4.6 Article

Zr-doped P2-Na0.75Mn0.55Ni0.25Co0.05Fe0.10Zr0.05O2 as high-rate performance cathode material for sodium ion batteries

期刊

ELECTROCHIMICA ACTA
卷 223, 期 -, 页码 92-99

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2016.12.019

关键词

layered oxides; cathode materials; P2-structure; sodium-ion battery; electrical conductivity

资金

  1. National Natural Science Foundation of China [11575192]
  2. State Key Project of Fundamental Research of Ministry of Science and Technology of the People's Republic of China [2012CB932504, 2014CB931900]
  3. Hundred Talents Project of the Chinese Academy of Sciences

向作者/读者索取更多资源

In this work, Zr4+ doped P2-Na0.75Mn0.55Ni0.25Co0.05Fe0.10Zr0.05O2 has been synthesized and investigated as high-rate sodium-ion battery cathode material for the first time. XRD results indicate thatZr-ion with a big size cannot completely dissolve into the crystal structure, but the residual ZrO2 shows little impact on the electrochemical performance in comparison with the post-added ZrO2. With the substitution of Zr4+ for Fe3+, the lattice parameter a decreases but c increases, resulting in the reduced lattice volume. In comparison with the Zr-free sample, Na0.75Mn0.55Ni0.25Co0.05Fe0.10Zr0.05O2 (Zr05) can deliver a discharge capacity of about 95, 74, 61 and 53 mAh g(-1) at 2C, 5C, 8C and 10C. At the current density of 2C, the capacity retention after 100 cycles has increased from 57% of Zr0 to 74% of Zr05. The results demonstrate that Zr-ion substitution can effectively improve the rate performance and cycling stability of P2-structure cathode materials. The role of Zr4+ can be summarized as follows: (1) Zr-0 (Delta H-f(298K)(Zr-0) = 760 kJ mol(-1)) has a stronger bond energy than that of Fe-O (Delta H-f(298K)(Fe-0)= 409 kJ mol(-1)), which enhances the structure stability and cycling performance; (2) the aliovalent substitution of Zr4+ for Fe3+ enhances the electronic conductivity, which is favorable for the rate capability; (3) the substitution of Zr4+ for Fe3+ can be beneficial to Na+ conduction because it increases disorder in the transition metal (TM) layers and can prevent Na+/vacancy ordering, which further enhances the rate capability. (C) 2016 Elsevier Ltd. All rights reserved.

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