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
Photocatalytic nitrogen reduction for the green synthesis of ammonia at ambient conditions has been slowed by the narrow light harvesting range,low activity and high charge recombination of photocatalysts.Plasmonic se...Photocatalytic nitrogen reduction for the green synthesis of ammonia at ambient conditions has been slowed by the narrow light harvesting range,low activity and high charge recombination of photocatalysts.Plasmonic semiconducting nanomaterials are becoming the promising candidates for nitrogen photofixation because of the broad absorption spectrum,rich defects and hot carriers.In the present study,plasmonic SrMoO_(4) is developed by regulating the concentration of oxygen vacancies that are accompanied in the reduction process from Mo^(6+) to Mo^(5+).The stable and tunable localized surface plasmon resonance(LSPR)absorption in visible and near infrared light range makes the wide bandgap SrMoO_(4) utilize the solar energy more efficiently.Energetic electrons from both the intrinsic band excitation and the LSPR excitation enable the reduction of dinitrogen molecules thermodynamically in ultrapure water to ammonia.This work provides a unique clue to design efficient photocatalysts for nitrogen fixation.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.
文摘Photocatalytic nitrogen reduction for the green synthesis of ammonia at ambient conditions has been slowed by the narrow light harvesting range,low activity and high charge recombination of photocatalysts.Plasmonic semiconducting nanomaterials are becoming the promising candidates for nitrogen photofixation because of the broad absorption spectrum,rich defects and hot carriers.In the present study,plasmonic SrMoO_(4) is developed by regulating the concentration of oxygen vacancies that are accompanied in the reduction process from Mo^(6+) to Mo^(5+).The stable and tunable localized surface plasmon resonance(LSPR)absorption in visible and near infrared light range makes the wide bandgap SrMoO_(4) utilize the solar energy more efficiently.Energetic electrons from both the intrinsic band excitation and the LSPR excitation enable the reduction of dinitrogen molecules thermodynamically in ultrapure water to ammonia.This work provides a unique clue to design efficient photocatalysts for nitrogen fixation.
