有机硫化合物
电解质
化学
硫黄
溶解度
锂(药物)
无机化学
电化学
多硫化物
有机化学
电极
医学
内分泌学
物理化学
作者
Abhay Gupta,Amruth Bhargav,Arumugam Manthiram
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-12-22
卷期号:6 (1): 224-231
被引量:52
标识
DOI:10.1021/acsenergylett.0c02461
摘要
The solution-mediated behavior of lithium–sulfur (Li–S) batteries presents a wide range of opportunity for evaluating and improving the performance at practical lean-electrolyte conditions. Here, we introduce methyl trifluoroacetate (CH3TFA) as an additive to the Li–S electrolyte to evaluate the joint effects of two distinct strategies: high donor number solvents/salts and organosulfur-mediated discharge. CH3TFA is shown to react with lithium polysulfides in situ to form lithium trifluoroacetate (LiTFA) and dimethyl polysulfides. We find that both the methyl group and trifluoroacetate anion considerably enhance Li–S discharge behavior over the course of cycling, though they have distinctly beneficial effects. The TFA anion impacts solution coordination behavior, improving polarization and discharge kinetics during cycling. Meanwhile, the derivatization to dimethyl polysulfides improves the solubility of intermediate species, enhancing overall utilization under lean-electrolyte conditions. CH3TFA thus represents a new class of additives for Li–S batteries, enabling an in situ systematic molecular engineering of intermediate species for improved performance.
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