五氧化二铁
钒
水合物
阴极
动力学
钠
无机化学
离子
材料科学
化学工程
铝硅酸钠
化学
冶金
物理化学
有机化学
催化作用
硅酸铝
物理
工程类
量子力学
作者
Yan Lin,Hemanth Neelgund Ramesh,Anthony J. Gironda,Liyan Lin,Xiaoxiao Jia,Yan-Dong Guo,Gerald T. Seidler,Tao Hu,Ulla Lassi,Guozhong Cao
标识
DOI:10.1016/j.jpowsour.2025.237766
摘要
Hydrate vanadium pentoxide (V 2 O 5 · n H 2 O, VOH) is a promising cathode material for rechargeable batteries, due to its high theoretical capacity, adjustable interlayer spacing, and the inherent multivalency of vanadium. However, the simultaneous intercalation and redox reactions during Na + storage poses challenges for structural stability during cycling. This work chemically pre-inserts potassium ions (K + ) to VOH, forming KVOH during hydrothermal synthesis. The pre-intercalated K + partially replaces weakly bound interlayer water, reducing the interlayer spacing and stabilizing the layered framework by mitigating the stress from repeated Na + insertion/extraction. X-ray absorption revealed the partial reduction of V 5+ to V 4+ to compensate the insertion of K + to maintain the electroneutrality. XPS analyses and DFT calculations corroborate the K + insertion. The resulting KVOH demonstrated enhanced rate capability with an energy efficiency of 76 % at 0.05 A g −1 , along with improved kinetics evidenced by lower electrochemical impedance, diminished polarization, and accelerated Na + diffusion. • K + partially replaces interlayer water in VOH, reducing the interlayer spacing. • Reduced spacing boosts electrostatic forces, improving stability and kinetics. • Increased V 4+ in KVOH enhances electron hopping and improving conductivity. • KVOH delivers superior rate capability and enhanced energy efficiency.
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