WELCOME MESSAGE
NanoTR VII - 7th Nanoscience and Nanotechnology ConferencePB 1
Contents
Plenary Talks ... 3
S1 - Advanced Nanomaterials THEME A ... 10
S1 - Advanced Nanomaterials THEME B ... 37
S1 - Advanced Nanomaterials THEME C ... 59
S2 - Nanodevices and Microsystems THEME E ... 72
S2 - Nanodevices and Microsystems THEME F ... 92
S2 - Nanodevices and Microsystems THEME G ... 98
S2 - Nanodevices and Microsystems THEME J ... 110
S2 - Nanodevices and Microsystems THEME O ... 117
S3 - Nanofabrication and Nanocharacterization THEME H ... 135
S3 - Nanofabrication and Nanocharacterization THEME I ... 154
S3 - Nanofabrication and Nanocharacterization THEME L ... 171
S4 - Nanotechnology in Life Sciences THEME D ... 177
S5 - Special Topics in Nanotechnology THEME K ... 208
S5 - Special Topics in Nanotechnology THEME N ... 210
S5 - Special Topics in Nanotechnology THEME P ... 222
S6 - Nanotechnology and Public THEME R ... 232
S6 - Nanotechnology and Public THEME S ... 238
Poster Session 1 THEME A ... 243
Poster Session 1 THEME D ... 317
Poster Session 2 THEME A ... 388
Poster Session 2 THEME B ... 465
Poster Session 2 THEME C ... 501
Poster Session 3 THEME E ... 516
Poster Session 3 THEME F ... 551
Poster Session 3 THEME G ... 571
Poster Session 3 THEME H ... 581
Poster Session 3 THEME I ... 589
Poster Session 3 THEME K ... 610
Poster Session 3 THEME L ... 613
Poster Session 3 THEME M ... 620
Poster Session 3 THEME N ... 622
Poster Session 3 THEME O ... 631
Poster Session 3 THEME P ... 646
Poster Session 3 THEME R ... 663
Poster Session 3 THEME S ... 666
Panel for Sectoral Nanotechnology Strategies and Policies ... 668
Industry Talks ... 670
Poster Presentations
Poster Session 1
THEME A
Nanomaterials; Nanoparticles, Nanocrystals, Nano-porous
materials, Molecular and supramolecular Materials
P1.A. 3
Comparison of Optical Properties for SnO
2, SnO
2: F and SnO
2:Sb Films Deposited on Glass
Substrates
Güven Turgut1*, Demet Tatar1, 2, Ahmet Battal3and Bahattin Düzgün1 1K. K. Education Faculty, Department of Physics, Ataturk University, Erzurum 25240, Turkey
2Health services vocational high school, 76300, Turkey
2Education Faculty, Department of Science Education, Mus Alparslan University, Mus 49100, Turkey
Abstract— Thin films of undoped, 20 wt. % flourine-doped and 2 wt. % antimony-doped tin oxide on glasses at 410 ( 5) C were prepared by spray pyrolysis technique. The effect of 20 wt. % fluorine and 2 wt. % antimony doping on the optical properties of tin oxide thin films were investigated. From the optical studies, it was found that the transmittance of undoped film increased from 52.46 % to a maximum 78 % and 69,56 % for 20 wt. % fluorine-doped and 2 wt. % antimony-doped film, respectively.
The undoped stoichiometric SnO2 films have very high
electrical resistivity because of their low intrinsic carrier density and mobility [1]. Therefore the challenge is to prepare non-stoichiometric doped thin films. The conductivity of weakly nonstoichiometric tin oxide films is supposed to be due to doubly ionized vacancies serving as donors [2]. Dopants as antimony (Sb), indium (In), and fluorine (F), are frequently used. The fluorine and low concentrations of Sb doped tin oxide, being an n-type, wide band gap semiconductor ( 3 eV) with special properties, high transmittance in the visible range and high reflectance in the infrared, excellent electrical conductivity, greater carrier mobility and good mechanical stability are used in different devices like solar cells as transparent, protective electrodes [3], flat panel collectors as spectral selective windows, sensors for detection of gases, sodium lamps, gas sensors, and varistors [4–6]. Undoped tin oxide (TO), fluorine doped tin oxide (FTO) and antimony doped tin oxide (ATO) thin films have been prepared by various techniques, such as chemical vapour deposition, metalorganic deposition, rf sputtering, sol– gel, and spray pyrolysis [7–9]. Spray pyrolysis is used to prepare films because of its simplicity, cheapness and commercial viability [10,11]. Moreover, the spray pyrolysis technique is well suited for the preparation of doped tin oxide thin films because of it is ease to adding various doping materials, controlling the texture via various deposition temperatures and mass production capability for uniform large area coatings.
The prime aim of this work is to produce high transmission in SnO2 thin films by cost-effective chemical spray pyrolysis
technique. Hence undoped, 20 wt. % F and 2% wt. Sb doped tin oxide thin films were deposited on glass substrates at 410 ( 5) C were prepared by spray pyrolysis technique.
The optical properties of the TO, FTO and ATO thin films were studied in the UV-Vis spectrophotometer (Perkin Elmer, Lambda 35).
After the film deposition with spray pyrolysis, it was observed that the colour of the films varied from milky white for undoped SnO2 to grayish white for 20 wt. % F doped SnO2
and light blue for 2 wt. % Sb doped SnO2.
The transmission spectra of the films was shown in Fig 1. It was observed that visible transmittance would increase with flourine or antimony doping of tin oxide. The maximum transmittance observed for the TO, FTO and ATO thin films was 52,46%, 77,39% and 69,56%, respectively at the wavelength 800nm. The figure clearly shows the increase in transmittance due to 20 wt. % F and 2 wt. % Sb doping at visible range of wavelength. Highest transmittance was obtained in FTO films, whereas a lower transmittance was observed in TO films. This important variation could be due to the optical scattering by doping of TO films in this work.
Fig. 1. Comparison of transmittance spectra of undoped, fluorine doped and antimony doped SnO2films
*Corresponding author: guventurgut@atauni.edu.tr
[1] A.V. Moholkar, et. al. Applied Surface Science 255 9358–9364 (2009). [2] G. Turgut, et. al. 6thNanoscience and Nanotechnology Conference June
15-18 370 (2010).
[3] S. Colen, Thin Solid Films 77 127 (1981). [4] P.S. Patil, et. al. Thin Solid Films 437 34 (2003). [5] A. Dima, et. al. Thin Solid Films 427 427 (2003). [6] D.S. Lee, et. al. Thin Solid Films 416 271 (2002).
[7] J. Kane, H.P. Schweizer, J. Electrochem. Soc. 123 270 (1976). [8] T.N. Blanton, M. Lelental, Mater. Res. Bull. 29 537 (1994). [9] K.Y. Rajpure, et. al. Mater. Chem. Phys. 64 184 (2000). [10] P.S. Patil, Mater Chem Phys. 59 158 (1999).