阴极
材料科学
动力学
扩散
微观结构
失真(音乐)
四面体
八面体
平面的
纳米技术
工作(物理)
兴奋剂
化学工程
压力(语言学)
化学物理
电极
活化能
原子扩散
表面扩散
作者
Pengxu Wang,Haifeng Yu,Ling Chen,Yaoguo Fang,Qian Cheng,Hao Jiang,Chunzhong Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-02-03
卷期号:20 (6): 5309-5317
被引量:1
标识
DOI:10.1021/acsnano.5c21496
摘要
Development of high-power LiMnxFe1-xPO4 (LMFP) cathodes is fundamentally challenged by the interplay between sluggish one-dimensional Li+ diffusion and severe Jahn–Teller distortion. Herein, we propose a synergistic substitution strategy to concurrently tackle these issues. Partial replacement of PO4 tetrahedra by planar BO3 groups creates three-dimensional interconnected Li-ion diffusion networks, while doping Nb5+ into transition-metal sites widens the diffusion channels. This tailored microstructure not only overcomes the intrinsic Li+ diffusion kinetics limitation but also dissipates the mechanical stress arising from high-rate operating conditions, suppressing the Jahn–Teller distortion in MnO6 octahedra by 36%. The optimized LMFP cathode delivers an ultrahigh reversible capacity of 126 mAh g–1 at 10C (about a 3.6-fold improvement over the pristine LMFP) and retains 80.2% of its initial capacity after 2000 cycles at 3C in pouch-type full cells. This work elucidates the critical link between Li+ diffusion kinetics and structural stability, providing an available paradigm for designing high-power, long-life Mn-based cathode materials.
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