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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-
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文摘
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 51V nuclear magnetic resonance spectroscopy (MAS NMR). It was shown that in the as-prepared nanocrystals V was deposited onto the surface, forming Ti鈥揙鈥揤 bonds. After heat treatment at 400 掳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鈥揙鈥揤 network. After heating at 500 掳C, V2O5 phase separation occurred, further evidenced by thermal analyses. The 400 掳C nanocrystals had a mean size of about 5 nm, proving the successful synthesis of the colloidal counterpart of the well-known TiO2鈥揤2O5 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.

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