多硫化物
电解质
硝酸锂
锂(药物)
阳极
硫黄
无机化学
溶解度
锂硫电池
分离器(采油)
化学
化学工程
材料科学
离子
电极
离子键合
有机化学
热力学
医学
物理
物理化学
工程类
内分泌学
作者
Ahmed Elabd,Jiheon Kim,Daniel Sethio,Sangho Kang,Taemin Kang,Jang Wook Choi,Ali Coşkun
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-07-07
卷期号:7 (8): 2459-2468
被引量:44
标识
DOI:10.1021/acsenergylett.2c00874
摘要
Electrolyte engineering is a highly promising strategy in lithium–sulfur batteries to increase the sulfur utilization and maintain a stable interface at the lithium metal anode for long-term cycling. Whereas high donor electrolytes can increase the solubility of polysulfides to promote the sulfur utilization and therefore operate under lean electrolyte conditions, their poor thermodynamic stability toward lithium metal anode causes uncontrolled decomposition at its interface and impair the cycle life severely. Here, we introduce a dual functional high donor electrolyte, 3-fluoropyridine (3-FPN), to simultaneously achieve high polysulfide solubility up to 1.5 M and compatibility with lithium metal. These features result in a high specific capacity of 1087.9 mAh gsulfur–1 and robust cycling under a lean electrolyte condition of 7 μLelectrolyte mgsulfur–1 in the absence of LiNO3. Remarkably, 3-FPN preserves stable cyclability even at a high areal sulfur loading of 8 mgsulfur cm–2, which opens a new avenue in advancing the electrolytes for lithium–sulfur batteries toward their high volumetric energy density and long cycle life.
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