Yongxu Du , Hongguang Fan , Yujing Zhu , Xianghua Zhang , Denghu Wei , Chuanyu Jin , Yongpeng Cui , Meiying Lv
{"title":"高效K-S /Se电池中具有多种化学亲和力的活性硫/硒锚定在增强碳宿主中†","authors":"Yongxu Du , Hongguang Fan , Yujing Zhu , Xianghua Zhang , Denghu Wei , Chuanyu Jin , Yongpeng Cui , Meiying Lv","doi":"10.1039/d4gc05818f","DOIUrl":null,"url":null,"abstract":"<div><div>Potassium–sulfur (K–S) and potassium–selenium (K–Se) batteries, with high energy density and low cost, are considered promising options for grid-scale energy storage systems. However, challenges such as the notorious dissolution of polysulfides/polyselenides result in corrosion of potassium and cycle life decay, limiting their practical application. Herein, enhanced carbon hosts with multiple chemical affinities are constructed for encapsulating S or Se species toward a stable potassium ion storage. The unique design allows for the high loading (∼60 wt%) of active S or Se via enhanced chemical affinities originating from abundant nitrogen and oxygen groups. Moreover, the introduction of an N-reinforced O-site on a carbon substance can provide good electrical conductivity and alleviate the shuttling effect during the electrochemical process. Besides, <em>in situ</em> Raman and visualization tests also verify that the electrodes exhibit excellent electrochemical reversibility and cycling stability. The optimized cathode exhibits conspicuous performance in K–S and K–Se batteries. This work provides a practical strategy and paves the way for viable applications of advanced alkali metal battery systems.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 8","pages":"Pages 2309-2318"},"PeriodicalIF":9.2000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anchoring active sulfur/selenium into enhanced carbon hosts with multiple chemical affinities for efficient K–S/Se batteries†\",\"authors\":\"Yongxu Du , Hongguang Fan , Yujing Zhu , Xianghua Zhang , Denghu Wei , Chuanyu Jin , Yongpeng Cui , Meiying Lv\",\"doi\":\"10.1039/d4gc05818f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Potassium–sulfur (K–S) and potassium–selenium (K–Se) batteries, with high energy density and low cost, are considered promising options for grid-scale energy storage systems. However, challenges such as the notorious dissolution of polysulfides/polyselenides result in corrosion of potassium and cycle life decay, limiting their practical application. Herein, enhanced carbon hosts with multiple chemical affinities are constructed for encapsulating S or Se species toward a stable potassium ion storage. The unique design allows for the high loading (∼60 wt%) of active S or Se via enhanced chemical affinities originating from abundant nitrogen and oxygen groups. Moreover, the introduction of an N-reinforced O-site on a carbon substance can provide good electrical conductivity and alleviate the shuttling effect during the electrochemical process. Besides, <em>in situ</em> Raman and visualization tests also verify that the electrodes exhibit excellent electrochemical reversibility and cycling stability. The optimized cathode exhibits conspicuous performance in K–S and K–Se batteries. This work provides a practical strategy and paves the way for viable applications of advanced alkali metal battery systems.</div></div>\",\"PeriodicalId\":78,\"journal\":{\"name\":\"Green Chemistry\",\"volume\":\"27 8\",\"pages\":\"Pages 2309-2318\"},\"PeriodicalIF\":9.2000,\"publicationDate\":\"2025-01-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1463926225000652\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926225000652","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Anchoring active sulfur/selenium into enhanced carbon hosts with multiple chemical affinities for efficient K–S/Se batteries†
Potassium–sulfur (K–S) and potassium–selenium (K–Se) batteries, with high energy density and low cost, are considered promising options for grid-scale energy storage systems. However, challenges such as the notorious dissolution of polysulfides/polyselenides result in corrosion of potassium and cycle life decay, limiting their practical application. Herein, enhanced carbon hosts with multiple chemical affinities are constructed for encapsulating S or Se species toward a stable potassium ion storage. The unique design allows for the high loading (∼60 wt%) of active S or Se via enhanced chemical affinities originating from abundant nitrogen and oxygen groups. Moreover, the introduction of an N-reinforced O-site on a carbon substance can provide good electrical conductivity and alleviate the shuttling effect during the electrochemical process. Besides, in situ Raman and visualization tests also verify that the electrodes exhibit excellent electrochemical reversibility and cycling stability. The optimized cathode exhibits conspicuous performance in K–S and K–Se batteries. This work provides a practical strategy and paves the way for viable applications of advanced alkali metal battery systems.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.