Article
Enhanced Photoactivity in Bilayer Films with Buried Rutile–Anatase Heterojunctions
Article first published online: 14 DEC 2010
DOI: 10.1002/cphc.201000734
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Romero-Gomez, P., Borras, A., Barranco, A., Espinos, J. P. and Gonzalez-Elipe, A. R. (2011), Enhanced Photoactivity in Bilayer Films with Buried Rutile–Anatase Heterojunctions. ChemPhysChem, 12: 191–196. doi: 10.1002/cphc.201000734
Publication History
- Issue published online: 12 JAN 2011
- Article first published online: 14 DEC 2010
- Manuscript Received: 8 SEP 2010
Funded by
- EU. Grant Number: NMP3-CT-2006–032583
- Spanish MICINN. Grant Numbers: MAT2010–21228, MAT2010–18447, CONSOLIDER 2010-CSD2008–00023
- Junta de Andalucia. Grant Number: P09-TEP5283 and CTS-5189
Keywords:
- crystal growth;
- photocatalysis;
- Raman spectroscopy;
- surface chemistry;
- thin films
Abstract
Herein, we study the photoactivity of anatase–rutile bilayer thin films consisting of an anatase overlayer of variable thickness from some tenths to some hundred nanometers deposited onto a rutile thin film. As references single anatase layers of equivalent thickness were deposited onto silicon. All the films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spectroscopy. The photoactivity of the samples was assessed by following the evolution with the UV illumination time of both the wetting angle on the thin film surface and the decoloration of a dye in a water solution. While a similar efficiency is found for the first type of experiments irrespective of the anatase thickness, in the second type a maximum in the photoactivity is found for a thickness of the anatase layer of about 130 nm. This enhanced photoactivity in bilayer systems with a buried anatase–rutile heterojunction is related to the formation of different Schottky potential barriers in the anatase layer, depending on its thickness and the substrate (i.e. rutile or SiO2) where it is deposited.

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