Inorganic-Rich Solid Electrolyte Interphase for Advanced Lithium-Metal Batteries in Carbonate Electrolytes

Sufu Liu (Co-first Author), Xiao Ji (Co-first Author), Nan Piao (Co-first Author), Ji Chen, Nico Eidson, Jijian Xu, Pengfei Wang, Long Chen, Jiaxun Zhang, Tao Deng, Singyuk Hou, Ting Jin, Hongli Wan, Jingru Li, Jiangping Tu, Chunsheng Wang*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

In carbonate electrolytes, the organic–inorganic solid electrolyte interphase (SEI) formed on the Li-metal anode surface is strongly bonded to Li and experiences the same volume change as Li, thus it undergoes continuous cracking/reformation during plating/stripping cycles. Here, an inorganic-rich SEI is designed on a Li-metal surface to reduce its bonding energy with Li metal by dissolving 4m concentrated LiNO3 in dimethyl sulfoxide (DMSO) as an additive for a fluoroethylene-carbonate (FEC)-based electrolyte. Due to the aggregate structure of NO3 ions and their participation in the primary Li+ solvation sheath, abundant Li2O, Li3N, and LiNxOy grains are formed in the resulting SEI, in addition to the uniform LiF distribution from the reduction of PF6 ions. The weak bonding of the SEI (high interface energy) to Li can effectively promote Li diffusion along the SEI/Li interface and prevent Li dendrite penetration into the SEI. As a result, our designed carbonate electrolyte enables a Li anode to achieve a high Li plating/stripping Coulombic efficiency of 99.55 % (1 mA cm−2, 1.0 mAh cm−2) and the electrolyte also enables a Li||LiNi0.8Co0.1Mn0.1O2 (NMC811) full cell (2.5 mAh cm−2) to retain 75 % of its initial capacity after 200 cycles with an outstanding CE of 99.83 %. © 2020 Wiley-VCH GmbH
Original languageEnglish
Pages (from-to)3661-3671
JournalAngewandte Chemie - International Edition
Volume60
Issue number7
Online published9 Nov 2020
DOIs
Publication statusPublished - 15 Feb 2021
Externally publishedYes

Funding

This work was supported the Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) through Battery500 Consortium under contract No. DE-EE0008202. We acknowledge the University of Maryland supercomputing resources (http://hpcc.umd.edu) made available for conducting DFT computations in this paper. We also thank the Maryland NanoCenter and its AIMLab for support.

Research Keywords

  • carbonate electrolytes
  • dendrite-free structures
  • electrode interphases
  • lithium nitrate
  • lithium-metal batteries

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