• 文献标题:   Plasmon-Sensitized Graphene/TiO2 Inverse Opal Nanostructures with Enhanced Charge Collection Efficiency for Water Splitting
  • 文献类型:   Article
  • 作  者:   BOPPELLA R, KOCHUVEEDU ST, KIM H, JEONG MJ, MOTA FM, PARK JH, KIM DH
  • 作者关键词:   tio2graphene, surface plasmon, inverse opal, photocatalysi, photoelectrochemical water splitting
  • 出版物名称:   ACS APPLIED MATERIALS INTERFACES
  • ISSN:   1944-8244
  • 通讯作者地址:   Ewha Womans Univ
  • 被引频次:   46
  • DOI:   10.1021/acsami.6b14618
  • 出版年:   2017

▎ 摘  要

In this contribution we have developed TiO2 inverse opal based photoelectrodes for photoelectrochemical (PEC) water splitting devices, in which Au nanoparticles (NPs) and reduced graphene oxide (rGO) have been strategically incorporated (TiO2@rGO@Au). The periodic hybrid nanostructure showed a photocurrent density of 1.29 mA cm(-2) at 1.23 V vs RHE, uncovering a 2-fold enhancement compared to a pristine TiO2 reference. The Au NPs were confirmed to extensively broaden the absorption spectrum of TiO2 into the visible range and to reduce the onset potential of these photoelectrodes. Most importantly, TiO2@rGO@Au hybrid exhibited a 14-fold enhanced PEC efficiency under visible light and a 2.5-fold enrichment in the applied bias photon-to-current efficiency at much lower bias potential compared with pristine TiO2. Incident photon-to electron conversion efficiency measurements highlighted a synergetic effect between Au plasmon sensitization and rGO-mediated facile charge separation/transportation, which is believed to significantly enhance the PEC activity of these nanostructures under simulated and visible light irradiation. Under the selected operating conditions the incorporation of Au NPs and rGO into TiO2 resulted in a remarkable boost in the H-2 evolution rate (17.8 mu mol/cm(2)) compared to a pristine TiO2 photoelectrode reference (7.6 mu mol/cm(2)). In line with these results and by showing excellent stability as a photoelectrode, these materials are herin underlined to be of promising interest in the PEC water splitting reaction.