Wanling Ji , Minghuang Li , Yutong Nong , Jie Luo , Xinglong Liang , Xiaowei Wang , Lei Ming , Xing Ou , Jiafeng Zhang , Bao Zhang , Xuwang Fu , Lei Dong , Jianmin Feng , Ji Liang
{"title":"Low-temperature de-alloying and unique self-filling interface optimization mechanism of layered silicon for enhanced lithium storage†","authors":"Wanling Ji , Minghuang Li , Yutong Nong , Jie Luo , Xinglong Liang , Xiaowei Wang , Lei Ming , Xing Ou , Jiafeng Zhang , Bao Zhang , Xuwang Fu , Lei Dong , Jianmin Feng , Ji Liang","doi":"10.1039/d4cc03857f","DOIUrl":null,"url":null,"abstract":"<div><div>Layered silicon (L–Si) anodes are celebrated for their high theoretical capacity but face significant challenges regarding safety and material purity during preparation. This study addresses these challenges by employing NH<sub>4</sub>Cl–CaSi<sub>2</sub> as the raw material in a gas-solid de-alloying process, which enhances both safety and purity compared to traditional methods. The L–Si anodes produced demonstrate outstanding electrochemical performance, delivering a high reversible lithium storage capacity of 1497.7 mA h g<sup>−1</sup> at a current density of 0.5 A g<sup>−1</sup>, and exhibiting stable performance over 1200 charge–discharge cycles. <em>In situ</em> and <em>ex situ</em> characterizations reveal that electrolyte decomposition products effectively fill the voids within the electrode, while the gradual disintegration of the L–Si structure contributes to the formation of a dense, conductive network. This process enhances lithium ion transport and exploits the capacitive storage benefits of layered silicon.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"60 76","pages":"Pages 10500-10503"},"PeriodicalIF":4.3000,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734524017725","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Layered silicon (L–Si) anodes are celebrated for their high theoretical capacity but face significant challenges regarding safety and material purity during preparation. This study addresses these challenges by employing NH4Cl–CaSi2 as the raw material in a gas-solid de-alloying process, which enhances both safety and purity compared to traditional methods. The L–Si anodes produced demonstrate outstanding electrochemical performance, delivering a high reversible lithium storage capacity of 1497.7 mA h g−1 at a current density of 0.5 A g−1, and exhibiting stable performance over 1200 charge–discharge cycles. In situ and ex situ characterizations reveal that electrolyte decomposition products effectively fill the voids within the electrode, while the gradual disintegration of the L–Si structure contributes to the formation of a dense, conductive network. This process enhances lithium ion transport and exploits the capacitive storage benefits of layered silicon.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.