多硫化物
电解质
化学工程
涂层
阴极
材料科学
硫黄
溶剂
锂(药物)
氟
电极
化学
无机化学
有机化学
纳米技术
医学
工程类
内分泌学
物理化学
作者
Florian Schmidt,Sebastian Kirchhoff,Karin Jägle,Ankita De,Sebastian Ehrling,Paul Härtel,Susanne Dörfler,Thomas Abendroth,Benjamin Schumm,Holger Althues,Stefan Kaskel
出处
期刊:Chemsuschem
[Wiley]
日期:2022-09-28
卷期号:15 (22)
被引量:16
标识
DOI:10.1002/cssc.202201320
摘要
In the market for next-generation energy storage, lithium-sulfur (Li-S) technology is one of the most promising candidates due to its high theoretical specific energy and cost-efficient ubiquitous active materials. In this study, this cell system was combined with a cost-efficient sustainable solvent-free electrode dry-coating process (DRYtraec®). So far, this process has been only feasible with polytetrafluoroethylene (PTFE)-based binders. To increase the sustainability of electrode processing and to decrease the undesired fluorine content of Li-S batteries, a renewable, biodegradable, and fluorine-free polypeptide was employed as a binder for solvent-free electrode manufacturing. The yielded sulfur/carbon dry-film cathodes were electrochemically evaluated under lean electrolyte conditions at coin and pouch cell level, using the state-of-the-art 1,2-dimethoxyethane/1,3-dioxolane electrolyte (DME/DOL) as well as the sparingly polysulfide-solvating electrolytes hexylmethylether (HME)/DOL and tetramethylene sulfone/1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TMS/TTE). These results demonstrated that the PTFE binder can be replaced by the biodegradable sericin as the cycle stability and performance of the cathodes was retained.
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