Polyaniline–Carbon Nanofiber Composite by a Chemical Grafting Approach and Its Supercapacitor Application
Unlike conventional routes by van der Waals forces, a facile and novel approach using covalent bonding is established in the present work to synthesize polyaniline (PANI)-grafted carbon nanofiber (CNF) composites as promising supercapacitors. For this purpose, toluenediisocyanate was initially funct...
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Veröffentlicht in: | ACS applied materials & interfaces 2013-09, Vol.5 (17), p.8374-8386 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Unlike conventional routes by van der Waals forces, a facile and novel approach using covalent bonding is established in the present work to synthesize polyaniline (PANI)-grafted carbon nanofiber (CNF) composites as promising supercapacitors. For this purpose, toluenediisocyanate was initially functionalized to carboxylated CNF via amidation followed by reaction with excess aniline to form a urea derivative and residual aniline, which was subsequently polymerized and grafted with a urea derivative. Amidation of CNF (TCNF) and, consequently, the grafting of PANI on TCNF were verified by IR, Raman, 1H NMR, X-ray photoelectron, and UV–visible spectroscopic methods, X-ray diffraction, and thermogravimetric analysis. Morphological analysis revealed uniform distribution of PANI on the surface of TCNF, indicating strong interaction between them. Electrochemical tests of the composite containing 6 wt % TCNF demonstrated efficient capacitance of ∼557 F g–1 with a capacity retention of 86% of its initial capacitance even after 2000 charge–discharge cycles at a current density of 0.3 A g–1, suggesting its superiority compared to the materials formed by van der Waals forces. The remarkably enhanced electrochemical performance showed the importance of the phenyl-substituted amide linkage in the development of a π-conjugated structure, which facilitated charge transfer and, consequently, made it attractive for efficient supercapacitors. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/am4014049 |