X射线光电子能谱
插层(化学)
阴极
电化学
离子
价(化学)
电解质
材料科学
密度泛函理论
无机化学
化学
化学工程
物理化学
电极
有机化学
计算化学
工程类
作者
Zixin Chen,Sisi Feng,Jiening Zheng,Chengkang Chang
标识
DOI:10.1002/cssc.202501500
摘要
This research provides a pioneering demonstration of LiFe 0.4 Mn 0.6 PO 4 @C (LFMP@C) as a cathode material for rechargeable aluminum‐ion batteries (AIBs). The composite delivers an initial discharge capacity of 156.5 mAh g −1 at 200 mA g −1 , with 148.2 mAh g −1 retained after 500 cycles. The Li + /Al 3+ (de)intercalation mechanisms and their structural impacts on the LFMP lattice are systematically investigated through density functional theory, inductively coupled plasma optical emission spectroscopy, X‐ray photoelectron spectroscopy, and ex situ X‐ray diffraction. The results show that aluminum and lithium ions successfully intercalate into the LFMP lattice and participate in the electrochemical reaction, while Fe and Mn undergo reversible valence state changes. The strong electrostatic interactions between Al 3+ and the host lattice (hindering ion migration) as well as Li + trapping by the acidic electrolyte jointly contribute to rapid capacity decay during initial cycles. Nevertheless, the LFMP@C composite demonstrates promising cycling stability.
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