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