优化 LiFePO4 中的锂离子扩散:掺杂 Ti4+ 对高速率能力和电化学稳定性的影响

IF 2.4 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2025-01-13 DOI:10.1007/s11581-025-06075-w
Tai Kang, Yanshuang Meng, Xingzhong Liu
{"title":"优化 LiFePO4 中的锂离子扩散:掺杂 Ti4+ 对高速率能力和电化学稳定性的影响","authors":"Tai Kang,&nbsp;Yanshuang Meng,&nbsp;Xingzhong Liu","doi":"10.1007/s11581-025-06075-w","DOIUrl":null,"url":null,"abstract":"<div><p>This study aims to enhance the electrochemical performance of lithium iron phosphate (LiFePO<sub>4</sub>) cathode materials through Ti<sup>4+</sup> ion doping strategy, in order to address the challenges of low conductivity and slow lithium-ion diffusion rates. We synthesized iron phosphate precursors with different Ti<sup>4+</sup> doping levels using the chemical precipitation method and successfully prepared LiFePO<sub>4</sub> material by the high-temperature solid-phase method, which improves the uniformity of ion doping. By systematically studying the effect of Ti<sup>4+</sup> doping on material structure, morphology, and electrochemical properties, we found that Ti<sup>4+</sup> successfully entered the LiFePO4, without affecting its morphology or lattice. This structural change had a positive impact on the electrochemical performance of the material. The discharge-specific capacities of 2% Ti<sup>4+</sup>-doped LiFePO<sub>4</sub> samples at 0.1, 1, 5, and 10 C reached 161.0, 132.4, 105.3, and 92.6 mAh g<sup>−1</sup>, respectively, demonstrating excellent electrochemical performance. Its lithium-ion diffusion coefficient was also significantly better than that of other samples. The comprehensive analysis results from XRD, SEM, XPS, and electrochemical testing show that the appropriate amount of Ti<sup>4+</sup> doping optimizes the diffusion path of lithium-ions and increases the charge transfer rate, thereby significantly improving the electrochemical performance of LiFePO<sub>4</sub>. This discovery not only enriches the understanding of the modification mechanism of lithium-ion battery cathode materials, but also provides important scientific basis and practical guidance for the development of high-performance lithium-ion battery cathode materials.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 3","pages":"2419 - 2428"},"PeriodicalIF":2.4000,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimizing lithium-ion diffusion in LiFePO4: the impact of Ti4+ doping on high-rate capability and electrochemical stability\",\"authors\":\"Tai Kang,&nbsp;Yanshuang Meng,&nbsp;Xingzhong Liu\",\"doi\":\"10.1007/s11581-025-06075-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This study aims to enhance the electrochemical performance of lithium iron phosphate (LiFePO<sub>4</sub>) cathode materials through Ti<sup>4+</sup> ion doping strategy, in order to address the challenges of low conductivity and slow lithium-ion diffusion rates. We synthesized iron phosphate precursors with different Ti<sup>4+</sup> doping levels using the chemical precipitation method and successfully prepared LiFePO<sub>4</sub> material by the high-temperature solid-phase method, which improves the uniformity of ion doping. By systematically studying the effect of Ti<sup>4+</sup> doping on material structure, morphology, and electrochemical properties, we found that Ti<sup>4+</sup> successfully entered the LiFePO4, without affecting its morphology or lattice. This structural change had a positive impact on the electrochemical performance of the material. The discharge-specific capacities of 2% Ti<sup>4+</sup>-doped LiFePO<sub>4</sub> samples at 0.1, 1, 5, and 10 C reached 161.0, 132.4, 105.3, and 92.6 mAh g<sup>−1</sup>, respectively, demonstrating excellent electrochemical performance. Its lithium-ion diffusion coefficient was also significantly better than that of other samples. The comprehensive analysis results from XRD, SEM, XPS, and electrochemical testing show that the appropriate amount of Ti<sup>4+</sup> doping optimizes the diffusion path of lithium-ions and increases the charge transfer rate, thereby significantly improving the electrochemical performance of LiFePO<sub>4</sub>. This discovery not only enriches the understanding of the modification mechanism of lithium-ion battery cathode materials, but also provides important scientific basis and practical guidance for the development of high-performance lithium-ion battery cathode materials.</p></div>\",\"PeriodicalId\":599,\"journal\":{\"name\":\"Ionics\",\"volume\":\"31 3\",\"pages\":\"2419 - 2428\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-01-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ionics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11581-025-06075-w\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ionics","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11581-025-06075-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimizing lithium-ion diffusion in LiFePO4: the impact of Ti4+ doping on high-rate capability and electrochemical stability

This study aims to enhance the electrochemical performance of lithium iron phosphate (LiFePO4) cathode materials through Ti4+ ion doping strategy, in order to address the challenges of low conductivity and slow lithium-ion diffusion rates. We synthesized iron phosphate precursors with different Ti4+ doping levels using the chemical precipitation method and successfully prepared LiFePO4 material by the high-temperature solid-phase method, which improves the uniformity of ion doping. By systematically studying the effect of Ti4+ doping on material structure, morphology, and electrochemical properties, we found that Ti4+ successfully entered the LiFePO4, without affecting its morphology or lattice. This structural change had a positive impact on the electrochemical performance of the material. The discharge-specific capacities of 2% Ti4+-doped LiFePO4 samples at 0.1, 1, 5, and 10 C reached 161.0, 132.4, 105.3, and 92.6 mAh g−1, respectively, demonstrating excellent electrochemical performance. Its lithium-ion diffusion coefficient was also significantly better than that of other samples. The comprehensive analysis results from XRD, SEM, XPS, and electrochemical testing show that the appropriate amount of Ti4+ doping optimizes the diffusion path of lithium-ions and increases the charge transfer rate, thereby significantly improving the electrochemical performance of LiFePO4. This discovery not only enriches the understanding of the modification mechanism of lithium-ion battery cathode materials, but also provides important scientific basis and practical guidance for the development of high-performance lithium-ion battery cathode materials.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
×
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