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通过铜、碘共掺杂激活硫化锂的氧化还原动力学以实现高性能全固态硫化锂基电池

Activating Redox Kinetics of LiS via Cu, I Co-Doping Toward High-Performance All-Solid-State Lithium Sulfide-Based Batteries.

作者信息

Gao Jing, Gao Yuan, Hao Jinghua, Sun Xiaolin, Zhao Fuhua, Zhang Yuan, Si Wenyan, Wu Jianfei

机构信息

Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, 189 Songling Road, Qingdao, 266101, P. R. China.

Shandong Energy Institute Qingdao, Qingdao New Energy Shandong Laboratory, 189 Songling Road, Qingdao, 266101, P. R. China.

出版信息

Small. 2024 Nov;20(47):e2404171. doi: 10.1002/smll.202404171. Epub 2024 Aug 26.

DOI:10.1002/smll.202404171
PMID:39185810
Abstract

All-solid-state lithium sulfide-based batteries (ASSLSBs) have drawn much attention due to their intrinsic safety and excellent performance in overcoming the polysulfide shuttle effect. However, the sluggish kinetics of LiS cathode severely impede commercial utilization. Here, a Cu, I co-doping strategy is employed to activate the kinetics of LiS to construct high-performance ASSLSBs. The electronic conductivity and Li-ion diffusion coefficient of the co-doped LiS are increased by five and two orders of magnitude, respectively. Cu as a redox medium greatly improves the reaction kinetics, which is supported by ex situ X-ray photoelectron spectroscopy. Density functional theory calculation (DFT) shows that Cu, I co-doping reduces the Li-ions diffusion energy barrier. The co-doped LiS exhibits a remarkable improvement in capacity (1165.23 mAh g (6.65 times that of pristine LiS) at 0.02 C and 592.75 mAh g at 2 C), and excellent cycling stability (84.58% capacity retention after 6200 cycles at 2 C) at room temperature. Moreover, an ASSLSB, fabricated with a lithium-free (Si─C) anode, obtains a high specific capacity of 1082.7 mAh g at 0.05 C and 97% capacity retention after 400 cycles at 0.5 C. This work provides a broad prospect for the development of ASSLSBs with practical energy density exceeding that of traditional lithium-ion batteries.

摘要

全固态硫化锂基电池(ASSLSBs)因其本质安全性以及在克服多硫化物穿梭效应方面的优异性能而备受关注。然而,LiS正极缓慢的动力学严重阻碍了其商业应用。在此,采用铜、碘共掺杂策略来激活LiS的动力学,以构建高性能的ASSLSBs。共掺杂LiS的电子电导率和锂离子扩散系数分别提高了五个和两个数量级。铜作为氧化还原介质极大地改善了反应动力学,这得到了非原位X射线光电子能谱的支持。密度泛函理论计算(DFT)表明,铜、碘共掺杂降低了锂离子扩散能垒。共掺杂LiS在容量方面有显著提升(在0.02 C时为1165.23 mAh g(是原始LiS的6.65倍),在2 C时为592.75 mAh g),并且在室温下具有优异的循环稳定性(在2 C下6200次循环后容量保持率为84.58%)。此外,采用无锂(Si─C)负极制造的ASSLSB在0.05 C时获得了1082.7 mAh g的高比容量,在0.5 C下400次循环后容量保持率为9七%。这项工作为开发实际能量密度超过传统锂离子电池的ASSLSBs提供了广阔前景。

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