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
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.
