Confining self-standing CoSe2 nanostructures and Fe3C wrapped N-doped carbon frameworks with enhanced energy storage performances

被引:28
作者
Khalafallah, Diab [1 ,2 ]
Miao, Jizhong [1 ]
Zhi, Mingjia [1 ]
Hong, Zhanglian [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, 38 Zheda Rd, Hangzhou 310027, Peoples R China
[2] Aswan Univ, Fac Energy Engn, Mech Design & Mat Dept, POB 81521, Aswan, Egypt
关键词
Self-supported CoSe2 nanostructures; Fe3C@N-CNTs composite; Hierarchical porous architectures; Faradic redox reactions; Battery-type supercapacitor hybrid devices; Energy storage; EFFICIENT ELECTROCATALYST; CO0.85SE NANOSHEETS; ELECTRODE MATERIAL; FACILE SYNTHESIS; COBALT SELENIDE; NANOPARTICLES; EVOLUTION; SUPERCAPACITORS; MECHANISMS; NANOARRAYS;
D O I
10.1016/j.apsusc.2021.150449
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
Transition metal selenides have been explored as suitable candidates for sustainable energy systems. More specific, designing battery-type and capacitor electrodes with exceptional structural, compositional and physiochemical properties is of a great significance to build battery-type supercapacitor hybrid (BSH) devices with high energy and power performances. In this study, a novel binder free positive electrode-based on nanostructured CoSe2 is prepared on a macroporous nickel foam (NF) current collector (CoSe2/NF) via a one-step chemical deposition route. A time-dependent in-situ growth reaction is executed to optimize the structural and electrochemical properties of electrodes. Interestingly, the uniformly constructed CoSe2/NF-9 crystallized into vertically aligned nanosheet arrays with unique porous features shows a higher specific capacitance (231 mAh g(-1) at a current density of 1 A g(-1)) and keeps about 83.7% of its initial capacitance after 3000 potential GCD cycles. As per strategy, Fe3C@N-CNTs composite is synthesized through a facile strategy and serves as a negative electrode material with a substantially high specific capacitance of 348 F g(-1) at 1 A g(-1) coupled with a remarkable rate capability. By paring the as-prepared CoSe2/NF-9 cathode and Fe3C@N-CNTs anode, an alkaline aqueous BSH system is fabricated with an enlarged potential window of 1.7 V. The integrated CoSe2/NF-9//Fe3C@N-CNTs BSH device exhibits a large energy density of 79.3 Wh kg(-1) at a power density of 1023.6 kW kg(-1). Moreover, the device has an improved cycling stability and retains around 80.7% of its initial capacitance after 8000 charge-discharge cycles. These results afford an effective rational guidance for developing materials with special compositional characteristics and electrochemical performances for energy storage applications.
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页数:13
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