材料科学
储能
插层(化学)
动力学
工作(物理)
氢气储存
降级(电信)
化学工程
电极
纳米技术
空位缺陷
水溶液
沉积(地质)
计算机数据存储
机制(生物学)
数码产品
兴奋剂
密度泛函理论
氢
结构稳定性
科技与社会
作者
Fei Long,Zhi Zhang,Changwu Liu,Yiming Ma,Yihua Gao
标识
DOI:10.1021/acsami.6c09981
摘要
Aqueous energy storage systems (AESS) offer advantages such as safety and environmental friendliness. Among them, the rapid charge-discharge capabilities of ammonium-ion batteries (AIBs) and the high energy density of zinc-ion batteries (ZIBs) complement each other. Although V2O5 holds promise as a key electrode material in both AIBs and ZIBs, it is limited by its slow kinetics and structural instability. Herein, V2O5·0.47H2O (HEVOH) with extended interlayer spacing and an optimized electronic structure is successfully constructed via a high-entropy doping strategy, effectively solving the issues of slow kinetics and structural instability of V2O5, and demonstrating outstanding performance in both AIBs and ZIBs. When used in AIBs, it delivers a capacity of 137.6 mAh g-1 at 0.20 A g-1, with a capacity retention of 92.7% at 1.00 A g-1 after 3000 cycles. When used in ZIBs, it achieves a capacity of 543.6 mAh g-1 at 0.10 A g-1, maintaining 76.6% capacity at 10.00 A g-1 after 7000 cycles. The NH4+ storage mechanism involves interlayer intercalation, hydrogen bond reconstruction, and oxygen vacancy generation. The Zn2+ storage mechanism is interlayer intercalation and reversible deposition of Zn4SO4(OH)6·4H2O to construct a dynamic interface protective layer. This work provides a direction for the universal design of high-performance AESS.
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