{"title":"亚微米硅阳极上氢键相互作用衍生的均质石墨烯涂层","authors":"Liewu Li, Yizhao Yang, Zhencheng Huang, Tao Huang, Weibin Chen, Xiaoyu Gong, Shenghua Ye, Hao Li, Shaoluan Huang, Wei Xiong, Jing Chen, Hongbin Wang, Xiangzhong Ren, Xiaoping Ouyang, Jionghui Wang, Qianling Zhang, Jiangtao Hu, Jianhong Liu","doi":"10.1002/bte2.20230068","DOIUrl":null,"url":null,"abstract":"<p>Silicon (Si) has emerged as a promising anode material in the pursuit of higher energy-density lithium-ion batteries (LIBs). The large-scale applications of Si anode, however, are hindered by its significant swelling, severe pulverization, and continuous electrode–electrolyte reaction. Therefore, the development of an efficient approach to mitigate Si particle swelling and minimize interface parasitic reactions has emerged as a prominent research focus in both academia and industry. Here, a facile and scalable strategy is reported for the preparation of a double-layer coated submicron Si anode, comprising ceramic (silicon oxide) and graphene layers, denoted as Si@SiO<sub>x</sub>@G. In this approach, SiO<sub>x</sub> is in situ synthesized on the surface of Si and bonded with graphene through hydrogen bond interactions. The prepared Si electrode shows exceptional structural integration and demonstrates outstanding electrochemical stability, with a capacity retention of 92.58% after 540 cycles at 1 A g<sup>−1</sup>, as well as remarkable rate capability, achieving a specific capacity of 875 mAh g<sup>−1</sup> at 2 A g<sup>−1</sup>. This study presents a straightforward yet pragmatic approach for the widespread implementation of high-energy-density silicon-based batteries.</p>","PeriodicalId":8807,"journal":{"name":"Battery Energy","volume":"3 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bte2.20230068","citationCount":"0","resultStr":"{\"title\":\"Hydrogen bond interaction derived homogeneous graphene coating on submicron silicon anode\",\"authors\":\"Liewu Li, Yizhao Yang, Zhencheng Huang, Tao Huang, Weibin Chen, Xiaoyu Gong, Shenghua Ye, Hao Li, Shaoluan Huang, Wei Xiong, Jing Chen, Hongbin Wang, Xiangzhong Ren, Xiaoping Ouyang, Jionghui Wang, Qianling Zhang, Jiangtao Hu, Jianhong Liu\",\"doi\":\"10.1002/bte2.20230068\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Silicon (Si) has emerged as a promising anode material in the pursuit of higher energy-density lithium-ion batteries (LIBs). The large-scale applications of Si anode, however, are hindered by its significant swelling, severe pulverization, and continuous electrode–electrolyte reaction. Therefore, the development of an efficient approach to mitigate Si particle swelling and minimize interface parasitic reactions has emerged as a prominent research focus in both academia and industry. Here, a facile and scalable strategy is reported for the preparation of a double-layer coated submicron Si anode, comprising ceramic (silicon oxide) and graphene layers, denoted as Si@SiO<sub>x</sub>@G. In this approach, SiO<sub>x</sub> is in situ synthesized on the surface of Si and bonded with graphene through hydrogen bond interactions. The prepared Si electrode shows exceptional structural integration and demonstrates outstanding electrochemical stability, with a capacity retention of 92.58% after 540 cycles at 1 A g<sup>−1</sup>, as well as remarkable rate capability, achieving a specific capacity of 875 mAh g<sup>−1</sup> at 2 A g<sup>−1</sup>. This study presents a straightforward yet pragmatic approach for the widespread implementation of high-energy-density silicon-based batteries.</p>\",\"PeriodicalId\":8807,\"journal\":{\"name\":\"Battery Energy\",\"volume\":\"3 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-02-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bte2.20230068\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Battery Energy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/bte2.20230068\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Battery Energy","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bte2.20230068","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
硅(Si)已成为一种前景广阔的负极材料,用于制造能量密度更高的锂离子电池(LIB)。然而,硅负极的大规模应用因其显著的膨胀、严重的粉化和持续的电极-电解质反应而受到阻碍。因此,开发一种有效的方法来缓解硅颗粒膨胀并最大限度地减少界面寄生反应已成为学术界和工业界的一个突出研究重点。本文报告了一种简便且可扩展的策略,用于制备双层涂层亚微米硅阳极,包括陶瓷层(氧化硅)和石墨烯层,命名为 Si@SiOx@G。在这种方法中,氧化硅在硅表面原位合成,并通过氢键相互作用与石墨烯结合。所制备的硅电极具有优异的结构整合性和出色的电化学稳定性,在 1 A g-1 条件下循环 540 次后容量保持率达到 92.58%,同时还具有出色的速率能力,在 2 A g-1 条件下比容量达到 875 mAh g-1。这项研究为高能量密度硅基电池的广泛应用提供了一种简单而实用的方法。
Hydrogen bond interaction derived homogeneous graphene coating on submicron silicon anode
Silicon (Si) has emerged as a promising anode material in the pursuit of higher energy-density lithium-ion batteries (LIBs). The large-scale applications of Si anode, however, are hindered by its significant swelling, severe pulverization, and continuous electrode–electrolyte reaction. Therefore, the development of an efficient approach to mitigate Si particle swelling and minimize interface parasitic reactions has emerged as a prominent research focus in both academia and industry. Here, a facile and scalable strategy is reported for the preparation of a double-layer coated submicron Si anode, comprising ceramic (silicon oxide) and graphene layers, denoted as Si@SiOx@G. In this approach, SiOx is in situ synthesized on the surface of Si and bonded with graphene through hydrogen bond interactions. The prepared Si electrode shows exceptional structural integration and demonstrates outstanding electrochemical stability, with a capacity retention of 92.58% after 540 cycles at 1 A g−1, as well as remarkable rate capability, achieving a specific capacity of 875 mAh g−1 at 2 A g−1. This study presents a straightforward yet pragmatic approach for the widespread implementation of high-energy-density silicon-based batteries.