{"title":"由二元金属-有机骨架衍生的锌/钴硫化物的异质结构界面构建与超稳定钠离子半/满电池","authors":"Yifan Zhang, Jingyu Guo, Xiao Liu, Yujie Gao, Zhongchao Bai, Nana Wang, Yunxiu Wang, Fuyi Jiang, Yanjun Zhai, Shi Xue Dou, Caifu Dong","doi":"10.1002/adfm.202504553","DOIUrl":null,"url":null,"abstract":"<p>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<sup>+</sup> 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<sup>−1</sup> at 10 A g<sup>−1</sup> over 1700 cycles) and superior rate performance (653.1/333.3 mAh g<sup>−1</sup> at 0.5/30 A g<sup>−1</sup>). 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<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub>@rGO are successfully assembled and demonstrated impressive performance (186.3 mAh g<sup>−1</sup> at 0.5 A g<sup>−1</sup> for 600 cycles). This study offers an easy way to design heterostructured anode materials for superior sodium-ion batteries.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"35 35","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Heterostructure Interface Construction of Zinc/Cobalt Sulfides Derived From Binary Metal–Organic Framework Toward Ultrastable Sodium-Ion Half/Full Batteries\",\"authors\":\"Yifan Zhang, Jingyu Guo, Xiao Liu, Yujie Gao, Zhongchao Bai, Nana Wang, Yunxiu Wang, Fuyi Jiang, Yanjun Zhai, Shi Xue Dou, Caifu Dong\",\"doi\":\"10.1002/adfm.202504553\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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<sup>+</sup> 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<sup>−1</sup> at 10 A g<sup>−1</sup> over 1700 cycles) and superior rate performance (653.1/333.3 mAh g<sup>−1</sup> at 0.5/30 A g<sup>−1</sup>). 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<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub>@rGO are successfully assembled and demonstrated impressive performance (186.3 mAh g<sup>−1</sup> at 0.5 A g<sup>−1</sup> for 600 cycles). 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引用次数: 0
摘要
发展稳定的材料结构和调制电子结构是提高金属硫化物电极电导率、减小体积变化、增强Na+电极反应动力学以实现稳定电化学性能的良好策略。然而,创建具有精确定义的架构和所需组合的混合结构仍然具有挑战性。因此,通过对锌/钴二元金属-有机骨架进行一步硫化处理,制备了碳包覆锌/硫化钴异质结构纳米棒(ZnS/CoS@C)。正如预期的那样,ZnS/CoS@C异质结构显示出超长的寿命(在10 A g−1下超过1700次循环的403 mAh g−1)和优越的倍率性能(在0.5/30 A g−1下653.1/333.3 mAh g−1)。动力学分析和密度泛函理论计算表明,优异的电化学性能归因于高赝电容性和快速的动力学行为。通过x射线衍射、非原位x射线光电子能谱和高分辨率透射电镜等手段揭示了ZnS/CoS@C的na离子储存机理。此外,成功组装了ZnS/CoS@C//Na3V2(PO4)3@rGO的完整电池,并展示了令人印象深刻的性能(186.3 mAh g−1,0.5 A g−1,600次循环)。本研究为设计高性能钠离子电池的异质结构负极材料提供了一种简便的方法。
Heterostructure Interface Construction of Zinc/Cobalt Sulfides Derived From Binary Metal–Organic Framework Toward Ultrastable Sodium-Ion Half/Full Batteries
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//Na3V2(PO4)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.
期刊介绍:
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