Colloidal Counterpart of the TiO2-Supported V2O5 System: A Case Study of Oxide-on-Oxide Deposition by Wet Chemical Techniques. Synthesis, Vanadium Speciation, and Gas-Sensing Enhancement
Abstract
TiO2 anatase nanocrystals were surface modified by deposition of V(V) species. The starting amorphous TiO2 nanoparticles were prepared by hydrolytic processing of TiCl4-derived solutions. A V-containing solution, prepared from methanolysis of VCl4, was added to the TiO2 suspension before a solvothermal crystallization step in oleic acid. The resulting materials were characterized by X-ray diffraction, transmission electron microscopy (TEM), Fourier transform infrared, Raman, and magic angle spinning solid-state V-51 nuclear magnetic resonance spectroscopy (MAS NMR). It was shown that in the as-prepared nanocrystals V was deposited onto the surface, forming Ti-O-V bonds. After heat treatment at 400 degrees C, TEM/electron energy loss spectroscopy and MAS NMR showed that V was partially inserted in the anatase lattice, while the surface was covered with a denser V-O-V network. After heating at 500 degrees C, V2O5 phase separation occurred, further evidenced by thermal analyses. The 400 degrees C nanocrystals had a mean size of about 5 nm, proving the successful synthesis of the colloidal counterpart of the well-known TiO2-V2O5 catalytic system. Hence, and also due to the complete elimination of organic residuals, this sample was used for processing chemoresistive devices. Ethanol was used as a test gas, and the results showed the beneficial effect of the V surface modification of anatase, with a response improvement up to almost 2 orders of magnitude with respect to pure TiO2. Moreover, simple comparison of the temperature dependence of the response clearly evidenced the catalytic effect of V addition.
Autore Pugliese
Tutti gli autori
-
Epifani M.; Diaz R.; Force C.; Comini E.; Andreu T.; Zamani R.R.; Arbiol J.; Siciliano P.; Faglia G.; Morante J.R.
Titolo volume/Rivista
Journal of physical chemistry. C
Anno di pubblicazione
2013
ISSN
1932-7447
ISBN
Non Disponibile
Numero di citazioni Wos
Nessuna citazione
Ultimo Aggiornamento Citazioni
Non Disponibile
Numero di citazioni Scopus
Non Disponibile
Ultimo Aggiornamento Citazioni
Non Disponibile
Settori ERC
Non Disponibile
Codici ASJC
Non Disponibile
Condividi questo sito sui social