In this contribution we have developed TiO inverse opal based photoelectrodes for photoelectrochemical (PEC) water splitting devices, in which Au nanoparticles (NPs) and reduced graphene oxide (rGO) have been strategically incorporated (TiO@rGO@Au). The periodic hybrid nanostructure showed a photocurrent density of 1.29 mA cm at 1.23 V vs RHE, uncovering a 2-fold enhancement compared to a pristine TiO reference. The Au NPs were confirmed to extensively broaden the absorption spectrum of TiO into the visible range and to reduce the onset potential of these photoelectrodes. Most importantly, TiO@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 TiO. 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 TiO resulted in a remarkable boost in the H evolution rate (17.8 μmol/cm) compared to a pristine TiO photoelectrode reference (7.6 μmol/cm). 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.

Comprehensive insight into the thermochemical, photochemical and electrochemical reduction of CO2 to methane and long-chain hydrocarbons as alternative fuels.

Hierarchically organized porous carbonized‐Co3O4 inverse opal nanostructures (C‐Co3O4 IO) are synthesized via complementary colloid and block copolymer self‐assembly, where the triblock copolymer Pluronic P123 acts as the template and the carbon source. These highly ordered porous inverse opal nanostructures with high surface area display synergistic properties of high energy density and promising bifunctional electrocatalytic activity toward both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). It is found that the as‐made C‐Co3O4 IO/Ketjen Black (KB) composite exhibits remarkably enhanced electrochemical performance, such as increased specific capacity (increase from 3591 to 6959 mA h g−1), lower charge overpotential (by 284.4 mV), lower discharge overpotential (by 19.0 mV), and enhanced cyclability (about nine times higher than KB in charge cyclability) in Li–O2 battery. An overall agreement is found with both C‐Co3O4 IO/KB and Co3O4 IO/KB in ORR and OER half‐cell tests using a rotating disk electrode. This enhanced catalytic performance is attributed to the porous structure with highly dispersed carbon moiety intact with the host Co3O4 catalyst.