4.8 Article

Enhanced Cathode Performance: Mixed Al2O3 and LiAlO2 Coating of Li1.2Ni0.13Co0.13Mn0.54O2

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 34, Pages 38153-38162

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c10459

Keywords

Li-rich; manganese-based cathode materials; mixed Al2O3 and LiAlO2 coating layer; density functional theory; electrochemical performance

Funding

  1. Joint Funds of the Innovation Academy for Green Manufacture, Chinese Academy of Sciences [IAGM2020C25]
  2. Qinghai Provincial Thousand Talents Program for High-level Innovative Professionals
  3. Natural Science Foundation of Qinghai Province of China for Youth Project [2019-ZJ-934Q]
  4. CAS Light of West China Program
  5. Major Science and Technology Projects of Qinghai Province [2018-GX-A9]

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Li-rich, manganese-based cathode materials are attractive candidates for Li-ion batteries because of their excellent capacity, but poor rate and cycle performance have limited their commercial applications. Herein, Li-rich, manganese-based cathode materials were modified with aluminum isopropoxide as an aluminum source modifier using a sol-gel technique followed by a wet chemical method. To investigate the structure, morphology, electronic state, and elemental composition of both pristine- and surface-modified Li1.2Ni0.13Co0.13Mn0.54O2, various characterizations were performed. Based on density functional theory simulations and the results of electrochemical tests, the surface of the modified cathode material was found to contain at least part of the LiAlO2 phase. This was attributed to the aluminum isopropoxide reacting with a Li2CO3/LiOH byproduct on the material surface to form LiAlO2 with a three-dimensional Li-ion channel structure. Electrochemical testing revealed that a 3 wt % aluminum isopropoxide coating of cathode materials exhibited excellent electrochemical performance. Furthermore, the initial Coulombic efficiency and discharge capacity at 0.1 C were up to 88.55% and 272.7 mAh g(-1), respectively. A final discharge capacity of 186.4 mAh g(-1) was achieved, corresponding to a capacity retention of 83.55% after 300 cycles at 0.5 C. This was attributed to LiAlO2 partially accelerating the diffusion of Li ions and Al2O3 aiding the avoidance of side reactions in the mixed coating layer by partially protecting the structure.

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