阴极
水溶液
电解质
无定形固体
材料科学
相间
图层(电子)
锌
纳米技术
化学工程
原子层沉积
无机化学
化学
电极
冶金
有机化学
物理化学
生物
工程类
遗传学
作者
Chen Hu,Binjie Li,Kunkun Nie,Ziyi Wang,Yujia Zhang,Lixin Yi,Xiaorong Hao,Huang Zhang,Shaokun Chong,Z.Y. Liu,Wei Huang
标识
DOI:10.1002/ange.202413173
摘要
Abstract Vanadium (V)‐based oxides as cathode materials for aqueous zinc‐ion batteries (AZIBs) still encounter challenges such as sluggish Zn 2+ diffusion kinetics and V‐dissolution, thus leading to severe capacity fading and limited life span. Here, we designed an ultrafast and facile colloidal chemical synthesis strategy based on crystalline Zn 0.25 V 2 O 5 ( c‐ ZVO) to successfully prepare a‐ ZVO@MoS 2 core@shell heterostructures, where atomic‐layer MoS 2 uniformly coats on the surface of amorphous a‐ ZVO. The tailored amorphous structure of a‐ ZVO provides more isotropic pathways and active sites for Zn 2+ , thus significantly enhancing the Zn 2+ diffusion kinetics during charge–discharge processes. Meanwhile, as an efficient artificial cathode electrolyte interphase, the precision‐engineered atomic‐layer MoS 2 with semi‐metallic 1T′ phase not only contributes to improved electron transport but also effectively inhibits the V‐dissolution of a‐ ZVO. Therefore, the prepared a‐ ZVO@MoS 2 and conceptually validated a‐ V 2 O 5 @MoS 2 derived from commercial c‐ V 2 O 5 exhibit excellent cycling stability at an ultralow current density (0.05 A g −1 ) while maintaining good rate capability and capacity retention. This research achievement provides a new effective strategy for various amorphous cathode designs for AZIBs with superior performance.
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