Heterocations Synergistic Doping for Kinetically Enhanced and Structurally Stable LiMn 0.6 Fe 0.4 PO 4

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Authors: Junjie Han, Na Tian, Siyun Wang, Jianhui Zhu, Yuan Gao, Xuanlong He, Chenxi Yan, Rongzheng Wang, Hongyong Dai, Xing Liu, Shibei Zhang, Dingtao Ma
+2 more Peixin Zhang, Lipeng Zhang
Cited by: 3
References: 32

Abstract

LiMn x Fe 1– x PO 4 (LMFP) is a promising olivine cathode material successor to LiFePO 4, offering a higher operating voltage platform for enhanced energy density. However, its commercial application is hindered by inherent poor kinetics. Herein, a dual-site doping strategy involving Na + and Co 2+ is proposed to synergistically enhance the ionic and electronic conductivity of LMFP. The codoped LMFP-Na-Co cathode delivers a specific capacity of 135.8 mAh/g at 1 C and exhibits outstanding cycling stability with 92.5% capacity retention after 200 cycles. Remarkably, it also maintains 90.2% capacity retention after 300 cycles even at 0 °C. Theoretical calculations reveal that Na + doping expands the one-dimensional lithium-ion diffusion channels, while Co 2+ doping elevates the intrinsic electronic conductivity and suppresses the Jahn–Teller distortion associated with Mn 3+, collectively lowering the Li + diffusion barrier and improving structural stability. This work demonstrates that Na + -Co 2+ dual-site doping is a highly promising strategy for developing high-performance LiMn x Fe 1– x PO 4 cathodes.

Fields of Study & Subjects

Advancements in Battery Materials Thermal Expansion and Ionic Conductivity Advanced Battery Materials and Technologies

Publication details

Journal / source
ACS Applied Materials & Interfaces
Publisher
American Chemical Society (ACS)
Volume
18
Issue
11
Pages
16481–16492
Publication date
14 March 2026
Language
EN