Heterostructure charge transfer dynamics on self-assembled ZnO on electronically different single-walled carbon nanotubes

The charge transfer kinetics of the catalyst particles play a key role in advanced oxidation processes (AOP) for the complete destruction of recalcitrant and persistent contaminants in water. Here, a significant improvement in the photocatalytic performance is observed in the Single-Walled Carbon Nanotube (SWCNT)-ZnO heterostructure photocatalyst. The charge transfer dynamics and factors affecting AOP are studied using ZnO nanoparticles self-assembled onto three electronically different SWCNTs (metallic, semiconducting, and pristine) via the precipitation method, introducing a heterojunction interface. The creation of the SWCNT/ZnO heterostructure interface improves charge transfer and separation, resulting in a charge carrier lifetime of 7.37 ns. Also, surface area, pore size, and pore volumes are increased by 4.2 times compared to those of ZnO. The nanoparticles-coated face-mask fabric used as the floating photocatalyst exhibited high stability and recyclability with 99% RhB degradation efficiency under natural sunlight and 94% under UV light after the 5th cycle. The surface and crystal defects-oxygen or zinc defects/interstitials open new reaction active sites that assist in charge carrier transfer and act as pollutant absorption and interaction sites for enhanced performance. The ideal band edge positions of the valence band and conduction band favor the generation of H2O/OH center dot, OH center dot/OH, and O-2/HO2 center dot reactive oxygen species. OH center dot radicals are found to play a vital role in this AOP by using ethanol as an OH center dot scavenger.