First principles study of the electronic structure and Li-ion diffusion properties of co-doped LIFex-1MxPyNy-1O4 (M=Co/Mn, N--S/Si) Li-ion battery cathode materials

被引:1
作者
Jiang, Kai [1 ]
Wang, Fazhan [1 ]
Liu, Menghui [1 ]
Fan, Yuan [1 ]
Chen, Zhanwen [1 ]
Li, Guangyuan [1 ]
Li, Pan [1 ]
Shi, Xiaohui [1 ]
Hong, Wu [1 ,2 ]
机构
[1] Xian Univ Architecture & Technol, Sch Mech & Elect Engn, Xian 710055, Peoples R China
[2] Shaanxi Engn Technol Res Ctr Wear Resistant Mat, Xian 710055, Peoples R China
来源
MICRO AND NANOSTRUCTURES | 2024年 / 196卷
关键词
Li-ion batteries; Doping; Electronic structure; Diffusion rate; First-principles calculation; LIFEPO4;
D O I
10.1016/j.micrna.2024.207988
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
In this work, a first-principles method based on density functional theory was systematically employed to investigate the stability, electronic properties, lithium-ion migration rates, and capacity-voltage curves of the LiFe x-1 M x P y N y-1 O 4 (M = Co/Mn, N--S/Si) system. The results indicate that the lattice constants of the LiFe x-1 M x P y N y-1 O 4 (M = Co/Mn, N--S/Si) system show little variation, and the system exhibits low formation and binding energies. Among the investigated systems, LFP-Mn/S demonstrates the best structural and thermodynamic stability. The bandgap of the doped systems decreases, leading to enhanced electronic conductivity. The LiFe 0.875 Co 0.125 P 0.875 Si 0.125 O 4 and LiFe 0.875 Mn 0.125 P 0.875 Si 0.125 O 4 systems remain semiconductors, while the LiFe 0.875 Co 0.125 P 0.875 S 0.125 O 4 and LiFe 0.875 Mn 0.125 P 0.875 S 0.125 O 4 systems exhibit semi-metallic properties due to the introduction of sulfur. Differential charge density calculations reveal changes in the covalent bond strength of the doped systems, with the introduction of Si and S respectively increasing and decreasing the covalency of their bonds with surrounding oxygen atoms. Additionally, doping reduces the Li-ion diffusion energy barriers, with the LiFe 0.875 Co 0.125 P 0.875 Si 0.125 O 4 system exhibiting the lowest migration energy barrier. The Li- ion diffusion rate is four orders of magnitude faster than that of the intrinsic system. This is attributed to changes in the average lengths of Li-O, Co-O, and Fe-O bonds. Finally, doping also alters the de-lithiation voltage, with values ranging from 2.69 V to 3.65 V for the doped systems, and the LiFe 0.875 Co 0.125 P 0.875 Si 0.125 O 4 system shows the highest complete de-lithiation voltage of 3.65 V. The overall performance improvements of the doped system have significant implications for enhancing the performance of Li-ion batteries.
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页数:12
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