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通过电聚合构建基于导电硫醇聚合物的无粘结剂和无碳添加剂的有机硫阴极用于锂硫电池

Constructing Binder- and Carbon Additive-Free Organosulfur Cathodes Based on Conducting Thiol-Polymers through Electropolymerization for Lithium-Sulfur Batteries.

作者信息

Ning Jiaoyi, Yu Hongtao, Mei Shilin, Schütze Yannik, Risse Sebastian, Kardjilov Nikolay, Hilger André, Manke Ingo, Bande Annika, Ruiz Victor G, Dzubiella Joachim, Meng Hong, Lu Yan

机构信息

Department for Electrochemical Energy Storage, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner Platz 1, 14109, Berlin, Germany.

School of Advanced Materials, Peking University Shenzhen Graduate School, Peking University, Lishui road 2199, Nanshan district, Shenzhen, 518055, P. R. China.

出版信息

ChemSusChem. 2022 Jul 21;15(14):e202200434. doi: 10.1002/cssc.202200434. Epub 2022 May 30.

Abstract

Herein, the concept of constructing binder- and carbon additive-free organosulfur cathode was proved based on thiol-containing conducting polymer poly(4-(thiophene-3-yl) benzenethiol) (PTBT). The PTBT featured the polythiophene-structure main chain as a highly conducting framework and the benzenethiol side chain to copolymerize with sulfur and form a crosslinked organosulfur polymer (namely S/PTBT). Meanwhile, it could be in-situ deposited on the current collector by electro-polymerization, making it a binder-free and free-standing cathode for Li-S batteries. The S/PTBT cathode exhibited a reversible capacity of around 870 mAh g at 0.1 C and improved cycling performance compared to the physically mixed cathode (namely S&PTBT). This multifunction cathode eliminated the influence of the additives (carbon/binder), making it suitable to be applied as a model electrode for operando analysis. Operando X-ray imaging revealed the remarkable effect in the suppression of polysulfides shuttle via introducing covalent bonds, paving the way for the study of the intrinsic mechanisms in Li-S batteries.

摘要

在此,基于含硫醇的导电聚合物聚(4-(噻吩-3-基)苯硫醇)(PTBT),证明了构建无粘结剂和无碳添加剂的有机硫阴极的概念。PTBT以聚噻吩结构主链作为高导电骨架,苯硫醇侧链与硫共聚形成交联有机硫聚合物(即S/PTBT)。同时,它可以通过电聚合原位沉积在集流体上,使其成为锂硫电池的无粘结剂自立式阴极。与物理混合阴极(即S&PTBT)相比,S/PTBT阴极在0.1 C时表现出约870 mAh g的可逆容量和改善的循环性能。这种多功能阴极消除了添加剂(碳/粘结剂)的影响,使其适合用作原位分析的模型电极。原位X射线成像揭示了通过引入共价键抑制多硫化物穿梭的显著效果,为锂硫电池内在机制的研究铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cfc/9401019/9edcb1201a42/CSSC-15-0-g001.jpg

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