MXenes induced formation of Ni-MOF microbelts for high-performance supercapacitors

被引:108
|
作者
Zhang, Xu [1 ,2 ]
Yang, Shixuan [1 ,2 ]
Lu, Wang [1 ,2 ]
Lei, Da [1 ,2 ]
Tian, Yuhan [1 ,2 ]
Guo, Minggang [3 ]
Mi, Panpan [3 ]
Qu, Ning [1 ,2 ]
Zhao, Yingyuan [4 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116023, Peoples R China
[2] Dalian Univ Technol, Sch Chem Engn, Panjin 124221, Liaoning, Peoples R China
[3] Dalian Univ Technol, Panjin Inst Ind Technol, Liaoning Key Lab Chem Addit Synth & Separat, Panjin 124221, Liaoning, Peoples R China
[4] Binzhou Univ, Coll Chem Engn & Safety, Binzhou 256603, Shandong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Ni-MOFs microbelts; MXenes; Supercapacitors; Inductive effect; METAL-ORGANIC FRAMEWORKS; SUPERIOR ELECTROCHEMICAL PERFORMANCE; CARBON NANOSHEETS; ELECTRODES; SPHERES;
D O I
10.1016/j.jcis.2021.02.042
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
For the sake of developing new energy storage devices for satisfying the energy needs of the modern society, we herein report an innovative MXene-induced strategy to synthesize Ti3C2Tx MXenes/Ni based metal-organic framework composites (Ti3C2Tx/Ni-MOFs) for high-performance supercapacitors. The two-dimensional (2D) MXenes with oxygen-containing groups on the surface can be used as structure-directing agents to tune the Ni-MOFs into 2D microbelts. The presence of MXenes cannot only improve conductivity of the composite but also provide additional electric double layer capacitance and faradaic pseudocapacitance. The 2D Ni-MOF microbelts can offer rich activity sites for the faradaic redox reactions and shorten the ion transport path. Taking advantages of synergistic effects of Ni-MOF microbelts and Ti3C2Tx MXenes, the prepared Ti3C2Tx/Ni-MOFs electrode shows a good electrochemical performance with 1124 F g(-1) at the current density of 1 Ag-1 and 62% rate capability at 20 A g(-1). This work can offer a new insight to design 2D MOF belts as high-performance electrode materials for supercapacitors. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:95 / 102
页数:8
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