电解质
溶剂化
化学
阳极
法拉第效率
锂(药物)
相间
硝酸锂
无机化学
电池(电)
化学工程
电化学
溶剂
电极
离子
物理化学
热力学
有机化学
离子键合
医学
生物
工程类
遗传学
内分泌学
功率(物理)
物理
作者
Jiahang Chen,Yu Zhang,Huichao Lü,Juan Ding,Xingchao Wang,Yudai Huang,Hui‐Yang Ma,Jiulin Wang
出处
期刊:eScience
[Elsevier]
日期:2023-04-22
卷期号:3 (4): 100135-100135
被引量:88
标识
DOI:10.1016/j.esci.2023.100135
摘要
Lithium metal batteries are regarded as promising alternative next-generation energy storage systems. However, the unstable anode interphase results in dendrite growth and irreversible lithium consumption with low Coulombic efficiency (CE). Herein, we rationally design a Li+ coordination structure via electrolyte solvation chemistry. Nitrate anions are aggregated in the solvation sheath, even at low concentration in a solvent with moderate solvation ability, which promotes Li+ desolvation and constructs a nitrate anion-tuned interphase. Meanwhile, a high-donor-number solvent is introduced as an additive to strongly coordinate with Li+, which accelerates the ion-transfer kinetics and rate performance. This not only results in micro-sized lithium deposition and a high CE of 99.5% over 3500 h, but also enables superior anode stability even under 50% depth plating/stripping and with a lean electrolyte of 3 g Ah–1 at 50 °C. A lithium–sulfur battery exhibits a prolonged lifespan of 2000 cycles with an average CE of 100%. A full battery using 1x excess lithium exhibits a high capacity near 1600 mAh gS–1 for 100 cycles without capacity loss. Moreover, a 0.55 Ah pouch cell delivers a reversible energy density of 423 Wh kg–1 based on these electrodes and electrolyte.
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