Lattice plainification flattens the crystal structure of nickel-rich layered cathodes
The extremely fast charging/discharging of nickel-rich LiNi<sub><i>x</i></sub>Co<sub><i>y</i></sub>Mn<sub>1-<i>x</i>-<i>y</i></sub>O<sub>2</sub> (NCM) cathodes has raised concerns about rapid capacity decay. The birth defects and fragile lattice result in the sluggish Li<sup>+</sup> diffusion kinetics and unfavorable structural degradation. Moreover, lattice strain, mechanical failures, surface reconstruction, and interfacial side reactions accelerate the decay process. Here, a proof-of-principle study of the lattice plainification (LP) strategy in a high-nickel NCM cathode is reported. The introduction of Al and Zr in transition metal layers by a wet chemistry and calcination method enables the simplification of the complex lattice structures to obtain an order phase and repair the various defects of NCM, thereby enhancing the lithium-ion transport. The modified LP-NCM exhibits a high initial discharge capacity of 157.3 mAh g<sup>-1</sup> with a capacity retention of 81% after 300 cycles at a 5C rate, significantly outperforming the pristine counterpart (50.9%). The LP-NCM/Gr pouch cells presented impressive cycling performance, achieving 80% capacity retention over 1000 cycles at 1C, which far surpasses the performance of the pristine NCM. Our method eliminates the rocksalt and disordered phases, and suppresses oxygen, lithium, and transition metal vacancies, as well as Li/Ni mixing. LP-NCM after cycling exhibits nanopores rather than cracks of pristine NCM. Our investigations reveal that the lattice plainification design approach flattens and toughens up the crystal lattice, which contributes to robust structural stability and improves the structure degradation, mechanical failures, and gas release. Our findings underscore the importance of lattice engineering and demonstrate the potential of the lattice plainification strategy for designing high-performance cathodes.
Authors
- Runsheng Yu (ORCID: https://orcid.org/0000-0001-6417-3910)
- Chengyu Li (ORCID: https://orcid.org/0009-0002-1947-5543)
- Jianjun Ma (ORCID: https://orcid.org/0000-0002-0016-6313)
- Cairong Jiang (ORCID: https://orcid.org/0000-0001-8499-4062)
- Wenge Yang (ORCID: https://orcid.org/0000-0001-8436-8731)
- Zhihao Sun (ORCID: https://orcid.org/0000-0001-5753-6680)
- Dongliang Chao (ORCID: https://orcid.org/0000-0001-7793-0044)
- Pengcheng Li (ORCID: https://orcid.org/0000-0002-1778-7095)
- Zhuo Peng
- Xiang Gao (ORCID: https://orcid.org/0000-0001-9277-1432)
- Yongjin Chen (ORCID: https://orcid.org/0000-0003-2540-6376)
- Jun Wang (ORCID: https://orcid.org/0009-0008-4092-479X)
Institutions
- Fudan University (CN)
- Chengdu University (CN)
- Tianjin Energy Investment Group (China) (CN)
- Center for High Pressure Science and Technology Advanced Research (CN)
- Shanghai Research Institute of Materials (CN)
- Collaborative Innovation Center of Chemistry for Energy Materials (CN)
- Xiangtan University (CN)
- Sichuan University of Science and Engineering (CN)
Publication Details
- Journal
- Materials Horizons
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5mh00975h
- Citations
- 2
- Primary Topic
- Advancements in Battery Materials
- Type
- article
- Field-Weighted Citation Impact
- 1.46
Funders
- National Natural Science Foundation of China