材料科学
电解质
锂(药物)
阴极
电池(电)
溶剂化
密度泛函理论
溶解
金属锂
氧化物
锂硫电池
福井函数
亲核细胞
无机化学
化学工程
可靠性(半导体)
电泳剂
功能(生物学)
工作(物理)
纳米技术
吸附
溶解度
过渡金属
自放电
化学稳定性
硫黄
金属
工作职能
储能
作者
Guohuang Kang,Yue Cao,Yue Cao,Qi Liu,Jiachao Duan,Yuanyuan Zhang,Feiyu Kang,Yidan Cao,Yidan Cao
标识
DOI:10.1002/adfm.202522713
摘要
Abstract Developing stable electrolytes for high‐voltage and high‐temperature lithium batteries remains a critical challenge due to severe interfacial degradation. This study presents a reactivity‐guided screening strategy based on density functional theory (DFT)‐derived Fukui functions to identify electrolyte additives that promote robust, inorganic‐rich electrode‐electrolyte interphases. Fukui function analysis achieves high prediction accuracy, outperforming conventional HOMO‐based screening, and demonstrates superior reliability in additive selection. By evaluating local electrophilic and nucleophilic reactivity, 4‐(Trifluoromethyl)thiobenzamide (TFSBN) is prioritized as a promising additive, with sulfur (S), fluorine (F), and nitrogen (N) sites facilitating oxidation. This, together with the preferential accumulation of TFSBN at the NCM811 interface, tailors the Li + solvation structure and enables the formation of a robust inorganic‐rich electrode‐electrolyte interphase, suppressing transition metal dissolution and cathode cracking. Experimental validation reveals that TFSBN‐modified electrolyte (1TF) significantly enhances battery performance for high‐voltage (≥4.8 V) and high‐temperature (≥55 °C) operational conditions. The cell with 1TF also demonstrates exceptional fast‐charging stability and pouch cell compatibility. This work establishes a generalizable computational‐experimental framework for electrolyte additive design, accelerating the development of high‐energy‐density batteries under extreme operational conditions.
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