The effect of growth parameters on photo-catalytic performance of the MAO-synthesized TiO2 nano-porous layers
- 1. Center of Excellence for Advanced Materials, Iran University of Science and Technology, P.O. Box 16845-195, Tehran (Iran, Islamic Republic of)
- 2. School of Metallurgy and Materials Engineering, Iran University of Science and Technology, P.O. Box 16845-161, Tehran (Iran, Islamic Republic of)
- 3. Institute for Nanoscience and Nanotechnology, Sharif University of Technology, P.O. Box 14588-89694, Tehran (Iran, Islamic Republic of)
- 4. Department of Physics, Sharif University of Technology, P.O. Box 11155-9161, Tehran (Iran, Islamic Republic of)
Description
In this research, the effect of applied voltage and electrolyte concentration on structure, chemical composition, optical properties, and especially photo-catalytic activity of the TiO2 layers containing micro/nano-sized pores are discussed. TiO2 layers were synthesized by micro arc oxidation (MAO) process using different electrolyte concentrations and applied voltages. Surface structure of the layers was studied by scanning electron microscope (SEM); furthermore, energy dispersive spectrophotometry (EDS), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) techniques were employed to determine phase structure and chemical composition of the layers. Photo-activity of the layers was also examined by measuring the decomposition rate of methylene blue on their surfaces. Band gap energy of the grown layers was also measured by a UV-vis spectrophotometer. It was found that there is a critical voltage at which electrical sparks begin to appear on the anode surface due to applying voltages higher than breakdown voltage of the surface gas layer. The critical voltage which was responsible for formation of structural pores decreased at higher concentrations of electrolyte. Meanwhile, surface pore size increased at higher applied voltages, or alternatively using electrolytes with higher concentrations. The layers contained the anatase and the rutile phases whose fractions varied with the synthesis parameters. It was also revealed that the band gap energy of the grown layers decreased with the applied voltage and electrolyte concentration. Moreover, the photo-catalytic performance of the layers synthesized at medium applied voltages was higher than that of the layers produced at lower or higher voltages. More than 90% of methylene blue solution was decomposed after 160 min UV irradiation on the layers produced in an electrolyte with a concentration of 10 g l-1.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.matchemphys.2009.12.005Additional details
Identifiers
- DOI
- 10.1016/j.matchemphys.2009.12.005;
- PII
- S0254-0584(09)00751-2;
Publishing Information
- Journal Title
- Materials Chemistry and Physics
- Journal Volume
- 120
- Journal Issue
- 2-3
- Journal Page Range
- p. 582-589
- ISSN
- 0254-0584
- CODEN
- MCHPDR
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44020088
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CHEMICAL COMPOSITION; DECOMPOSITION; ELECTROLYTES; ENERGY GAP; IRRADIATION; LAYERS; METHYLENE BLUE; NANOSTRUCTURES; OPTICAL PROPERTIES; OXIDATION; PHOTOCATALYSIS; POROUS MATERIALS; SCANNING ELECTRON MICROSCOPY; SPECTROPHOTOMETRY; SURFACES; TITANIUM OXIDES; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- AMINES; ANTI-INFECTIVE AGENTS; ANTIMICROBIAL AGENTS; AZINES; CATALYSIS; CHALCOGENIDES; CHEMICAL REACTIONS; CHLORIDES; CHLORINE COMPOUNDS; COHERENT SCATTERING; DIFFRACTION; DRUGS; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; HALIDES; HALOGEN COMPOUNDS; HETEROCYCLIC COMPOUNDS; MATERIALS; MICROSCOPY; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PHENOTHIAZINES; PHOTOELECTRON SPECTROSCOPY; PHYSICAL PROPERTIES; SCATTERING; SPECTROSCOPY; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.