• 文献标题:   Synthesis of frost-like CuO combined graphene-TiO2 by self-assembly method and its high photocatalytic performance
  • 文献类型:   Article
  • 作  者:   NGUYEN DCT, CHO KY, OH WC
  • 作者关键词:   graphene nanocomposite, selfassembly, organic dye photodegradation, frostlike, cuo
  • 出版物名称:   APPLIED SURFACE SCIENCE
  • ISSN:   0169-4332 EI 1873-5584
  • 通讯作者地址:   Hanseo Univ
  • 被引频次:   30
  • DOI:   10.1016/j.apsusc.2017.03.248
  • 出版年:   2017

▎ 摘  要

A novel material, frost-like CuO combined-graphene-TiO2 composite, was successfully synthesized using a self-assembly method. During the reaction, the loading of CuO and TiO2 nanoparticles on graphene sheets was achieved. The obtained CuO-graphene-TiO2 composite photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis, transmission electron microscopy (TEM), Raman spectroscopy, ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS), and X-ray photoelectron spectroscopy (XPS). The frost-like CuO nanoparticles combined with the small TiO2 rods were successfully loaded on the transparent graphene sheets. The photocatalytic degradation of rhodamine B (RhB), methylene blue trihydrate (MB), and reactive black B (RBB) in an aqueous solution under visible light irradiation was observed by UV spectrophotometry after measurement of the decrease of their concentrations. Through the photocatalytic test and TOC results, the CuO-graphene-TiO2 is expected to become a new potential material for photodegradation activity with excellent photodegradation. The scavenging experiments confirmed that center dot OH and h(+) play a major role in the photocatalytic reaction than O-2 center dot- or both hydroxyl and holes are the active species responsible for the RBB degradation under visible light irradiation. After five repeated cycles to investigate the stability of photocatalytic performance, the CuO-graphene-TiO2 had high stability under visible light irradiation. (C) 2017 Elsevier B.V. All rights reserved.