Elsevier

Powder Technology

Volume 217, February 2012, Pages 7-10
Powder Technology

Thermoluminescence of combustion synthesized yttrium oxide

https://doi.org/10.1016/j.powtec.2011.09.042Get rights and content

Abstract

Pure yttrium oxide (Y2O3) was prepared by solution combustion technique using disodium ethylene diamine tetra acetic acid (EDTA-Na2) as fuel at ~ 350 °C. Powder X-ray diffraction (PXRD) pattern of Y2O3 revealed cubic crystalline structure with crystallite size in the range of 18–23 nm. The scanning electron microscopy (SEM) indicated the foamy and fluffy nature of the sample. Fourier transformed infrared spectroscopy (FTIR) revealed four prominent absorption with peaks at 3395, 1433, 875 and 566 cm 1. From the optical absorption studies the energy gap of the synthesized sample was found to be 5.72 eV. Two well resolved thermoluminescence (TL) glows with peaks at 475 and 626 K were observed in γ-irradiated Y2O3. The glow curves were analyzed and the average activation energy was found to be 0.505 and 0.977 eV respectively.

Graphical abstract

Yttrium oxide with nanophase was prepared by solution combustion technique. Powder X-ray diffraction pattern revealed the cubic crystalline structure in the range 18–23 nm. The morphology as revealed from SEM showed with spatial structure, loosely agglomerated particles with fluffy, crispy, pores and voids. Thermoluminescence of γ-irradiated Y2O3 shows good response with general order kinetics.

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Highlights

► Y2O3 nanoparticles have been synthesized by combustion technique. ► The crystallite size was found to be ~ 19.32 nm. ► The energy gap of the sample is found to be ~ 5.72 eV. ► Y2O3 nanophophor shows good TL response. ► Two luminescence centers corresponding to 475 K and 626 K are analyzed.

Introduction

Different techniques are applied to prepare nanocrystals. They include solid state reaction [1], wet chemical methods such as chemical vapor deposition [2], combustion [3], [4], sol–gel [5], aerosol pyrolysis [6] etc. The solid state reaction method has several shortcomings such as prolonged reaction time, larger size grain growth and poor homogeneity. However, the salient features of wet chemical methods are that the starting materials can be mixed at molecular level and the temperature of formation of the final products is as low as that of conventional solid-state reactions techniques. Among wet chemical methods, ‘solution combustion synthesis’ has several advantages. It requires simple apparatus and the materials used are more economical [7], [8]. It requires low energy, short time and this technique may also be employed to produce homogeneous, high-purity, crystalline oxides. The nature of crystallinity, surface area and agglomeration of the synthesized products are primarily governed by flame temperature during combustion which itself dependents on the nature of the fuel and the fuel-to-oxidizer ratio [9]. It is known that, a good fuel should react non-violently without producing toxic gasses and act as a complexing agent for metal ions [10]. EDTA-Na2 is one such compound which serves as a fuel during the combustion reaction and gets oxidized by nitrate ions and this is used as a new technology for material synthesis [11]. This EDTA has several remarkable advantages in comparison with other fuels and it has the greater ability to chelate metal cations and forming very stable and soluble complexes. In this technique, the starting materials are mixed at the molecular or the atomic level in a solution and it is easy to control the composition and a high degree of homogeneity is obtained. It is an exothermic reaction and occurs with the evolution of heat and light. When the mixture of fuel and oxidizer is ignited, combustion takes place at high temperature and leads to growth of materials with nano crystalline form. Metal nitrates and hydrazine based compounds are used as oxidizer and fuels respectively to synthesize metal oxides [12].

Oxide phosphors are found to be suitable for field emission display (FED), vacuum fluorescent display (VFD), plasma panel display (PDP) and electroluminescence (EL) devices. Luminescence efficiency is found to increase as the size of the phosphor particle is decreased and the preparation of phosphor powders becomes very important in technological application [13]. When thermoluminescent material is exposed to γ-radiation, it absorbs and stores energy in the form of defects. A part of the stored energy is released in the form of visible light when the two types of defect centers are recombined upon warming the material.

Metal oxide matrix is proved to be an excellent host material for lasing action. The Y2O3 possesses high refractory properties, a high melting point (~ 2450 °C) and a high thermal conductivity (33 Wm 1 K 1). It is a suitable material for photonic waveguide due to its high band gap (5.72 eV), with a very high refractive index (~ 2) and a wide transmission range (280–8000 nm) [14]. Numerous techniques are applied on the synthesis of rare earth doped nanocrystalline Y2O3 [15], [16], [17], [18].

In the present work, Y2O3 nanopowder was synthesized by solution combustion technique in which EDTA-Na2 was used as the chelating-fuel. Further, the TL behavior of the γ-irradiated Y2O3 has been studied and the enhancement in TL intensity with γ-ray dose was found. In addition the material was found to be a potential candidate in TL dosimetry.

Section snippets

Experimental

The stoichiometry of the redox mixture used for combustion process was calculated using the total oxidizing and reducing valencies of the ingredients which serve as numerical co-efficients for the stoichiometric balance. The equivalence ratio, i.e. the ratio of the oxidizing valency to reducing valency was maintained at unity. According to the concept used in propellant chemistry, the valency of C is + 4, H is + 1, O is + 2, divalent metal ions is + 2, trivalent metal ions is + 3 and so on. Based on

Results and discussion

Fig. 1 shows the PXRD patterns of as-synthesized Y2O3. The peaks were found to be in agreement with the JCPDS 41-1105 reference, corresponding to the [222], [400], [411], [332], [431], [440], [611], and [622] planes. It confirms the formation of single-phase cubic crystalline yttrium nanoparticles. The formation of a single phase is attributed to the high in-situ temperature generated during combustion reaction. The crystallites sizes were calculated using Scherer's formula and were found to be

Conclusions

Y2O3 nanoparticles have been synthesized by the EDTA-Na2 assist combustion technique at low temperature and in a very short time. PXRD pattern of this sample confirms the cubic phase. The crystallites size and the particle density were found to be 18–23 nm and ~ 5.059 g cm 3 respectively. The SEM picture of Y2O3 indicated the spatial structure of the loosely agglomerated particles which were fluffy and crispy with pores and voids. The energy gap of Y2O3 synthesized in the present work was found to

Acknowledgments

One of the authors, J.R. Jayaramaiah is thankful to “ISRO-ISEC, advanced devices and radiation cell, Bangalore” for providing facilities for γ-irradiation.

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