Gold Nanoparticles Located at the Interface of Anatase/Rutile TiO2 Particles as Active Plasmonic Photocatalysts for Aerobic Oxidation
Titanium
Binding Sites
Time Factors
Light
Photochemistry
Temperature
Metal Nanoparticles
Electrons
02 engineering and technology
01 natural sciences
7. Clean energy
Catalysis
0104 chemical sciences
Oxygen
Models, Chemical
Alcohols
Gold
0210 nano-technology
DOI:
10.1021/ja2120647
Publication Date:
2012-03-23T12:21:48Z
AUTHORS (6)
ABSTRACT
Visible-light irradiation (λ > 450 nm) of gold nanoparticles loaded on a mixture of anatase/rutile TiO(2) particles (Degussa, P25) promotes efficient aerobic oxidation at room temperature. The photocatalytic activity critically depends on the catalyst architecture: Au particles with <5 nm diameter located at the interface of anatase/rutile TiO(2) particles behave as the active sites for reaction. This photocatalysis is promoted via plasmon activation of the Au particles by visible light followed by consecutive electron transfer in the Au/rutile/anatase contact site. The activated Au particles transfer their conduction electrons to rutile and then to adjacent anatase TiO(2). This catalyzes the oxidation of substrates by the positively charged Au particles along with reduction of O(2) by the conduction band electrons on the surface of anatase TiO(2). This plasmonic photocatalysis is successfully promoted by sunlight exposure and enables efficient and selective aerobic oxidation of alcohols at ambient temperature.
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