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Title: | Enhanced Li-ion intercalation kinetics and lattice oxygen stability in single-crystalline Ni-rich Co-poor layered cathodes | ||||||||||
Author: | Zhang, Hujun; Qin, Li; Sedlačík, Michal; Sáha, Petr; Cheng, Qilin; Yu, Haifeng; Jiang, Hao | ||||||||||
Document type: | Peer-reviewed article (English) | ||||||||||
Source document: | Journal of Materials Chemistry A. 2024, vol. 2024, issue 12, p. 3682-3688 | ||||||||||
ISSN: | 2050-7488 (Sherpa/RoMEO, JCR) | ||||||||||
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DOI: | https://doi.org/10.1039/d3ta07156a | ||||||||||
Abstract: | Single-crystalline nickel-rich cobalt-poor layered oxides are promising cathode materials for lithium-ion batteries due to their high safety and competitive cost. However, the severe cation disorder and lithium/oxygen (Li/O) loss during the high-temperature calcination process result in slow Li-ion diffusion and inferior O stability. Herein, a LiNi0.85Co0.05Mn0.10O2 (NCM85) single-crystalline cathode was prepared at relatively lower lithiation temperatures by barium/aluminum (Ba/Al) co-doping. The increase in the c-axis caused by Ba doping with a larger ion radius and the reduction in Li/Ni disorder can enhance the Li-ion diffusion kinetics, while the strong Ba-O and Al-O bonds considerably boost the lattice O stability to alleviate O escape during the charging process. The optimized cathode exhibits a high reversible capacity of 206.5 mA h g−1 at 0.1C and 115.6 mA h g−1 at 5C. Impressively, 87.5% of initial capacity is still maintained after 500 cycles at 1C in a pouch-type full cell. This finding provides a viable and flexible method to resolve the kinetics and stability issues of other layered oxide cathodes. | ||||||||||
Full text: | https://pubs.rsc.org/en/content/articlelanding/2024/ta/d3ta07156a | ||||||||||
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