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用于锂硫电池的卤化物季铵电解质添加剂实现的激进途径和稳定锂负极

A Radical Pathway and Stabilized Li Anode Enabled by Halide Quaternary Ammonium Electrolyte Additives for Lithium-Sulfur Batteries.

作者信息

Meng Ruijin, He Xin, Ong Samuel Jun Hoong, Cui Chenxu, Song Shufeng, Paoprasert Peerasak, Pang Quanquan, Xu Zhichuan J, Liang Xiao

机构信息

Department State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, China.

School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore, 639798, Singapore.

出版信息

Angew Chem Int Ed Engl. 2023 Sep 18;62(38):e202309046. doi: 10.1002/anie.202309046. Epub 2023 Aug 9.

Abstract

Passivation of the sulfur cathode by insulating lithium sulfide restricts the reversibility and sulfur utilization of Li-S batteries. 3D nucleation of Li S enabled by radical conversion may significantly boost the redox kinetics. Electrolytes with high donor number (DN) solvents allow for tri-sulfur (S ⋅ ) 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 ⋅ 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  mg . This work opens a new avenue for the development of electrolyte additives for Li-S batteries.

摘要

绝缘的硫化锂对硫阴极的钝化作用限制了锂硫电池的可逆性和硫利用率。通过自由基转化实现的硫化锂三维成核可能会显著提高氧化还原动力学。具有高给体数(DN)溶剂的电解质允许三硫(S⋅)自由基作为中间体,然而,此类溶剂与锂阳极的剧烈反应性对其实际应用构成了巨大挑战。在此,我们提出使用季铵盐作为电解质添加剂,其可以保留触发S⋅自由基途径的部分高DN特性,并抑制锂枝晶的生长。含有溴化四丙基铵(T3Br)电解质添加剂的锂硫电池具有出色的循环稳定性(在1 C下循环700次,每循环的低容量衰减率为0.049 %),并且在5 μL  mg 的贫电解质条件下具有高容量。这项工作为锂硫电池电解质添加剂的开发开辟了一条新途径。

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