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锂硫电池中硫的演化过程及其对可逆容量影响的直接监测

Direct Monitoring of Li S Evolution and Its Influence on the Reversible Capacities of Lithium-Sulfur Batteries.

作者信息

Luo Yufeng, Fang Zhenhan, Duan Shaorong, Wu Hengcai, Liu Haitao, Zhao Yuxing, Wang Ke, Li Qunqing, Fan Shoushan, Zheng Zijian, Duan Wenhui, Zhang Yuegang, Wang Jiaping

机构信息

Tsinghua-Foxconn Nanotechnology Research Center, Tsinghua University, Beijing, 100084, China.

Laboratory for Advanced Interfacial Materials and Devices, School of Fashion and Textiles, The Hong Kong Polytechnic University, Hong Kong, SAR 99077, China.

出版信息

Angew Chem Int Ed Engl. 2023 Mar 6;62(11):e202215802. doi: 10.1002/anie.202215802. Epub 2023 Feb 1.

Abstract

The polysulfide (PS) dissolution and low conductivity of lithium sulfides (Li S) are generally considered the main reasons for limiting the reversible capacity of the lithium-sulfur (Li-S) system. However, as the inevitable intermediate between PSs and Li S, lithium disulfide (Li S ) evolutions are always overlooked. Herein, Li S evolutions are monitored from the operando measurements on the pouch cell level. Results indicate that Li S undergoes slow electrochemical reduction and chemical disproportionation simultaneously during the discharging process, leading to further PS dissolution and Li S generation without capacity contribution. Compared with the fully oxidized Li S, Li S still residues at the end of the charging state. Therefore, instead of the considered Li S and PSs, slow electrochemical conversions and side chemical reactions of Li S are the determining factors in limiting the sulfur utilization, corresponding to the poor reversible capacity of Li-S batteries.

摘要

多硫化物(PS)的溶解和硫化锂(Li₂S)的低导电性通常被认为是限制锂硫(Li-S)体系可逆容量的主要原因。然而,作为PSs和Li₂S之间不可避免的中间体,二硫化锂(Li₂S₂)的演变总是被忽视。在此,通过软包电池层面的原位测量来监测Li₂S₂的演变。结果表明,在放电过程中,Li₂S₂同时经历缓慢的电化学还原和化学歧化反应,导致进一步的PS溶解和Li₂S生成,而没有容量贡献。与完全氧化的Li₂S相比,Li₂S₂在充电状态结束时仍然残留。因此,限制硫利用率的决定因素是Li₂S₂缓慢的电化学转化和副化学反应,而非之前所认为的Li₂S和PSs,这也对应了Li-S电池较差的可逆容量。

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