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Thermal coupled photocatalysis to enhance CO2 reduction activities on Ag loaded g-C3N4 catalysts
- Source :
- Surfaces and Interfaces. 23:101006
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- The contribution of heat input in traditional photocatalytic processes is rarely studied. Herein, a series of the Ag nanoparticles deposited g-C3N4 (Ag-CN) was prepared by photochemical method and used for photocatalytic CO2 reduction with the assistance of thermal energy. The photocatalytic properties were investigated under light-emitting diode light (420 nm, on the order of solar intensity) irradiation at temperatures up to 200 oC, confirming that the CO evolution rate was strongly dependent on the reaction temperature. The CO production reached to a maximum value of 179.6 μmol•g−1•h−1 (about 4.2 times higher than that of CN) on the 20%Ag loaded CN at 190 °C although negligible photocatalytic activity was observed under light illumination at ambient temperature. The enhancement of the temperature could not only improve the transfer rate and energy of the excited electrons, but also increase the population of the activated molecules, which might contribute to the enhancement on the CO production. Our finding provides an alternative way for integrating infrared light (accounting for ~50% of the solar light) in photocatalysis considering the thermal effect of the infrared light.
- Subjects :
- education.field_of_study
Materials science
business.industry
Infrared
Population
General Physics and Astronomy
02 engineering and technology
Surfaces and Interfaces
General Chemistry
010402 general chemistry
021001 nanoscience & nanotechnology
Condensed Matter Physics
Photochemistry
01 natural sciences
0104 chemical sciences
Surfaces, Coatings and Films
Catalysis
Excited state
Thermal
Photocatalysis
Irradiation
0210 nano-technology
business
education
Thermal energy
Subjects
Details
- ISSN :
- 24680230
- Volume :
- 23
- Database :
- OpenAIRE
- Journal :
- Surfaces and Interfaces
- Accession number :
- edsair.doi...........d8c316cb464a937f1c985289ea32e901