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Journal of Materials Science
Erschienen in: Journal of Materials Science 8/2016

08.01.2016 | Original Paper

Facile preparation of halloysite/polyaniline nanocomposites via in situ polymerization and layer-by-layer assembly with good supercapacitor performance

verfasst von: Huabo Huang, Junlong Yao, Hongyan Chen, Xiaoping Zeng, Changlian Chen, Xiao She, Liang Li

Erschienen in: Journal of Materials Science | Ausgabe 8/2016

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Abstract

The functionalization of halloysite nanotubes (HNTs) has attracted much attention in recent years due to the nano-tubular structure and particular features. Here, we report a conductive nanohybrids of HNTs, polyaniline (PANI), and poly(sodium-p-styrenesulfonate) (PSS) with high electrical conductivity (0.11 S/cm) prepared by in situ polymerization and layer-by-layer assembly. The chemical structures and morphologies were characterized by FT-IR, UV–Vis, FE-SEM, and TEM, which confirmed that the layers of PANI, PSS, and PANI were sequentially coated onto the HNTs as expected. A study of cyclic voltammetry suggested the typical pseudocapacitance and good rate performance of the as-prepared nanocomposites. The results of galvanostatic charge/discharge and electrochemical impedance spectroscopy further demonstrated its favorable capacitive behavior and low resistance. The easily fabricated halloysite/polyaniline nanocomposites show great potential as electrode materials for supercapacitors.
Vorheriger Artikel Effect of morphological state of graphene on mechanical properties of nanocomposites
Nächster Artikel Effect of ion beam irradiation on dielectric properties of BaTiO3 thin film using surface plasmon resonance

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Metadaten
Titel
Facile preparation of halloysite/polyaniline nanocomposites via in situ polymerization and layer-by-layer assembly with good supercapacitor performance
verfasst von
Huabo Huang
Junlong Yao
Hongyan Chen
Xiaoping Zeng
Changlian Chen
Xiao She
Liang Li
Publikationsdatum
08.01.2016
Verlag
Springer US
Erschienen in
Journal of Materials Science / Ausgabe 8/2016
Print ISSN: 0022-2461
Elektronische ISSN: 1573-4803
DOI
https://doi.org/10.1007/s10853-016-9724-y

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