Chengjin Liu , Jiaxiang Wan , Linling Jiang , Zhicheng Yi , Zhiyan Wang , Jiajun Chen , Rui Li , Wei Xiao
{"title":"高效协同策略使高性能富镍单晶lini0.83 co0.11 mn0.060 o2阴极的界面和晶体结构稳定","authors":"Chengjin Liu , Jiaxiang Wan , Linling Jiang , Zhicheng Yi , Zhiyan Wang , Jiajun Chen , Rui Li , Wei Xiao","doi":"10.1016/j.electacta.2025.147469","DOIUrl":null,"url":null,"abstract":"<div><div>To address the structural and interfacial degradation of Ni-rich layered cathodes, a collaborative strategy combining Ti<sup>4+</sup> ions doping with <em>in situ</em>-formed Li<sub>3</sub>PO<sub>4</sub> coating is designed to regulate and optimize Ni-rich single-crystal LiNi<sub>0.83</sub>Co<sub>0.11</sub>Mn<sub>0.06</sub>O<sub>2</sub> (SC-NCM-TP) cathode. The introduced Ti<sup>4+</sup> ions not only strengthen the crystal framework and inhibit harmful phase transition by forming stronger Ti-O bonds, but also boost Li<sup>+</sup> ions kinetics by expanding migration channels. Moreover, a uniform Li<sub>3</sub>PO<sub>4</sub> conductive coating with a thickness of about 3 nm, generated by converting surface residual lithium salts through NH<sub>4</sub>H<sub>2</sub>PO<sub>4</sub> treatment, enhances cathode/electrolyte interfacial stability. Benefiting from these advantages, the SC-NCM-TP based cell demonstrates exceptional capacity retention ratio of 90.3 % at 25 °C and 84.6 % at 60 °C after 100 cycles under 1.0 <em>C</em>, and maintains excellent capacity retention ratio of 81.3 % after 200 cycles even at 5.0 <em>C</em>. Hence, this work sheds new light on the design of advanced single-crystal cathodes for lithium-ion batteries.</div></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"542 ","pages":"Article 147469"},"PeriodicalIF":5.6000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effective collaborative strategy enabling stable interphase and crystal structure for high-performance Ni-rich single-crystal LiNi0.83Co0.11Mn0.06O2 cathode\",\"authors\":\"Chengjin Liu , Jiaxiang Wan , Linling Jiang , Zhicheng Yi , Zhiyan Wang , Jiajun Chen , Rui Li , Wei Xiao\",\"doi\":\"10.1016/j.electacta.2025.147469\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>To address the structural and interfacial degradation of Ni-rich layered cathodes, a collaborative strategy combining Ti<sup>4+</sup> ions doping with <em>in situ</em>-formed Li<sub>3</sub>PO<sub>4</sub> coating is designed to regulate and optimize Ni-rich single-crystal LiNi<sub>0.83</sub>Co<sub>0.11</sub>Mn<sub>0.06</sub>O<sub>2</sub> (SC-NCM-TP) cathode. The introduced Ti<sup>4+</sup> ions not only strengthen the crystal framework and inhibit harmful phase transition by forming stronger Ti-O bonds, but also boost Li<sup>+</sup> ions kinetics by expanding migration channels. Moreover, a uniform Li<sub>3</sub>PO<sub>4</sub> conductive coating with a thickness of about 3 nm, generated by converting surface residual lithium salts through NH<sub>4</sub>H<sub>2</sub>PO<sub>4</sub> treatment, enhances cathode/electrolyte interfacial stability. Benefiting from these advantages, the SC-NCM-TP based cell demonstrates exceptional capacity retention ratio of 90.3 % at 25 °C and 84.6 % at 60 °C after 100 cycles under 1.0 <em>C</em>, and maintains excellent capacity retention ratio of 81.3 % after 200 cycles even at 5.0 <em>C</em>. Hence, this work sheds new light on the design of advanced single-crystal cathodes for lithium-ion batteries.</div></div>\",\"PeriodicalId\":305,\"journal\":{\"name\":\"Electrochimica Acta\",\"volume\":\"542 \",\"pages\":\"Article 147469\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-09-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Electrochimica Acta\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0013468625018262\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0013468625018262","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
Effective collaborative strategy enabling stable interphase and crystal structure for high-performance Ni-rich single-crystal LiNi0.83Co0.11Mn0.06O2 cathode
To address the structural and interfacial degradation of Ni-rich layered cathodes, a collaborative strategy combining Ti4+ ions doping with in situ-formed Li3PO4 coating is designed to regulate and optimize Ni-rich single-crystal LiNi0.83Co0.11Mn0.06O2 (SC-NCM-TP) cathode. The introduced Ti4+ ions not only strengthen the crystal framework and inhibit harmful phase transition by forming stronger Ti-O bonds, but also boost Li+ ions kinetics by expanding migration channels. Moreover, a uniform Li3PO4 conductive coating with a thickness of about 3 nm, generated by converting surface residual lithium salts through NH4H2PO4 treatment, enhances cathode/electrolyte interfacial stability. Benefiting from these advantages, the SC-NCM-TP based cell demonstrates exceptional capacity retention ratio of 90.3 % at 25 °C and 84.6 % at 60 °C after 100 cycles under 1.0 C, and maintains excellent capacity retention ratio of 81.3 % after 200 cycles even at 5.0 C. Hence, this work sheds new light on the design of advanced single-crystal cathodes for lithium-ion batteries.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.