Ultralow Iridium Dopant (&lt;0.5 at. %) in LiNiO<sub>2</sub> Oxide for Improved Structure Stability

The structural instability of LiNiO<sub>2</sub> (LNO) during charge-discharge cycles is a significant challenge in developing high-capacity cathodes for lithium-ion batteries. In this work, we doped a trace amount of Ir (0.5 at. %) into the LNO structure (LNO-Ir) to enhance its stability. Operando XRD reveals that the formation of the H3 phase, which typically occurs at high voltages upon delithiation in LNO, was completely suppressed in the LNO-Ir cathode, resulting in a minimal lattice contraction (<0.1 Å). TEM images reveal that cation migration and surface structural reconstruction can also be significantly reduced in LNO-Ir. DFT calculations confirm that Ir doping not only increases the formation energy of oxygen vacancies but also the energy barrier for Ni migration. Collectively, these effects endow the LNO-Ir cathode with promising structural stability over extended cycling, highlighting a potential strategy for stabilizing high-nickel-content cathodes.

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Publication Details

Journal
Nano Letters
Published
2025-04-01
DOI
https://doi.org/10.1021/acs.nanolett.4c05411
Citations
1
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.73

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article

Ultralow Iridium Dopant (<0.5 at. %) in LiNiO2 Oxide for Improved Structure Stability

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article

Ultralow Iridium Dopant (<0.5 at. %) in LiNiO2 Oxide for Improved Structure Stability

Jianwen Wang, Yixiang Li, Chunzhen Yang, Haobin Song, Wen J. Li, Jiajun Chen, Hui Ying Yang, Long Gu, Chao Wang, Yuying Zhang, Weixin Chen, Wencheng Su
article en
1 citations

Abstract

The structural instability of LiNiO<sub>2</sub> (LNO) during charge-discharge cycles is a significant challenge in developing high-capacity cathodes for lithium-ion batteries. In this work, we doped a trace amount of Ir (0.5 at. %) into the LNO structure (LNO-Ir) to enhance its stability. Operando XRD reveals that the formation of the H3 phase, which typically occurs at high voltages upon delithiation in LNO, was completely suppressed in the LNO-Ir cathode, resulting in a minimal lattice contraction (<0.1 Å). TEM images reveal that cation migration and surface structural reconstruction can also be significantly reduced in LNO-Ir. DFT calculations confirm that Ir doping not only increases the formation energy of oxygen vacancies but also the energy barrier for Ni migration. Collectively, these effects endow the LNO-Ir cathode with promising structural stability over extended cycling, highlighting a potential strategy for stabilizing high-nickel-content cathodes.

Nano LettersVol. 25(15)
Singapore University of Technology and Design (SG), Sun Yat-sen University (CN)
National Natural Science Foundation of China, China Scholarship Council
Affordable and clean energy
Openalex Percentile: Top 30%
Advancements in Battery Materials
0.73
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