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Bulk-surface dual modification via Mg/Zr doping and Li3PO4coating for suppressing phase transition and side reaction in 4.6 V LiCoO2 AITranslate

Faculty of Materials Metallurgy and Chemistry;Faculty of Materials Metallurgy and Chemistry;Faculty of Materials Metallurgy and Chemistry;Faculty of Materials Metallurgy and Chemistry;Faculty of Materials Metallurgy and Chemistry;Faculty of Materials Metallurgy and Chemistry;Faculty of Materials Metallurgy and Chemistry
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Publisher: Youke Publish Co., Ltd.
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Abstract AITranslate

The rapid advancement of electronic devices has resulted in increasingly demanding performance requirements for highvoltage LiCoO2(LCO)cathodes.However,LCO exhibits significant irreversible phase transitions and detrimental side reactions under high voltages.Herein,Mg/Zr co-doped and Li3PO4-coated LiCoO2(denoted as MZP-LCO)was synthesized through an element self-diffusion reaction at a high temperature.Mg2+and Zr4+can partially replace Li+in the LCO structure,creating a homogeneous concentration distribution with a 60 nm thickness from the surface to the interior.Mg2+serves as a stabilizing"pillar"to suppress Co-O layer sliding during deep delithiation,enhancing the structural integrity of LCO,while Zr4+expands the Li+deintercalation channels,thereby increasing the capacity.Furthermore,a Li3PO4nano-coating layer forms in situ on the surface of the LCO,improving Li+transport efficiency and successfully inhibiting harmful side reactions at the electrode surface.The half-cell of MZP-LCO exhibits a capacity of 154.7 mAh·g-1after 200 cycles at 0.5C within 3.0-4.6 V,and demonstrates superior rate capability,maintaining a capacity of 156.1 mAh·g-1at 10C.The exceptional electrochemical performance can be attributed to the synergistic effects of the uniform Mg/Zr doping within the LCO and the Li3PO4coating nanolayer on the surface.These findings offer valuable insights for resolving the issues related to LCO cathode performance degradation at high voltages.

KeyWords AITranslate

High-voltage LiCoO2 Synergistic modification Mg/Zr co-doping Li3PO4coating Structural stability
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DOI:

Chinese Library Classification Number:TM912[电气工程—电力电子与电力传动];TQ131.1[化学工程—无机化工]

Citation Information:

The rapid advancement of electronic devices has resulted in increasingly demanding performance requirements for highvoltage LiCoO2(LCO)cathodes.However,LCO exhibits significant irreversible phase transitions and detrimental side reactions under high voltages.Herein,Mg/Zr co-doped and Li3PO4-coated LiCoO2(denoted as MZP-LCO)was synthesized through an element self-diffusion reaction at a high temperature.Mg2+and Zr4+can partially replace Li+in the LCO structure,creating a homogeneous concentration distribution with a 60 nm thickness from the surface to the interior.Mg2+serves as a stabilizing"pillar"to suppress Co-O layer sliding during deep delithiation,enhancing the structural integrity of LCO,while Zr4+expands the Li+deintercalation channels,thereby increasing the capacity.Furthermore,a Li3PO4nano-coating layer forms in situ on the surface of the LCO,improving Li+transport efficiency and successfully inhibiting harmful side reactions at the electrode surface.The half-cell of MZP-LCO exhibits a capacity of 154.7 mAh·g-1after 200 cycles at 0.5C within 3.0-4.6 V,and demonstrates superior rate capability,maintaining a capacity of 156.1 mAh·g-1at 10C.The exceptional electrochemical performance can be attributed to the synergistic effects of the uniform Mg/Zr doping within the LCO and the Li3PO4coating nanolayer on the surface.These findings offer valuable insights for resolving the issues related to LCO cathode performance degradation at high voltages.

quote

GB/T 7714-2015 [1] Li-Mei Ma, Yi Liu, Meng-Hui Qiu, et al. Tungsten, 2025(4): 817-830.
MLA [1] Li-Mei Ma, et al., Tungsten, no. 4, 2025, pp. 817-830.
APA [1] Li-Mei Ma, Yi Liu, Meng-Hui Qiu, Yan-Hong Yin, Xian-Bin Liu, Ting Liu, & Ye-Sheng Li. (2025). Tungsten(4), 817-830.
IEEE [1] Li-Mei Ma, Yi Liu, Meng-Hui Qiu, Yan-Hong Yin, Xian-Bin Liu, Ting Liu, and Ye-Sheng Li, Tungsten, no. 4, pp. 817-830, 2025.