Skip to main content

Enhancement of luminescence in white emitting strontium fluoride core @ calcium fluoride shell nanoparticles


Synthesis of lanthanide-doped fluoride SrF2:3Dy and SrF2:3Dy@CaF2 nanoparticles with different ratios of core to shell (1:0.5, 1:1 and 1:2) has been carried out by employing ethylene glycol route. X-ray diffraction (XRD) patterns reveal that the structure of the prepared nanoparticles was of cubical shape, which is also evident in TEM images. The size of the nanoparticles for core (SrF2:3Dy) is found to increase when core is covered by shell (CaF2). It is also evident from Fourier transform infrared spectroscopy (FTIR) that ethylene glycol successfully controls the growth and acts as a shape modifier by regulating growth rate. In the photoluminescence investigation, emission spectra of SrF2:3Dy is found to be highly enhanced when SrF2:3Dy is covered by CaF2 due to the decrease of cross relaxation amongst the Dy3+-Dy3+ ions. Such type of enhancement of luminescence in homonanostructure SrF2:3Dy@CaF2 (core@shell) has not been studied so far, to the best of the authors’ knowledge. This luminescent material exhibits prominently white light emitting properties as shown by the Commission Internationale d’Eclairage (CIE) chromaticity diagram. The calculated correlate colour temperature (CCT) values for SrF2:3Dy, SrF2:3Dy@CaF2 (1:0.05), SrF2:3Dy@CaF2 (1:1) and SrF2:3Dy@CaF2 (1:2) are 5475, 5476, 5384 and 5525 K, respectively, which lie in the cold white region.

White light emitting homonanostructure material SrF2:3Dy@CaF2(core@shell).


Fluorides have wide applications in optics as windows, lenses and scintillation crystals and also exhibit interesting properties in optoelectronics such as lasing [1, 2], light amplification, and upconversion [35] as host crystals for lanthanide ions. The solid fluoride materials have drawn attention due to their unique properties, like low-energy phonons, high ionicity, electron-acceptor behaviour, high resistivity and anionic conductivity [68] and also have wide range of potential optical applications in optics, biological labels and lenses [9, 10]. Fluoride base system possesses very low vibrational energy comparing oxide-base system therefore quenching of excite states of the lanthanide ions is minimal in fluoride-based system [11, 12].

Strontium fluoride (SrF2) has immense applications in microelectric and optoelectric devices because of its dielectric properties and is used as an attractive host for phosphors [13, 14]. There are two main fluorescence transitions of trivalent dysprosium (Dy+3 ion) having 4f9 electronic configuration, which are 4F9/2 → 6H15/2 (blue) and 4F9/2 → 6H13/2 (yellow-orange wavelength region) [15, 16]. 4F9/2 → 6H13/2 is hypersensitive transition and strongly depend on crystal-field environment. White light emission can also achieved by doping with lanthanide ions (Ln3+) which emit primary colour (red, blue and green). White emitter characteristics are also exhibited by nanomaterials prepared by surfactant route with multiple lanthanide doping [17]. However, Dy3+ ion emits white light at a suitable yellow-to-blue intensity ratio [18, 19].

Enhancement of luminescence intensity of the lanthanide-doped nanoparticles has potential applications in optoelectronic devices. A core-shell formation in lanthanide-doped nanoparticles is one of the useful methods for enhancing luminescence.

In this present work, we have reported dysprosium ion (3 at.% )-doped SrF2 (SrF2:3Dy) nanoparticles and studied its photoluminescence properties. In order to enhance luminescence intensity, SrF2:3Dy (core) is covered by CaF2 (shell) at different ratios of shells (1:0.5, 1:1, 1:2). The Commission Internationale d’Eclairage (CIE) colour coordinates are found to be very close to ideal white values.


Chemicals and reagents

Strontium nitrate (Sr(NO3)2, 99.9 %), dysprosium (III) nitrate pentahydrade (Dy(NO3)3·5H2O, 99.99 %), from Sigma-Aldrich, ethylene glycol, ammonium fluoride NH4F and calcium chloride, CaCl2 from Merck, and methanol were used as received without further purification. Double distilled water was used throughout the experiment.

Preparation of SrF2:3Dy and SrF2:3Dy core @CaF2 shell nanoparticles

Pure SrF2 and Dy3+ ion (3 at.%)-doped SrF2 nanoparticles were synthesised by ethylene glycol route. In a typical synthesis procedure, stoichiometric amount of precursor of Dy3+ ions and strontium nitrate were heated at 40 °C for 30 min and ammonium fluoride was added. The resulting precipitate solution was allowed to mix with 50 ml of ethylene glycol and refluxed at 120 °C for 2 h. The resulting white precipitate was collected by centrifugation at 10,000 rpm after washing with methanol. In case of core-shell, i.e., SrF2:3Dy@CaF2 (1:0.5), SrF2:3Dy@CaF2 (1:1) and SrF2:3Dy@CaF2 (1:2), once the above procedure of lanthanide doping is done, requisite amount of calcium chloride solution is added and refluxed at 40 °C for about 30 min. Further, ammonium fluoride solution is added, and whole content is refluxed again at 120 °C about 2 h.

Characterisation of nanoparticles

Philips x-ray diffractometer (PW 1071) with Cuk α (1.5 Å) radiation having Ni filter was used for x-ray diffraction (XRD) study. All patterns were recorded over the angular range 10 ≤ 2θ/deg ≤ 70 with a step size of ∆2θ = 0.02. The powder samples were ground and dispersed in methanol on a glass slide and allowed to dry. The average crystallite size and strain were calculated using Williamson-Hall model. The lattice parameters were calculated from the least square fitting of the diffraction peaks.

For the characterisation of the nanoparticles, Fourier transform infrared spectroscopy (FTIR) spectra were recorded on a Perkin Elmer Spectrum 400 FT-IR spectrometer. Powder samples were studied by making thin pellets with KBr.

JEOL 2000 FX transmission electron microscope was used for recording TEM images. For the TEM measurement, the powder samples were ground and dispersed in methanol. A drop of the dispersed particles was put over the carbon coated copper grid and evaporated to dryness at room temperature.

All the luminescence spectra were recorded using LS-55 Photoluminescence Spectrometer. Powder samples were dispersed in methanol and spread over the quartz slide and dried at room temperature.

Results and discussion

X-ray analysis

Figure 1 shows the XRD pattern of SrF2, SrF2:3Dy and SrF2:3Dy@CaF2 at two different ratios of shell (1:1 and 1:2). All the peaks pattern for pure and SrF2:3Dy can be index with the Joint Committee on Powder Diffraction Standards (JCPDS) card number 06-0262 having cubical structure with space group Fm3m (225). In case of SrF2:3Dy@CaF2 core-shell, the peak patterns are found coexisting for both SrF2 and CaF2 phases, indicating the CaF2 coated on the SrF2.The star mark in the Fig. 1 indicates the SrF2 phase,and the hutch mark indicates the CaF2 phases. For CaF2, the peaks patterns are found to be face centre cubical structure with space group Fm3m (225) (JCPDS No. 35-0816). All the prepared samples are found to be crystalline structure, and there is no extra impurity peaks from the precursors of core SrF2 and shell CaF2. The lattice parameter and unit cell volume of the prepared samples are given in the Table 1. Williamson-Hall model [20] has been used to calculate the microstrain (ε) for the system under study.

Fig. 1

XRD pattern of pure, doped (3 at.% Dy3+ ion) SrF2 core and CaF2 shell at different ratios of shell

Table 1 Lattice parameter, unit cell volume and crystallite sizes of SrF2, SrF2:3Dy and SrF2:3Dy@CaF2 nanoparticles
$$ \beta \cos \uptheta = 0.9\lambda /D + 4\upvarepsilon\ \sin \uptheta $$

Here, β is the full width at half maxima (FWHM) at Bragg’s angle (2θ), with λ being the x-ray wavelength (CuKα = 1.54 Å). The calculated crystallite sizes are in the ranges of 20–40 nm (Table 2). From the Table 1, we observed that the unit cell volumes of the SrF2:3Dy is larger than SrF2 this can be explained as follows. The ionic radii of the Sr2+ (rSr 2+ = 1.27 Å) [21] is larger than the size of Dy3+ ( rDy 3+ = 1.03 Å) [22], and according to Vegard’s law, incorporation of Dy3+ ion in SrF2 results in shrinking of unit cell volume as compared to the standard data (JCPDS No. 01-1274). But from the data (lattice parameter, unit cell volume and crystallite sizes of SrF2, SrF2:3Dy and SrF2:3Dy@CaF2 nanoparticles) given in Table 1, we observed that there is slight increase in unit cell volume from the reported value. This is due to the formation of the interstitials fluoride ions, i.e., when Sr2+ is substituted by a trivalent Dy3+ ion, excess positive charges are compensated by interstitial fluoride ions where electronic repulsion between F ions also exist leading to the increase in unit cell volume [23] which indicates the incorporation of the Dy3+ ion into the SrF2 crystal lattice. Full width at half of maximum values for SrF2, SrF2:3Dy and SrF2:3Dy@CaF2 (1:1 and 1:2) are 0.24696, 0.26582, 0.3437 and 0.52442° in 2θ. The full width at half-maximum values increased gradually, which indicated the decrease of crystallinity (decreasing of crystallite size) and increase of disorder extent. Decrease in crystallinity of the SrF2:3Dy when covered with CaF2 can explained as there is possibility of substitution of some Sr2+ ions with Ca2+ ions (rCa 2+ = 1.50 Å) because they are almost having similar sizes and same charges. This type of substitution creates deformation in the crystal, which results in decreases of peak sharpness. Further, when SrF2:3Dy is covered with CaF2, there is decrease in penetration depth of x-ray passing through core (SrF2). This is reflected in the intensity of peaks corresponding to SrF2 of core-shell to decrease when compared to SrF2 without covering shell. The unit cell volume also decreases when SrF2:3Dy is covered with CaF2 which can be explained as, some of Dy3+ ion located near the surface gets distributed into CaF2 leading to decrease in electronic repulsion between F ions and unit cell volume decreases. Moreover, with increased coating of CaF2 over SrF2 particle, there is decrease of penetration depth of x-ray passing through the core. This results in decrease of intensity of peaks corresponding to SrF2, and this is possible only when SrF2 is cover by CaF2 rather than they are existing as two separated phases.

Table 2 The strain and crystallite size for of SrF2, SrF2:3Dy and SrF2:3Dy@CaF2 nanoparticles

FTIR study

Figure 2 shows the FTIR spectra of SrF2, SrF2:3Dy core and its shell with CaF2 nanoparticles at different ratios of shell component. FTIR spectra of ethylene glycol is attribute by O–H stretching and bending vibrations around 3300–3600 cm−1 and 1500–1600 cm−1; the broadening around 3300–3600 cm−1 is due to the O-H stretching vibration. Stretching vibration corresponds to C–O and C–C linkage appearing around 1000–1100 cm−1 and 1000–1200 cm−1, respectively. The C–C vibration is dominant over the C–O vibration. The peak around 2900 cm−1 has been corresponds to the C–H stretching vibrations [24]. The FTIR pattern of SrF2 nanoparticles shows the peak characterise of O–H, C–C, C–O and C–H indicating that the nanoparticles are capped by ethylene glycol molecule which was used as capping agent.

Fig. 2

FTIR spectrum of SrF2, SrF2:3Dy and SrF2:3Dy@CaF2 nanoparticles

TEM study

TEM image of SrF2:3Dy (core) shows that the prepared nanoparticles are of cubical shape and some spherical particles (Fig. 3a), and the core particles size are in the range of 8–30 nm. HRTEM image (upper inset Fig. 3a) gives the value of d = 3.3 Å which is correspond to (111) plane of SrF2:3Dy according to JCPDS No. 06-0262. The selected area electron diffraction (SAED) pattern of SrF2:3Dy (Fig. 3b) shows crystallinity of the prepared nanoparticles exhibiting clear spots on the rings. In case of SrF2:3Dy@CaF2 (core@shell) with the ratio 1:2, the shape of the particles is still cubical and spherical (Fig. 3c). The size of the core@shell nanoparticles were found to be larger than core where the size of the cubical shaped core@shell particles is 50 nm and that of spherical is 37 nm. The cubical shape appears to be covered by another cube, but image is not clear and similar thing happens in case of spherical particles also. This indicates that CaF2 shell covers the SrF2:3Dy core. From the HRTEM image (lower inset Fig. 3c), we observed two kinds of plane, one gives the value of d = 2.8 Å which corresponds to (200) plane of core (SrF2:3Dy) according to JCPDS No. 06-0262, and the other one gives the value of d = 3.2 Å corresponding to (111) plane of shell (CaF2) according to JCPDS No. 35-0816. These data indicated that core (SrF2:3Dy) is well covered by shell (CaF2). The SAED pattern of core@shell is also shown in Fig. 3d, and particles are still crystalline.

Fig. 3

a TEM image of SrF2 :3Dy (core) and b its SAED pattern. c TEM image of SrF2:3Dy@CaF2 (1:2) and d its SAED pattern

In order to see the crystallinity of shell CaF2, the TEM image and SAED pattern of shell alone are shown in Fig. 4. The shape of shell is found to be cubic (Fig. 4a) with particle size of 20 nm. The HRTEM of shell (inset Fig. 4a) clearly indicates crystallinity of CaF2 and gives the value of d = 1.9 Å which corresponds to (220) plane of CaF2 according to JCPDS No. 35-016. In the SAED pattern also (Fig. 4b), the spots in the rings indicate crystallinity of shell and diffraction rings are labelled accordingly.

Fig. 4

a TEM image of shell CaF2 (inset HRTEM of shell) and b SAED of shell

Photoluminescence study

Figure 5a shows the excitation spectra of the SrF2:3Dy and SrF2:3Dy@CaF2 at two different ratios of shell monitored at 575-nm emission wavelength. In order to study the excitation spectra, we can divide the whole spectrum into two regions, one in the range 200–280 nm and another is 280–400 nm. The region from 200–280 nm corresponds to the transition from 2p orbital of F ions to the 4f orbital of Dy3+ ions (charge transfer transition) and consists of peaks at 239, 256 and 277 nm. The peaks from 280–400 nm are related with the 4f-4f transition of Dy3+ ion. The peak at 349, 363, 386, 435, 453 and 474 nm can be assigned to the transition from 6H15/2 to 6P7/2 , 6P5/2 , 4I13/2 , 4G11/2 , 4I15/2 and from 4F9/2 to 4H15/2 of Dy3+ ion [25].

Fig. 5

a Excitation spectra of SrF2:3Dy core nanoparticles and its CaF2 shell at different ratios of shells monitor at 575-nm emission wavelength. b Emission spectra of SrF2:3Dy@CaF2 (1:2) monitor at two different excitation wavelengths 240 and 349 nm

The emission spectra monitored at two different excitation wavelengths 240 and 349 nm (Fig. 5b) for the SrF2:3Dy@CaF2 (1:2) nanoparticles shows the characteristic emission peaks of Dy3+ ion at 475 and 570; 612 nm originating from 4F9/2 → 6H15/2 (blue) and 4F9/2 → 6H13/2 (yellow-orange), as we know that the yellow part of Dy3+ ion is in the range extended from 560–610 nm [22]. So 612-nm peak is related to the yellow part of the Dy3+ ion and consists of some red part also. The peak of 612-nm emission is seen in case of 240-nm excitation, but for 349-nm excitation, only two peaks at 475 and 570 nm are seen since the intensity of the peaks are higher when excited at host (charge transfer transition), indicating good energy transfer from host to Dy3+ ion. In case of 349 nm excitation, the peak of 570 nm emission is predominant so the peak of 612 nm cannott be seen. The peak at 475 nm is most intense as compared to other peaks.

In case of all nanoparticles excited at 240 nm (Fig. 6a), the peaks at 475 nm, i.e. 4F9/2 → 6H15/2 transition, are most intense and they have same peak pattern except their intensities are different. From the figure, we observed that the intensity of the peak for the core SrF2:3Dy is less than the intensity of the peak for core@shell SrF2:3Dy@CaF2 and increase in intensity is also seen for the emission peaks of Dy3+ ion with increasing concentration of the shell. The intensity of the emission peaks increases when core (SrF2:3Dy) is covered with CaF2 (shell); this can be explained as, Dy3+ ion have strong cross relaxation amongst Dy3+-Dy3+ ions resulting in decrease in luminescence intensity. But SrF2:3Dy is covered by CaF2 where some part of Dy3+ ion is diffused to the CaF2 so that Dy3+ ion concentration decreases resulting in decreases of the cross relaxation amongst the Dy3+-Dy3+ ions leading to increase in emission intensity. Moreover –OH present on the surface of the core is less in number when core is covered by shell. Because of the removal of –OH/dangling bond from the surface of the core, the non-radiative decay diminishes, and hence, the emission intensity increases when core is covered by shell. We know that –OH decreases luminescence intensity through multiphonon relaxation [17]. Enhancement of emission intensity can also be assigned to decreasing tensile strain value as reported elsewhere [26], and this has been also observed in our prepared nanoparticles. Tensile strain value for core@shell is decreased as compared to core itself. The values of strain are given in Table 2. Because of above factors, the emission intensity of SrF2:3Dy (core) is enhanced when it is covered by shell (CaF2).

Fig. 6

Emission spectra of SrF2:3Dy core nanoparticles and its CaF2 shell at different ratios of shells excited at a 240 nm and b 349 nm

Upon excitation at 240 nm, the emission spectrum of core SrF2:3Dy is broadened. This is related to defect-induced emission from host. There is large difference in ionic sizes in Sr2+ and Dy3+, which creates defects in lattice. When shell of CaF2 is introduced, some parts of Dy3+ occupy Ca2+ sites. Ionic size difference between Ca2+ and Dy3+ is much less than that between Sr2+ and Dy3+. Thus, defect in lattice decreases after formation of core@shell. The emission peak intensity arising from defects decreases. In case of core@shell (1:2), broad emission peak almost disappears; instead, emission peaks of Dy3+ are observed. Emission spectrum gives sharp peaks corresponding to Dy3+ when excitation is chosen at 349 nm (direct excitation) irrespective of samples (core or core@shell) as shown in Fig. 6b. It means that 349-nm excitation cannot create electron-hole pairs from lattice defects. The energy associated with 349 nm is much less than that of 240 nm, and thus, it is insufficient to generate electron-hole pairs. In case of 240-nm CT excitation, there are various ways of excited electrons returning to the ground state, and in the meantime, energy diffusion may also occur. But in the case of 349-nm direct excitation, there is a limited path for returning of excited electron to ground state [27]. The emission intensity of the 240-nm excitation is slightly less than that of 349-nm excitation indicating that energy transfer from charge transfer band is less than direct excitation. Such type of enhancement of luminescence in homonanostructure SrF2:3Dy@CaF2 (core@shell) has not been studied so far, to the best of the authors’ knowledge.

Figure 7 shows the Commission Internationale d’Eclairage (CIE) coordinate diagram of SrF2:3Dy and SrF2:3Dy@CaF2 at different ratios excited at two different excitation wavelengths 240 and 349 nm emitting white light. The corresponding chromaticity coordinates for 240-nm excitation (Fig. 7a) are (A) SrF2:3Dy (x = 0.334, y = 0.348), (B) SrF2:3Dy@CaF2 (1:0.5) (x = 0.338, y = 0.346), (C) SrF2:3Dy@CaF2 (1:1) (x = 0.333, y = 0.334) and (D) SrF2:3Dy@CaF2 (1:2) (x = 0.334, y = 0.335) and for 349-nm excitation (Fig. 7b) are (A) SrF2:3Dy (x = 0.333, y = 0.337), (B) SrF2:3Dy@CaF2 (1:0.5) (x = 0.333, y = 0.338), (C) SrF2:3Dy@CaF2 (1:1) (x = 0.335, y = 0.336) and (D) SrF2:3Dy@CaF2 (1:2) (x = 0.331, y = 0.334). The calculated chromaticity coordinates are very close to the other reported values [28]. The quality of the white light calculated by using Mc Camy empirical formula [29] in terms of correlate colour temperature (CCT) values, which is given below:

$$ \mathrm{C}\mathrm{C}\mathrm{T} = -449{n}^3 + 352\ {n}^2\hbox{--}\ 6823n+5520.33 $$
Fig. 7

CIE diagram of SrF2:3Dy, SrF2:3Dy@CaF2 (1:0.5, 1:1 and 1:2) nanoparticles excited at two different excitation wavelengths a 240 and b 349 nm

Where, \( n = \frac{x - {x}_c}{y - {y}_c} \) is negative inverse slope line, x c = 0.332, and y c = 0.186. The CCT values for excitation at 240 nm, for SrF2:3Dy, SrF2:3Dy@CaF2 (1:0.05), SrF2:3Dy@CaF2 (1:1) and SrF2:3Dy@CaF2 (1:2) are 5436, 5264, 5474 and 5428 K, respectively. For excitation at 349 nm, the CCT values for SrF2:3Dy, SrF2:3Dy@CaF2 (1:0.05), SrF2:3Dy@CaF2 (1:1) and SrF2:3Dy@CaF2 (1:2) are 5475, 5476, 5384 and 5525 K, respectively. These CCT values lie in the cold white region. Thus, the prepared nanomaterials exhibit the characteristics of white emitter.


Lanthanide ion (Dy3+)-doped SrF2 core and SrF2:3Dy@CaF2 shell at different ratios of shell (CaF2) have been successfully synthesised by using ethylene glycol as capping agent. The XRD pattern indicates that the synthesised nanoparticles have mainly cubical structure SrF2 (JCPDS 06-0262) and substitution of Dy3+ ion into SrF2 sites. Unit cell volume of the SrF2:3Dy decreases when it is covered by CaF2, since some parts of Dy3+ ions are distributed into the shell (CaF2) thereby decreasing both the electronic repulsion between F ions and unit cell volume. FTIR studies show the capping of SrF2 by ethylene glycol which is used as capping agent. The emission spectrum of the SrF2:3Dy core is weak due to the strong cross relaxation amongst the Dy3+-Dy3+ ions, which has been overcome by covering a layer of CaF2 shell over SrF2:3Dy (i.e., core@shell formation). Thus, in such core@shell system, the emission intensity of Dy3+ ion is enhanced effectively. Luminescence properties of such type of homonanostructure SrF2:3Dy@CaF2 have not been investigated so far, to the best of the authors’ knowledge. The emission spectra lies in the white region in CIE diagram and CCT calculated using Mc Camy empirical formula shows the prepared nanoparticles are found to be lying in the cold white region.


  1. 1.

    Slunga EB, Cederwall E, Ideguchi A, Kerek W, Klamra J, Marel VD, et al. Scintillation response of BaF2 and YAlO3:Ce (YAP: Ce) to energetic ions. Phys Res Sect A. 2001;469:70–6.

  2. 2.

    Basiev TT, Orlovskii YV, Galagan BI, Doroshenko ME, Vorob’ev IN, Dmitruk LN, et al. Evaluation of rare-earth doped crystals and glasses for 4-5-μm lasing. Laser Phys. 2002;12:859–77.

    Google Scholar 

  3. 3.

    Goldner P, Mortier M. Effect of rare earth impurities on fluorescent cooling in ZBLAN glass. J Non-Cryst Solids. 2001;284:249–54.

    Article  Google Scholar 

  4. 4.

    Bouffard M, Jouart JP, Joubert MF. Red-to-blue up conversion spectroscopy of Tm3+ in SrF2, CaF2, BaF2 and CdF2. Opt Mater. 2000;14:73–9.

    Article  Google Scholar 

  5. 5.

    Zhang X, Liu XR, Jouart JP, Mary G. Upconversion fluorescence of Ho3+ ions in a BaF2 crystal. Chem Phys Lett. 1998;287:659–62.

    Article  Google Scholar 

  6. 6.

    Feldmann C, Roming M, Trampert K. Polyol-mediated synthesis of nanoscale CaF2 and CaF2:Ce,Tb. Small. 2006;2:1248–50.

    Article  Google Scholar 

  7. 7.

    Zewei Q, Dongmei Y, Piaoping Y, Xiaoming Z, Hongzhou L, Xiaoming L, et al. Uniform collodial alkaline earth metal fluoride nanocrystals: nonhydrolytic synthesis and luminescence properties. Inorg Chem. 2008;47:9509–17.

  8. 8.

    Peng G, Yi X, Zhen L. Controlling the size of BaF2 nanotubes from 1000 to 10 nm. Eur J Inorg Chem. 2006;16:3261–5.

    Google Scholar 

  9. 9.

    Yuanbing M, Fen Z, Stanislaus WS. Ambient template-directed synthesis of single-crystalline alkaline-earth metal fluoride nanowires. Adv Mater. 2006;18:1895–9.

    Article  Google Scholar 

  10. 10.

    Wen SW, Liang Z, Cheng YX, Jun ZC, Wen ZS. Aqueous solution synthesis of CaF2 hollow microspheres via the ostwald ripening process at room temperature. Appl Mater Interfaces. 2009;1:780–8.

    Article  Google Scholar 

  11. 11.

    Christopher BM, James BM. Synthesis and fluorescence of neodymium-doped barium fluoride nanoparticles. Chem Mater. 2000;12:1969–76.

    Article  Google Scholar 

  12. 12.

    Laishram PS, Srivastava SK, Ratikant M, Raghumani NS. Multifunctional hybrid nanomaterials from water dispersible CaF2:3Eu3+, Mn2+ and Fe3O4 luminescence and hyperthermia application. J Phys Chem C. 2014;118:18087–96.

    Article  Google Scholar 

  13. 13.

    Zewei Q, Dongmei Y, Chunxia L, Piaoping Y, Ziyong C, Jun Y, et al. SrF2 hierarchical flowerlike structures: solvothermal synthesis, formation mechanism and optical properties. Mater Res Bull. 2009;44:1009–16.

  14. 14.

    Ivanovskikh KV, Pustovarov VA, Kirm M, Shulgin BV. Luminescent VUV spectroscopy of Er3+ and Tm3+ ions in fluoride crystals. J Lumin. 2007;122–123:28–31.

    Article  Google Scholar 

  15. 15.

    John GB, Bahram Z, Uygun VV, Rakhimov SA. Energy levels of Dy3+ (4fn) in orthoaluminate crystals. J Appl Phys. 2003;94:1030–4.

    Article  Google Scholar 

  16. 16.

    Bo L, Chaoshu S, Zemimg Q. Potential white-light long-lasting phosphor: Dy3+-doped aluminate. Appl Phys Lett. 2005;86:19111–3.

    Article  Google Scholar 

  17. 17.

    Meitram NL, Raghumani NS, Srivastava SK, Rakesh KV. Preparation of white light emitting YVO4:Ln3+ and silica-coated YVO4:Ln3 + (Ln3+ = Eu3+, Dy3+, Tm3+) nanoparticles by CTAB/n-butanol/hexane/water microemulsion route: energy transfer and site symmetry studies. J Mater Chem C. 2011;21:5326–37.

    Article  Google Scholar 

  18. 18.

    Qiang S, Zhiwu P, Lisheng C, Hongjie Z, Zhongyi Z, Feng Z. The yellow-to-blue intensity ratio (Y/B) of Dy3+ emission. J Electrochem Soc. 2005;192:25–7.

    Google Scholar 

  19. 19.

    Qiang S, Zhiwu P, Jun L, Feng X. Luminescence of Dy3+ enhanced by sensitization. J Alloys Comp. 1995;225:103–6.

    Article  Google Scholar 

  20. 20.

    Williamson GK, Hall WH. X-ray line broading from filed aluminium and wolfram. Actametall. 1953;1:22–31.

    Google Scholar 

  21. 21.

    Ryu O, Yousuke O, Seiji K. Inelastic light scattering of divalent ions (Ca2+, Sr2+ and Ba2+) substituted (Na1/2Bi1/2) TiO2 single crystal. J Kore Phys Soc. 2011;59:2471–4.

    Article  Google Scholar 

  22. 22.

    Satapathy KK, Khan F. Impulsive excitation of mechanoluminescence in γ-ray irradiated ZnAl2O4:Dy phosphors synthesized by solution combustion technique. Adv Mat Lett. 2013;4(4):323–6.

    Google Scholar 

  23. 23.

    Bing H, Hongbin L, Yan H, Ye T, Qiang S. Vacuum ultraviolet-visible spectroscopic properties of Tb3+ in Li(Y, Gd)(PO3)4: tunable emission, quantum cutting and energy transfer. J Phys Chem C. 2010;114:6770–7.

    Google Scholar 

  24. 24.

    Kemp W. Organic spectroscopy. Hampshire: Macmillan Educational Ltd.; 1987.

    Google Scholar 

  25. 25.

    Carnall WT, Fields PR, Rajnak K. Electronic energy levels in the trivalent lanthanide aqua ions (Pr3+, Nd3+, Pm3+, Sm3+, Dy3+, Ho3+, Er3+ and Tm3+). J Chem Phys. 2002;49:65–653.

    Google Scholar 

  26. 26.

    Aumer ME, LeBoeuf SF, Bedair SM, Smith M, Lin JY, Jiang HX. Effects of tensile and compressive strain on the luminescence properties of AllnGaN/InGaN quantum well structures. Appl Phys Lett. 2000;77:821–3.

    Article  Google Scholar 

  27. 27.

    Pushpal G, Amitava P. Influence of crystal phase and excitation wavelength on luminescence properties of Eu3+-doped sodium yttrium fluoride nanocrystals. J Phys Chem C. 2008;112:19283–92.

    Article  Google Scholar 

  28. 28.

    Godhuli S, Amitava P. Generation of green, red and white light from rare-earth doped Ga2O3 nanoparticles. Chem Phys Lett. 2009;473:151–4.

    Article  Google Scholar 

  29. 29.

    Mc Camy CS. Correlated color temperature as an explicit function of chromaticity coordinates. Color Res Appl. 1992;17:142–4.

    Article  Google Scholar 

Download references


Nandini Kumam thanks the University Grants Commission, New Delhi, India for providing the UGC-BSR Meritorious Fellowship. Ningthoujam Premananda Singh would like to thank the Council of Scientific and Industrial Research (CSIR), New Delhi for Junior Research Fellowship.

Author information



Corresponding author

Correspondence to Sri Krishna Srivastava.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

SKS conceived and designed the experiments. NK, NPS and LPS performed the experiments. NK, NPS, LPS and SKS analysed the data. NK, NPS, LPS and SKS wrote the paper. All authors read and approved the final manuscript.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Kumam, N., Singh, N.P., Singh, L.P. et al. Enhancement of luminescence in white emitting strontium fluoride core @ calcium fluoride shell nanoparticles. Nanoscale Res Lett 10, 347 (2015).

Download citation


  • Core shell fluoride nanomaterials
  • Luminescence
  • White emitter