Architecture design of yolk-shell heterostructured bimetallic selenide confined in polydopamine for high efficiency sodium/potassium ion storage

被引:8
|
作者
Hou, Yun-Lei [1 ,2 ]
Zhang, Lei [3 ]
Gao, Fen [1 ,2 ]
Wen, Wan-Xin [1 ,2 ]
Wang, Hua-Ying [1 ,2 ]
Zhang, Bo-Han [1 ,2 ]
Zhao, Dong-Lin [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Key Lab Carbon Fiber & Funct Polymers, Minist Educ, Beijing 100029, Peoples R China
[3] China Acad Bldg Res Co Ltd, Beijing 100013, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic framework; Yolk-shell structure; Anode material; Sodium/potassium ion batteries; Energy density; METAL-ORGANIC FRAMEWORK; HYDROGEN EVOLUTION; MOSE2; NANOSHEETS; ANODE MATERIALS; SODIUM; LITHIUM; PERFORMANCE; COMPOSITES; ELECTROCATALYST; NANOCOMPOSITE;
D O I
10.1016/j.electacta.2023.142602
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Benefiting from the enriched resources and satisfactory electrochemical performance, sodium/potassium ion batteries (SIBs/PIBs) are attracting significant attention and promising to be an ideal energy storage alternative to lithium-ion batteries (LIBs). Transition metal selenides are regarded as ideal anodes on account of their high theoretical capacity. Yet the weak reaction kinetics and the volume expansion still hinder its further development. Reasonable structural design and surface optimization are commonly used to address this challenge. Herein, a yolk-shell heterostructured bimetallic selenide derived from metal-organic framework (MOF) and confined in polydopamine plastic layer (ZnSe/CoSe2@PDA) is successfully synthesized. The unique structure and the polydopamine layer can release internal stress during the cycling process and effectively relieve the volume expansion. The construction of heterostructure can bring abundant active energy storage sites for Na+/K+ while shortening the diffusion paths of ions/electrons, thereby accelerating the reaction kinetics. Consequently, the ZnSe/CoSe2@PDA electrode exhibits an extremely high capacity of 914 mA h g(-1) at 0.1 A g(-1) in SIBs. Furthermore, it also possesses 182 mA h g(-11) at 1 A g(-1) after 250 cycles in PIBs. This strategy significantly increases the energy density of the anodes. Providing a new way for metal selenide anodes toward high-performance SIBs/PIBs.
引用
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页数:11
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