Enhanced Li-ion intercalation kinetics and lattice oxygen stability in single-crystalline Ni-rich Co-poor layered cathodes

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...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2024-02, Vol.12 (6), p.3682-3688
Hauptverfasser: Zhang, Hujun, Qin, Li, Sedlacik, Michal, Saha, Petr, Cheng, Qilin, Yu, Haifeng, Jiang, Hao
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Sprache:eng
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Zusammenfassung: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 LiNi 0.85 Co 0.05 Mn 0.10 O 2 (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. Ba/Al co-doping effectively lower the calcination temperature, greatly reduces Li/Ni mixing and expands the c -axis parameter, and stabilizes the lattice oxygen, resulting in enhanced Li-diffusion kinetics and excellent cycle life.
ISSN:2050-7488
2050-7496
DOI:10.1039/d3ta07156a