Abstract
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 H2 evolution rate (17.8 μmol/cm2) compared to a pristine TiO2 photoelectrode reference (7.6 μmol/cm2). 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.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.