Abstract
In this work, the attapulgite-supported nitrogen-doped carbon (ANC) was prepared by in-situ chemically polymerizing polyaniline coating upon attapulgite, followed by high temperature heat treatment, and then NiCo2O4was reacted onto the surface of ANC by a combination of hydrothermal reaction and calcination to synthesize ANC@NiCo2O4 composites. The chemical composition and morphology of the samples were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and N2 adsorption/desorption. The electrochemical properties were evaluated by means of constant current charge discharge (GCD) and cyclic voltammetry (CV). The results showed that due to the high specific surface area and porous structure of ANC, the NiCo2O4 particles were uniformly located on the surface, resulting in large contact reaction areas with the electrolyte and improved electrochemical performance. At a current density of 1 A·g-1, the specific capacitance was up to 945.5 F·g-1, while at a current density of 16 A·g-1, it was 587.6 F·g-1, i.e., the capacitance retention was 62.1%, revealing a better rate performance. After 2000 cycles of charge-discharge process at a high current of 12 A·g-1, the capacitance retention was 74.1%, higher than 48.7% of pure NiCo2O4, which indicated that the as-prepared composite electrode materials had excellent electrochemical durability.
Graphical Abstract
Keywords
Attapulgite, Carbon, Nitrogen-doped, NiCo2O4, Electrode material, Supercapacitor
Publication Date
2017-02-28
Online Available Date
2016-07-29
Revised Date
2016-07-05
Received Date
2016-05-23
Recommended Citation
Hui WAN, Zong-rong YING, Xin-dong LIU, Jian-jian LU, Wen-wen ZHANG.
Preparation and Electrochemical Properties of Attapulgite-Supported Nitrogen-Doped Carbon@NiCo2O4Composites for Supercapacitors[J]. Journal of Electrochemistry,
2017
,
23(1): 28-35.
DOI: 10.13208/j.electrochem.160523
Available at:
https://jelectrochem.xmu.edu.cn/journal/vol23/iss1/5
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