Effect of titanium dioxide crystalline structure on the photocatalytic production of hydrogen
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The Effect of Interfacial Chemical Bonding in TiO2-SiO2 Composites on Their Photocatalytic NOx Abatement Performance
Published on: July 4, 2017
Gian Luca Chiarello1, Agatino Di Paola, Leonardo Palmisano
1Dipartimento di Chimica Fisica ed Elettrochimica, CIMaINa and ISTM-CNR, Università degli Studi di Milano, via Golgi 19, I-20133, Milano, Italy.
Abstract:
The effect of the crystalline phase of TiO(2) (anatase, rutile and brookite) on its photocatalytic activity in hydrogen production from methanol-water vapours has been investigated by testing a series of both home-made and commercial TiO(2) photocatalysts, either bare or surface-modified by deposition of a fixed amount, i.e. 1 wt%, of platinum as co-catalyst. For all of the TiO(2) samples the rate of hydrogen production increased by one order of magnitude upon Pt deposition, because of the ability of Pt to enhance the separation of photoproduced electron-hole pairs. Under irradiation in the 350-450 nm wavelength range, brookite and anatase showed similar photoactivities, both superior to that of rutile. By contrast, rutile, possessing a narrower band gap, was active also under visible light (λ > 400 nm), whereas no hydrogen evolution was observed with anatase and brookite under such conditions. Surface area proved to be a key parameter, strongly influencing photoactivity. However, as the particle size became ultra-small, the semiconductor absorption edge was blue-shifted because of size quantisation effects, with a consequent decrease in hydrogen production rate due to the smaller portion of incident photons absorbed by the photocatalyst.

