Fan Wang , Pengfei Lou , Suqin Chen, Zihao Cha, Xiaoyan Zhang
{"title":"Preparation and electrochemical lithium storage properties of Cu2SnS3@C nanocomposites","authors":"Fan Wang , Pengfei Lou , Suqin Chen, Zihao Cha, Xiaoyan Zhang","doi":"10.1016/j.jssc.2025.125326","DOIUrl":null,"url":null,"abstract":"<div><div>Cu<sub>2</sub>SnS<sub>3</sub>, recognized as a conversion and alloy type anode material for lithium-ion batteries, possesses a high theoretical specific capacity of 784 mAh g<sup>−1</sup> and exhibits a distinct lithium storage mechanism. However, its intrinsically low electrical conductivity and pronounced volume expansion during cycling pose significant challenges to its practical battery performance. To address these limitations, Cu<sub>2</sub>SnS<sub>3</sub>@C (CTS@C) nanomaterials were synthesized by a one-step microwave-assisted method, utilizing ethylene glycol as a solvent and glucose as a carbon precursor. The incorporation of a carbon coating has been demonstrated to markedly improve the conductivity of the material and mitigate the volume expansion associated with lithium insertion and extraction. Electrochemical tests revealed that the CTS@C electrode exhibits superior electrochemical performance. Specifically, the CTS@C electrodes exhibited an initial discharge capacity of 612.8 mAh g<sup>−1</sup>, with a retention of 295.8 mAh g<sup>−1</sup> after 500 cycles at a current density of 500 mA g<sup>−1</sup>. The carbon coating not only effectively enhances the conductivity of the electrode material, but also accelerates the electrochemical reaction rate, and enhances the diffusion rate of lithium ions, thereby significantly improving the electrochemical performance of the battery.</div></div>","PeriodicalId":378,"journal":{"name":"Journal of Solid State Chemistry","volume":"347 ","pages":"Article 125326"},"PeriodicalIF":3.2000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid State Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022459625001495","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Cu2SnS3, recognized as a conversion and alloy type anode material for lithium-ion batteries, possesses a high theoretical specific capacity of 784 mAh g−1 and exhibits a distinct lithium storage mechanism. However, its intrinsically low electrical conductivity and pronounced volume expansion during cycling pose significant challenges to its practical battery performance. To address these limitations, Cu2SnS3@C (CTS@C) nanomaterials were synthesized by a one-step microwave-assisted method, utilizing ethylene glycol as a solvent and glucose as a carbon precursor. The incorporation of a carbon coating has been demonstrated to markedly improve the conductivity of the material and mitigate the volume expansion associated with lithium insertion and extraction. Electrochemical tests revealed that the CTS@C electrode exhibits superior electrochemical performance. Specifically, the CTS@C electrodes exhibited an initial discharge capacity of 612.8 mAh g−1, with a retention of 295.8 mAh g−1 after 500 cycles at a current density of 500 mA g−1. The carbon coating not only effectively enhances the conductivity of the electrode material, but also accelerates the electrochemical reaction rate, and enhances the diffusion rate of lithium ions, thereby significantly improving the electrochemical performance of the battery.
期刊介绍:
Covering major developments in the field of solid state chemistry and related areas such as ceramics and amorphous materials, the Journal of Solid State Chemistry features studies of chemical, structural, thermodynamic, electronic, magnetic, and optical properties and processes in solids.