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High-performance lithium-ion batteries (LIB) are important in powering emerging technologies. Cathodes are regarded as the bottleneck of increasing battery energy density, among which layered oxides are the most promising candidates for LIB. However, a limitation with layered oxides cathodes is the transition metal and Li site mixing, which significantly impacts battery capacity and cycling stability. Despite recent research on Li/Ni mixing, there is a lack of comprehensive understanding of the origin of cation mixing between the transition metal and Li; therefore, practical means to address it. Here, a critical review of cation mixing in layered cathodes has been provided, emphasising the understanding of cation mixing mechanisms and their impact on cathode material design. We list and compare advanced characterisation techniques to detect cation mixing in the material structure; examine methods to regulate the degree of cation mixing in layered oxides to boost battery capacity and cycling performance, and critically assess how these can be applied practically. An appraisal of future research directions, including superexchange interaction to stabilise structures and boost capacity retention has also been concluded. Findings will be of immediate benefit in the design of layered cathodes for high-performance rechargeable LIB and, therefore, of interest to researchers and manufacturers.

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Publication history

Received: 13 July 2022
Accepted: 21 September 2022
Published: 09 October 2022
Issue date: December 2023

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© 2022 Chongqing University.

Acknowledgements

Acknowledgements

J. X. Li acknowledges the University of Adelaide for providing scholarship to support the Doctor of Philosophy candidature. Dr G.M. Liang acknowledges the Australian Institute of Nuclear Science and Engineering (AINSE) Limited for providing financial assistance in the form of a Post Graduate Research Award (PGRA) to carry out this work. This work is supported by the Australian Research Council under grants DP200101862, DP210101486, and FL210100050.

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This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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