Enhanced microwave absorption properties of PMMA modified MnFe2O4-polyaniline nanocomposites.

A manganese based spinel ferrite, chemically modified with polymethyl methacrylate (PMMA) and polyaniline (PANI) are synthesized and their composites are used as electromagnetic interference (EMI) shielding materials. X-ray diffraction studies show that the as-prepared manganese ferrite crystallizes in a cubic spinel structure. The particles are highly agglomerated and nanocrystalline as indicated by transmission electron microscopy. Manganese exists in +2 and +4 oxidation states and Fe in +2 and +3 oxidation states. Modified manganese ferrite and polyaniline composites in different weight ratios are evaluated for their EMI shielding properties. It is observed that composites containing the PMMA modified ferrite show enhanced total shielding effectiveness (SET) compared to those containing the unmodified ferrite in the X band frequency range (8-12 GHz). The optimized ratio of the PMMA modified ferrite and PANI demonstrates SET values as high as ∼44 dB in the X band frequency range.

Synthesis, luminescence properties and EPR investigation of hydrothermally derived uniform ZnO hexagonal rods.

One-dimensional (1D) zinc oxide (ZnO) hexagonal rods have been successfully synthesized by surfactant free hydrothermal process at different temperatures. It can be found that the reaction temperature play a crucial role in the formation of ZnO uniform hexagonal rods. The possible formation processes of 1-D ZnO hexagonal rods were investigated. The zinc hydroxide acts as the morphology-formative intermediate for the formation of ZnO nanorods. Upon excitation at 325 nm, the sample prepared at 180°C show several emission bands at 400 nm (∼3.10 eV), 420 nm (∼2.95 eV), 482 nm (∼2.57 eV) and 524 nm (∼2.36 eV) corresponding to different kind of defects. TL studies were carried out by pre-irradiating samples with γ-rays ranging from 1 to 7 kGy at room temperature. A well resolved glow peak at ∼354°C was recorded which can be ascribed to deep traps. Furthermore, the defects associated with surface states in ZnO nano-structures are characterized by electron paramagnetic resonance.

Luminescence studies and EPR investigation of solution combustion derived Eu doped ZnO.

ZnO:Eu (0.1 mol%) nanopowders have been synthesized by auto ignition based low temperature solution combustion method. Powder X-ray diffraction (PXRD) patterns confirm the nanosized particles which exhibit hexagonal wurtzite structure. The crystallite size estimated from Scherrer's formula was found to be in the range 35-39 nm. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies reveal particles are agglomerated with quasi-hexagonal morphology. A blue shift of absorption edge with increase in band gap is observed for Eu doped ZnO samples. Upon 254 nm excitation, ZnO:Eu nanopowders show peaks in regions blue (420-484 nm), green (528 nm) and red (600 nm) which corresponds to both Eu2+ and Eu3+ ions. The electron paramagnetic resonance (EPR) spectrum exhibits a broad resonance signal at g=4.195 which is attributed to Eu2+ ions. Further, EPR and thermoluminescence (TL) studies reveal presence of native defects in this phosphor. Using TL glow peaks the trap parameters have been evaluated and discussed.

Synthesis and luminescence properties of Sm3+ doped CaTiO3 nanophosphor for application in white LED under NUV excitation.

CaTiO3:Sm(3+) (1-11 mol%) nanophosphors were successfully synthesized by a low temperature solution combustion method [LCS]. The structural and morphological properties of the phosphors were studied by using Powder X-ray diffractometer (PXRD), Fourier transform infrared (FTIR), X-ray photo electron spectroscopy (XPS), scanning electron microscope (SEM) and transmission electron microscopy (TEM). TEM studies indicate that the size of the phosphor is ∼20-35 nm. Photoluminescence (PL) properties of Sm(3+) (1-11 mol%) doped CaTiO3 for NUV excitation (407 nm) was studied in order to investigate the possibility of its use in White light emitting diode (WLED) applications. The emission spectra consists of intra 4f transitions of Sm(3+), such as (4)G5/2→(6)H5/2 (561 nm), (4)G5/2→(6)H7/2 (601-611 nm), (4)G5/2→(6)H9/2 (648 nm) and (4)G5/2→(6)H11/2 (703 nm) respectively. Further, the emission at 601-611 nm show strong orange-red emission and can be applied to the orange-red emission of phosphor for the application for near ultra violet (NUV) excitation. Thermoluminescence (TL) of the samples irradiated with gamma source in the dose range 100-500 Gy was recorded at a heating rate of 5°Cs(-1). Two well resolved glow peaks at 164°C and 214°C along with shouldered peak at 186°C were recorded. TL intensity increases up to 300 Gy and thereafter, it decreases with further increase of dose. The kinetic parameters namely activation energy (E), frequency factor (s) and order of kinetics were estimated and results were discussed in detail.

Gd(1.96-x)Y(x)Eu0.04O3 (x = 0.0, 0.49, 0.98, 1.47, 1.96 mol%) nanophosphors: propellant combustion synthesis, structural and luminescence studies.

Gd(1.96-x)Y(x)Eu0.04O3 (x = 0.0, 0.49, 0.98, 1.47, 1.96 mol%) nanophosphors were synthesized by propellant combustion method at low temperature (400°C). The powder X-ray diffraction patterns of as formed Gd1.96Eu0.04O3 showed monoclinic phase, however with the addition of yttria it transforms from monoclinic to pure cubic phase. The porous nature increases with increase of yttria content. The particle size was estimated from Scherrer's and W-H plots which was found to be in the range 30-40 nm. These results were in well agreement with transmission electron microscopy studies. The optical band gap energies estimated were found to be in the range 5.32-5.49 eV. PL emission was recorded under 305 nm excitation show an intense emission peak at 611 nm along with other emission peaks at 582, 641 nm. These emission peaks were attributed to the transition of (5)D0→(7)FJ (J = 0, 1, 2, 3) of Eu(3+) ions. It was observed that PL intensity increases with increase of Y content up to x = 0.98 and thereafter intensity decreases. CIE color co-ordinates indicates that at x = 1.47 an intense red bright color can be achieved, which could find a promising application in flat panel displays. The cubic and monoclinic phases show different thermoluminescence glow peak values measured under identical conditions. The response of the cubic phase to the applied dose showed good linearity, negligible fading, and simple glow curve structure than monoclinic phase indicating that suitability of this phosphor in dosimetric applications.

Study on low temperature solution combustion synthesized Sr(2)SiO(4):Dy(3+) nano phosphor for white LED.

A series of Dy(3+) (1-5mol.%) activated Sr2SiO4 nanophosphors were prepared by low temperature solution combustion method using oxalyl dihydrazide (ODH) as a fuel. The obtained phosphor was well characterized by powder X-ray diffraction, scanning electron microscopy, and UV-visible spectroscopy. The average crystallite sizes were estimated by Debye-Scherrer formula and Williamson-Hall plots and found to be in the range 20-32nm. Energy band gap was found to be widened with increase of Dy(3+) ion dopant. Photoluminescence spectra consist of three main groups of peaks in 460-500nm (blue), 555-610nm (yellow) and 677nm (red) respectively. These peaks were assigned to transition of (4)F9/2→(6)H15/2,13/2,11/2. The critical distance between Dy(3+) ions and quenching site was found to be ∼16.71Ǻ. The chromaticity co-ordinates of all the prepared phosphors were located in white light; as a result Dy(3+) activated Sr2SiO4 is a promising single phased phosphor for white light emitting diodes. Thermoluminescence (TL) of Dy(3+) doped Sr2SiO4 nanophosphors were investigated using γ-irradiation in the dose range 1-6kGy at a warming rate of 2.5°Cs(-1). The phosphors show a well resolved single glow peak at ∼145°C. The kinetic parameters were estimated by different methods and the results discussed. The TL intensity increases linearly with γ-dose at room temperature. The effect of fading with storage time was found to be ∼66% which is highly useful in radiation dosimetry.

Synthesis, EPR and luminescent properties of YAlO3:Fe3+ (0.1-0.9mol%) nanopowders.

A simple and inexpensive combustion method was used to prepare Fe(3+) doped YAlO3 perovskite within few minutes at low temperature (400±10°C). This might be useful in lowering the cost of the material. The final products were well characterized by various spectroscopic techniques such as PXRD, SEM, TEM, FTIR and UV-Visible. The average crystallite size was estimated from the broadening of the PXRD peaks and found to be in the range 45-90nm, the results were in good agreement with the W-H plots and TEM. The crystallites show dumbbell shape, agglomerated particles with different size. The TL glow curves of 1-5kGy γ-irradiated YAlO3:Fe(3+) (0.1mol%) nanopowder warmed at a heating rate of 3°Cs(-1) records a single glow peak at ∼260°C. The kinetic parameters namely activation energy (E), order of kinetics (b) and frequency factor (s) were determined at different gamma doses using the Chens glow peak shape method and the results were discussed in detail. The photoluminescence spectra for Fe(3+) (0.1-0.9mol%) doped YAlO3 records the lower energy band at 720nm ((4)T1 (4G)→(6)A1 (6S)) and the intermediate band located at 620nm ((4)T2 ((4)G)→(6)A1 (6S)) with the excitation of 378nm. The higher energy band located at 514nm was associated to (4)E+(4)A1 ((4)G)→(6)A1 (6S) transition. The resonance signals at g values 7.6, 4.97, 4.10, 2.94, 2.33 and 1.98 were observed in EPR spectra of Fe(3+) (0.1-0.9mol%) doped YAlO3 recorded at room temperature. The g values indicate that the iron ions were in trivalent state and distorted octahedral site symmetry was observed.

Investigation of structural and luminescence properties of Ho(3+) doped YAlO3 nanophosphors synthesized through solution combustion route.

YAlO3:Ho(3+) (1-5mol%) nanophosphors have been prepared by solution combustion route using oxalyl dihydrazide (ODH) as a fuel. The final product was well characterized by powder X-ray diffraction (PXRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), UV-Vis, etc. PXRD patterns confirm the formation of highly crystalline orthorhombic phase structure. SEM and TEM studies show the particles are dumbbell shape, highly agglomerated and nano-size (∼30nm). The direct energy band gap (Eg) values estimated from Tauc's relation were found to be in the range 5.76-5.99eV. Photoluminescence (PL) studies show green (540 and 548nm) and red (645 and 742nm) emissions upon excited at 452nm wavelength. The emission peaks at ∼742 and 645nm was associated with the transitions of (5)F4→(5)I7 and (5)F5→(5)I8 respectively. The higher energy bands located at 540 and 548nm were associated with (5)F4, (5)S2→(5)I8 transitions. Thermoluminescence (TL) studies of γ-irradiated YAlO3:Ho(3+) (1-5mol%) show two glow peaks at 223 and 325°C recorded at a heating rate of 2.5°Cs(-1). The 223°C glow peak follow linear behavior up to 1kGy and after that, it showed sub-linearity. Up to 1kGy, the phosphor is quite useful in radiation dosimetry. The kinetic parameters (E, b and s) were estimated from glow peak shape method. The CIE coordinate values lies within the green region. Therefore, the present phosphors may have potential application in WLEDs as green phosphor.

Photoluminescence study of nanocrystalline Y2O3:Ho3+ phosphor.

The Y2O3:Ho(3+) powder phosphors have been prepared by using low temperature combustion method. Powder X-ray diffraction, scanning electron microscope and transmission electron microscopy techniques were used to characterize the as-prepared phosphor. The UV-Vis-NIR absorption, excitation and emission studies have been performed and the phenomenological Judd-Ofelt intensity parameters which are critically important in calculating the radiative properties and stimulated emission crosssection have been calculated by using Judd-Ofelt theory. Based on the calculated values of the inter electronic parameter, covalency and bonding parameter the bonding between the Ho(3+) ions and surrounding oxygen atoms have been found to be covalent in nature. The color purity has also been verified by using the chromaticity diagram. The analysis shows that the Y2O3:Ho(3+) phosphor may be used for producing the green light emitting diodes and display applications.

Structural, EPR, optical and magnetic properties of α-Fe2O3 nanoparticles.

α-Fe(2)O(3) nanoparticles were synthesized by a low temperature solution combustion method. The structural, magnetic and luminescence properties were studied. Powder X-ray diffraction (PXRD) pattern of α-Fe(2)O(3) exhibits pure rhombohedral structure. SEM micrographs reveal the dumbbell shaped particles. The EPR spectrum shows an intense resonance signal at g≈5.61 corresponding to isolated Fe(3+) ions situated in axially distorted sites, whereas the g≈2.30 is due to Fe(3+) ions coupled by exchange interaction. Raman studies show A(1g) (225 cm(-1)) and E(g) (293 and 409 cm(-1)) phonon modes. The absorption at 300 nm results from the ligand to metal charge transfer transitions whereas the 540 nm peak is mainly due to the (6)A(1)+(6)A(1)→(4)T(1)(4 G)+(4)T(1)(4 G) excitation of an Fe(3+)-Fe(3+) pair. A prominent TL glow peak was observed at 140°C at heating rate of 5 °Cs(-1). The trapping parameters namely activation energy (E), frequency factor (s) and order of kinetics (b) were evaluated and discussed.

CdSiO3:Pr³âº nanophosphor: synthesis, characterization and thermoluminescence studies.

A series of Pr(3+) (1-9 mol%) doped CdSiO(3) nanophosphors have been prepared for the first time by a low temperature solution combustion method using oxalyldihydrizide (ODH) as a fuel. The final product was characterized by Powder X-ray diffraction (PXRD), Fourier Transform Infrared Spectroscopy (FTIR), scanning electron microscopy (SEM), and UV-Vis spectroscopy. The average crystallite size was calculated using Debye-Scherrer's formula and Williamson-Hall (W-H) plots and found to be in the range 31-37 nm. The optical energy band gap (E(g)) of undoped for Pr(3+) doped samples were estimated from Tauc relation which varies from 5.15-5.36 eV. Thermoluminescence (TL) properties of Pr(3+) doped CdSiO(3) nanophosphor has been investigated using γ-irradiation in the dose range 1-6 kGy at a heating rate of 5 °C s(-1). The phosphor shows a well resolved glow peak at ∼171 °C along with shouldered peak at 223 °C in the higher temperature side. It is observed that TL intensity increase with increase of Pr(3+) concentration. Further, the TL intensity at 171 °C is found to be increase linearly with increase in γ-dose which is highly useful in radiation dosimetry. The kinetic parameters such as activation energy (E), frequency factor (s) and order of kinetics was estimated by Luschiks method and the results are discussed.

Influence of annealing temperature on Raman and photoluminescence spectra of electron beam evaporated TiO2 thin films.

Titanium dioxide (TiO(2)) thin films were deposited on fused quartz substrates by electron beam evaporation method at room temperature. The films were annealed at different temperatures in ambient air. The surface morphology/roughness at different annealing temperatures were analyzed by atomic force microscopy (AFM). The crystallinity of the film has improved with the increase of annealing temperature. The effect of annealing temperature on optical, photoluminescence and Raman spectra of TiO(2) films were investigated. The refractive index of TiO(2) films were studied by envelope method and reflectance spectra and it is observed that the refractive index of the films was high. The photoluminescence intensity corresponding to green emission was enhanced with increase of annealing temperature. The peaks in Raman spectra depicts that the TiO(2) film is of anatase phase after annealing at 300°C and higher. The films show high refractive index, good optical quality and photoluminescence characteristics suggest that possible usage in opto-electronic and optical coating applications.

Effect of different fuels on structural, thermo and photoluminescent properties of Gd2O3 nanoparticles.

Gd(2)O(3) nanoparticles (27-60 nm) have been synthesized by the low temperature solution combustion method using citric acid, urea, glycine and oxalyl dihydrazide (ODH) as fuels in a short time. The structural and luminescence properties have been carried out using powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), Raman, UV-Vis, photoluminescence (PL) and thermoluminescence (TL) techniques. The optical band gap values were estimated for as formed and 800 °C calcined samples. The band gap values in as-formed and calcined samples were found to be in the range 4.89-5.59 eV. It is observed that, the band gap values are lower for as-formed products and it has been attributed to high degree of structural defects. However, in calcined samples, structure becomes more order with reduced structure defects. Upon 270 nm excitation, deep blue UV-band at ~390nm along with blue (420-482 nm), green (532 nm) and red emission (612 nm) was observed. The 390 nm emission peak may be attributed to recombination of delocalized electron close to the conduction band with a single charged state of surface oxygen vacancy. TL measurements were carried out on Gd(2)O(3) prepared by different fuels by irradiating with γ-rays (1 kGy). A well resolved glow peak at 230 °C was observed for all the samples. It is observed that TL intensity is found to be higher in for urea fuel when compared to others. From TL glow curves the kinetic parameters were estimated using Chen's peak shape method and results are discussed in detail.

YAlO3:Cr3+ nanophosphor: synthesis, photoluminescence, EPR, dosimetric studies.

YAlO(3):Cr(3+) (0.1 mol%) nanophosphor has been synthesized by low temperature solution combustion method. The X-ray diffraction studies reveal an orthorhombic structure. Transmission electron microscopy reveals that the particles are spherical in shape with nano-size ~40-65 nm. Electron paramagnetic resonance (EPR) spectrum shows a resonance signal with effective g value at g=1.978 which can be attributed to the exchange coupled Cr(3+) ion pairs in weakly distorted sites. The photoluminescence spectrum shows an intense doublet at 677 nm and 694 nm (R lines) assigned to spin-forbidden (2)E(g)→(4)A(2)(g) transition of Cr(3+) ions. EPR and PL studies reveal that the Cr(3+) ions occupy Al(3+) sites in YAlO(3). The interesting feature reported in this work concerns the linearity with gamma dose in the wide range (0.1-6 kGy). Prominent TL glow peaks at 226 °C and 346 °C were observed for both γ and UV-rays respectively. It is observed that the peaks at 226 °C and 346 °C eventually show a linear response up to 5 kGy which makes them a candidate for high dose dosimetry of ionizing radiation. The kinetic parameters namely activation energy (E), order of kinetics (b), frequency factor (s) of undoped and Cr doped samples were determined using Chens glow peak shape method and the results are discussed in detail.

Water-repellent coatings prepared by modification of ZnO nanoparticles.

Superhydrophobic coatings with a static water contact angle (WCA)>150° were prepared by modifying ZnO nanoparticles with stearic acid (ZnO@SA). ZnO nanoparticles of size ∼14nm were prepared by solution combustion method. X-ray diffraction (XRD) studies reveal that as prepared ZnO has hexagonal wurtzite structure whereas the modified coatings convert to zinc stearate. Field emission scanning electron micrographs (FE-SEM) show the dual morphology of the coatings exhibiting both particles and flakes. The flakes are highly fluffy in nature with voids and nanopores. Fourier transformed infrared (FTIR) spectrum shows the stearate ion co-ordinates with Zn(2+) in the bidentate form. The surface properties such as surface free energy (γ(p)) and work of adhesion (W) of the unmodified and modified ZnO coatings have been evaluated. The electron paramagnetic resonance (EPR) spectroscopy reveals that surface defects play a major role in the wetting behavior.

Influence of Sn doping on structural, optical and electrical properties of ZnO thin films prepared by cost effective sol-gel process.

Tin (Sn) doped zinc oxide (ZnO) thin films were synthesized by sol-gel spin coating method using zinc acetate di-hydrate and tin chloride di-hydrate as the precursor materials. The films were deposited on glass and silicon substrates and annealed at different temperatures in air ambient. The agglomeration of grains was observed by the addition of Sn in ZnO film with an average grain size of 60 nm. The optical properties of the films were studied using UV-VIS-NIR spectrophotometer. The optical band gap energies were estimated at different concentrations of Sn. The MOS capacitors were fabricated using Sn doped ZnO films. The capacitance-voltage (C-V), dissipation vs. voltage (D-V) and current-voltage (I-V) characteristics were studied and the electrical resistivity and dielectric constant were estimated. The porosity and surface area of the films were increased with the doping of Sn which makes these films suitable for opto-electronic applications.

Structural, EPR, optical and Raman studies of Nd2O3:Cu2+ nanophosphors.

Nanocrystalline Nd(2)O(3):Cu(2+) (2mol %) phosphors have been prepared by a low temperature solution combustion technique. Powder X-ray diffraction (PXRD) results confirm that hexagonal A-type Nd(2)O(3) (900°C, 3h) and the lattice parameters have been evaluated by Rietveld refinement. Surface morphology of as-formed and Cu(2+) doped Nd(2)O(3) phosphors show that the particles are irregular in shape and porous in nature. TEM results also confirm the nature and size of the particles. The EPR spectrum exhibits two resonance signals with effective g values at g(ǀǀ)≈2.12 and g(⊥)≈2.04. The g values indicate that the site symmetry of Cu(2+) ions is octahedral symmetry with elongated tetragonal distortion. Raman studies show major peaks, which are assigned, to F(g) and combination of A(g)+E(g) modes. It is observed that the Raman peaks and intensity have been reduced in Cu(2+) doped samples. UV-Visible absorption spectra exhibit a strong and broad absorption band at ∼240nm. Further, the absorption peak shifts to ∼14nm in Cu(2+) doped samples. The optical band gap is estimated to be 5.28eV for Cu doped Nd(2)O(3) nanoparticles which are higher than the bulk Nd(2)O(3) (4.7eV). This can be attributed to the quantum confinement effect of the nanoparticles.

Combustion synthesis, structural characterization, thermo and photoluminescence studies of CdSiO3:Dy³âº nanophosphor.

CdSiO(3):Dy(3+) (1-9mol%) nanophosphors were prepared for the first time using the solution combustion method. The process of monoclinic phase formation was investigated by PXRD, TG-DTA and FTIR. The results show that the phase formation temperature of combustion-derived monoclinic CdSiO(3) is found to be lower as compared to the powders prepared by solid-state and sol-gel methods. It was observed that the average crystallite size calculated by Debye-Scherrer's formula and Williamson-Hall (W-H) plot are well comparable and was found to be in the range of 35-70 nm. Scanning electron micrographs indicate that there exist circular microcrystalline particles. It is observed that the optical energy gap is widened with the increase of Dy(3+) ion dopant. The photoluminescence (PL) spectra exhibit characteristic transitions of Dy(3+) due to (4)F(9/2)→(6)H(15/2) (blue) and (4)F(9/2)→(6)H(13/2) (yellow) regions. The thermoluminescence (TL) glow curve of CdSiO(3):Dy(3+) nano powder exposed to UV irradiation exhibited one main peak centered at 170°C. The intensity of the main peak increases up to the dose of 20 min then it decreases. The glow curves were analyzed by the glow peak shape method and the estimated trap parameters are discussed.

Thermoluminescence and EPR studies of nanocrystalline Nd2O3:Ni²âº phosphor.

Nanocrystalline Nd(2)O(3):Ni(2+) (2 mol%) phosphor has been prepared by a low temperature (∼400°C) solution combustion method, in a very short time (<5 min). Powder X-ray diffraction results confirm the single hexagonal phase of nanopowders. Scanning electron micrographs show that nanophosphor has porous nature and the particles are agglomerated. Transmission electron microscopy confirms the nanosize (20-25 nm) of the crystallites. The electron paramagnetic resonance (EPR) spectrum exhibits a symmetric absorption at g≈2.77 which suggests that the site symmetry around Ni(2+) ions is predominantly octahedral. The number of spins participating in resonance (N) and the paramagnetic susceptibility (χ) has been evaluated. Raman study show major peaks, which are assigned to F(g) and combination of A(g)+E(g) modes. Thermoluminescence (TL) studies reveal well resolved glow peaks at 169°C along with shoulder peak at around 236°C. The activation energy (E in eV), order of kinetics (b) and frequency factor (s) were estimated using glow peak shape method. It is observed that the glow peak intensity at 169°C increases linearly with γ-dose which suggest that Nd(2)O(3):Ni(2+) is suitable for radiation dosimetry applications.

Swift heavy ion induced structural, iono and photoluminescence properties of ß-CaSiO3:Dy³âº nanophosphor.

CaSiO(3):Dy(3+) (1-5 mol%) nanophosphors have been prepared by a low temperature solution combustion method. The structural and luminescence (ionoluminescence; IL and photoluminescence; PL) studies have been carried out for pristine and ion irradiated samples. The XRD patterns of pristine sample show a prominent peak at (320) for the monoclinic structure of ß-CaSiO(3). Upon ion irradiation, the intensity of the prominent peak is decreased at the fluence of 7.81 × 10(12)ions cm(-2) and at higher fluence of 15.62 × 10(12)ions cm(-2), the prominent peak completely vanishes. The decrease in peak intensity might be due to the stress induced point defects. On-line IL and in situ PL studies have been carried out on pelletized samples bombarded with 100 MeV Si(7+) ions with fluences in the range (7.81-15.62)×10(12)ions cm(-2). The characteristic emission peaks at 481,574, 664 and 754 nm recorded in both IL and PL are attributed to the luminescence centers activated by Dy(3+) ions. It is found that IL and PL emissions intensity decreases with increase in Si(7+) ion fluence. The decrease in intensity can be due to the destruction of Si-O-Si and O-Si-O type species present on the surface of the sample. FTIR studies also confirm the Si-O-Si and O-Si-O type species observed to be sensitive for swift heavy ion (SHI) irradiated samples.