Studying photochemical evolution of H2 from ethanol occurred only from illuminated catalyst. The core/shell structure performed better under Vis, while alloy structure (after calcination) performed better under UV
Bimodal size distribution 1 to 8 (Au) and 40 to 70 (Au-Pd)
n.d.
Two types of catalysts were synthesized and investigated. The active catalysts contained relatively large alloy particles with Au core surrounded by a Pd-rich shell. The photocatalytic activity was not studied
Medium pressure Hg lamp with a cut-off filter at nm
Synergetic effect of Au-Pt/TiO2 NPs under simulated sunlight compared to monometallic Pt-TiO2 and Au-TiO2 was reported. Higher activity of Au0.5-Pt0.5/TiO2 results from interaction between Au and Pt which can induce a decrease in metal-hydrogen bond strength and improve the electron trapping ability of NPs
The role of Pd was to split H2 into absorbed Pd–H atoms, which can reduce nitrite to other nitric species, but also reduce the adjacent copper oxides into metal copper. The highest activity was achieved by using Pd-Cu/TiO2 (Pd : Cu = 2 : 1, 3 wt.%) catalyst
The addition of a small amount of Ni onto Cu/TiO2 (10 wt.%, Cu : Ni mass composition of 9 : 1) enhanced the performance of photocatalyst from producing 5.0 cm3 to 6.1 cm3 of hydrogen
Cu-Ni/TiO2 nanoparticles revealed about 1.2 times and 2.6 times higher photoactivity than bimetallic photocatalysts Pt-Cu/TiO2 and Pd-Cu/TiO2 obtained using the same preparation procedure
Among the prepared TiO2 supported bimetallic (Pt-Pd/TiO2 and Pt-Ru/TiO2 and Pt-Au/TiO2) nanocatalysts Pt-Ru/TiO2 showed the best overall conversion and selectivity towards geraniol and nerol