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Polymer matrix mediated solvation of LiNO3 in carbonate electrolytes for quasi-solid high-voltage lithium metal batteries.

Authors :
Wang, Zijian
Yang, Kai
Song, Yongli
Lin, Hai
Li, Ke
Cui, Yanhui
Yang, Luyi
Pan, Feng
Source :
Nano Research; Sep2020, Vol. 13 Issue 9, p2431-2437, 7p
Publication Year :
2020

Abstract

Lithium (Li) metal is one of the most promising anodes for next-generation energy storage systems. However, the Li dendrite formation and unstable solid-electrolyte interface (SEI) have hindered its further application. Lithium nitrate (LiNO<subscript>3</subscript>) is extensively used as an effective electrolyte additive in ether-based electrolytes to improve the stability of lithium metal. Nevertheless, it is rarely utilized in carbonate electrolytes due to its low solubility. Here, a novel gel polymer electrolyte (GPE) consisting of poly(vinylidene fluoride) (PVDF), poly(methyl methacrylate) (PMMA), poly(ethylene oxide) (PEO) with LiNO<subscript>3</subscript> additive is proposed to solve this issue. In this GPE, polyether-based PEO serves as a matrix for dissolving LiNO<subscript>3</subscript> which can be decomposed into a fast Li-ion conductor (Li<subscript>3</subscript>N) in conventional carbonate electrolytes to enhance the stability and Li<superscript>+</superscript> conductivity of the SEI film. As a result, dendrite formation is effectively suppressed, and a significantly improved average Coulombic efficiency (CE) of 97.2% in Li-Cu cell is achieved. By using this novel GPE coupled with Li anode and LiNi<subscript>0.5</subscript>Mn<subscript>0.3</subscript>Co<subscript>0.2</subscript>O<subscript>2</subscript> (NMC532), excellent capacity retention of 94.1% and high average CE of over 99.2% are obtained after 200 cycles at 0.5 C. This work presents fresh insight into practical modification strategies on high-voltage Li metal batteries. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19980124
Volume :
13
Issue :
9
Database :
Complementary Index
Journal :
Nano Research
Publication Type :
Academic Journal
Accession number :
144920883
Full Text :
https://doi.org/10.1007/s12274-020-2871-0