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将受限的硫化钴纳米晶体嵌入氮/硫共掺杂碳纳米纤维中,作为一种类似锁子甲的电催化剂,用于高硫负载的高性能锂硫电池。

Confined CoS nanocrystals into N/S-Co-doped carbon nanofibers as a chainmail-like electrocatalyst for high-performance lithium-sulfur batteries with high sulfur loading.

作者信息

Zhou Wei, Chen Minzhe, Zhao Dengke, Wu Qikai, Dan Jiacheng, Zhu Chuheng, Qiu Wanwen, Lei Wen, Ma Li-Jun, Li Ligui

机构信息

New Energy Research Institute, School of Environment and Energy, South China University of Technology, Higher Education Mega Center, 382 East Waihuan Road, Guangzhou 510006, China.

The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, China.

出版信息

J Colloid Interface Sci. 2022 Nov;625:187-196. doi: 10.1016/j.jcis.2022.04.042. Epub 2022 Apr 12.

DOI:10.1016/j.jcis.2022.04.042
PMID:35716614
Abstract

Accelerating phase transposition efficiency of lithium polysulfides (LiPSs) to LS and hampering the solution of LiPSs are the keys to stabilizing lithium-sulfur (Li-S) batteries. Hence, the sulfiphilic ultrafine CoS nanoparticles embedded lithiophilic N, S co-doping carbon nanofibers (CoS/NSCNF) are prepared via the dual-template method, which are then used as sulfur host in Li-S batteries. Particularly, the double active sites (CoS and N, S) in CoS/NSCNF are prone to form "Co-S", "Li-O" or "Li-N" bonds, and then simultaneously improving the chemisorption and interface transposition capability of LiPSs. In case of the S@ CoS/NSCNF composites with high sulfur loading of 89% are employed as cathode, the cell possesses optimized "sulfiphilicity" and "lithiophilicity", which achieves remarkable sulfur electrochemistry, including outstanding reversibility of 816.8mAhg over 500 cycles at 1.0C, excellent rate property of 742.2mAhgat 5.0C, and long-term cycling with a low attenuation of 0.011% per cycle over 1800 cycles at 3.0C. Impressively, a remarkable areal capacity of 11.51mAhcm is retained under the sulfur loading of 15.3 mg cm for 50 cycles. This research will deepen the understanding of the complex LiPSs interface transposition procedure and provide new ideas for the design of new host materials.

摘要

提高多硫化锂(LiPSs)向硫化锂(LS)的相转变效率并抑制LiPSs的溶解是稳定锂硫(Li-S)电池的关键。因此,通过双模板法制备了嵌入亲锂氮、硫共掺杂碳纳米纤维(CoS/NSCNF)的亲硫超细微CoS纳米颗粒,并将其用作Li-S电池中的硫宿主。特别地,CoS/NSCNF中的双活性位点(CoS和N、S)易于形成“Co-S”、“Li-O”或“Li-N”键,进而同时提高LiPSs的化学吸附和界面转位能力。当使用硫负载量高达89%的S@CoS/NSCNF复合材料作为阴极时,电池具有优化的“亲硫性”和“亲锂性”,实现了卓越的硫电化学性能,包括在1.0C下500次循环中816.8mAhg的出色可逆性、在5.0C下742.2mAhg的优异倍率性能以及在3.0C下1800次循环中每循环0.011%的低衰减长期循环。令人印象深刻的是,在硫负载量为15.3mg cm的情况下,50次循环后仍保留了11.51mAhcm的显著面积容量。本研究将加深对复杂的LiPSs界面转位过程的理解,并为新型宿主材料的设计提供新思路。

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