A strongly coupled FeS2@TiO2 heterostructure with an island-like structure for high-efficiency lithium storage†

IF 6 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Luchao Yue, Wei Song, Yu Feng, Lixin Zhang, Ruina Shi, Lin Jiang, Jing Song, Guisheng Qi and Xuping Sun
{"title":"A strongly coupled FeS2@TiO2 heterostructure with an island-like structure for high-efficiency lithium storage†","authors":"Luchao Yue, Wei Song, Yu Feng, Lixin Zhang, Ruina Shi, Lin Jiang, Jing Song, Guisheng Qi and Xuping Sun","doi":"10.1039/D4QM00675E","DOIUrl":null,"url":null,"abstract":"<p >Titanium dioxide (TiO<small><sub>2</sub></small>) has garnered substantial interest as a potential anode material for advanced lithium-ion batteries (LIBs) owing to its superior structural stability, rapid pseudocapacitive kinetics, economic viability, and nontoxicity. Nevertheless, its practical application is significantly curtailed by the limitations in specific capacity and inferior intrinsic electronic conductivity. Although carbonaceous materials can enhance electronic conductivity to a certain extent, the deficiency in lithium storage capacity persists as a critical issue requiring amelioration. Herein, we introduce a unique heterostructure composed of TiO<small><sub>2</sub></small> nanobelts and FeS<small><sub>2</sub></small> nanoparticles, fabricated through a hydrothermal method, followed by cation exchange and a sulfidation process. For the heterostructure, FeS<small><sub>2</sub></small> nanoparticles are <em>in situ</em> anchored on the surface of TiO<small><sub>2</sub></small> nanobelts, forming an island-like p–n heterostructure (FeS<small><sub>2</sub></small>@TiO<small><sub>2</sub></small>). The incorporation of FeS<small><sub>2</sub></small> featuring high specific capacity facilitates the emergence of a built-in electric field at the interface between the two compounds, thereby expediting the charge transport during the lithium storage process. As a consequence, the island-like FeS<small><sub>2</sub></small>@TiO<small><sub>2</sub></small> p–n heterostructure delivers a remarkable reversible capacity of 584.9 mA h g<small><sup>−1</sup></small> at 1.0 A g<small><sup>−1</sup></small> after 300 cycles, along with superior rate capability (average capacity of 204.8 mA h g<small><sup>−1</sup></small> at 10.0 A g<small><sup>−1</sup></small>). Even at 5.0 A g<small><sup>−1</sup></small>, the FeS<small><sub>2</sub></small>@TiO<small><sub>2</sub></small> anode maintains a substantial specific capacity of 251.2 mA h g<small><sup>−1</sup></small> over 3000 cycles, revealing its outstanding cycling stability. This study suggests that the design strategy coupling TiO<small><sub>2</sub></small> with other materials that possess high specific capacity could be broadly applied to enhance its electrochemical performance.</p>","PeriodicalId":86,"journal":{"name":"Materials Chemistry Frontiers","volume":" 5","pages":" 800-808"},"PeriodicalIF":6.0000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Chemistry Frontiers","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/qm/d4qm00675e","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Titanium dioxide (TiO2) has garnered substantial interest as a potential anode material for advanced lithium-ion batteries (LIBs) owing to its superior structural stability, rapid pseudocapacitive kinetics, economic viability, and nontoxicity. Nevertheless, its practical application is significantly curtailed by the limitations in specific capacity and inferior intrinsic electronic conductivity. Although carbonaceous materials can enhance electronic conductivity to a certain extent, the deficiency in lithium storage capacity persists as a critical issue requiring amelioration. Herein, we introduce a unique heterostructure composed of TiO2 nanobelts and FeS2 nanoparticles, fabricated through a hydrothermal method, followed by cation exchange and a sulfidation process. For the heterostructure, FeS2 nanoparticles are in situ anchored on the surface of TiO2 nanobelts, forming an island-like p–n heterostructure (FeS2@TiO2). The incorporation of FeS2 featuring high specific capacity facilitates the emergence of a built-in electric field at the interface between the two compounds, thereby expediting the charge transport during the lithium storage process. As a consequence, the island-like FeS2@TiO2 p–n heterostructure delivers a remarkable reversible capacity of 584.9 mA h g−1 at 1.0 A g−1 after 300 cycles, along with superior rate capability (average capacity of 204.8 mA h g−1 at 10.0 A g−1). Even at 5.0 A g−1, the FeS2@TiO2 anode maintains a substantial specific capacity of 251.2 mA h g−1 over 3000 cycles, revealing its outstanding cycling stability. This study suggests that the design strategy coupling TiO2 with other materials that possess high specific capacity could be broadly applied to enhance its electrochemical performance.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Materials Chemistry Frontiers
Materials Chemistry Frontiers Materials Science-Materials Chemistry
CiteScore
12.00
自引率
2.90%
发文量
313
期刊介绍: Materials Chemistry Frontiers focuses on the synthesis and chemistry of exciting new materials, and the development of improved fabrication techniques. Characterisation and fundamental studies that are of broad appeal are also welcome. This is the ideal home for studies of a significant nature that further the development of organic, inorganic, composite and nano-materials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信