Freestanding carbon nanofibers encapsulating MOF-derived NiSe with in-situ porous carbon protective layer for sodium storage

被引:21
|
作者
Cu, Qiao [1 ]
Shang, Chaoqun [2 ,3 ]
Hu, Le [1 ]
Zhou, Guofu [1 ,4 ]
Wang, Xin [1 ,4 ]
机构
[1] South China Normal Univ, Guangdong Prov Key Lab Opt Informat Mat, Guangzhou 510006, Peoples R China
[2] Wuhan Inst Technol, Sch Mat Sci & Engn, Wuhan 430205, Peoples R China
[3] Wuhan Inst Technol, Hubei Key Lab Plasma Chem & Adv Mat, Wuhan 430205, Peoples R China
[4] South China Normal Univ, Int Acad Optoelect Zhaoqing, Zhaoqing 526060, Peoples R China
基金
中国国家自然科学基金;
关键词
NiSe; Freestanding electrode; 1D carbon nanofibers; Cycling stability; Sodium storage; ANODE MATERIAL; ION; LITHIUM; PERFORMANCE; NANOPARTICLES; ELECTRODE; GRAPHENE; MOSE2;
D O I
10.1016/j.apsusc.2021.152181
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
NiSe is considered to be an effective sodium storage electrode material due to its eminent theoretical capacity and ultra-long-term cycle life. Nonetheless, the large volume fluctuation and slow reaction kinetics cause NiSe to exhibit poor rate performance and cycle stability. Furthermore, the conventional electrode preparation technique necessitates the use of conductive and binder chemicals, resulting in poor electrochemical performance. To address these issues, freestanding NiSe-based electrodes (NiSe@C@NCNFs) are successfully fabricated via electrospinning Ni-MOF precursors and subsequent selenization reactions that NiSe nanoparticles are in-situ protected by MOF-derived porous carbon, thus ensuring the long-term cycling stability for sodium storage. Furthermore, the unique electrode structure design can improve the anode-electrolyte interface contact, short-ening the sodium ionic transport path and quickening reaction kinetics. According to corresponding kinetics analysis, the sodiation/desodiation process of NiSe@C@NCNFs is a dominant surface pseudo-capacitance pro -cess, guaranteeing their prominent rate capability.
引用
收藏
页数:7
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