Abstract
The present work explores palladium sensitized Titania nanotubes (Pd/TiO2 NTs) as a potential sensor material for detecting hydrogen (H2). TiO2 NTs powder was prepared as bundles via rapid breakdown anodization. Pd nanoparticles (NPs) were deposited over TiO2 NTs by sodium borohydride-based chemical reduction of palladium chloride (PdCl2) to form nanocomposite materials. Morphological analysis exposed the tubular architecture and provided the nanoscale dimensions of the synthesized materials. Structural analysis revealed the anatase phase and face-centered cubic crystal structure for TiO2 NTs and Pd nanoparticles (NPs), respectively. The presence of Pd over TiO2 NTs was established with compositional analysis. Thermal stability analysis confirmed that the deformation of phase takes place only after 550 °C, thereby indicating the suitability of the material to sense H2 up to the required 350 °C temperature. A paste of Pd/TiO2 NTs was used to make a thick film sensor to sense H2 in argon (Ar) as a function of Pd loading and temperature. A tremendous change in the sensor response of the sample was witnessed with different percentages of Pd. The sensor material was insensitive to H2 up to a threshold temperature of 100 °C owing to the formation of a surface oxide over Pd NPs. The sensors displayed an elevated response beyond the threshold temperature. The sensing behavior was selective only to H2 gas, amid the presence of reducing gases like ammonia and methane and oxidizing gas like nitrogen oxide.
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.