Reinforcing the stability of cobalt-free lithium-rich layered oxides via Li-poor Ni-rich surface transformation

Abstract

Lithium-rich layered oxides are one of the most promising cathode materials for lithium-ion batteries due to their super-high capacity and low cost. However, extensive surface destruction, which originates from side reactions between the oxidative surface and the reductive electrolyte, leads to fast capacity fading along with the inevitable voltage drop. Here, we report a cobalt-free lithium-rich layered oxide Li1.2Mn0.6Ni0.2O2 (LMNO) with an electrochemically stable Li-poor nickel-rich surface by simple excessive calcination treatment. We show that the Li-poor nickel-rich surface possesses a rock-salt structure, greatly enhancing the interface stability and suppressing surface side reactions and Mn-ion dissolution. As a result, the modified LMNO, with a Li-poor nickel-rich surface of 4.2 nm thickness, can gain an improved resistance against extensive surface destruction, which delivers a stable capacity of 239.5 mA h g−1 after 100 cycles at 0.1C and a mitigated voltage decay of only 3.885 mV per cycle. This work provides a facile and feasible strategy to enhance the surface properties of LMNO cathode materials without using heteroatom dopants or heterogeneous coatings, which is conducive to the design of high-performance cathode materials.

Graphical abstract: Reinforcing the stability of cobalt-free lithium-rich layered oxides via Li-poor Ni-rich surface transformation

Supplementary files

Article information

Article type
Paper
Submitted
29 feb 2024
Accepted
20 jun 2024
First published
25 jun 2024

J. Mater. Chem. A, 2024, Advance Article

Reinforcing the stability of cobalt-free lithium-rich layered oxides via Li-poor Ni-rich surface transformation

G. Chen, L. Yu, Y. Gan, C. Zeng, X. Cheng, L. Xian, L. Li, Q. Zhang, C. Dai, Y. Li, R. Zhao, Z. Yang, J. Qiu, W. Tang, W. Zeng, F. Liu, J. Wan and J. Yang, J. Mater. Chem. A, 2024, Advance Article , DOI: 10.1039/D4TA01403K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements