Indian Journal of Materials Science

Volume 2014 (2014), Article ID 794680, 4 pages

http://dx.doi.org/10.1155/2014/794680

Research Article

A Promising Orange-Red Nanocrystalline Potassium Lanthanum Orthophosphate for White Light-Emitting Diodes

Palvi Gupta,¹ A. K. Bedyal,¹ Vinay Kumar,1,2 Y. Khajuria,¹ O. M. Ntwaeaborwa,² and H. C. Swart²

¹School of Physics, Shri Mata Vaishno Devi University, Katra 182320, India

²Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein 9300, South Africa

Received 23 November 2013; Accepted 15 January 2014; Published 19 February 2014

Academic Editors: S. Ghosh, F. Gourbilleau, and M. Razeghi

Copyright © 2014 Palvi Gupta et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The spectral properties of the K₃La(PO₄)₂:Eu³⁺ nanophosphors synthesized by the combustion method are reported. The phosphors were characterized by X-ray diffraction, transmission electron microscopy, and optical spectroscopy. The XRD pattern reveals a pure monoclinic phase of the K₃La(PO₄)₂ with the average particle size of 30 nm in diameter. Under UV excitation, the phosphors exhibited several emission bands which were assigned to 4f-4f transitions of Eu³⁺ ions. The red shade of the Eu³⁺ ion with the CIE coordinates (x, y) as (0.63, 0.37) suggests that this material is a promising phosphor for near-UV InGaN-based LED lighting.

1. Introduction

In recent years, white light-emitting diodes (LEDs) have attracted more attention as possible replacement of the incandescent and fluorescent light sources due to their extraordinary characteristics such as high luminous efficiency, low cost synthesis, energy saving, long lifetime, reliability, mercury free, and environmental friendliness [1–4]. The rare earth doped phosphates are an important family of luminescent materials for solid state lighting applications as they possess excellent properties such as large band gap, moderate phonon energy, high thermal and chemical stability, exceptional optical damage threshold, and high absorption of in the VUV region [5–7]. Among the phosphates families, orthophosphate is considered to be an excellent host material to accommodate large amount of dopants due to its large band gap. Very often, orthophosphate crystallizes in the monoclinic phase with space group Pc/m or Pc/n [8].

The electronic transitions in the inner 4f orbitals, which are not influenced by the 5s and 5p electrons, are only found in the lanthanide. This leads to narrow and intense emission bands which are useful sources of the individual colors in multiphosphor devices. Therefore, in many commercial phosphors the blue (450 nm), green (545 nm), and red (610 nm) emissions of Eu²⁺, Tb³⁺, and Eu³⁺ have been widely used [9, 10]. Currently, there are several techniques used to synthesize these materials, like colloidal [11, 12], sonochemical [13], spray pyrolysis [14], and high temperature solid-state reactions [15, 16].

In the present paper, we report on the structure and photoluminescence (PL) properties of Eu³⁺ activated K₃La(PO₄)₂ nanophosphors synthesized by the combustion technique.

2. Experimental

K₃La(PO₄)₂:Eu³⁺ (2 mol%) phosphors were synthesized via the combustion method using urea as a fuel. All the chemicals used in the preparation were of analytical grade and were used without further purification. The starting materials were potassium nitrate (KNO₃·4H₂O), lanthanum (III) nitrate hexahydrate (La(NO₃)₃·6H₂O), ammonium dihydrogen tetraoxophosphate(V) (NH₄H₂PO₄), urea (NH₂CONH₂), and europium nitrate (Eu(NO₃)₃·6H₂O). The reagents were weighed according to the balanced chemical reaction given below. The ratio of the metal nitrates (oxidizers) and urea (fuel) was calculated using the total oxidizing and reducing valences of the components to get an equivalent ratio of unity to enable complete combustion. The ratio of an oxidizer and fuel is expressed as follows:

In the reaction (3), KNO₃. 4H₂O (-5) and La(NO₃)₃·6H₂O (-15) are oxidizing elements, whereas NH₄H₂PO₄ (+3) and NH₂CONH₂ (+6) are reducing elements. By using the oxidising and reducing values in (1), we have

The weighed reactants were dissolved in few drops of distilled water and thoroughly mixed in agate mortar to obtain thick paste. The paste was transferred to alumina crucible and placed in a furnace, preheated to a temperature of 550°C. The paste underwent volumetric combustion with evolution of large amounts of gasses. The reaction took 3–5 minutes to be completed. The final white foamy product was cooled to room temperature and ground to obtain a fine powder. The powder was annealed at 800°C for 2 h to improve the crystallinity and also to remove reactants which could not be decomposed at lower temperature. Consider

The structure of the product was examined by using a Bruker Advance D8 X-ray diffractometer with Cu, Kα irradiation (). Transmission electron microscopy (TEM) was used to examine the particle size and morphology of the phosphor. The TEM images were taken with a JEM-2100 at an accelerating voltage of 200 kV. The emission and excitation spectra (PL) of the phosphors were recorded by using a Cary-Eclipse spectrofluorometer.

3. Results and Discussion

Figure 1 shows the X-ray diffraction (XRD) pattern of the annealed K₃La(PO₄)₂:Eu³⁺ nanophosphor. The characteristic reflections confirm the monoclinic phase of the K₃La(PO₄)₂ orthophosphates. The crystal structure of the host matrix was not affected by the addition of small amount of Eu³⁺ dopant ions. Since the ionic radii of Eu³⁺ () and La³⁺ () are approximately the same, the Eu³⁺ ions can therefore easily incorporate in La³⁺ sites in host lattice. The XRD pattern was compared with those of the standard JCPDS data (47-0468) and the peaks were indexed accordingly. The diffraction peaks at 23.7°, 28.5°, and 25.5° (in terms of 2) indicate that some impurity phases were present in the host. The average crystallite size calculated by the well-known Debye-Scherrer equation [17] was 30 nm.

Figure 1: XRD pattern of the K₃La(PO₄)₂:Eu³⁺ nanophosphors.

The morphology of the K₃La(PO₄)₂:Eu³⁺ nanophosphors was analyzed using TEM as shown in Figure 2. From the micrograph, the particles were mostly spheroidal and the average particle size was estimated to be in the range of ~2 nm. This result is consistent with the XRD data. It is well known that the morphological characteristics of the combustion derived products are strongly dependent on the heat and gas generated during the reaction. Large amounts of gases generated during the combustion process are suitable for preparation of fine particles, while the heat released is an important factor for crystal growth. This type of porous network is typically the characteristic of combustion synthesized powders. The porous powders are highly friable which facilitates easy grinding to obtain finer particles. The evolution of gas with high pressure leads to the formation of pores along with the simultaneous growth of small particles near the pores [16].

Figure 2: TEM image of the K₃La(PO₄)₂:Eu³⁺ nanophosphors.

Figure 3 shows the photoluminescence excitation spectrum of the K₃La(PO₄)₂:Eu³⁺ phosphor. The spectrum has a broad band ranging from 200 to 310 nm with a set of sharp lines protruding from the band. The broad band is attributed to charge transfer (CTB) from u3+, while the sharp lines at wavelengths of 318, 360, 382, and 392 nm are assigned to (⁷F₀ ⁵H₃, ⁵D₄, ⁵, ⁵L₇, ⁵L₆) intraconfigurational 4f-4f transitions of Eu³⁺ ion.

Figure 3: PL excitation spectrum of the K₃La(PO₄)₂:Eu³⁺ nanophosphors.

The PL emission spectra at different excitation wavelengths are presented in Figure 4 and it is clear that the peak positions and shapes of the spectra did not change for all the excitation wavelengths. The emission spectrum consists of four typical emission peaks at 591, 617, 653, and 703 nm, which results from the intraconfigurational 4f-4f characteristic transitions (⁵D₀ → ⁷, , 2, 3, 4) of the Eu³⁺ ion, respectively. The emission line at 591 nm is due to magnetic dipole transition ⁵D₀⁷F₁ which is insensitive to the site symmetry, whereas the emission at 617 nm is due to the electric dipole transition of ⁵D₀ → ⁷F₂ and it is induced by the lack of inversion symmetry at the Eu³⁺ site. Generally, the forced electric dipole transitions arise from the lack of centre of symmetry and it is much stronger than that of the ⁵D₀ → ⁷F₁ transition. Also, the ⁵D₀ → ⁷F₂ transition is dependent upon the local symmetry, while the ⁵D₀ → ⁷F₁ emission is related to the local symmetry due to insensitivity to the site symmetry. Therefore, in the present case, the Eu³⁺ ion occupies a symmetric and a nonsymmetric site almost equally, as both the peak intensities of Eu³⁺ ion due to ⁵D₀ → ⁷F₂ and ⁵D₀ → ⁷F₁ transitions are the same [18, 19]. The CIE 1931 color space chromaticity coordinates were calculated and are presented in the CIE diagram in Figure 5. The diagram was constructed using the Commission International de L’Eclairage (CIE) coordinate calculator. The calculated CIE coordinates of our materials were (0.63, 0.37) which correspond to the shade of orange-red emission of the Eu³⁺ ion. Bright orange-red light-emitting diodes may be fabricated by the combination of the synthesized K₃La(PO₄)₂:Eu³⁺ with 392 nm emitting InGaN-based chips.

Figure 4: PL emission spectra of the K₃La(PO₄)₂:Eu³⁺ nanophosphors.

Figure 5: The CIE 1931 chromaticity diagram for K₃La(PO₄)₂:Eu³⁺ nanophosphors under 392 nm excitation.

4. Conclusions

K₃La(PO₄)₂:Eu³⁺ nanophosphors were synthesized by the combustion method and its luminescence properties were investigated under UV excitation. The emission spectrum consists of two prominent peaks at 591 and 617 nm which corresponds to magnetic-dipole transitions (⁵D₀ → ⁷F₁) and electric-dipole transitions (⁵D₀ → ⁷F₂) of the Eu³⁺ ion. The CIE chromaticity coordinates were calculated to be (.63, .37) which corresponds to the orange-red shade. The maximum emission from 392 nm excitation makes this material a potential candidate for the near-UV-light-emitting diode applications.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

A. K. Bedyal would like to thank Inter University Accelerator Centre, New Delhi, for the financial support in the form of fellowship under UFR Project code—MS/30505. Vinay Kumar is grateful to the Department of Science and Technology (DST), Government of India, for funding the Fast Track Project reference no. SR/FTP/PS-043/2011 under DST Young Scientist Scheme.

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