磷腈
材料科学
电解质
锂(药物)
碳酸乙烯酯
碳酸丙烯酯
阳极
硅
电化学
环氧乙烷
锂离子电池
化学工程
电池(电)
无机化学
复合材料
共聚物
聚合物
化学
物理化学
电极
冶金
功率(物理)
内分泌学
工程类
物理
医学
量子力学
作者
Adjmal Ghaur,Christoph Peschel,Iris Dienwiebel,Lukas Haneke,Leilei Du,Laurin Profanter,Aurora Gómez-Martín,Martin Winter,Sascha Nowak,Tobias Placke
标识
DOI:10.1002/aenm.202203503
摘要
Abstract Silicon, as potential next‐generation anode material for high‐energy lithium‐ion batteries (LIBs), suffers from substantial volume changes during (dis)charging, resulting in continuous breakage and (re‐)formation of the solid electrolyte interphase (SEI), as well as from consumption of electrolyte and active lithium, which negatively impacts long‐term performance and prevents silicon‐rich anodes from practical application. In this work, fluorinated phosphazene compounds are investigated as electrolyte additives concerning their SEI‐forming ability for boosting the performance of silicon oxide (SiO x )‐based LIB cells. In detail, the electrochemical performance of NCM523 || SiO x /C pouch cells is studied, in combination with analyses regarding gas evolution properties, post‐mortem morphological changes of the anode electrode and the SEI, as well as possible electrolyte degradation. Introducing the dual‐additive approach in state‐of‐the‐art electrolytes leads to synergistic effects between fluoroethylene carbonate and hexafluorocyclotriphosphazene‐derivatives (HFPN), as well as enhanced electrochemical performance. The formation of a more effective SEI and increased electrolyte stabilization improves lifetime and results in an overall lower cell impedance. Furthermore, gas chromatography‐mass spectrometry measurements of the aged electrolyte with HFPN‐derivatives as an additive compound show suppressed ethylene carbonate and ethyl methyl carbonate decomposition, as well as reduced trans‐ esterification and oligomerization products in the aged electrolyte.
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