{"title":"小型微晶SiO2催化na2s2转化为na2s用于高性能室温钠硫电池","authors":"Jianfeng Huang, Yalin Zhang, Liyun Cao, Dewei Chu, Qingqing Huang, Yijun Liu, Yong Zhao, Junle Dong, Chunyi Cai, Shuzhuo Bai, Wen Wen, Jiayin Li","doi":"10.1039/d5qi01291k","DOIUrl":null,"url":null,"abstract":"Biomass-derived carbon materials are widely employed as cathode carriers for RT-Na/S batteries. However, their limited surface activity and scarcity of catalytic sites hinder stable long-term cycling performance, particularly under high current densities. In this work, we successfully synthesized large-sized, microcrystalline, and amorphous SiO2 structures via in situ growth on carbon substrates, utilizing the natural silicate components inherent to the biomass precursors. The designed C/M-SiO₂@S cathode demonstrates remarkable electrochemical performance, retaining a specific capacity of 1021 mAh g-1 after 5000 cycles at a high current density of 5 A g<small><sup>-1</sup></small>. The microcrystalline SiO₂ exhibits pronounced catalytic activity, significantly facilitating the conversion kinetics from Na2S2 to Na2S and enabling a shortened sodium-ion diffusion pathway. This study provides valuable insights for engineering catalytic architectures within biomass-derived carbon.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"23 1","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Small-Sized Microcrystalline SiO2 Catalyzed Na2S2-to-Na2S Conversion for High-Performance Room-Temperature Sodium-Sulfur Batteries\",\"authors\":\"Jianfeng Huang, Yalin Zhang, Liyun Cao, Dewei Chu, Qingqing Huang, Yijun Liu, Yong Zhao, Junle Dong, Chunyi Cai, Shuzhuo Bai, Wen Wen, Jiayin Li\",\"doi\":\"10.1039/d5qi01291k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Biomass-derived carbon materials are widely employed as cathode carriers for RT-Na/S batteries. However, their limited surface activity and scarcity of catalytic sites hinder stable long-term cycling performance, particularly under high current densities. In this work, we successfully synthesized large-sized, microcrystalline, and amorphous SiO2 structures via in situ growth on carbon substrates, utilizing the natural silicate components inherent to the biomass precursors. The designed C/M-SiO₂@S cathode demonstrates remarkable electrochemical performance, retaining a specific capacity of 1021 mAh g-1 after 5000 cycles at a high current density of 5 A g<small><sup>-1</sup></small>. The microcrystalline SiO₂ exhibits pronounced catalytic activity, significantly facilitating the conversion kinetics from Na2S2 to Na2S and enabling a shortened sodium-ion diffusion pathway. This study provides valuable insights for engineering catalytic architectures within biomass-derived carbon.\",\"PeriodicalId\":79,\"journal\":{\"name\":\"Inorganic Chemistry Frontiers\",\"volume\":\"23 1\",\"pages\":\"\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2025-08-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5qi01291k\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qi01291k","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
摘要
生物质衍生碳材料被广泛用作RT-Na/S电池的正极载体。然而,它们有限的表面活性和催化位点的稀缺性阻碍了稳定的长期循环性能,特别是在高电流密度下。在这项工作中,我们利用生物质前驱体中固有的天然硅酸盐成分,通过在碳基质上原位生长成功地合成了大尺寸、微晶和非晶SiO2结构。所设计的C/M-SiO₂@S阴极具有出色的电化学性能,在5 a g-1的高电流密度下,经过5000次循环后保持1021 mAh g-1的比容量。微晶sio2具有明显的催化活性,显著促进了Na2S2到Na2S的转化动力学,缩短了钠离子的扩散途径。这项研究为生物质衍生碳的工程催化结构提供了有价值的见解。
Biomass-derived carbon materials are widely employed as cathode carriers for RT-Na/S batteries. However, their limited surface activity and scarcity of catalytic sites hinder stable long-term cycling performance, particularly under high current densities. In this work, we successfully synthesized large-sized, microcrystalline, and amorphous SiO2 structures via in situ growth on carbon substrates, utilizing the natural silicate components inherent to the biomass precursors. The designed C/M-SiO₂@S cathode demonstrates remarkable electrochemical performance, retaining a specific capacity of 1021 mAh g-1 after 5000 cycles at a high current density of 5 A g-1. The microcrystalline SiO₂ exhibits pronounced catalytic activity, significantly facilitating the conversion kinetics from Na2S2 to Na2S and enabling a shortened sodium-ion diffusion pathway. This study provides valuable insights for engineering catalytic architectures within biomass-derived carbon.