{"title":"原位构建Mo2C-MoS2纳米球形异质结构加速锂硫电池动力学","authors":"Ao Zhang, Junzhi Li, Guangshe Li, Liping Li","doi":"10.1002/smll.202504580","DOIUrl":null,"url":null,"abstract":"<p>The interaction between catalysts and polysulfides plays a crucial role in the redox kinetics of lithium-sulfur batteries (LSBs). However, the role of nanoscale heterostructures formed by non-metal atoms in regulating the electronic state of catalysts is often overlooked. In this work, these electronic states are modulated by in situ constructing a Mo─S heterostructure in a Mo<sub>2</sub>C nanosphere. The introduction of sulfur atoms forms the anion heterointerface, altering the coordination environment of interfacial Mo atoms and strengthening Mo─S interactions. This modification significantly enhances lithium polysulfide (LiPS) adsorption and conversion kinetics when using a Mo<sub>2</sub>C-MoS<sub>2</sub> heterostructure-modified separator (Mo<sub>2</sub>C-MoS<sub>2</sub>/PP) in LSBs. Furthermore, Mo<sub>2</sub>C-MoS<sub>2</sub>/PP effectively suppresses the LiPS shuttle effect and improves cycling stability, achieving a low capacity decay rate of 0.036% per cycle over 500 cycles at 1C. This study proposes a comprehensive approach to modulate metal electronic states by non-metal atoms nanoheterostructure, aiming to enhance the catalytic reaction kinetics of LSBs.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 29","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In Situ Construction of Mo2C-MoS2 Nanospherical Heterostructure for Accelerating the Kinetics of Lithium-Sulfur Batteries\",\"authors\":\"Ao Zhang, Junzhi Li, Guangshe Li, Liping Li\",\"doi\":\"10.1002/smll.202504580\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The interaction between catalysts and polysulfides plays a crucial role in the redox kinetics of lithium-sulfur batteries (LSBs). However, the role of nanoscale heterostructures formed by non-metal atoms in regulating the electronic state of catalysts is often overlooked. In this work, these electronic states are modulated by in situ constructing a Mo─S heterostructure in a Mo<sub>2</sub>C nanosphere. The introduction of sulfur atoms forms the anion heterointerface, altering the coordination environment of interfacial Mo atoms and strengthening Mo─S interactions. This modification significantly enhances lithium polysulfide (LiPS) adsorption and conversion kinetics when using a Mo<sub>2</sub>C-MoS<sub>2</sub> heterostructure-modified separator (Mo<sub>2</sub>C-MoS<sub>2</sub>/PP) in LSBs. Furthermore, Mo<sub>2</sub>C-MoS<sub>2</sub>/PP effectively suppresses the LiPS shuttle effect and improves cycling stability, achieving a low capacity decay rate of 0.036% per cycle over 500 cycles at 1C. This study proposes a comprehensive approach to modulate metal electronic states by non-metal atoms nanoheterostructure, aiming to enhance the catalytic reaction kinetics of LSBs.</p>\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"21 29\",\"pages\":\"\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2025-05-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smll.202504580\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202504580","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
In Situ Construction of Mo2C-MoS2 Nanospherical Heterostructure for Accelerating the Kinetics of Lithium-Sulfur Batteries
The interaction between catalysts and polysulfides plays a crucial role in the redox kinetics of lithium-sulfur batteries (LSBs). However, the role of nanoscale heterostructures formed by non-metal atoms in regulating the electronic state of catalysts is often overlooked. In this work, these electronic states are modulated by in situ constructing a Mo─S heterostructure in a Mo2C nanosphere. The introduction of sulfur atoms forms the anion heterointerface, altering the coordination environment of interfacial Mo atoms and strengthening Mo─S interactions. This modification significantly enhances lithium polysulfide (LiPS) adsorption and conversion kinetics when using a Mo2C-MoS2 heterostructure-modified separator (Mo2C-MoS2/PP) in LSBs. Furthermore, Mo2C-MoS2/PP effectively suppresses the LiPS shuttle effect and improves cycling stability, achieving a low capacity decay rate of 0.036% per cycle over 500 cycles at 1C. This study proposes a comprehensive approach to modulate metal electronic states by non-metal atoms nanoheterostructure, aiming to enhance the catalytic reaction kinetics of LSBs.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.