电解质
材料科学
溶剂化
相间
锂(药物)
电化学
沉积(地质)
电镀(地质)
金属锂
储能
充电周期
纳米技术
能量密度
工作(物理)
锂电池
化学工程
光电子学
锂离子电池
脉搏(音乐)
离子
电极
金属
电流密度
化学物理
电池(电)
剥离(纤维)
过电位
作者
Zhongxian Sun,Anqi Ren,Jiaqi Wang,Sha Luo,Ming Li,Wei Sun,Bao Zhang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-02-13
卷期号:11 (3): 2778-2788
被引量:2
标识
DOI:10.1021/acsenergylett.5c03883
摘要
Anode-free lithium metal batteries promise exceptional energy density but suffer from unstable lithium plating and a short cycle life. While pulse charging is known to influence deposition morphology, we demonstrate it can also reshape the local solvation environment at the electrode interface─without altering bulk electrolyte composition─to favor anion-derived solid electrolyte interphase (SEI) formation. By integrating electrochemical insight with Bayesian optimization, we rapidly identify high-performance pulse protocols in one month─five times faster than conventional screening. The optimal protocol boosts the cycle performance by over 60%, enabling uniform lithium deposition and a LiF-rich SEI. Molecular simulations reveal that the pulse charging enhances specific anion coordination in the lithium-ion solvation structure, rationalizing the SEI chemistry. Crucially, the same design strategy transfers successfully to a different electrolyte system, underscoring its generality. This work establishes intelligent charging as a powerful, chemistry-agnostic tool for interfacial engineering in next-generation batteries.
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