4.6 Article

Preparation of graphene-carbon nanotube-TiO2 composites with enhanced photocatalytic activity for the removal of dye and Cr (VI)

Journal

APPLIED CATALYSIS A-GENERAL
Volume 473, Issue -, Pages 83-89

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcata.2013.12.028

Keywords

Carbon nanotubes; Graphene; Titania; Photocatalysis

Funding

  1. National Science Fund for Distinguished Young Scholars [51225901]
  2. National Key Basic Research Development Program (973 project) of China [2010CB429006]
  3. National Natural Science Foundation of China [51108158]
  4. Outstanding Youth Fund of Jiangsu Province [BK2012037]
  5. Fundamental Research Funds for the Central Universities [2013832114]
  6. Project of 333 High Level Talents of Jiangsu Province [BRA2010121]
  7. Research Fund for innovation team of Ministry of education [IRT13061]

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Graphene-carbon nanotubes (CNTs)-TiO2 composites were successfully synthesized by a one-pot solvothermal method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and diffuse reflectance UV-vis spectra. The photocatalytic activity of as-prepared composite photocatalysts was tested by degradation of dye methylene blue (MB) and photoreduction of Cr(VI) in aqueous solution under UV light irradiation. The experiment results showed that the composites exhibited enhanced photocatalytic performance compared to binary one (i.e. graphene-TiO2) and pristine TiO2. The effect of CNTs content on the photocatalytic activity was also studied. It showed that the photocatalytic performance of the graphene-CNTs-TiO2 hybrids was dependent on the proportion of CNTs in the composite. The mass ratio of CNTs:TiO2 = 5% was proved to be the optimal ratio. The apparent rate constants k for MB degradation and Cr(VI) reduction were 2.2 and 1.9 times as graphene-TiO2 composite, respectively. The enhanced activity can be ascribed to the addition of CNTs, which can be severed as charge transmitting paths thus decrease the recombination rate of photoinduced electron-hole pairs. This mechanism for the enhanced photoactivity was further confirmed by measuring the hydroxyl radical and transient photocurrent. (C) 2014 Elsevier B.V. All rights reserved.

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