Abstract
The facilitation of charge transport toward the targeted chemical reaction is a challenging task for two-dimensional (2D) nanomaterials. We demonstrate the effectiveness of two different strategies, non-metal doping and heterojunction formation, to adjust the electronic and molecular structures of g-C3N4 nanosheets (CN), which could widen the visible-light response and improve the photo-induced electron–hole separation. The g-C3N4 nanosheets containing impurity levels (boron doping (BCN)) were prepared by a high-temperature solid-state reaction. Additionally, by anchoring the 3D dichalcogenide structures (CdIn2S4) elicited by a wet chemical route, hybrid BCN/CdIn2S4 nanostructures were obtained. The resulting BCN/CdIn2S4 (BCN–CIS3) nanostructures exhibited an excellent degradation efficiency (95%) for methyl orange (MO) compared to pristine g-C3N4 nanosheets (CN) (28%) and boron-doped g-C3N4 (BCN) (35%). All the optimized photocatalysts were thoroughly characterized using various techniques and investigated for comparative structural, optical, morphological, and catalytic properties. Our results reveal that introducing boron atoms into the lattice of g-C3N4 nanosheets leads to reduction in the band-gap energy and rapid electron transfer. The formation of heterojunctions with the 3D CdIn2S4 further assists in improving the degradation efficiency by minimizing the undesired electron–hole recombination, as confirmed by time-resolved photoluminescence (TRPL) analysis. This work proposes feasible strategies and their synergy to develop innovative materials for sustainable energy conversion and 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.