Abstract

Abstract Titanium substrate was subjected to anodization and electrodeposition techniques to prepare tin oxide decorated tungsten oxide doped TiO2 nanotube (Sn-WTNT) films. Then, they were used as photoanodes in photoelectrochemical (PEC) water splitting to produce hydrogen. The samples were characterized by different techniques including field emission scanning and transmission electron microscopies (FE-SEM and TEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), UV–Vis DRS and Raman spectroscopies. The photoelectrochemical behavior of the samples was studied by linear sweep voltammetry (LSV) and chronoamperometry. Furthermore, the impact of tin electrodeposition time on the photocatalytic behavior of the Sn-WTNT photoelectrodes in PEC water splitting has been investigated. The highest PEC activity was shown by WT5 photoelectrode, (WT5 = Sn-WTNT which was prepared after 10 min of tin electrodeposition and subsequent treatments). Also, the photochemical stability of all samples was maintained in all photocatalytic tests, even after four cycles. The effect of different alcohol additives on the electrolyte was also studied. The rate of hydrogen evolution by Sn-WTNT decreased as follows: ethylene glycol > glycerol > methanol > ethanol > propanol > butanol > pentanol. H2 production rates were observed to be influenced by the number of hydroxyl groups, polarity, and relative hole scavenging capability of the alcohols.

Full Text
Paper version not known

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.