The effect of anatase crystal morphology on the photocatalytic conversion of NO by TiO2-based nanomaterials

15Citations
Citations of this article
29Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Hydrogen titanate nanotubes (H-TTNT) were synthesized by the alkali hydrothermal method followed by proton exchange and then submitted either to thermal treatment or to acid hydrothermal reaction to generate TiO 2-anatase nanocrystals of different morphologies. The samples were characterized by XRPD, TGA, sulfur analysis, N2 physisorption, UV-Vis spectroscopy and TEM. Their photocatalytic activities were determined by measuring the NO conversion in inert gas stream passed through the powder catalyst bed under UV radiation. Incomplete transformation into anatase resulted in nanomaterials with low activity due to coexistence with H-TTNT or TiO 2-B precursors. Anatase specimens derived from H-TTNT aged in strong sulfuric acid media contained equidimensional nanoparticles, but retention of sulfate negatively affected their photocatalytic activity. Combining milder acidic pH with higher aging temperature, allowed synthesis of a sulfate free anatase with the same optical properties and specific surface area as the counterpart produced by calcination of H-TTNT at 550°C; however, the former exhibited truncated bi-pyramid nanocrystals and the other adopted the form of nanorods. This latter showed the highest photocatalytic activity for NO abatement, outperforming the benchmark photocatatyst TiO2-P25; this improved activity was tentatively ascribed to the maximization of high energy {001} facets in anatase nanorods formed during calcination of H-TTNT. © Versita Sp. z o.o.

Cite

CITATION STYLE

APA

De Abreu, M. A. S., Morgado, E., Jardim, P. M., & Marinkovic, B. A. (2012). The effect of anatase crystal morphology on the photocatalytic conversion of NO by TiO2-based nanomaterials. Central European Journal of Chemistry, 10(4), 1183–1198. https://doi.org/10.2478/s11532-012-0040-3

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free