Effect of Mg and Zr co-doping on the Co-less Ni-rich cathode materials for advanced lithium-ion batteries

The Co-less Ni-rich (Ni ≥ 90 %) layered cathode materials are attracting attention because of their high specific capacity and relatively low cost. However, its application is hampered by low cycling stability and structural susceptibility to deterioration. To resolve these issues, the Li0.994Mg0.00...

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Veröffentlicht in:Journal of energy storage 2023-09, Vol.68, p.107777, Article 107777
Hauptverfasser: Luo, Zhongyuan, Hu, Guorong, Wang, Weigang, Peng, Zhongdong, Fang, Zijun, Zhao, Baibin, Li, Huan, Du, Ke, Cao, Yanbing
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Sprache:eng
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Zusammenfassung:The Co-less Ni-rich (Ni ≥ 90 %) layered cathode materials are attracting attention because of their high specific capacity and relatively low cost. However, its application is hampered by low cycling stability and structural susceptibility to deterioration. To resolve these issues, the Li0.994Mg0.006(Ni0.925Co0.03Mn0.045)0.996Zr0.004O2 (MZ-NCM) cathode material co-doped with magnesium and zirconium ions was synthesized by the solid-phase method through optimization of the formulation. The physicochemical properties of the materials were investigated in detail by XRD, SEM, EDS, XPS and HR-TEM. Compared with the bare NCM, the MZ-NCM exhibits excellent electrochemical performance with capacity retention of 82.03 % after 150 cycles and discharge specific capacity of 171.81 mAh g−1 at rate of 10C. Comparison of dQ/dV, XRD, SEM and HR-TEM of the electrodes after cycling indicated that the Mg2+ and Zr4+ co-doped cathode maintains intact spherical morphology and relatively stable layered structure. •Diffusion during calcination results in a uniform distribution of Mg2+ and Zr4+ in the cathode particles.•The original particles undergo severe phase transformation and shape destruction during cycling.•The MZ-NCM sample exhibits an excellent rate performance and cycling life.•A simple strategy for large-scale production of nickel-rich electrode materials is provided.
ISSN:2352-152X
DOI:10.1016/j.est.2023.107777