Abstract

Copper-based films (Cu2(OH)3NO3, Cu2O, and CuO) were successfully synthesized using a sparking process under an external magnetic field, without requiring an annealing process. We thoroughly investigate the impact of magnetic field orientation on the structural, morphological, and optical properties of the films, along with their performance in photocatalytic degradation of methylene blue (MB) and carbon dioxide (CO2) reduction. Field-emission scanning electron microscopy (FE-SEM) images reveal that the CuEB(S) sample displays secondary particles forming spherical, dense clusters, whereas the CuEB(N) sample exhibits larger, loosely packed clusters. In contrast, the cluster-like structures disperse in the CuEB(P) sample, resulting in a smoother film surface aligned with the parallel magnetic flux direction. Upon close observation, rice-shaped particles of varying sizes (26.3–60.3 nm) were found stacked together. This study presents a facile method to selectively fabricate films comprising single-phase Cu2(OH)3NO3, a CuO/Cu2O composite, or a combination of all phases by manipulating the external magnetic field orientation during the sparking process. All synthesized materials exhibit photocatalytic activity, with the heterojunction composed of CuO, Cu2O, and Cu2(OH)3NO3 demonstrating superior performance. This heterostructure achieved up to a 180 % enhancement in MB degradation and approximately doubled the CO2-to-CO conversion rate to 16.09 μmol g–¹ h–¹ compared to the sample prepared without a magnetic field.

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 call

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.