Heterostructure Interface Construction of Zinc/Cobalt Sulfides Derived From Binary Metal–Organic Framework Toward Ultrastable Sodium‐Ion Half/Full Batteries

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 · 发表于：Advanced Functional Materials · 年份：2025 · DOI：10.1002/adfm.202504553 · 被引用次数：35 · 研究领域：Advancements in Battery Materials、Advanced battery technologies research、Extraction and Separation Processes

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.