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  5. Oxygen Vacancy Introduction to Increase the Capacity and Voltage Retention in Li‐Excess Cathode Materials

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Article
en
2022

Oxygen Vacancy Introduction to Increase the Capacity and Voltage Retention in Li‐Excess Cathode Materials

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en
2022
Vol 4 (1)
Vol. 4
DOI: 10.1002/sstr.202200343

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Gerbrand Ceder
Gerbrand Ceder

University of California, Berkeley

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Jianping Huang
Peichen Zhong
Yang Ha
+5 more

Abstract

Li‐rich rocksalt oxides are promising cathode materials for lithium‐ion batteries due to their large capacity and energy density, and their ability to use earth‐abundant elements. The excess Li in the rocksalt, needed to achieve good Li transport, reduces the theoretical transition metal redox capacity and introduces a labile oxygen state, both of which lead to increased oxygen oxidation and concomitant capacity loss with cycling. Herein, it is demonstrated that substituting the labile oxygen in Li‐rich cation‐disordered rocksalt materials with a vacancy is an effective strategy to inhibit oxygen oxidation. It is found that the oxygen vacancy in cation‐disordered lithium manganese oxide favors high Li coordination thereby reducing the concentration of unhybridized oxygen states, while increasing the theoretical Mn capacity. It is shown that in the vacancy‐containing compound, synthesized by ball milling, the Mn valence is lowered to less than +3, providing access to more than 300 mAh g −1 capacity from the Mn 2+ /Mn 4+ redox reservoir. The increased transition metal redox and decreased O oxidation are found to improve the capacity and voltage retention, indicating that oxygen vacancy creation to remove the most vulnerable oxygen ions and reduce transition metal valence provides a new opportunity for the design of high‐performance Li‐rich rocksalt cathodes.

How to cite this publication

Jianping Huang, Peichen Zhong, Yang Ha, Zhengyan Lun, Yaosen Tian, Mahalingam Balasubramanian, Wanli Yang, Gerbrand Ceder (2022). Oxygen Vacancy Introduction to Increase the Capacity and Voltage Retention in Li‐Excess Cathode Materials. , 4(1), DOI: https://doi.org/10.1002/sstr.202200343.

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Publication Details

Type

Article

Year

2022

Authors

8

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1002/sstr.202200343

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