Flower-like MnNi2O4-MnNi2S4 core@shell composite electrode as battery-type supercapacitors

被引:12
|
作者
Lv, Xinrong [1 ]
Chen, Lu [1 ]
Min, Xiaoqin [1 ]
Lin, Xiaoyun [1 ,2 ]
Ni, Yongnian [1 ]
机构
[1] Nanchang Univ, Coll Chem & Chem Engn, Nanchang 330031, Peoples R China
[2] Nanchang Univ, Jiangxi Prov Key Lab Modern Analyt Sci, Nanchang 330031, Peoples R China
基金
中国国家自然科学基金;
关键词
electrode; In-situ growth reaction; Battery-type supercapacitors; Electrochemical performance; MICROWAVE-ASSISTED SYNTHESIS; SOLID-STATE SUPERCAPACITORS; REDUCED GRAPHENE OXIDE; FACILE SYNTHESIS; PERFORMANCE; NANOSHEETS; NANOCOMPOSITE; NANOPARTICLES; MICROSPHERES; ARCHITECTURE;
D O I
10.1016/j.est.2022.105792
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
A novel flower-like MnNi2O4-MnNi2S4 core@shell composite electrode was synthesized by a simple hydrother-mal in -situ growth reaction and used as battery-type supercapacitors. MnNi2S4 nanosheets as "shell" were observed to be evenly grown onto the surface of MnNi2O4 nanoflower as "core" to form a typical core@shell structure. Such structures greatly increase the abundant electrochemically active sites of materials. In addition, the X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscope (TEM) test results showed that MnNi2S4 is an amorphous structure, which can provide more channels for electron transmission and ion diffusion. Consequently, the MnNi2O4-MnNi2S4 electrode shows outstanding electro-chemical performance. When a current density is 1 A g-, 1 the specific capacity for the MnNi2O4-MnNi2S4 reaches up to 1302.0C g-1, which is 2.7 times higher than that of the MnNi2O4. Furthermore, the MnNi2O4-MnNi2S4 shows preeminent cycling performance, and its specific capacity retention rate can still be maintained at 96.67 % after 5000 cycles at 20 A g-1. Additionally, when the power density is 774.95 W kg-, 1 the energy density for the MnNi2O4-MnNi2S4 is up to be 57.26 Wh kg-1. Therefore, the device-MnNi2O4-MnNi2S4//AC shows good prac-tical application prospect.
引用
收藏
页数:10
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