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Erschienen in: Journal of Materials Science 9/2017

11.01.2017 | Original Paper

A donor–acceptor–donor-type conjugated polymer-modified TiO2 with enhanced photocatalytic activity under simulated sunlight and natural sunlight

verfasst von: Yujie Wang, Ruxangul Jamal, Minchao Wang, Lei Yang, Fangfang Liu, Tursun Abdiryim

Erschienen in: Journal of Materials Science | Ausgabe 9/2017

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Abstract

A low bandgap donor–acceptor–donor (D–A–D)-type conjugated polymer, poly(3,6-bis(3,4-ethylenedioxythienyl)pyridazine) (poly(EPE)), including 3,4-ethylenedioxythiophene as donor (D) and pyridazine as acceptor (A) units were synthesized. The nanocomposites (poly(EPE)/TiO2) of D–A–D-type conjugated polymer and TiO2 with different weight percentage of poly(EPE) were successfully prepared by an in situ chemical oxidative polymerization method. The structure and morphology of nanocomposites were investigated by Fourier transform infrared spectroscopy, UV–Vis diffuse reflectance spectra (UV–Vis/DRS), scanning electron microscopy images and transmission electron microscopy images. The structural and morphological studies revealed that the poly(EPE) was entrapped in the TiO2 nanoparticles. The photocatalytic activities of nanocomposites were measured by the photodegradation of methyl orange (MO) aqueous solutions under simulated sunlight and natural sunlight irradiation, respectively. The pseudo-first-order kinetic constants of photocatalytic degradation of MO under simulated sunlight and natural sunlight irradiation with 8 wt% poly(EPE)/TiO2 were 4.39 and 4.04 times as great as that of pure TiO2, respectively, exhibiting greater photocatalytic performance.

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Metadaten
Titel
A donor–acceptor–donor-type conjugated polymer-modified TiO2 with enhanced photocatalytic activity under simulated sunlight and natural sunlight
verfasst von
Yujie Wang
Ruxangul Jamal
Minchao Wang
Lei Yang
Fangfang Liu
Tursun Abdiryim
Publikationsdatum
11.01.2017
Verlag
Springer US
Erschienen in
Journal of Materials Science / Ausgabe 9/2017
Print ISSN: 0022-2461
Elektronische ISSN: 1573-4803
DOI
https://doi.org/10.1007/s10853-016-0717-7

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