Plasmonic photocatalysis with tunable light absorption has aroused significant attention in so-lar-to-chemical energy conversion.However,the energy conversion efficiency of plasmonic photo-catalysts is impeded by inef...Plasmonic photocatalysis with tunable light absorption has aroused significant attention in so-lar-to-chemical energy conversion.However,the energy conversion efficiency of plasmonic photo-catalysts is impeded by ineffective charge separation and the lack of highly active sites for redox reactions.In this work,the Au nanoparticle size and Au-TiO2 interaction of the Au/TiO2 plasmonic photocatalyst were adjusted simultaneously using a post-calcination treatment.The visi-ble-ight-induced water oxidation activity exhibited a volcano-like relationship with the calcination temperature;the treated photocatalyst at 600°C manifested the highest activity.Characterization with UV-visible spectra,XRD,SEM,and XPS revealed that the effect of the Au nanoparticle size and Au-TiO2 interaction were both responsible for the increase in plasmon-induced water oxidation activity.展开更多
基金supported by the National Natural Science Foundation of China (21633010)the National Basic Research Program of China (973 pro‐gram, 2014CB239400)the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB01020300)~~
文摘Plasmonic photocatalysis with tunable light absorption has aroused significant attention in so-lar-to-chemical energy conversion.However,the energy conversion efficiency of plasmonic photo-catalysts is impeded by ineffective charge separation and the lack of highly active sites for redox reactions.In this work,the Au nanoparticle size and Au-TiO2 interaction of the Au/TiO2 plasmonic photocatalyst were adjusted simultaneously using a post-calcination treatment.The visi-ble-ight-induced water oxidation activity exhibited a volcano-like relationship with the calcination temperature;the treated photocatalyst at 600°C manifested the highest activity.Characterization with UV-visible spectra,XRD,SEM,and XPS revealed that the effect of the Au nanoparticle size and Au-TiO2 interaction were both responsible for the increase in plasmon-induced water oxidation activity.
