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Photonic crystals in biology

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Poster Session, Tuesday, June 15<br />

Theme A1 - B702<br />

Synthesis of anatase TiO 2 nanotubes at high temperature by sol-gel template method<br />

Elaheh Ghorbani 1, * , Leili Motevalizadeh 1, * , Nasser Shahtahmassebi 2 , Ebrahim Attaran 2<br />

1 Department of physics, Faculty of science, Islamic Azad university, Mashhad branch, Mashhad, Iran.<br />

2 Department of physics, Ferdowsi university of Mashhad, Mashhad, Iran.<br />

Abstract—The anatase phase of TiO 2 nanotubes have been synthesized by sol-gel template method us<strong>in</strong>g alum<strong>in</strong>a membrane<br />

as a template after anneal<strong>in</strong>g at 800°C for 2 hours. Transmission electron microscopy (TEM) and X-ray diffraction were used<br />

to <strong>in</strong>vestigate the structure and morphology of the TiO 2 nanotubes. TEM image showed that the obta<strong>in</strong>ed TiO 2 nanotubes were<br />

highly ordered and uniform. The diameter and length of the obta<strong>in</strong>ed nanotubes were determ<strong>in</strong>ed by the pore size and the<br />

thickness of AAO template. XRD results showed that the TiO 2 nanotubes were crystallized <strong>in</strong> anatase phase after anneal<strong>in</strong>g at<br />

800°C for 2 hours.<br />

TiO 2 is one of the semiconductor materials that are widely<br />

<strong>in</strong>vestigated due to important applications <strong>in</strong> many fields such<br />

as gas sensors, solar cells and photocatalysts [1, 2]. Most of<br />

these applications are a consequence of its chemical stability,<br />

high photocatalytic activity and surface reactivity [3, 4].<br />

Recently, much effort has been devoted to preparation of TiO 2<br />

nanotubes that have larger surface area compared to TiO 2<br />

nanoparticles and bulks. These structures should enhance<br />

surface related properties such as catalytic activity and surface<br />

adsorption [5].<br />

One of the most important methods for synthesis TiO 2<br />

nanotubes is the template assisted method due to controll<strong>in</strong>g<br />

the morphology and arrangement (1D) nanostructures <strong>in</strong><br />

which the diameter, length and aspect ratio of the obta<strong>in</strong>ed<br />

structures are fully controlled by the templates used [6]. This<br />

method comb<strong>in</strong>es the sol-gel process<strong>in</strong>g and template-based<br />

growth. In this manner, the template is dipped directly <strong>in</strong>to<br />

TiO 2 -sol solution with an appropriate deposition time, sol<br />

particles can fill channels of template and form structures with<br />

high aspect ratio. The f<strong>in</strong>al product will be obta<strong>in</strong>ed after a<br />

thermal treatment to remove the gel [7].<br />

In this paper the TiO 2 -sol is formed by mix<strong>in</strong>g of<br />

titanium tetra isopropoxide and 2-propanol at molar ratios of<br />

1:20. The mixture was then stirred for 3 h at the room<br />

temperature.<br />

For the synthesis of nanotubes, the porous anodic<br />

alum<strong>in</strong>a membranes (Whatman Anodisc 25) were used as the<br />

template. The average thickness, and pore size of these<br />

templates were 60 μm and 150–200 nm, respectively. The<br />

alum<strong>in</strong>a template membranes were dipped <strong>in</strong>to sol solution for<br />

5 m<strong>in</strong>, then the samples were dried <strong>in</strong> air at room temperature<br />

for 30 m<strong>in</strong>. For thermal treatment, the prepared specimens<br />

were placed <strong>in</strong> a furnace (<strong>in</strong> air) and the samples warm up to<br />

200°C <strong>in</strong> less than 5 m<strong>in</strong>, then they were heated up at a rate of<br />

2°C/m<strong>in</strong> <strong>in</strong> 800°C and were held <strong>in</strong> this temperature for 2 h.<br />

F<strong>in</strong>ally, the furnace was shut down and the samples were<br />

cooled down to room temperature. The fig 1 shows the XRD<br />

patterns of samples annealed at 800°C for 2 h. we have to<br />

notice that these samples are <strong>in</strong>clude of AAO membrane and<br />

polycrystall<strong>in</strong>e TiO 2 nanotubes. The peak positions and their<br />

relative <strong>in</strong>tensities are consistent with the standard powder<br />

diffraction pattern of anatase TiO 2 . Sadeghzade Attar et al.<br />

reported the formation of anatase TiO 2 <strong>in</strong> anneal<strong>in</strong>g<br />

temperature between 400 to 600°C and <strong>in</strong> 800°C the phase of<br />

TiO 2 was reported rutile[8]. But <strong>in</strong> this work the phase of TiO 2<br />

has been changed from rutile to anatase <strong>in</strong> this anneal<strong>in</strong>g<br />

temperature.<br />

Fig. 2 shows TEM images of obta<strong>in</strong>ed TiO 2 nanotubes.<br />

They have a wall thickness about 10 nm and a diameter of<br />

around 200 nm, which correspond exactly with the pore size<br />

of the AAO membrane. This <strong>in</strong>dicates that the diameter of the<br />

nanotube synthesized is controlled by the pore size of<br />

alum<strong>in</strong>um oxide membrane.<br />

Fig. 1 XRD pattern of sample that <strong>in</strong>clude TiO 2 nanotubes and AAO<br />

template.<br />

200 nm 500 nm<br />

Fig. 2 TEM images of TiO2 nanotubes<br />

In this study, TiO 2 nanotubes have been synthesized by<br />

sol-gel chemical method with<strong>in</strong> the pores of AAO template<br />

membrane. The results of XRD showed that the obta<strong>in</strong>ed TiO 2<br />

nanotubes are polycrystall<strong>in</strong>e with anatase phase after<br />

anneal<strong>in</strong>g at 800ºC for 2h. The TEM images showed the<br />

average diameter of nanotubes were about 200 nm <strong>in</strong> diameter<br />

with several micrometers <strong>in</strong> length. It was shown that the<br />

dimension of nanotubes depends on the pore size of the<br />

template.<br />

*Correspond<strong>in</strong>g author: lmotevali@mshdiau.ac.ir, e.ghorbani80@gmail.com<br />

[1] E. Palomares, R. Vilar, J.R. Durrant, Chem. Commun. 4 (2004) 362.<br />

[2] B. O , Regan, M. Gratzel, Nature (1991) 353.<br />

[3] A-W. Xu, Y. Gao, H-Q. Liu, J Catal 207(2002)151.<br />

doi:10.1006/jeat.2002.3539.<br />

[4] M. Keshmiri, M. Mohseni, T. Troczynski, Appl Catal Environ<br />

53(2004)209. doi: 10.1016/j.apcatb.2004.05.016<br />

[5] E. Com<strong>in</strong>i, C. Baratto, G. Fglia, M. Ferroni, A. Vomiero, G. Sberveglieri,<br />

Progress <strong>in</strong> material science 54 (2009) 1.<br />

[6] John C. Hulteen and Charles R. Mart<strong>in</strong>, J. Mater. Chem. 7 (1997) 1075.<br />

[7] B.B. Lakshmi, C.J. Patrissi, C.R. Mart<strong>in</strong>, Chem. Mater. 9 (1997) 2544.<br />

[8] A. Sadeghzadeh Attar, M. Sasani, F. Hajiesmaeilbaigi, Sh. Mirdamadi,<br />

K.Katagiri, K. Koumoto; J Mater Sci 43 (2008) 5924.<br />

6th Nanoscience and Nanotechnology Conference, zmir, 2010 379

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