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化学接枝法制备聚苯胺-碳纳米纤维复合材料及其超级电容器应用。

Polyaniline-carbon nanofiber composite by a chemical grafting approach and its supercapacitor application.

机构信息

Department of Chemistry and ‡Department of Physics, Indian Institute of Technology , Patna 800013, India.

出版信息

ACS Appl Mater Interfaces. 2013 Sep 11;5(17):8374-86. doi: 10.1021/am4014049. Epub 2013 Aug 21.

DOI:10.1021/am4014049
PMID:23911041
Abstract

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.

摘要

与通过范德华力的常规途径不同,本工作建立了一种使用共价键的简便新颖方法,用于合成聚苯胺(PANI)接枝碳纳米纤维(CNF)复合材料,作为有前途的超级电容器。为此,首先通过酰胺化将甲苯二异氰酸酯官能化至羧基化的 CNF,然后与过量苯胺反应形成脲衍生物和残留苯胺,随后将其聚合并接枝脲衍生物。通过 IR、拉曼、1H NMR、X 射线光电子能谱和紫外-可见光谱、X 射线衍射和热重分析验证了 CNF 的酰胺化(TCNF)以及随后在 TCNF 上接枝 PANI。形态分析表明 PANI 在 TCNF 表面上均匀分布,表明它们之间存在强烈相互作用。在电流密度为 0.3 A g(-1) 时,含有 6 wt % TCNF 的复合材料的电化学测试表明,其电容约为 557 F g(-1),初始电容的容量保持率为 86%,即使在 2000 次充放电循环后也是如此,这表明与通过范德华力形成的材料相比,其具有优越性。显著增强的电化学性能表明了苯基取代酰胺键在开发π共轭结构中的重要性,这促进了电荷转移,因此使其成为高效超级电容器的有吸引力的选择。

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