卤化物
电解质
阳极
铵
锂(药物)
无机化学
硫黄
化学
材料科学
有机化学
电极
内分泌学
医学
物理化学
作者
Ruijin Meng,Xin He,Samuel Jun Hoong Ong,Chenxu Cui,Shufeng Song,Peerasak Paoprasert,Quanquan Pang,Zhichuan J. Xu,Xiao Liang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-08-02
卷期号:62 (38): e202309046-e202309046
被引量:45
标识
DOI:10.1002/anie.202309046
摘要
Abstract Passivation of the sulfur cathode by insulating lithium sulfide restricts the reversibility and sulfur utilization of Li−S batteries. 3D nucleation of Li 2 S enabled by radical conversion may significantly boost the redox kinetics. Electrolytes with high donor number (DN) solvents allow for tri‐sulfur (S 3 ⋅ − ) radicals as intermediates, however, the catastrophic reactivity of such solvents with Li anodes pose a great challenge for their practical application. Here, we propose the use of quaternary ammonium salts as electrolyte additives, which can preserve the partial high‐DN characteristics that trigger the S 3 ⋅ − radical pathway, and inhibit the growth of Li dendrites. Li−S batteries with tetrapropylammonium bromide (T3Br) electrolyte additive deliver the outstanding cycling stability (700 cycles at 1 C with a low‐capacity decay rate of 0.049 % per cycle), and high capacity under a lean electrolyte of 5 μL electrolyte mg sulfur −1 . This work opens a new avenue for the development of electrolyte additives for Li−S batteries.
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