Cu2O/SiC photocatalytic reduction of carbon dioxide to methanol using visible light on InTaO4

Photo-catalytic reduction of CO2 to methanol is a direct path to producing energy from the sun. The production of methanol via photocatalytic reduction of CO2 using a modified catalyst was investigated. The photo-catalytic reduction of CO2 to methanol is considered a direct path to producing energy...

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Veröffentlicht in:Materials science in semiconductor processing 2024-05, Vol.174, p.108235, Article 108235
Hauptverfasser: Oni, Babalola Aisosa, Sanni, Samuel Eshorame, Tomomewo, Olusegun Stanley, Bade, Shree Om
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Sprache:eng
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Zusammenfassung:Photo-catalytic reduction of CO2 to methanol is a direct path to producing energy from the sun. The production of methanol via photocatalytic reduction of CO2 using a modified catalyst was investigated. The photo-catalytic reduction of CO2 to methanol is considered a direct path to producing energy from the sun since it involves using solar energy to drive a chemical reaction that converts CO2 into methanol. The sol-gel method was used to produce Cu2O/SiC catalyst loaded onto InTaO4 photo-catalyst support. The Cu2O/SiC photo-catalyst was made from Cu2O-modified SiC nanoparticles (NPs). An optical-fiber photo-reactor (0.14 m thick) comprising of Cu2O·SiC-NPs/InTaO4-coated fibers was used to evenly spread and transmit light inside the reactor. The ultraviolet–visible spectra of powdered Cu2O/SiC, InTaO4, and Cu2O/SiC–InTaO4 were all examined. CO2 was photo-catalytically reduced to CH3OH using sunlight irradiation, visible-light, and the optical-fiber reactor. At 80 °C, the CH3OH produced was 21.0 μ mol/g using energy with light intensity of 327 mW/cm2. The CH3OH production rate from sunlight was 3.43 μ mol/g. The optical-fiber reactor and quantum efficiencies in aqueous-phase were about 0.0045% and 0.063%, per gram of 1 wt%Cu2O+1 wt% SiC on InTaO4 photo-catalyst support. Under visible-light irradiation, a high CH3OH yield of 430 μmol/g with 1 wt%Cu2O + 1 wt% SiC on InTaO4 was achieved.
ISSN:1369-8001
1873-4081
DOI:10.1016/j.mssp.2024.108235