硫黄
锂(药物)
溶剂
尿素
化学
无机化学
锂硫电池
材料科学
有机化学
电化学
物理化学
电极
医学
内分泌学
作者
Lin Peng,Yilu Liu,Pengcheng Xue,Chenxi Lei,Xiao Yang,Lishan Lin,Liang Ma,Luyi Chen,Yue‐Peng Cai,Jian Wang,Lingzhi Zhao,Qifeng Zheng
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-07-28
卷期号:10 (8): 4004-4012
被引量:7
标识
DOI:10.1021/acsenergylett.5c00974
摘要
Highly solvating electrolytes hold great prospects for achieving the goal of practically high-energy-density lithium–sulfur batteries, yet they suffer from short cycle life due to their poor compatibility with Li-metal anode (LMA). Herein, a new six-membered cyclic urea, N, N′-dimethylpropyleneurea (DMPU), was rationally proposed as an electrolyte solvent to conquer this longstanding contradiction. The DMPU with high electron donicity preferentially coordinates with Li+ to dominate the inner-solvation shell, which not only initiates and stabilizes the S3•– radical to facilitate S redox kinetics and 3D Li2S deposition but also suppresses its contact reaction with LMA kinetically. More encouragingly, the DMPU molecule with a six-membered ring bears small ring strain, thus weakening their reactivity with LMA thermodynamically. Consequently, the DMPU-based electrolyte bestows an extremely high area capacity of 8.4 mAh cm–2 for a practical lithium–sulfur cell under a high S mass loading of 8.2 mg cm–2 and ultralow E/S ratio of 3.8 μL mgsulfur–1.
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