4.7 Article

Enhanced Electrochemical Performance of LiNi0.5Mn1.5O4 Composite Cathodes for Lithium-Ion Batteries by Selective Doping of K+/Cl- and K+/F-

期刊

NANOMATERIALS
卷 11, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/nano11092323

关键词

LiNi0; 5Mn1; 54; K; Cl co-doping; K; F co-doping; rate capability; cycling stability

资金

  1. Project of Hebei Academy of Sciences [21709, 21708]
  2. Hebei Province Major Scientific and Technological Achievements Transformation Project [20284401Z]
  3. China Postdoctoral Science Foundation [2021M693813]
  4. Natural Science Foundation of Guangxi [2020GXNSFBA297029]
  5. Foundation of Guilin University of Technology [GLUTQDJJ2020003]
  6. Foundation of Key Laboratory of New Processing Technology for Nonferrous Metal & Materials, Ministry of Education/Guangxi Key Laboratory of Optical and Electronic Materials and Devices, Guilin University of Technology [20AA-13]

向作者/读者索取更多资源

K+/Cl- and K+/F- co-doped LNMO materials were synthesized successfully, reducing impurities, enlarging lattice parameters, and improving cycling performance. Co-doping decreased particle size, enhanced Li+ diffusion, modified crystal structures, and increased electrochemical kinetics. The co-doped samples exhibited improved rate capability and cycling stability.
K+/Cl- and K+/F- co-doped LiNi0.5Mn1.5O4 (LNMO) materials were successfully synthesized via a solid-state method. Structural characterization revealed that both K+/Cl- and K+/F- co-doping reduced the LixNi1-xO impurities and enlarged the lattice parameters compared to those of pure LNMO. Besides this, the K+/F- co-doping decreased the Mn3+ ion content, which could inhibit the Jahn-Teller distortion and was beneficial to the cycling performance. Furthermore, both the K+/Cl- and the K+/F- co-doping reduced the particle size and made the particles more uniform. The K+/Cl- co-doped particles possessed a similar octahedral structure to that of pure LNMO. In contrast, as the K+/F- co-doping amount increased, the crystal structure became a truncated octahedral shape. The Li+ diffusion coefficient calculated from the CV tests showed that both K+/Cl- and K+/F- co-doping facilitated Li+ diffusion in the LNMO. The impedance tests showed that the charge transfer resistances were reduced by the co-doping. These results indicated that both the K+/Cl- and the K+/F- co-doping stabilized the crystal structures, facilitated Li+ diffusion, modified the particle morphologies, and increased the electrochemical kinetics. Benefiting from the unique advantages of the co-doping, the K+/Cl- and K+/F- co-doped samples exhibited improved rate and cycling performances. The K+/Cl- co-doped Li0.97K0.03Ni0.5Mn1.5O3.97Cl0.03 (LNMO-KCl0.03) exhibited the best rate capability with discharge capacities of 116.1, 109.3, and 93.9 mAh g(-1) at high C-rates of 5C, 7C, and 10C, respectively. Moreover, the K+/F- co-doped Li0.98K0.02Ni0.5Mn1.5O3.98F0.02 (LNMO-KF0.02) delivered excellent cycling stability, maintaining 85.8% of its initial discharge capacity after circulation for 500 cycles at 5C. Therefore, the K+/Cl- or K+/F- co-doping strategy proposed herein will play a significant role in the further construction of other high-voltage cathodes for high-energy LIBs.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据