Abstract
The precise detection of flammable and explosive gases and vapors remains an important issue because of the increasing demand for renewable energy sources and safety requirements in industrial processes. Metal oxides (TiO2, SnO2, ZnO, etc.) are very attractive materials for the manufacturing of chemical gas sensors. However, their gas selectivity issues and further improvement in the sensing response remain a significant challenge. The incorporation of metal oxides with two-dimensional (2D) graphene oxide (GO) is considered to be a promising approach to obtaining hybrid structures with improved gas-sensing performance. Herein, we report the development of GO and niobium-doped titanium dioxide nanotube (NT) hybrid structures with a tunable selectivity and sensing response against hydrogen gas, achieved by properly controlling the degree of reduction and concentration of GO. The effects of these parameters are systematically studied in terms of the response amplitude and selectivity. It was found that, compared to undoped titanium dioxide nanotubes, the hybrid material with an optimal concentration of reduced-GO and the introduction of niobium shows an increase in hydrogen response of about an order of magnitude and a simultaneous reduction of the response to possible interfering compounds such as carbon monoxide and acetone, thus providing enhanced selectivity. This research may provide an efficient way to enhance the chemical sensing performance of metal oxide nanomaterials.
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.