4.6 Article

Boosting the electrochemical performance of LiNiO2 by extra low content of Mn-doping and its mechanism

Journal

ELECTROCHIMICA ACTA
Volume 417, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2022.140345

Keywords

Lithium nickelate; Manganese doping; Li+; Ni2+ cation mixing; Minimal modification; Lithium ion battery

Funding

  1. Innovation District of Military China [18-163-13-ZD-008-005-02]
  2. National Key R&D Program of China [2019YFC1604605]
  3. National Natural Science Foundation of China [51974190]

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The addition of a small amount of manganese can greatly stabilize the crystal structure and integrity of the secondary particles of LiNiO2 material, resulting in excellent electrochemical cycling performance and thermal stability. However, a high content of manganese doping can deteriorate the rate performance of the material, emphasizing the importance of optimizing the amount of doping.
The urgent demands of developing Co-free materials for lithium ion batteries with high energy density for next generation electric vehicles have driven the attention of researches to LiNiO2 stabilized by doping of common elements. Among those elements, manganese is usually used to stabilize cathode material crystal structures to achieve better electrochemical performances. However, the Li+/Ni2+ cation disorder causing by Mn doping is greatly neglected of the effect on electrochemical behaviors. In order to elucidate the exact effect of Mn-doping, herein, we synthesize Mn-doped LiNiO2 with extra low Mn content by using the solid-state element thermal interdiffusion strategy. Under calcination at high temperature, with the spherical species coated with Mncontaining gel as the precursor, Mn can be evenly doped into the framework of LiNiO2 material. It is demonstrated that the small amount of Mn-doping can greatly stabilize both the crystal structure of LiNiO2 and integrity of the secondary particles during the electrochemical cycling to provide the excellent electrochemical cycling performance and thermal stability of the materials. Nevertheless, the rate capability of the materials is strongly dependent on the amount of the doped Mn, due to the Li+/Ni2+ cation mixing formed in the synthesis process and introduced in the electrochemical cycling. In the presence of a tiny quantity of the doped Mn, the enlarged crystal lattice would be favorable to the diffusion of the Li+ ions in the crystal. However, serious Li+/Ni2+ cation mixing of the materials with high content of the Mn-doping deteriorates the rate performance of the materials. Thus, in this case, the Mn content is optimized to be 4 mol%, endowing the material with an initial capacity of 202 mAh g-1 at 0.1 C, and a capacity retention of 85.41% after 200 cycles at 0.5 C. For the Mn-doped LiNiO2 materials, it is suggested that to control the Li+/Ni2+ cation mixing would be crucial for gaining the materials with superior electrochemical performance.

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