材料科学
再分配(选举)
密度泛函理论
阴极
电化学
八面体
结构完整性
兴奋剂
氧化还原
铝
化学工程
电压
电荷密度
格子(音乐)
粘结长度
化学物理
纳米技术
相(物质)
晶体结构
分子
结晶学
结构变化
电流密度
晶格常数
无机化学
电池电压
电极
化学
功率密度
作者
Phongsit Krabao,Sujeera Pleuksachat,Natthapong Kamma,Somratchanee Puarsa,Thanayut Kaewmaraya,Songyoot Kaewmala,Wanwisa Limphirat,Nonglak Meethong
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-12-18
卷期号:40 (1): 857-864
被引量:1
标识
DOI:10.1021/acs.energyfuels.5c03311
摘要
In this work, we report the synthesis of aluminum-doped Na4–xVMn1–xAlx(PO4)3/C cathodes via a solid-state reaction and evaluate their structural and electrochemical performances for sodium-ion batteries. Structural analyses reveal that Al incorporation modifies both the long-range lattice and the local coordination of V and Mn sites. Electrochemical results show that although the specific capacity varies nonlinearly with Al content, moderate Al substitution yields smoother voltage profiles, reduced polarization, and markedly enhanced cycling stability, with doped electrodes retaining over 92% of their initial capacity after 500 cycles at 2C. Density functional theory (DFT) calculations further clarify that Al substitution distorts the MnO6 and VO6 octahedra and alters V–O and Mn–O bonding through modified cation–oxygen hybridization. The projected density of states (PDOS) and Bader charge analyses reveal pronounced charge redistribution around V atoms, accounting for the merged redox potentials and improved structural stability. Overall, electrochemically inactive Al3+ substitution effectively stabilizes the NASICON framework and mitigates phase transitions, offering atomic-level insights for the design of durable, high-performance sodium-ion batteries.
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