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

被引:35
作者
Meng, Ruijin [1 ,2 ]
He, Xin [1 ]
Ong, Samuel Jun Hoong [2 ]
Cui, Chenxu [1 ]
Song, Shufeng [3 ]
Paoprasert, Peerasak [4 ]
Pang, Quanquan [5 ]
Xu, Zhichuan J. [2 ]
Liang, Xiao [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, Dept State Key Lab Chem Biosensing & Chemometr, Changsha 410082, Peoples R China
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore
[3] Chongqing Univ, Coll Aerosp Engn, Chongqing 400044, Peoples R China
[4] Thammasat Univ, Fac Sci & Technol, Dept Chem, Pathum Thani 12120, Thailand
[5] Peking Univ, Sch Mat Sci & Engn, Beijing 100871, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Li-S Batteries; Quaternary Ammonium Salts; Solid Electrolyte Interface; Solvation Structure; Tri-Sulfur Radical; METAL ANODE; PRODUCTS; SULFIDE;
D O I
10.1002/anie.202309046
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Passivation of the sulfur cathode by insulating lithium sulfide restricts the reversibility and sulfur utilization of Li-S batteries. 3D nucleation of Li2S enabled by radical conversion may significantly boost the redox kinetics. Electrolytes with high donor number (DN) solvents allow for tri-sulfur (S-3(center dot-)) 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(center dot-) 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 mu L(electrolyte)mg(sulfur)(-1). This work opens a new avenue for the development of electrolyte additives for Li-S batteries.
引用
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页数:12
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