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将CeO纳米晶体界面组装成氮化钴用于协同促进锂硫电池中多硫化物转化和稳定锂沉积

Interfacial assembly of CeO nanocrystals into cobalt nitride for synergistic promotion of polysulfide conversion and stable lithium deposition in Li-S batteries.

作者信息

Yuan Long, Liu Xinyun, Peng Xiaoli, Li Shilan, Jing Shengdong, Lu Shengjun, Lei Hua, Zhang Yufei, Fan Haosen

机构信息

College of Materials Science and Metallurgy Engineering, Guizhou University, Guiyang 550025, China.

College of Materials Science and Metallurgy Engineering, Guizhou University, Guiyang 550025, China.

出版信息

J Colloid Interface Sci. 2025 Nov 15;698:138065. doi: 10.1016/j.jcis.2025.138065. Epub 2025 Jun 2.

DOI:10.1016/j.jcis.2025.138065
PMID:40466599
Abstract

Lithium-sulfur batteries (LSBs), as the promising next-generation energy storage devices, have attracted great research interests owing to their outstanding theoretical energy density, abundant reserves of sulfur and environmental friendliness. However, the commercial application of lithium-sulfur batteries still faces many challenges such as the heavy shuttle effect of polysulfides and lithium dendrite growth. In this work, CoN@CeO heterostructures were successfully prepared through interfacial assembly of CeO nanocrystals into cobalt nitride from a hydrothermal-nitriding process. The CoN@CeO heterostructure exhibits excellent adsorption-catalytic properties and effectively immobilizes soluble LiPS and promotes its electrochemical conversion. When CoN@CeO was used to modify commercial polypropylene (PP) separators, the results indicated that the LSBs still delivers a high discharge specific capacity of 621.86 mAh g after 600 cycles at 0.5C with low capacity decay rate of only 0.066 % per cycle. Meanwhile, the CoN@CeO also exhibited a high cell capacity after 250 cycles at a high sulfur loading of 4.352 mg. In addition, it also presents excellent resistance to self-discharge. The capacity retention rate was as high as 99.04 % after 72 h resting. The preparation of CoN@CeO heterostructure pave a bright way for the construction of high-performance LSBs through separator modification.

摘要

锂硫电池(LSBs)作为很有前景的下一代储能装置,因其出色的理论能量密度、丰富的硫储量和环境友好性而吸引了大量的研究兴趣。然而,锂硫电池的商业应用仍面临许多挑战,如多硫化物的严重穿梭效应和锂枝晶生长。在这项工作中,通过水热氮化过程将CeO纳米晶体界面组装到氮化钴中,成功制备了CoN@CeO异质结构。CoN@CeO异质结构表现出优异的吸附催化性能,有效地固定了可溶性锂多硫化物(LiPS)并促进其电化学转化。当使用CoN@CeO修饰商用聚丙烯(PP)隔膜时,结果表明,锂硫电池在0.5C下循环600次后仍具有621.86 mAh g的高放电比容量,容量衰减率仅为每循环0.066%。同时,在4.352 mg的高硫负载下循环250次后,CoN@CeO也表现出高电池容量。此外,它还具有优异的抗自放电性能。静置72小时后,容量保持率高达99.04%。CoN@CeO异质结构的制备为通过隔膜修饰构建高性能锂硫电池铺平了光明的道路。

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