Abstract
A novel hybrid photocatalyst, ZnWO4/Ag2O@Ag heterostructure was synthesized using a simple one-pot microwave treatment with varying concentrations of silver. Physico-chemical characterization was performed to elucidate the synthesized nanohybrids' properties. The photocatalytic activity of both pristine and heterostructure samples was evaluated through the degradation of cationic MB dye. Among the varied Ag concentrations, the 9 % Ag-doped ZnWO4/Ag2O heterostructure exhibited superior degradation performance, with a degradation rate of 93 % achieved within 45 min, surpassing both other Ag concentrations (89 % (90 min) for 1 % Ag, 87 % (80 min) for 3 % Ag, 90 % (80 min) for 5 % Ag and 91 % (45 min) for 7 % Ag) and pristine ZnWO4 (91 % (90 min)) samples. This catalytic enhancement can be attributed to the formation of heterostructures, plasmon-induced absorption enhancement within specific wavelength ranges, and reduced charge recombination rates. UV–visible studies revealed Ag nanoparticles of various sizes in the heterostructures, supported by surface plasmon resonance (SPR) peaks at 480 and 550 nm, respectively. Trapping experiments indicated that •OH and •O2− were the active species in MB reduction for pure and heterostructure samples. Furthermore, the hybrid heterostructure samples exhibited high stability and reusability in photocatalytic degradation. These findings suggest that the ZnWO4/Ag2O heterostructure photocatalysts are promising candidates for environmental remediation applications.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: 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.