钒酸盐
阴极
钒
材料科学
格子(音乐)
氧化钒
钠
储能
化学物理
价(化学)
结构稳定性
空位缺陷
电导率
电子结构
容量损失
氧化物
无机化学
八面体
化学工程
衰减
氧气
钠离子电池
电极
晶体结构
凝聚态物理
密度泛函理论
离子
晶格常数
作者
Haofei Yang,Wenbin Li,Jintao Xu,Yetong Li,Mengjiao Li,Jianhua Zhang,Yangyang Luo,Qinting Jiang,Lingkun Yang,Jiaxuan Zuo,Xuexia Song,Jingjing Wang,Xifei Li
出处
期刊:eScience
[Elsevier]
日期:2025-12-01
卷期号:: 100512-100512
标识
DOI:10.1016/j.esci.2025.100512
摘要
Layered sodium vanadate has attracted considerable attention as a promising cathode material for sodium-ion batteries, due to its multiple accessible vanadium valence states and large interlayer spacing. However, its inherent limitations in electronic/ionic conductivity and lattice stability result in poor Na + storage stability. To address these challenges, a coupled electronic and lattice modulation strategy is proposed, in which metal-ion pre-intercalation is employed to tune the electronic structure of lattice oxygen. It is revealed that Zn 2+ pre-intercalation elevates the p-band center of lattice O (Oεp) by forming the interlayer local coordination structure of ZnO 4 tetrahedral. This electronic modulation simultaneously increases both oxygen vacancy formation energy and Na + adsorption energy, leading to two critical improvements of significant suppression of potential attenuation and enhanced Na + transport kinetics. Furthermore, the Oεp position serves as a critical descriptor for Na + storage stability, exhibiting an approximately linear correlation with both average potential retention and capacity retention. Consequently, Zn 2+ pre-intercalated cathode exhibits outstanding long-term cycling stability, achieving a high capacity retention of 81.2% after 500 cycles at 1.65 A g −1 , with potential attenuation nearly eliminated. This study advances both the fundamental understanding and practical design of layered oxide cathodes through structural modification for enhanced cycling stability. • The newly developed layered sodium vanadate cathode demonstrates an outstanding capacity retention of 81.2% after 500 cycles at a high current density of 1.65 A g −1 . • Zn 2+ pre-intercalation effectively elevates the O p-band center (Oεp) by forming the interlayer local coordination structure of ZnO 4 tetrahedral. • The p-band center of lattice O (Oεp) is found to be a key descriptor for Na + storage stability, exhibiting approximate linear correlation with both average potential retention and capacity retention.
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