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Third Day Poster Session, 17 June 2010 - NanoTR-VI

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<strong>Poster</strong> <strong>Session</strong>, Thursday, <strong>June</strong> <strong>17</strong><br />

Theme F686 - N1123<br />

Optical and Structural Characterization of Y 2 O 3 :Nd 3+ Phosphors via Thermal Decomposition Method<br />

G. Bilir* and G. Özen<br />

Department of Physics, stanbul Technical University, Maslak-stanbul 34469, Turkey<br />

Abstract: The Y 2 O 3 :Nd 3+ nanophosphors were synthesized by using thermal decomposition method. The powders were annealed at different<br />

temperatures to investigate annealing temperature dependence of the crystallite size. Average particle size of the products were calculated by<br />

using Scherrer Formula from the X-ray diffractograms Luminescence measurement were performed for all samples at room temperature. Also<br />

SEM/EDS measurements were confirmed the calculated particle sizes from XRD diffractograms.<br />

Materials with nanostructure attracted considerable attention<br />

because of potential applications in optoelectronics and<br />

photonics[1-4]. Phosphor materials find wide applications<br />

ranging from fluorescent lamp to luminescence immunoassay.<br />

These materials essentially convert one type of energy into<br />

visible radiation and hence, phosphor materials are called<br />

optical transducer[5].<br />

In this work nanosized Y 2 O 3 samples doped with x=0.2, 0.5,<br />

1, 2, 5, 10 mol% Nd 3+ ions (Y 2-x Nd x O 3 ) were prepared by<br />

thermal decomposition of yttrium-neodymium alginate.<br />

Obtained products were annealed at 600, 800 and 1000 to<br />

investigate particle size dependence on annealing temperature.<br />

X-ray diffraction investigations were carried out with<br />

Philips TM model(Cu-K) diffractometer at 40 kV in the 2 range<br />

from 20 o to 60 o . Also SEM images of the samples were taken by<br />

using JEOL 6335F model scanning electron microscope(SEM).<br />

Both of XRD and SEM measurements show that the particle<br />

sizes of Y 2 O 3 :Nd 3+ samples were ranging from 20nm to 40 nm<br />

which are consistent with the values reported in literature[6].<br />

Representative X-ray diffractograms and SEM images are given<br />

in Figs.1-2.<br />

Princeton Instruments SP2500i model monochromator and<br />

Acton series ID441-C Model InGaAs detector for the<br />

detection.<br />

PL measurements were performed at room temperature and<br />

strong PL intensities were obtained for all Nd 3+ doped<br />

samples. The PL spectra of all samples are consist of three<br />

spectral regions which were correspond to the 4 F 3/2 4 I 9/2 ,<br />

4 F 3/2 4 I 11/2 and 4 F 3/2 4 I 13/2 transitions of theNd 3+ . In Fig.2<br />

representative of PL of 0.5% Nd 3+ doped sample are given.<br />

Figure 3: PL of 0.5% Nd 3+ doped Y 2O 3<br />

Also in Fig. 4, the dependence of FWHM(full width at half<br />

maxima) of the transitions on annealing temperature is given.<br />

Figure 1: XRD patterns of the non-annealed Y 2O 3:Nd 3+ nanopowders<br />

Figure 2: SEM images of the %0,5Nd doped Y 2O 3 annealed at 1000C (left) and<br />

non-annealed (right)<br />

From SEM images also seen that the organic<br />

component(alginate) from synthesis method which used to<br />

form yttrium alginate gels is exist for non-annealed samples<br />

and it was observed for all samples. The emission spectra were<br />

collected by using Apollo Instruments diode laser (Model No:<br />

S30-808-6) with 805.2 nm wavelength as an excitation source,<br />

Figure 4:Annealing temperature dependence of the FWHM<br />

SEM measurements were supported by Science Institute of<br />

Marmara University with the project number FEN-CDRP-<br />

090409-0079<br />

*bilirg@itu.edu.tr<br />

References<br />

[1]Promod and et al, Journal of Luminescence, 82 (1999) 187-193<br />

[2] Hai Huang and et al, Nanotechnology, 13 (2002) 318-323<br />

[3] Gino Tessari, Marco Bettinelli and et al., Applied Surface Science,<br />

144-145 (1999) 686-689<br />

[4] Michael Nazarov and et al, Optical Materials, 27 (2005) 1587-1592<br />

[5] T. Kim Anh and et al, Journal of Luminescence, 102-103 (2003)<br />

391-394<br />

[6] D. Tatar, H. Kaygusuz, F. Tezcan, FB. Erim, ML. Oveçolu, G.<br />

Ozen “Y2O3 Nanophosphors Synthesized by Combustion and Thermal<br />

Decomposition Techniques” 11th Annual Conference on NanoScience<br />

and NanoTechnology, NSTI-NanoTech, Boston-USA (MO81-919)<br />

(<strong>June</strong> 1-5/2008)<br />

6th Nanoscience and Nanotechnology Conference, zmir, <strong>2010</strong> 6<strong>17</strong>

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