Abstract

In this study, cobalt-based metal-organic framework (MOF) powder was prepared via the solvothermal method using 2,6-naphthalenedicarboxylic acid (NDC) as the organic linker and N,N-dimethylformamide (DMF) as the solvent. The thermal decomposition of the pristine cobalt-based MOF sample (CN-R) was identified using a thermogravimetric examination (TGA). The morphology and structure of the MOFs were modified during the pyrolysis process at three different temperatures: 300, 400, and 500 °C, which labeled as CN-300, CN-400, and CN-500, respectively. The results were evidenced via field-emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD). The crystallite size of all samples was calculated using Scherrer’s equation. The smallest crystallite size of 7.77 nm was calculated for the CN-300 sample. Fourier transform infrared spectroscopy (FTIR) spectra were acquired for all the samples. The graphical study of the cyclic voltammogram (CV) gave the reduction and oxidation peaks. The charge transfer resistance and ionic conductivity were studied using electrical impedance spectroscopy (EIS). The galvanostatic charge–discharge (GCD) responses of all samples were analyzed. The relatively high specific capacitance of 229 F g−1 at 0.5 A g−1 was achieved in the sample CN-300, whereby 110% of capacitance was retained after 5000 cycles. These findings highlighted the durability of the electrode materials at high current densities over a long cycle.

Highlights

  • Previous reports established that porous carbon materials are crucial for energy storage application [1,2,3,4]

  • The product was placed in an oven to evaporate the ethanol before implement analysis of cobalt-based metal-organic framework (MOF) (Co-MOF)

  • A sharp decrease in sample weight can be observed in the 100 ◦ C up to 150 ◦ C region, which was caused by moisture vaporization due to the presence of water molecules (H2 O), solvent (DMF), and alcohol in the sample

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Summary

Introduction

Previous reports established that porous carbon materials are crucial for energy storage application [1,2,3,4]. Porous carbon material was selected like the electrode material for electrochemical capacitors as a result of its large surface area of 3000 m2 g−1 , chemical resistance, and high conductivity [5]. The porous carbon capacity has arrived its bottleneck in getting the necessities of application in high energy storage [6]. Porous structure will provide extra space inside the electrode with a high surface area. The additional spacious area stores more ion at the electrode/electrolyte interface, which is important for energy storage application

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