{"title":"高熵硫代硒化物作为钠离子电池负极,具有快速动力学和高稳定性","authors":"Shengfeng Zhang, Wenhua Zuo, Xiaoguang Fu, Juntao Li, Qiuwen Zhang, Weihua Yang, Hongwei Chen, Junyu Zhang, Xianghui Xiao, Khalil Amine, Shi-Gang Sun, Fang Fu, Meidan Ye, Gui-Liang Xu","doi":"10.1038/s41467-025-59078-6","DOIUrl":null,"url":null,"abstract":"<p>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 Cu<sub>0.88</sub>Sn<sub>0.02</sub>Sb<sub>0.02</sub>Bi<sub>0.02</sub>Mn<sub>0.02</sub>S<sub>0.9</sub>Se<sub>0.1</sub> 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<sup>−1</sup> and a high reversible capacity of 365.7 mAh g<sup>−1</sup> under fast charging in 13 seconds at 100 A g<sup>−1</sup>. 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.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"33 1","pages":""},"PeriodicalIF":14.7000,"publicationDate":"2025-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"High-entropy sulfoselenide as negative electrodes with fast kinetics and high stability for sodium-ion batteries\",\"authors\":\"Shengfeng Zhang, Wenhua Zuo, Xiaoguang Fu, Juntao Li, Qiuwen Zhang, Weihua Yang, Hongwei Chen, Junyu Zhang, Xianghui Xiao, Khalil Amine, Shi-Gang Sun, Fang Fu, Meidan Ye, Gui-Liang Xu\",\"doi\":\"10.1038/s41467-025-59078-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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 Cu<sub>0.88</sub>Sn<sub>0.02</sub>Sb<sub>0.02</sub>Bi<sub>0.02</sub>Mn<sub>0.02</sub>S<sub>0.9</sub>Se<sub>0.1</sub> 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<sup>−1</sup> and a high reversible capacity of 365.7 mAh g<sup>−1</sup> under fast charging in 13 seconds at 100 A g<sup>−1</sup>. 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.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"33 1\",\"pages\":\"\"},\"PeriodicalIF\":14.7000,\"publicationDate\":\"2025-04-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-59078-6\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-59078-6","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
与传统的插层化学电极相比,转化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体积膨胀大的问题。尽管付出了巨大的努力,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。本研究利用高熵掺杂和形态裁剪的优势,开发了一种具有熵驱动快速充电能力的高熵层次化微纳米结构硫硒化物Cu0.88Sn0.02Sb0.02Bi0.02Mn0.02S0.9Se0.1电极。作为钠离子电池的负极材料,在30 a g - 1条件下可达到10000次的稳定循环寿命,在100 a g - 1条件下13秒快速充电可达到365.7 mAh g - 1的高可逆容量。此外,作为锂金属电池的正极材料,高熵硫代硒化物也表现出稳定的循环和良好的倍率能力,实现了37秒的快速充电能力,与最先进的层状阴极相当。高熵硫代硒化物具有坚固的晶体结构、低离子扩散势垒、有效抑制循环过程中与电解质的副反应等特点。重要的是,透射x射线显微镜证实了HESSe的化学稳定性,这是其快速充电性能的基础。
High-entropy sulfoselenide as negative electrodes with fast kinetics and high stability for sodium-ion batteries
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 Cu0.88Sn0.02Sb0.02Bi0.02Mn0.02S0.9Se0.1 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−1 and a high reversible capacity of 365.7 mAh g−1 under fast charging in 13 seconds at 100 A g−1. 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.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.