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用于钠离子电池的具有快速动力学和高稳定性的高熵硫硒化物负极材料

High-entropy sulfoselenide as negative electrodes with fast kinetics and high stability for sodium-ion batteries.

作者信息

Zhang Shengfeng, Zuo Wenhua, Fu Xiaoguang, Li Juntao, Zhang Qiuwen, Yang Weihua, Chen Hongwei, Zhang Junyu, Xiao Xianghui, Amine Khalil, Sun Shi-Gang, Fu Fang, Ye Meidan, Xu Gui-Liang

机构信息

College of Materials Science and Engineering, Huaqiao University, Xiamen, China.

Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, IL, USA.

出版信息

Nat Commun. 2025 Apr 30;16(1):4052. doi: 10.1038/s41467-025-59078-6.

DOI:10.1038/s41467-025-59078-6
PMID:40307247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12044082/
Abstract

Conversion electrodes offer higher reversible capacity and lower cost than conventional intercalation chemistry electrodes, but suffer from kinetic limitation and large volume expansion. Despite significant efforts, developing conversion electrodes with fast charging capability and extended lifespan remains challenging. Here, by leveraging the advantages of high-entropy doping and morphology tailoring, we develop a high-entropy hierarchical micro/nanostructured sulfoselenide CuSnSbBiMnSSe electrode with entropy-driven fast-charging capability. When used as a negative electrode material for sodium-ion batteries, it achieves a stable cycle life of 10,000 cycles at 30 A g and a high reversible capacity of 365.7 mAh g under fast charging in 13 seconds at 100 A g. Moreover, high-entropy sulfoselenide also demonstrates stable cycling and good rate capability as a positive electrode material for lithium metal batteries, achieving a fast-charging capability of 37 seconds that is comparable with state-of-the-art layered cathodes. High-entropy sulfoselenide is characterized by its robust crystal structure, low ion diffusion barrier, and effective suppression of side reactions with electrolytes during cycling. Importantly, transmission X-ray microscopy affirms the chemical stability of HESSe, which underpins its fast-charging performance.

摘要

与传统的嵌入化学电极相比,转换电极具有更高的可逆容量和更低的成本,但存在动力学限制和较大的体积膨胀问题。尽管付出了巨大努力,但开发具有快速充电能力和延长使用寿命的转换电极仍然具有挑战性。在这里,通过利用高熵掺杂和形貌调控的优势,我们开发了一种具有熵驱动快速充电能力的高熵分级微/纳米结构硫硒化物CuSnSbBiMnSSe电极。当用作钠离子电池的负极材料时,它在30 A g下实现了10000次循环的稳定循环寿命,在100 A g下13秒快速充电时具有365.7 mAh g的高可逆容量。此外,高熵硫硒化物作为锂金属电池的正极材料也表现出稳定的循环性能和良好的倍率性能,实现了37秒的快速充电能力,与目前最先进的层状阴极相当。高熵硫硒化物的特点是其坚固的晶体结构、低离子扩散势垒以及在循环过程中有效抑制与电解质的副反应。重要的是,透射X射线显微镜证实了HESSe的化学稳定性,这支撑了其快速充电性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/fec2338d8c7c/41467_2025_59078_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/491b9654551f/41467_2025_59078_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/4a4c5c8d690d/41467_2025_59078_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/3435e19ef93d/41467_2025_59078_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/b06e043b8c64/41467_2025_59078_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/e1aa32d42bc6/41467_2025_59078_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/71a317cd578b/41467_2025_59078_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/9fed43191afd/41467_2025_59078_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/fec2338d8c7c/41467_2025_59078_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/491b9654551f/41467_2025_59078_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/4a4c5c8d690d/41467_2025_59078_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/3435e19ef93d/41467_2025_59078_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/b06e043b8c64/41467_2025_59078_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/e1aa32d42bc6/41467_2025_59078_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/71a317cd578b/41467_2025_59078_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/9fed43191afd/41467_2025_59078_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4025/12044082/fec2338d8c7c/41467_2025_59078_Fig8_HTML.jpg

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本文引用的文献

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