Highly Solvating Electrolytes with Core-Shell Solvation Structure for Lean-Electrolyte Lithium-Sulfur Batteries

被引:0
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作者
He, Mengxue [1 ]
Zhu, Lujun [1 ]
Liu, Yatao [1 ]
Jia, Yongfeng [1 ]
Hao, Yizhou [2 ]
Ye, Guo [1 ]
Hong, Xufeng [1 ]
Xiao, Zhitong [1 ]
Ma, Yue [1 ]
Chen, Jianhao [2 ,3 ]
Shafqat, Muhammad Burhan [2 ]
Pang, Quanquan [1 ]
机构
[1] Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering, Peking University, Beijing,100871, China
[2] Key Laboratory for the Physics and Chemistry of Nanodevices, Peking University, Beijing,100871, China
[3] International Center for Quantum Materials, Collaborative Innovation Center of Quantum Matter, Peking University, Beijing, China
关键词
D O I
10.1002/anie.202415053
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学科分类号
摘要
The practical energy density of lithium-sulfur batteries is limited by the low sulfur utilization at lean electrolyte conditions. The highly solvating electrolytes (HSEs) promise to address the issue at harsh conditions, but the conflicting challenges of long-term stability of radical-mediated sulfur redox reactions (SRR) and the poor stability with lithium metal anode (LMA) have dimmed the efforts. We now present a unique core–shell solvation structured HSE formulated with classical ether-based solvents and phosphoramide co-solvent. The unique core–shell solvation structure features confinement of the phosphoramide in the first solvation shell, which prohibits severe contact reactions with LMA and endows prolonged stability for [S3]⋅− radical, favoring a rapid radical-mediated solution-based SRR. The cell with the proposed electrolyte showing a high capacity of 864 mAh gsulfur−1 under high sulfur loading of 5.5 mgsulfur cm−2 and low E/S ratio of 4 μL mgsulfur−1. The strategy further enables steady cycling of a 2.71-A h pouch cell with a high specific energy of 307 W h kg−1. Our work highlights the fundamental chemical concept of tuning the solvation structure to simultaneously tame the SRR and LMA stability for metal-sulfur batteries wherein the electrode reactions are heavily coupled with electrolyte chemistry. © 2024 Wiley-VCH GmbH.
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