电解质
材料科学
阴极
相间
电池(电)
电化学
电极
化学工程
制作
电导率
钒
纳米技术
电流密度
容量损失
功率密度
涂层
离子
导电体
图层(电子)
电化学动力学
储能
复合材料
动力学
结构稳定性
电阻率和电导率
电化学电池
作者
Yu Zhang,Yaoyu Gu,Yang Wang,Hang Ye,Xiaorui Li,Shaojie Qu,Kuan Hu,Rui Wu,Juanjuan Zhang,Chunsheng Liu,Dianzeng Jia,He Lin
出处
期刊:Small
[Wiley]
日期:2025-11-26
卷期号:22 (4): e11424-e11424
被引量:1
标识
DOI:10.1002/smll.202511424
摘要
The practical application of vanadium oxide-based cathodes in high-performance aqueous zinc-ion batteries (AZIBs) is impeded by inherent interfacial instability, material dissolution, structural degradation, and sluggish kinetics. This study proposes a dual-functional stabilization strategy combining dual-ion pre-intercalation with electrolyte optimization. This approach involves the fabrication of Ca2+/Na+ co-inserted CaNaVO electrodes and use of an electrolyte enriched with trace SO4 2-, which collectively enhance the structural stability and reaction kinetics of the electrode material. Additionally, it promotes the in situ formation of a CaSO4-rich interphase layer via differential ion migration, achieving simultaneous improvement in both interfacial protection and bulk stability. Density functional theory (DFT) calculations confirm the superior electrical conductivity and accelerated ion transport of CaNaVO. The CaNaVO||Zn cell demonstrates exceptional electrochemical performance, exhibiting over 20 000 cycles at 10 A g-1 with minimal capacity decay (87.4%, only 0.00063% per cycle). Additionally, it demonstrates significant areal capacity (10 mA cm-2, 2.3 mAh cm-2) and cycle life under high mass loading conditions. Notably, the battery operates effectively with a low-concentration electrolyte (2 m), offering significant cost advantages. This work provides an innovative approach to improving the structural stability and long-term cycling performance of AZIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI