Plasmon-Sensitized Graphene/TiO2 Inverse Opal Nanostructures with Enhanced Charge Collection Efficiency for Water Splitting

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 photo...

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Veröffentlicht in:ACS applied materials & interfaces 2017-03, Vol.9 (8), p.7075-7083
Hauptverfasser: Boppella, Ramireddy, Kochuveedu, Saji Thomas, Kim, Heejun, Jeong, Myung Jin, Marques Mota, Filipe, Park, Jong Hyeok, Kim, Dong Ha
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container_end_page 7083
container_issue 8
container_start_page 7075
container_title ACS applied materials & interfaces
container_volume 9
creator Boppella, Ramireddy
Kochuveedu, Saji Thomas
Kim, Heejun
Jeong, Myung Jin
Marques Mota, Filipe
Park, Jong Hyeok
Kim, Dong Ha
description 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.
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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). 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Mater. Interfaces</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>9</volume><issue>8</issue><spage>7075</spage><epage>7083</epage><pages>7075-7083</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><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. 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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.</abstract><pub>American Chemical Society</pub><doi>10.1021/acsami.6b14618</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-0444-0479</orcidid><orcidid>https://orcid.org/0000-0002-0370-5490</orcidid><orcidid>https://orcid.org/0000-0002-6629-3147</orcidid><orcidid>https://orcid.org/0000-0002-0928-3583</orcidid></addata></record>
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