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Effective Oxygen‐Deficient Li 4 Ti 5 O 12 Anode Material Displaying Excellent Rate Performance and Outstanding Cyclic Stability

Currently, developing materials with high power capability is crucial to the rapid deployment of electric vehicles. The Li 4 Ti 5 O 12 (LTO) anode material with zero strain rate upon lithium insertion and extraction. The successful implementation of this anode material depends on strategies to overc...

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Bibliographic Details
Published in:ChemistrySelect (Weinheim) 2024-10, Vol.9 (37)
Main Authors: Pratheeksha, P. M., Sivakanali, S., Kashyap, Shreyas J., Chandra, Gowthami, Joseph, D. Paul, Vijay, R., Rao, T. N., Anandan, S.
Format: Article
Language:English
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Summary:Currently, developing materials with high power capability is crucial to the rapid deployment of electric vehicles. The Li 4 Ti 5 O 12 (LTO) anode material with zero strain rate upon lithium insertion and extraction. The successful implementation of this anode material depends on strategies to overcome the low electronic and ionic conductivity. In this study, Li 4 Ti 5 O 12 was synthesized using solid‐state approach in which different phases (anatase and rutile) of TiO 2 as precursors were used. X‐ray photoelectron spectroscopy (XPS) and Raman analysis confirmed the formation of oxygen vacancies with the existence of Ti 3+ ions, which is believed to greatly enhance the electronic conductivity of Li 4 Ti 5 O 12 . The electrochemical performance revealed that the rutile TiO 2 precursor concentration significantly affects the resultant Li 4 Ti 5 O 12 capacity and power capability. The Li 4 Ti 5 O 12 synthesized using 80% anatase and 20% rutile TiO 2 (N2‐LTO) exhibits a specific capacity of 169, 145, 140, 133, 122, 101, and 84 mAh g −1 at 1C, 3C, 5C, 7C, 10C, 20C, and 30C. In addition, LFP||N2‐LTO pouch‐cell was fabricated which showed promising results with 95% capacity retention after 1000 cycles at 1C rate. The oxygen vacancies created due to the presence of Ti 3+ /Ti 4+ mixed valances and reduced particle size for faster lithium‐ion diffusion significantly enhanced the overall electrochemical performance.
ISSN:2365-6549
2365-6549
DOI:10.1002/slct.202403479