Abstract
NiO-TiO2 (TN) nanocomposite is synthesized from an assembly of p-type nickel oxide (NiO) and n-type titanium oxide (TiO2) in an ultrasound assisted operation. Transmission electron microscopy (TEM) demonstrates the existence of hexagonal particles in the nanocomposite. Dynamic light scattering (DLS) measurements show stable TN nanoparticles (NPs) at a negative zeta potential (−18.5 ± 0.8 mV). The nanocomposite is tested for its catalytic activity towards degrading malachite green (MG), a known water toxicant and methylene blue (MB) under ultraviolet (UV) irradiation. Response surface methodology (RSM) is employed to optimise the influence of significant variables such as initial dye concentration, catalyst dose and time. Their mutual interactions are mapped by response surface and contour plots and correlated with degradation process by a designed model. The best photocatalytic efficiency (87%) is observed at an optimised concentration of 5 ppm dye with 10 ppm catalyst. The presence of inorganic ions and organic matter hardly affected the aggregate size of TN but caused a decline in photoactivity. The catalyst is found effective even in real water system (Hooghly River). A (Fluorine doped tin oxide) FTO/TN/Al heterojunction is fabricated. TN showed enhanced carrier mobility (1.03.10−4 m2V-1s-1) and low transit time (1.76.10-6 s) evaluated using space charge limited current (SCLC) theory. The nanocomposite appears suitable for energy preservation and environmental 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.