Abstract
• Photo-thermal-magnetic three-field coupling for enhanced CO 2 photo-reduction. • Nickel foam was used as nickel source and catalyst support. • 0.01 wt% Cu/Cu 2 O/HNF exhibited the best catalytic activity and CH 4 selectivity. • The heat of the reaction system came from magnetic-thermal and photo-thermal effects. Aiming at the bottleneck of thermodynamics, kinetics and reaction systems in photothermal catalytic CO 2 reduction conversion, a three-field coupling method based on the efficient utilization of solar energy and the application of a photo-thermal-magnetic three-field was proposed to achieve efficient and highly selective CO 2 conversion. The composite monolithic catalyst with three field response functions and multiple active reaction interfaces was prepared by using photoactive copper supported by nickel foam. The effect of an external alternating magnetic field on photocatalytic CO 2 reduction was studied using a range between 0.005 and 0.1 wt% Cu/Cu 2 O/Ni(OH) 2 /NF as catalysts. The results showed that 0.01 wt% Cu/Cu 2 O/Ni(OH) 2 /NF exhibited the best catalytic activity and CH 4 selectivity under alternating magnetic field enhanced photocatalysis. The main products were CO (6.76 μmol g −1 ) and CH 4 (167 μmol g −1 ). The selectivity of CH 4 was 96.1%. The yields of CH 4 using this method were 11 and 6 times higher than the yields obtained with photocatalysis (14.58 μmol g −1 ) and magnetic-thermal catalysis (26.75 μmol g −1 ), respectively. According to the analysis of temperature measurements and electrochemical measurements, the surface temperature of the three-field coupled catalyst reaches about 230 °C. Applying an alternating magnetic field can effectively reduce the recombination of photogenerated electron holes. Alternating magnetic field enhanced photocatalytic CO 2 reduction conversion provides a new and promising method for the efficient conversion and utilization of solar energy.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
