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Influence of pore structures on the electrochemical performance of asphaltene-based ordered mesoporous carbons

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Indexed by:期刊论文

Date of Publication:2013-07-01

Journal:MICROPOROUS AND MESOPOROUS MATERIALS

Included Journals:SCIE、EI

Volume:174

Page Number:67-73

ISSN No.:1387-1811

Key Words:Ordered mesoporous carbon; Structure; Supercapacitor; Charge storage ability; Ion transfer behavior

Abstract:Three ordered mesoporous carbons (OMCs) with different pore structures and pore arrangements were synthesized by template method using silicas as template and asphaltene as carbon source. The microstructures of the OMCs were characterized by X-ray diffraction and nitrogen adsorption techniques. The as-made OMCs had two-dimensional (2D) hexagonal symmetry, 3D body-centered cubic Im (3) over barm symmetry and 3D bicontinuous cubic Ia (3) over bard symmetry. All of the OMCs exhibit similar pore volume, pore size distribution and BET surface area. Their electrochemical performance as electrode materials for supercapacitors was investigated by cyclic voltammetry, galvanostactic charge-discharge, and electrochemical impedance spectroscopy techniques to assess the ion transfer behavior and charge storage capacity in different mesopore structures. The OMCs with different mesopore shapes and connectivity show different capacitances and ion transport behaviors. In terms of the ion transport kinetics, OMC with 2D hexagonal symmetry has the best ionic diffusion performance and lowest impedance for the long ordered pore channels. However, the OMC with 3D bicontinuous cubic Ia (3) over bard symmetry exhibits the best charge storage capacity because of the tortuosity of bicontinuous mesostructure. (C) 2013 Elsevier Inc. All rights reserved.

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