| Literature DB >> 29178154 |
Xiang Chen1, Xin Shen1, Bo Li2, Hong-Jie Peng1, Xin-Bing Cheng1, Bo-Quan Li1, Xue-Qiang Zhang1, Jia-Qi Huang3, Qiang Zhang1,4.
Abstract
Lithium and sodium metal batteries are considered as promising next-generation energy storage devices due to their ultrahigh energy densities. The high reactivity of alkali metal toward organic solvents and salts results in side reactions, which further lead to undesirable electrolyte depletion, cell failure, and evolution of flammable gas. Herein, first-principles calculations and in situ optical microscopy are used to study the mechanism of organic electrolyte decomposition and gas evolution on a sodium metal anode. Once complexed with sodium ions, solvent molecules show a reduced LUMO, which facilitates the electrolyte decomposition and gas evolution. Such a general mechanism is also applicable to lithium and other metal anodes. We uncover the critical role of ion-solvent complexation for the stability of alkali metal anodes, reveal the mechanism of electrolyte gassing, and provide a mechanistic guidance to electrolyte and lithium/sodium anode design for safe rechargeable batteries.Entities:
Keywords: alkali metal batteries; electrochemistry; electrolytes; first-principles calculations; gas evolution
Year: 2017 PMID: 29178154 DOI: 10.1002/anie.201711552
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336