Ternary Inert Element Co‐Doping: a New Approach to Stable 4.7 V LiCoO 2
Source abstract
Abstract
Abstract LiCoO 2 (LCO) has long dominated the cathode materials in portable electronic batteries due to its high volumetric energy density. However, the pursuit of higher voltages to achieve larger capacities remains a challenge due to severer structural degradation. Herein, a ternary inert element co‐doping strategy that can greatly improve the structure stability of LCOs at elevated voltages is reported. Mg and Ni doping at Li site support the layered structure in the highly delithiated state, while Ni also facilitates the separation of O 2p and Co 3d orbits, thereby suppressing oxygen loss. Meanwhile, Al doping at Co site suppresses the distortion of Co–O octahedra and stabilizes the Co layers. The synergistic effects of Al, Mg and Ni co‐doping inhibit the irreversible H3–H1‐3 phase transitions and mitigate internal stress accumulation. The Al–Mg–Ni co‐doped LCO exhibits a capacity of 221 mAh g −1 with a capacity retention of 65.5% after 1500 cycles at 4.6 V. At a higher voltage of 4.7 V, it delivers a capacity of 225.8 mAh g −1 with a capacity retention of 58.6% after 600 cycles. This multiple inert elements co‐doping strategy gives an effective method for stabilizing the high‐voltage LCO and other related layered oxide materials.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Semiconductor materials and interfaces · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing Advanced Innovation Center for Soft Matter Science and Engineering, State Key Laboratory of Organic–Inorganic Composites Beijing University of Chemical Technology Beijing 100029 China
Funding
Key Technologies Research and Development Program · National Natural Science Foundation of China · Natural Science Foundation of Beijing Municipality
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