Advances in Optical TechnologiesVolume 2014 (2014), Article ID 706459, 5 pageshttp://dx.doi.org/10.1155/2014/706459

Research Article

A Potential Candidate for Lamp Phosphor: Eu³⁺ Activated K₂Y₂B₂O₇

K. A. Koparkar, N. S. Bajaj, and S. K. Omanwar

Department of Physics, SGB Amravati University, Amravati 444602, India

Received 2 February 2014; Revised 15 March 2014; Accepted 28 March 2014; Published 10 April 2014

Academic Editor: Zoran Ikonic

Copyright © 2014 K. A. Koparkar 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 novel phosphor K₂Y₂B₂O₇ doped with europium is studied for its photoluminescence properties. The studies show that the phosphor gives strong red emission (PL) at 613 nm related to ⁵D₀-⁷F₂ transition of Eu³⁺ under the 260 nm excitation (PLE) related to the charge transfer (CT) from the 2p orbital of the O²⁻ ions to the 4f orbital of Eu³⁺ ions with CIE coordinates (; ). The results of PL and PLE spectra indicate the applicability of K₂Y₂B₂O₇:Eu as a red component in lamp phosphor. The phosphor is characterized through XRD pattern analysis, and morphology is explained on the basis of SEM image. Optimum concentration of Eu³⁺ required for the highest intensity of emission is also studied.

1. Introduction

Borates as host for light emitting materials under UV excitation have attracted much attention. The reason behind their being in a focus of research is their variety of structure types, transparency to a wide range of wavelengths, and high optical quality [1–4]. Also borates possess excellent properties as host due to the inherent attributes of the large band gap and covalent bond energy. A variety of borate host materials doped with rare earth and other ions have been studied and reported [5]. Moreover, B–O bond generally has no absorption in near UV region and has absorption in deep UV region because of its large covalent bond energy. Some previous works show that Eu³⁺ doped borates exhibit relatively strong absorption in the UV region and intense red emission with good color purity [6, 7].

Recently the alkali earth metal (M) yttrium borates (M₂Y₂B₂O₇) have been well known hosts for luminescent material with better crystallinity, lower synthesis temperature, and higher radiation efficiency, as compared to the corresponding simple alkali earth metal borates [8]. The Na₂Y₂B₂O₇ is an excellent host for luminescent materials which supports all the possible trivalent rare earth dopants and shows intense emission from violet region to red region [9]. In the present work, we investigate, for the first time, the photoluminescence characteristics of Eu³⁺ doped K₂Y₂B₂O₇. The purpose of replacing the mostly studied Na⁺ by K⁺ is to find the ion type dependence of Eu³⁺ luminescence in M₂Y₂B₂O₇ host. The photoluminescence properties of the synthesized materials were studied using a fluorescence spectrometer (Hitachi F-7000).

2. Experimental

2.1. Sample Preparation

The powder samples of the phosphor K₂Y₂B₂O₇ with different concentrations of Eu³⁺ (0.001, 0.002, 0.005, 0.01, and 0.02) have been prepared by solution combustion technique. The method is based on the exothermic reaction between the fuel (urea) and oxidizer (ammonium nitrate). The detailed description of the method regarding the measurement of stoichiometric quantities of fuel and oxidizer is reported in our earlier work [10–13].

All the ingredients, yttrium nitrate (Y(NO₃)₃), boric acid (H₃BO₃), potassium nitrate (KNO₃), urea (NH₂–CO–NH₂), and ammonium nitrate (NH₄NO₃) used, are of AR grade and the rare earth Eu₂O₃ (99.99% purity) used is from the Indian Rare Earths. The stoichiometric amounts of the ingredients are thoroughly mixed in an agate mortar. Later, little amount of double distilled water was added to get an aqueous homogeneous solution. The solution is then transferred into a China Basin and slowly heated at lower temperature at 90°C in order to remove the excess of water contents. The thick paste obtained after heating is then transferred into a preheated muffle furnace maintained at ()°C. The paste boils foams and ignites to burn with flame; lastly, a voluminous, foamy powder is obtained. This entire combustion process is over in about 5 min. Following the combustion, the resulting fine powders were annealed in slightly reducing atmosphere (produced by burning charcoal) at a temperature of 750°C for about 60 min and suddenly cooled to room temperature [14]. The same process of synthesis is repeated for different concentrations of activator.

2.2. Characterization Techniques

K₂Y₂B₂O₇:Eu³⁺ materials were characterized by using Rigaku Miniflex II X-ray diffractometer with scan speed of 2.000°/min and with Cu Kα radiation. SEM images are produced on Philips XL 30 SEM system having a resolution of 2.0 nm at 30 kV and 0.5 nm at 1 kV. The PL and PLE spectra are recorded on Hitachi F-7000 fluorescence spectrometer by keeping slit window at 1.0 nm for excitation and emission and PMT voltage at 400 V.

3. Results and Discussion

3.1. XRD Pattern for K₂Y₂B₂O₇

The studies on novel yttrium based borate phosphor become a hot issue in exploring new phosphor materials, which have also been proved to be efficient in the application of light conversion. Na₂Y₂B₂O₇ phosphor was first reported by Zhang and Li [15] as a near-UV white LEDs phosphor prepared by high temperature solid state synthesis method. The material was described in the monoclinic crystal system. In this paper it has been decided to replace sodium by potassium (having the same valence) to get K₂Y₂B₂O₇.

The X-ray diffraction patterns of K₂Y₂B₂O₇ with different concentrations of activator Eu³⁺ are shown in Figure 1 to verify the phase purity and crystal similarity. All the peaks in different patterns are in good agreement with each other, which indicates that all the prepared samples are in a similar phase, and the increasing concentration of dopants does not affect the crystal structure. However, the obtained diffraction peaks of compound are in some agreement with the two different phases in the ICDD database, namely, Y₂B₂O₆(~80%) and K₂O (~20%). Having in mind that the quantities of the starting materials are chosen according to the given chemical composition of K₂Y₂B₂O7:Eu³⁺ matrix, therefore (even if in a mixed phase) this was named as K₂Y₂B₂O₇:Eu³⁺ phosphor in this paper [16].

Figure 1: XRD patterns for K₂Y₂B₂O₇ doped with different concentrations of Eu.

The results also imply that the prepared samples are not the simple physical mixtures of precursor used but may be a new single-host K₂Y₂B₂O₇ material. The detailed studies on structures of these materials are still under investigation. Therefore, only XRD data of K₂Y₂B₂O₇ is reported in this paper.

3.2. Surface Morphology of K₂Y₂B₂O₇:Eu³⁺

The SEM photographs of K₂Y₂B₂O₇:Eu³⁺ phosphor clearly show that the grains are irregular in shape and have a size less than 1 μm. The typical morphological images are represented in Figure 2. The particles possess foamy like morphology formed from highly agglomerated crystallites. An average crystallite size is in submicrometer range of K₂Y₂B₂O₇:Eu³⁺ phosphors.

Figure 2: Representative SEM image for K₂Y₂B₂O₇.

3.3. Luminescence Properties of Eu³⁺ Activated K₂Y₂B₂O₇

Figure 3 represents excitation and emission behaviors of Eu³⁺ activated K₂Y₂B₂O₇ prepared at 750°C. The excitation spectra exhibit a broad band centered at 260 nm related to the charge transfer (CT) from the 2p orbital of the O²⁻ ions to the 4f orbital of Eu³⁺ ions [17]. Other minor peaks, 300–400 nm, are associated with the direct excitation of electrons for the f-f shell transitions in Eu³⁺ ions.

Figure 3: Excitation and emission spectra for K₂Y₂B₂O₇ doped with 0.01 mole of Eu.

The emission spectra of Eu doped K₂Y₂B₂O₇ under the charge transfer (CT) band excitation at 260 nm essentially contain groups of lines between 500 and 650 nm. The lines in the 500–550 nm range (shown in Figure 3 (inset)) are attributed to ⁵D₁ to ⁷ transition of Eu³⁺ and are found to be very weak. The lines in the 550–650 nm range correspond to transitions from the first excited state ⁵D₀ to the ⁷ levels (). It is well known that the relative intensity of the ⁵D₀-⁷F₁ and ⁵D₀-⁷F₂ transitions strongly depends on the local symmetry of the Eu³⁺ ions. When the Eu³⁺ ions occupy sites with inversion centers, the ⁵D₀-⁷F₁ (the magnetic dipole) transition should be relatively strong, while the ⁵D₀-⁷F₂ (the electric dipole) transition is parity-forbidden and should be very weak. The emission spectra of the compound K₂Y₂B₂O₇ exhibit strong red luminescence of ⁵D₀-⁷F₂ at 613 nm indicating that the Eu³⁺ ion is located in a noncentrosymmetric position in the matrix. For Eu³⁺ doped Na₂Y₂B₂O₇, after the Eu³⁺ ions have entered the crystal lattice, they will occupy Y sites and Y ions indeed occupy very low symmetry sites, C₁. According to group theory selection rules, the magnetic dipole and the electric dipole are permitted and the electric dipole transition is the stronger one [18]. Taking the same reference in account it may be suggested that in Eu³⁺ doped K₂Y₂B₂O₇ phosphor Eu³⁺ also takes the same low symmetry site.

3.4. Concentration Quenching Effect

Generally speaking, the doping concentration has a significant effect on the phosphor performance. The effect of Eu³⁺ doping concentration () in the K₂Y₂B₂O₇:Eu³⁺ (, 0.002, 0.005, 0.01, and 0.02) phosphors on the relative intensity of the electronic dipole transition (⁵D₀-⁷F₂) is shown in Figure 4. The result shows that, as the concentration of Eu³⁺ increases, the luminescent intensity also increases and reaches the highest intensity when the doping concentration of Eu³⁺ increases to 0.01. However, the luminescent intensity slightly decreases as long as the concentration is over 0.01 due to concentration quenching. The energy transfer within the same rare earth ions results in the concentration quenching associated with the exchange interaction [5].

Figure 4: Peak intensity versus concentration of Eu in K₂Y₂B₂O₇ ( nm).

The concentration quenching phenomenon can be theoretically supported by the relationship between luminescent intensity and doping concentration mathematically expressed as where is the intrinsic transition probability of the sensitizer and is the index of electric multipole, for electric dipole-electric dipole, electric dipole-electric quadrapole, and electric quadrapole-electric quadrapole corresponding to 6, 8, and 10, respectively. denotes a dimension of the sample, and here owing to the energy transfer between Eu³⁺ inside the grains. and are constants, and is a function. From (1), it can be obtained that where is independent of the doping concentration. Figure 5 presents the plots for the ⁵D₀-⁷F₂ transition of Eu³⁺ in the K₂Y₂B₂O₇ host. According to (2), the value of the slope parameter is calculated to be −0.89 (close to −1) corresponding to by linear approximation idea [19]. This suggests that the exchange interaction mechanism plays a central role in the energy transfer among Eu³⁺ ions in the phosphors K₂Y₂B₂O₇.

Figure 5: The relation of the concentration of Eu³⁺ ions and for the ⁵D₀ → ⁷F₂ transition in the K₂Y₂B₂O₇ phosphor.

3.5. CIE Diagram

The CIE 1931 color space chromaticity diagram to illustrate the chromaticity of K₂Y₂B₂O₇:Eu³⁺ phosphors. Figure 6 represents that the CIE coordinates of K₂Y₂B₂O₇:Eu³⁺ were measured as (; ). The location of coordinate has been marked in Figure 3 with a green circle. The CIE coordinates of K₂Y₂B₂O₇:Eu³⁺ are in the bright red area.

Figure 6: CIE coordinate for 613 nm emission of K₂Y₂B₂O₇:Eu³⁺.

4. Conclusion

For K₂Y₂B₂O₇ doped with europium, the XRD pattern shows that the material was highly crystalline, having multiple peaks related to precursor or dopants, and the SEM image indicates the crystalline nature of this phosphor, with agglomerated regular morphology. Photoluminescence properties show that the phosphor gives strong red emission (PL) at 613 nm related to ⁵D₀-⁷F₂ transition of Eu³⁺ under the 260 nm excitation (PLE) related to the charge transfer (CT) from the 2p orbital of the O²⁻ ions to the 4f orbital of Eu³⁺ ions with CIE coordinates (; ). The results of PL and PLE spectra indicate the applicability of K₂Y₂B₂O₇:Eu³⁺ as a red component in lamp phosphor.

Conflict of Interests

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

Acknowledgment

One of the authors, K. A. Koparkar, is thankful to the head of Department of Physics for providing XRD facility implemented under FIST Program-2010.

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