材料科学
钴
异质结
接口(物质)
锌
钠
金属
二进制数
无机化学
化学工程
离子
纳米技术
冶金
光电子学
有机化学
复合材料
毛细管数
化学
毛细管作用
工程类
算术
数学
作者
Yifan Zhang,Jingyu Guo,Xiao Liu,Yujie Gao,Zhongchao Bai,Nana Wang,Yunxiu Wang,Fuyi Jiang,Yanjun Zhai,Shi Xue Dou,Caifu Dong
标识
DOI:10.1002/adfm.202504553
摘要
Abstract Developing stable material structures and modulating electronic structures is a good strategy for improving metal‐sulfide electrode conductivity, reducing volume change, and enhancing the reaction kinetics of Na + electrodes to achieve stable electrochemical performance. However, it continues to be challenging to create hybrid structures with precisely defined architectures and desired compositions. Thus, the carbon‐coated Zinc/Cobalt sulfide heterostructure nanorods (ZnS/CoS@C) are prepared by sulfidation treatment of the Zinc/Cobalt binary metal–organic framework in one step. As expected, ZnS/CoS@C heterostructure displayed an ultra‐long lifespan (403 mAh g −1 at 10 A g −1 over 1700 cycles) and superior rate performance (653.1/333.3 mAh g −1 at 0.5/30 A g −1 ). The kinetic analysis and Density functional theory calculations show that the excellent electrochemical performance is attributed to the high pseudocapacitive and fast kinetic behavior. The Na‐ion storage mechanism of ZnS/CoS@C is revealed by in X‐ray diffraction, ex situ X‐ray photoelectron spectroscopy, and high‐resolution transmission electron microscopy. Furthermore, the full cells of ZnS/CoS@C//Na 3 V 2 (PO 4 ) 3 @rGO are successfully assembled and demonstrated impressive performance (186.3 mAh g −1 at 0.5 A g −1 for 600 cycles). This study offers an easy way to design heterostructured anode materials for superior sodium‐ion batteries.
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