{"title":"In situ formation of NaTi2(PO4)3 coating layers to enhance the high-temperature performance of NaNi1/3Fe1/3Mn1/3O2 cathode materials†","authors":"Wu Meng, Huajun Guo, Zhixing Wang, Guangchao Li, Bichao Wu, Jiexi Wang, Wenjie Peng, Xinhai Li, Hui Duan and Guochun Yan","doi":"10.1039/D4MH01766H","DOIUrl":null,"url":null,"abstract":"<p >The insufficient structure and interfacial stability of O3-type layered oxide cathode materials hinder their practical application in sodium-ion batteries, particularly at high temperatures. In this study, a thin, island-like NaTi<small><sub>2</sub></small>(PO<small><sub>4</sub></small>)<small><sub>3</sub></small> coating layer (∼15 nm) is constructed on the surface of NaNi<small><sub>1/3</sub></small>Fe<small><sub>1/3</sub></small>Mn<small><sub>1/3</sub></small>O<small><sub>2</sub></small> through an <em>in situ</em> reaction involving nano-TiO<small><sub>2</sub></small>, Na<small><sub>2</sub></small>CO<small><sub>3</sub></small> and NH<small><sub>4</sub></small>H<small><sub>2</sub></small>PO<small><sub>4</sub></small>. During the high-temperature calcination process, partial Ti-atom diffusion into the NaNi<small><sub>1/3</sub></small>Fe<small><sub>1/3</sub></small>Mn<small><sub>1/3</sub></small>O<small><sub>2</sub></small> lattice results in the expansion of the interslab of the sodium layer and a reduction in lattice oxygen vacancies. Benefitting from the stable NaTi<small><sub>2</sub></small>(PO<small><sub>4</sub></small>)<small><sub>3</sub></small>-modified interface and enhanced structural stability, the NaNi<small><sub>1/3</sub></small>Fe<small><sub>1/3</sub></small>Mn<small><sub>1/3</sub></small>O<small><sub>2</sub></small> coated with 2 wt% NaTi<small><sub>2</sub></small>(PO<small><sub>4</sub></small>)<small><sub>3</sub></small> exhibits optimal cycle stability at high temperature. It retains 90.3% of its initial capacity after 100 cycles at 0.5C (1C = 130 mA g<small><sup>−1</sup></small>, 45 °C). This dual-modification strategy, obtained from a facile approach, has the potential to facilitate the practical application of O3-type layered oxide cathode materials.</p>","PeriodicalId":87,"journal":{"name":"Materials Horizons","volume":" 9","pages":" 3160-3170"},"PeriodicalIF":10.7000,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Horizons","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/mh/d4mh01766h","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
The insufficient structure and interfacial stability of O3-type layered oxide cathode materials hinder their practical application in sodium-ion batteries, particularly at high temperatures. In this study, a thin, island-like NaTi2(PO4)3 coating layer (∼15 nm) is constructed on the surface of NaNi1/3Fe1/3Mn1/3O2 through an in situ reaction involving nano-TiO2, Na2CO3 and NH4H2PO4. During the high-temperature calcination process, partial Ti-atom diffusion into the NaNi1/3Fe1/3Mn1/3O2 lattice results in the expansion of the interslab of the sodium layer and a reduction in lattice oxygen vacancies. Benefitting from the stable NaTi2(PO4)3-modified interface and enhanced structural stability, the NaNi1/3Fe1/3Mn1/3O2 coated with 2 wt% NaTi2(PO4)3 exhibits optimal cycle stability at high temperature. It retains 90.3% of its initial capacity after 100 cycles at 0.5C (1C = 130 mA g−1, 45 °C). This dual-modification strategy, obtained from a facile approach, has the potential to facilitate the practical application of O3-type layered oxide cathode materials.