Jyun-Siang Wang , Guan-Bo Liao , Zhen Chong , Cheng-Hsun Ho , Po-Chia Huang , Jow-Lay Huang , Chia-Chin Chang , Dipti R. Sahu , Yu-Min Shen
{"title":"碳包覆非化学计量TiOx在锂离子电池阳极快速充电中的应用——原位XRD研究","authors":"Jyun-Siang Wang , Guan-Bo Liao , Zhen Chong , Cheng-Hsun Ho , Po-Chia Huang , Jow-Lay Huang , Chia-Chin Chang , Dipti R. Sahu , Yu-Min Shen","doi":"10.1016/j.jelechem.2025.119127","DOIUrl":null,"url":null,"abstract":"<div><div>Lithium-ion batteries have emerged as a promising solution for electric vehicles, owing to their high specific capacity. However, the commonly used carbon anodes suffer from poor high-rate capability, which restricts their wider application. In this work carbon-coated nonstoichiometric TiO<sub>x</sub> (C@TiO<sub>1</sub><em>.</em><sub>944</sub>) nanopowder was synthesized using a two-step annealing method. The performances of batteries show that the C@TiO<sub>1.944</sub> electrode has a remarkable initial capacity of 246.3 mAh/g with 71.5 % ICE and retains 166.2 mAh/g at a rate of 0.2C with 100 % CE and 109.0 mAh/g at 5C after formation. In contrast, the TiO<em>x</em> battery's initial capacity is 264.3 mAh/g with a 67.4 % ICE with a retention of 156.6 mAh/g at the same rate and 79.2 mAh/g at a discharge rate of 5C. Additionally, in situ X-ray diffraction (XRD) experiments was conducted with a potentiostat for elucidating the reaction mechanism which enables to track the phase transition in real-time during charge and discharge. The carbon coating protects the inner TiO<em>x</em> core from phase transition and lattice distortion occurs when Li ions are intercalated in the rutile TiO<sub>2</sub> matrix. The Li storage mechanism of rutile TiO<sub>2</sub> indicates it is not phase-transformed that can be taken as extra evidence for the high Coulombic efficiency. Further, the carbon coating enhanced the Coulombic efficiency by preventing dead Li ions while retaining in the anatase phase. The results shows that carbon-coated nonstoichiometric TiO<sub>2</sub> (C@TiO<em>x</em>) used in LIBs will be a solution for rapid charge application.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"988 ","pages":"Article 119127"},"PeriodicalIF":4.1000,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Carbon-coated nonstoichiometric TiOx for application of Li-ion battery anodes in fast charging-in situ XRD study\",\"authors\":\"Jyun-Siang Wang , Guan-Bo Liao , Zhen Chong , Cheng-Hsun Ho , Po-Chia Huang , Jow-Lay Huang , Chia-Chin Chang , Dipti R. Sahu , Yu-Min Shen\",\"doi\":\"10.1016/j.jelechem.2025.119127\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Lithium-ion batteries have emerged as a promising solution for electric vehicles, owing to their high specific capacity. However, the commonly used carbon anodes suffer from poor high-rate capability, which restricts their wider application. In this work carbon-coated nonstoichiometric TiO<sub>x</sub> (C@TiO<sub>1</sub><em>.</em><sub>944</sub>) nanopowder was synthesized using a two-step annealing method. The performances of batteries show that the C@TiO<sub>1.944</sub> electrode has a remarkable initial capacity of 246.3 mAh/g with 71.5 % ICE and retains 166.2 mAh/g at a rate of 0.2C with 100 % CE and 109.0 mAh/g at 5C after formation. In contrast, the TiO<em>x</em> battery's initial capacity is 264.3 mAh/g with a 67.4 % ICE with a retention of 156.6 mAh/g at the same rate and 79.2 mAh/g at a discharge rate of 5C. Additionally, in situ X-ray diffraction (XRD) experiments was conducted with a potentiostat for elucidating the reaction mechanism which enables to track the phase transition in real-time during charge and discharge. The carbon coating protects the inner TiO<em>x</em> core from phase transition and lattice distortion occurs when Li ions are intercalated in the rutile TiO<sub>2</sub> matrix. The Li storage mechanism of rutile TiO<sub>2</sub> indicates it is not phase-transformed that can be taken as extra evidence for the high Coulombic efficiency. Further, the carbon coating enhanced the Coulombic efficiency by preventing dead Li ions while retaining in the anatase phase. The results shows that carbon-coated nonstoichiometric TiO<sub>2</sub> (C@TiO<em>x</em>) used in LIBs will be a solution for rapid charge application.</div></div>\",\"PeriodicalId\":355,\"journal\":{\"name\":\"Journal of Electroanalytical Chemistry\",\"volume\":\"988 \",\"pages\":\"Article 119127\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-04-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Electroanalytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1572665725002012\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665725002012","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Carbon-coated nonstoichiometric TiOx for application of Li-ion battery anodes in fast charging-in situ XRD study
Lithium-ion batteries have emerged as a promising solution for electric vehicles, owing to their high specific capacity. However, the commonly used carbon anodes suffer from poor high-rate capability, which restricts their wider application. In this work carbon-coated nonstoichiometric TiOx (C@TiO1.944) nanopowder was synthesized using a two-step annealing method. The performances of batteries show that the C@TiO1.944 electrode has a remarkable initial capacity of 246.3 mAh/g with 71.5 % ICE and retains 166.2 mAh/g at a rate of 0.2C with 100 % CE and 109.0 mAh/g at 5C after formation. In contrast, the TiOx battery's initial capacity is 264.3 mAh/g with a 67.4 % ICE with a retention of 156.6 mAh/g at the same rate and 79.2 mAh/g at a discharge rate of 5C. Additionally, in situ X-ray diffraction (XRD) experiments was conducted with a potentiostat for elucidating the reaction mechanism which enables to track the phase transition in real-time during charge and discharge. The carbon coating protects the inner TiOx core from phase transition and lattice distortion occurs when Li ions are intercalated in the rutile TiO2 matrix. The Li storage mechanism of rutile TiO2 indicates it is not phase-transformed that can be taken as extra evidence for the high Coulombic efficiency. Further, the carbon coating enhanced the Coulombic efficiency by preventing dead Li ions while retaining in the anatase phase. The results shows that carbon-coated nonstoichiometric TiO2 (C@TiOx) used in LIBs will be a solution for rapid charge application.
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.