电解质
锂(药物)
金属锂
金属
电荷(物理)
材料科学
联动装置(软件)
化学
化学工程
化学物理
电极
物理
工程类
物理化学
冶金
生物化学
量子力学
医学
基因
内分泌学
作者
Chao Qiu,Jiajie Pan,Wenzhi Huang,Zihao Yang,Kaixiang Shi,Zikang Chen,Tianxiang Yang,Rui Zhang,Zhouguang Lu,Quanbing Liu,Zhenxing Liang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-10-08
标识
DOI:10.1021/acs.nanolett.4c02330
摘要
Lithium metal batteries are booming because of their inherent preponderance, but a negative electric field from concentration dipolarization and slow solid-phase transfer at the electrode interface become blocking modules for extreme fast charging. Achieving an anion-rich solvation shell with a high dielectric constant (ε) is a feasible strategy to bootstrap an interface microenvironment for mass-transport reaction, but it is still an uncultivated field. Herein, the superposition, including the donor number values, the high ε, and the spatial potential resistance, are complementarily considered; we propose a low-cost electrolyte with an internal excluding external tactic to answer the above issue. Explanatorily, an optimized solvation shell follows the cascading exclusion relationship of nitrate ion (NO
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