Morphology- and size-dependent spectroscopic properties of Eu3+-doped Gd2O3 colloidal nanocrystals

  • Dominika Wawrzynczyk
  • Marcin Nyk
  • Artur Bednarkiewicz
  • Wiesław Strek
  • Marek Samoc
Open Access
Research Paper

Abstract

The synthesis, morphological characterization, and optical properties of colloidal, Eu(III) doped Gd2O3 nanoparticles with different sizes and shapes are presented. Utilizing wet chemical techniques and various synthesis routes, we were able to obtain spherical, nanodisk, nanotripod, and nanotriangle-like morphology of Gd2O3:Eu3+ nanoparticles. Various concentrations of Eu3+ ions in the crystal matrix of the nanoparticles were tested in order to establish the levels at which the concentration quenching effect is negligible. Based on the luminescence spectra, luminescence lifetimes and optical parameters, which were calculated using the simplified Judd–Ofelt theory, correlations between the Gd2O3 nanoparticles morphology and Eu3+ ions luminescence were established, and allowed to predict the theoretical maximum quantum efficiency to reach from 61 to 98 %. We have also discussed the impact of the crystal structure of Gd2O3 nanoparticles, as well as coordinating environment of luminescent ions located at the surface, on the emission spectra. With the use of a tunable femtosecond laser system and the Z-scan measurement technique, the values of the effective two-photon absorption cross-section in the wavelength range from 550 to 1,200 nm were also calculated. The nonlinear optical measurements revealed maximum multi-photon absorption in the wavelength range from 600 to 750 nm.

Keywords

Oxide nanoparticles Lanthanide luminescence Judd–Ofelt theory Z-scan technique Nonlinear optics Colloidal stability 

Introduction

The precise control of both morphology and spectroscopic properties of lanthanide-doped nanoparticles (NPs) is of great importance for their use in sensing and labeling applications. Among various factors pertinent to optimizing the properties, it is essential to consider the influence of NPs size and shape on spectroscopic properties of optically active ions embedded in the fabricated materials (Yan and Yan 2008; Zhang et al. 2009). With well-optimized synthesis protocols, it is possible to obtain NPs with narrow size and shape distributions, and further investigate their optical properties. Several reports showed the possibility of obtaining lanthanide-doped NPs with various morphologies such as spheres, plates, rods, nanotubes, nanowires, and even 3D flowers (Cao 2004; Gai et al. 2011; Paik et al. 2013; Paik and Murray 2013; Yang et al. 2008; Zheng et al. 2010). Additionally, the combination of unique optical features of lanthanide ions (Bünzli and Eliseeva 2011), i.e., long luminescence lifetimes, sharp excitation, and emission lines, with chosen crystal matrices and the nanometric size provides effective performance of the synthesized NPs. In particular, Eu3+ ions-doped oxide NPs have shown unique luminescent properties, owing to different possible narrowband luminescence excitation pathways. The Eu3+ ions have been excited by either direct 4f-4f electronic transitions in Eu3+ ions, through the host matrix absorption, Eu–O charge transfer, indirect Gd3+ or Ce3+ ions absorption, or even with the sensitization through the organic ligands attached to the NPs surface (Chen et al. 2013; Du et al. 2013; Grzyb et al. 2013; Kumar et al. 2013; Liu et al. 2006). As a result, the Eu3+ ions-doped oxide NPs showed intense, narrowband luminescence with excited state lifetimes up to 1 ms, suitable for applications as red emitting phosphors (Blasse 1994). Another interesting feature of Eu3+-doped oxide NPs is the possibility to excite the emission through multi-photon absorption processes. Although extensive literature regarding nonlinear optical (NLO) properties of Eu3+ organic complexes is available (Andraud and Maury 2009), the reports regarding NLO properties of inorganic lanthanide-doped NPs are scarce (Nyk et al. 2011; Wawrzynczyk et al. 2013b). The measured and calculated NLO parameters are usually limited to a single wavelength, thus the dispersions of these parameters are lacking, while wide-wavelength range measurements are essential for finding optimum wavelengths for multi-photon excitation of lanthanide luminescence. Additionally, since the 4f-4f photon transitions in lanthanides are two-photon allowed (Lakowicz et al. 2001; Sztucki and Strek 1986), the NLO spectroscopy can provide additional information regarding the electronic structure of the investigated materials.

Apart from being efficient luminescence centers, Eu3+ ions are also very good luminescent probes of local crystalline environment, which enable correlation between spectral and structural properties of lanthanide-doped hosts. It has been proved that the ratio of the intensities of 5D0 → 7F2 and 5D0 → 7F1 transitions in Eu3+ ions (asymmetry ratio, R) together with Judd–Ofelt intensity parameters (Ω2 and Ω4) can be considered indicative of the distortion in the symmetry of the local environment of the Eu3+ emitters (Boyer et al. 2004; Judd 1962; Kumar et al. 2013; Ofelt 1962). The intensity parameters Ω2 and Ω4 were successfully related with NaGdF4 and Gd2O3 NPs sizes (Bednarkiewicz et al. 2005; Liu et al. 2006), while Eu3+ ions luminescence was successfully used to probe the surface effects, originating from high surface to volume ratio in nanosized materials (Banski et al. 2013; Chang et al. 2007; Jia et al. 2010). Furthermore, Wiglusz et al. (Wiglusz et al. 2010) showed elegant correlation between Eu3+ luminescence decays and relative amount of Eu3+ ions located at different crystallographic sites of hydroxyapatites.

Here we report the synthesis and spectroscopic investigations of Gd2O3 NPs doped with Eu3+ ions. The obtained nanosized Gd2O3:Eu3+ NPs presented spherical, nanodisk, nanotripod, and nanotriangle-like morphologies. The various sizes and shapes of those NPs resulted from changes introduced in the thermal decomposition reaction, through modifying lanthanide precursors to capping ligands ratio, or by addition of Li+ ions. In order to perform detailed spectroscopic investigation, we have synthesized those NPs with various concentrations (0.5, 1, 2, 3, 4, and 5 mol%) of Eu3+ ions. The analysis of luminescence spectra, luminescence lifetimes, and Judd–Ofelt parameters revealed different concentration quenching for Eu3+ ions depending on the size and shape of Gd2O3 nanocrystals. We have also performed wide-wavelength range Z-scan measurements in order to calculate the values of effective two-photon absorption cross-section (σ2,eff) for representative Gd2O3 NPs of different shapes. The Z-scan experiments revealed multi-photon absorption in the wavelength range from 600 to 750 nm. Furthermore, the values of σ2,eff and molecular mass scaled parameters (σ2,eff/M) obtained for Gd2O3:Eu3+ NPs were compared with the values obtained for other types of inorganic NPs.

Experimental

Materials and methods

Transmission Electron Microscopy (TEM) images and Selected Area Diffraction (SEAD) patterns were obtained by a FEI Tecnai G2 20 X-TWIN microscope. X-ray powder diffraction (XRD) measurements were recorded on a STOE diffractometer with Ge-filtered CuKα1 radiation. The excitation spectra were recorded with a Hitachi F-4500 spectrofluorimeter. The emission spectra and luminescence decay curves were obtained under excitation from the third harmonic (266 nm) of a Ti:Sapphire laser pumped by a Nd:YAG LOTIS TII laser (Belarus). The luminescence signals were detected by a Synapse CCD camera (HORIBA JOBIN–YVON). Fluorescence decay curves were recorded with a photomultiplier (HAMAMATSU R928) whose output was fed into a LeCroy Wave Surfer 425 digital oscilloscope. The NLO measurements were performed using a femtosecond laser system consisting of a Quantronix Integra-C Ti:Sapphire regenerative amplifier which produces ~130 fs, 800 nm pulses with 1 kHz repetition rate, and 1 mJ energy per pulse, pumping a Quantronix Palitra-FS optical parametric amplifier (OPA). Details of the experiment were described in our previous papers (Nyk et al. 2011, 2012). Samples for Z-scan measurements were prepared in 1-mm-thick sealed glass cuvettes. Scans of the investigated Gd2O3:Eu3+ NPs were preceded by scans of a 4.6 mm-thick silica glass plate used as a reference, and a cuvette with pure solvent, the latter being used in order to eliminate the contributions of the cuvette walls and the solvent itself to the signals (Samoc et al. 2003). The open-aperture (OA) Z-scan traces were fitted using expressions derived by Sheik-Bahae (Sheikbahae et al. 1990). This allowed us to calculate the values of effective two-photon absorption cross-section σ2,eff referring to individual Gd2O3:Eu3+ NPs.

Synthesis of Eu3+ doped Gd2O3 nanocrystals

All chemicals for synthesis of Gd2O3:Eu3+ NPs were purchased from Sigma Aldrich or POCH S.A. (Poland), and used without further purification. In order to study the dependence of NPs sizes and shapes on Eu3+ optical properties, we synthesized Gd2O3 NPs with spherical, nanodisk, nanotripod, and nanotriangle-like NPs morphology. For nanosphere- and nanodisk-shaped Gd2O3 NPs, we utilized the synthesis protocol reported by Cao (Cao 2004). In a typical synthesis procedure, gadolinium acetate hydrate (1 or 2 mM) and europium acetate hydrate (1 or 2 mM) were dissolved in a mixture of 1.7 ml oleylamine, 1 ml oleic acid, and 2.7 ml octadecene at ~100 °C. The solution was degassed and heated to temperature around 300 °C, and then cooled to room temperature after 1 h. The obtained Gd2O3 NPs were precipitated with a mixture of methanol and acetone (2:1 v/v), and washed several times with methanol. Finally, the NPs were dissolved in 4 ml of CHCl3. For nanotripod- and nanotriangle-shaped Gd2O3 NPs, we followed the report by Paik et al. (Paik et al. 2013). In a typical synthesis procedure, lithium hydroxide (6 mM) was dissolved and degassed in a mixture of 12 ml of oleic acid, 18 ml of oleylamine, and 30 ml of 1-octadecene at ~100 °C. Next, gadolinium acetate (3 mM) and europium acetate (3 mM) were added into the solution, followed by the evaporation at ~100 °C. The yellowish, transparent solution was then heated to ~300 °C under N2 flow. Identical amounts of the reaction solution were picked up with a syringe after 45 min, 1.5, and 3.5 h, cooled to room temperature, precipitated with a mixture of methanol and acetone (2:1 v/v), and washed several times with methanol. Finally, the NPs were dissolved in 4 ml of CHCl3. The intentional Eu3+ ions content in the crystal matrix in the prepared samples was as follows: Gd2O3:x %Eu3+ (x = 0.5, 1, 2, 3, 4, and 5).

Results and discussion

Morphology and crystal structure

Figures 1 and 2 present the morphological and crystallographic characterization of Eu3+-doped Gd2O3 NPs obtained by the synthesis protocols described by (Cao 2004) and (Paik et al. 2013), respectively. As can be seen from Fig. 1, when low volumes of coordinating solvents are used and no Li+ ions are added to the reaction, the synthesis results in formation of nanospheres and nanodiscs. In particular, smaller amount of Gd3+ and Eu3+ acetates (1 mM) with respect to the constant coordinating solvents volume results in formation of small, spherical Gd2O3 NPs with average sizes below 5 nm (Fig. 1a). The increase of the lanthanide acetates amount (2 mM) results in formation of thin nanodiscs with average dimensions ~10 nm/~1.3 nm (Fig. 1b). Based on the SAED patterns (insets in Fig. 1a, b), and comparisons of XRD patterns for nanospheres and nanodiscs (Fig. 1c) with standard (JCPDS 12-797) pattern of cubic Gd2O3, we have assigned the obtained NPs to the Gd2O3 cubic phase. We have observed significant broadening of the XRD peaks and diffraction rings diameters related to the lattice plane spacing, being a result of small sizes of the NPs.
Fig. 1

TEM images and SAED patterns for Gd2O3:Eu3+ NPs synthesized following (Cao 2004), with addition of 1 mM (a) and 2 mM (b) of lanthanide acetates. XRD patterns of Gd2O3:Eu3+ NPs with nanosphere and nano-disks like morphology compared with standard (JCPDS 12-797) pattern of cubic Gd2O3 (c)

Fig. 2

TEM images and SAED patterns for Gd2O3:Eu3+ NPs synthesized following Paik et al. (2013) obtained after 45 min (a), 1.5 h (b), and 3.5 h (c) time of synthesis. XRD patterns of nanotriangle, intermediate form, and nanotripod shaped Gd2O3:Eu3+ NPs compared with standard (JCPDS 12-797) pattern of cubic Gd2O3 (d)

Fig. 3

Luminescence spectra of Gd2O3:Eu3+ nanospheres (a) and nanodiscs (b) doped with different amounts of Eu3+ ions; measured at room temperature under 266 nm laser light excitation

Introducing Li+ ions into the reaction results in the formation of thin nanotripod- and nanotriangle-shaped Gd2O3:Eu3+ NPs. As it was previously shown by Paik et al. (2013), by prolonging the reaction time the NPs shape is transformed from nanotripods (Fig. 2a) to nanotriangles (Fig. 2c) throughout the transitional form (Fig. 2b). The obtained Gd2O3:Eu3+ NPs possessed much narrower size and shape distribution and, in comparison with previously obtained nanospheres and nanodiscs, were much bigger. The average diameter of Gd2O3:Eu3+ NPs was ~40 nm. Based on the SAED (insets in Fig. 2a–c) and XRD patterns (Fig. 2d), we could again assign the obtained NPs to the Gd2O3 cubic form, as expected for the case of bigger NPs, and the diffraction pattern rings were sharp and more intense. The broadening of the peaks at the XRD patterns results from the small thickness of obtained Gd2O3:Eu3+ NP, which did not exceed 2 nm. The influence of the Li+ ions on the size and shape of the obtained Gd2O3 NPs may be related to the direct doping of Li+ ions into the crystal matrix, causing lattice expansion (Paik et al. 2013). Extensive work concerning the influence of alkali ions (Li+, Na+, and K+) on the formation of fluoride NPs has been performed by (Xue et al. 2013) showing that, depending on the ionic radius of the added alkali ions, formation of various fluoride NPs morphologies may occur.

Photoluminescence properties and Judd–Ofelt parameters of Gd2O3:Eu3+ nanocrystals

The main purpose of this work was to search for correlation between spectroscopic properties of Eu3+ ions doped the Gd2O3 matrix with the size and shape of the respective NPs. The investigated Gd2O3:Eu3+ NPs showed intense red luminescence under 266 nm laser excitation, and the observed luminescence lines (Figs. 3, 4) resulted from the electronic 4f-4f transitions from 5D0 level of Eu3+ ions to 7FJ=0,1,2,3,4 ground state components, from which the most intensive ones could be observed at ~613 and ~625 nm (5D0 → 7F2). In order to study the possible Eu3+ luminescence excitation pathways, we recorded excitation spectra, monitoring the most intense emission line at 613 nm (5D0 → 7F2). The representative results for nanospheres, nanodiscs, nanotripods, and nanotriangles are shown in Fig. 4. The excitation spectra are dominated by the Gd2O3 (maximum at ~200 nm) host absorption for smaller nanospheres and nanodiscs, and by the charge-transfer (CT) absorption (~260 nm) for the nanotripods and nanotriangles with larger average sizes. With increasing the size of Gd2O3:Eu3+ NPs, the excitation from host matrix gets less dominant, and the CT band occurs. This fact can be well understood, since the CT relies on electron transfer between the O2- and Eu3+, and many more of such optically active centers can be found in bigger NPs. A similar effect was observed by (Li and Hong 2007) for nanocrystalline Gd2O3:Eu3+ powders, where the ratio of host absorption to CT band of smaller NPs was much bigger, compared with that for larger NPs. Additionally, we could observe characteristic narrowband excitation peaks corresponding to the direct 4f-4f electronic transitions in Gd3+ (8S7/2 → 6I7/2) and in the Eu3+ ions (inset in the Fig. 5). The intensity of the excitation peak from the Gd3+ ions was much higher than for the case of Eu3+ ions, owing to very low (from 0.5 to 5 %) Eu3+ ions concentration in the Gd2O3 matrix.
Fig. 4

Luminescence spectra of nanotripods (a) intermediate form (b) and nanotriangles (c) shaped Gd2O3 NPs doped with different amounts of Eu3+ ions and excited with 266 nm laser light

Fig. 5

Excitation spectra of representative Gd2O3:Eu3+ NPs with the shapes of nanospheres, nanodiscs, nanotripods, and nanotriangles obtained by monitoring 5D0 → 7F2 transition of Eu3+ emission at 613 nm

Fig. 6

Luminescence lifetime values corresponding to the long τ1 (black) and short τ2 (blue) components for 5D0 excited state in Eu3+ ions measured for Gd2O3:Eu3+ nanospheres (a) and nanodiscs (b) excited with 266 nm laser light. (Color figure online)

In order to find Eu3+ ions doping level at which the concentration quenching is the weakest in the Gd2O3 matrix, as well as to investigate the influence of nanocrystals’ shape and crystal structure on Eu3+ emission, we have measured luminescence spectra and 5D0 excited state lifetimes for Gd2O3:Eu3+ NPs of different shapes, as a function of rising Eu3+ concentrations. In the case of nanospheres, the observed luminescence lines were considerably broadened in comparison with the larger Gd2O3:Eu3+ NPs (Fig. 3a). Those Gd2O3:Eu3+ NPs had the highest surface to volume ratio, and the largest number of Eu3+ ions was exposed to the interaction with organic ligands as well as solvent molecules (Liu et al. 2006; Wawrzynczyk et al. 2013a). The slight increase in Gd2O3:Eu3+ NPs’ size resulted in evident narrowing of the emission lines for the nanodiscs, nanotripods, and nanotriangles (Fig. 3b and Fig. 4). We have also observed roughly even intensity of the two peaks characteristic for the 5D0 → 7F2 electronic transition in Eu3+ ions. The Gd2O3 NPs are obtained either in the monoclinic or cubic crystal structure of nanopowders, with emission spectra maximum at longer wavelengths (~620 nm) for the monoclinic form, and blue-shifted (~610 nm) for the cubic one (Seo et al. 2009). The increased ratio of Eu3+ emission intensities at 620 nm to the peak at 610 nm for the investigated cubic Gd2O3 NPs may be rationalized by high surface to volume ratio. In such a case, a significant number of Eu3+ ions are located at NPs’ surface, and thus, Eu3+ display a lower coordination number and emission spectra similar to monoclinic polycrystalline powders, in which Eu3+ ions occupy lower symmetry. The same relationships were observed by (Si et al. 2005) for Eu2O3 NPs. Gd2O3:Eu3+ colloidal NPs emission spectra, with peaks at 610 and 620 nm having roughly even intensities, have been also reported by (Paik et al. 2013). The highest luminescence intensity was observed at 4 % Eu3+ doping level for nanospheres and nanodiscs (Fig. 3), at 5 % for nanotripods and at 4 % for nanotriangles (Fig. 4). However, these values were found somewhat susceptible to the concentration of the Gd2O3:Eu3+ NPs in the chloroform colloidal dispersion, sample experimental setup alignment, and fluctuation in the excitation light intensity.

The luminescence lifetime measurements provide more reliable information regarding optimum Eu3+ concentration in the host matrix. In general, longer 5D0 excited state luminescence lifetimes indicate lower quenching arising from surface defects, vibrational modes of ligands molecules, and impurities inside the crystal matrix. Apart from these external quenching mechanisms, additional concentration quenching may occur in heavily Eu3+ doped hosts, which originates from the distance dependent non-radiative cross relaxation between neighbor Eu3+ ions (Blasse 1994; Singh et al. 2008). For nanospheres and nanodiscs, the observed luminescence decays were double exponential, with the short lifetime component in the range from 271 ± 4 μs up to 761 ± 5 μs, and from 535 ± 6 μs up to 926 ± 2 μs in the case of nanospheres and nanodiscs, respectively (Fig. 6). The long luminescence lifetime components varied in the range from 1.18 ± 0.01 μs up to 1.60 ± 0.02 μs, and from 1.34 ± 0.01 μs up to 1.59 ± 0.02 μs in the case of nanospheres and nanodiscs, respectively (Fig. 6). The longest decay times, for both τ1 and τ2, were measured for 3 and 4 % of Eu3+ doping level concentration for nanospheres and nanodiscs, respectively. The relative maximum changes of the measured long lifetime components in relation to the Eu3+ level concentration in the matrix were found to be ~30 and ~20 % for nanospheres and nanodiscs, respectively.

For bigger Gd2O3:Eu3+ NPs shaped as nanotripods and nanotriangles, the observed luminescence decays were single exponential (Fig. 7), and the lifetimes varied in the range from 1.22 ± 0.01 μs up to 1.39 ± 0.01 μs, from 1.15 ± 0.01 μs up to 1.40 ± 0.01 μs, and from 1.15 ± 0.01 μs up to 1.34 ± 0.01 μs, for nanotripods, intermediate form (nanotripods → nanotriangles), and nanotriangles, respectively. The longest luminescence lifetime values were measured for 0.5 %Eu3+ doping for nanotripods, and for 1 %Eu3+ for nanotriangles, and intermediate form of Gd2O3 NPs. The relative maximum rate of changes in measured luminescence lifetimes varied in the range from ~10 to 20 %, with changing the Eu3+ doping level in the Gd2O3 crystal matrix. The less significant changes of the observed Eu3+5D0 excited state lifetimes in bigger Gd2O3 NPs show that in NPs with lower surface to volume ratio (i.e., in larger NPs) the Eu3+ ions are less susceptible to the changes in the local environment.
Fig. 7

Luminescence lifetimes values of 5D0 excited state in Eu3+ ions measured for Gd2O3 NPs shaped as nanotripods (a), intermediate form (b), and nanotriangles (c) with 266 nm laser light excitation

The observed lower Eu3+ concentration quenching in nanotripods and nanotriangles could be attributed to the size of the Gd2O3 NPs. In smaller nanosized particles, the non-radiative quenching centers distribute randomly with a considerable fluctuation within the particle, and at the same time, the increased surface quenching effect in smaller particles effectively competes with cross-relaxation between Eu3+ ions (Li and Hong 2007). Additionally, in smaller NPs, the quenching traps distribute randomly, and resonance energy transfer between neighbor Eu3+ ions can occur only within one particle due to the hindrance by the particle surface. When increasing the concentration of luminescence centers, quenching occurs first in particles containing many traps, while those particles containing fewer traps quench only at high concentration (Jiang et al. 2003). Therefore, quenching occurs preferentially at higher Eu3+ concentration in smaller NPs. For gaining better insight into the spectroscopic properties of synthesized Gd2O3:Eu3+ NPs, we have also calculated and analyzed Judd–Ofelt intensity parameters (Judd 1962; Ofelt 1962).

The Judd–Ofelt intensity parameters: Ω2 and Ω4, can be used to investigate the spectroscopic properties of Eu3+ ions embedded in Gd2O3 crystal matrix. Following Kodaira et al. (Kodaira et al. 2003), we have calculated the Ω2 and Ω4 parameters, as well as transition rates and quantum efficiencies, from emission spectra and luminescence decays time. The proposed approach uses the integral intensity of 5D0 → 7F1 magnetic dipole transition as a reference for calculating experimental intensity parameters for 5D0 → 7F2 and 5D0 → 7F4 ones. According to the Judd–Ofelt theory, the rates of 5D0 → 7FJ transition can be expressed as
$$ A_{0J} = \frac{{64\pi^{4} \upsilon_{J}^{3} }}{{3h\left( {2J + 1} \right)}}e^{2} \frac{{n\left( {n^{2} + 2} \right)^{2} }}{9}\mathop {\sum_{\lambda = 2,4,6} }\limits \,\varOmega_{\lambda } \left| {\langle \,^{5} D_{0} ||U^{\left( \lambda \right)} ||\,^{7} F_{J} \rangle } \right|^{2} , $$
(1)
where e is the electronic charge, νJ is the wavenumber of the corresponding transition, (2 J + 1) is equal to 1 for 5D0 transition, h is the Planck constant, and n is the refractive index of the investigated material. For calculations of the effective refractive index (Meltzer et al. 1999) of the investigated CHCl3 solution of Gd2O3:Eu3+ NPs, we have estimated the filling factor to be approximately 5 %, based on Gd2O3:Eu3+ NPs morphology measurements and gravimetric analysis after evaporating solvent from a certain amount of the solution. The wavelength dependent refractive index of cubic Gd2O3 was calculated using Sellmeier equation (Liu et al. 2007; Medenbach et al. 2001). 〈5D0||U(λ)||7FJ=2,4〉 are the squared reduced matrix elements, with values independent of the chemical environment of the Eu3+ ions, and equal to 0.0032 and 0.0023 for J = 2 and 4 (Kaminskii 1996), respectively. The A0–1 coefficient is a constant and independent of the medium, being equal to 50 s−1 (Hreniak et al. 2004). The relation between the integral intensity of transition (I0-J), the transition energy (hυ0–J), emission coefficient (A0–J), and 5D0 energy level population N is I0–J = hυ0–JA0–JN. Comparison of the relation for 5D0 → 7F2 and 5D0 → 7F4 transitions versus 5D0 → 7F2 allows one to rewrite the expression for A0–J as
$$ A_{0 - J} = A_{0 - 1} \frac{{I_{0 - J} }}{{I_{0 - 1} }}\frac{{\upsilon_{0 - J} }}{{\upsilon_{0 - 1} }}. $$
(2)
Combination of Eq. (1) and (2) allows for calculation of Ω2 and Ω4 intensity parameters, which are collected in Table 1. Table 1 presents also emission quantum efficiency (η), lifetimes (τ), non-radiative (Anrad), radiative (Arad), and total (Atotal) decay rates for the observed transitions in all the investigated Eu3+ doped Gd2O3 NPs of different shapes. The above spectroscopic parameters have been calculated based on following equations: \( A_{rad} = \sum _{j} A_{0 - J} \), \( A_{total} = \frac{1}{\tau } = A_{rad} + A_{nrad} \), \( \eta = \frac{{A_{rad} }}{{A_{rad} + A_{nrad} }}. \) In the case of nanospheres and nanodiscs, which showed double-exponential luminescence decays, we have calculated the average luminescence lifetime (τavg) based on equation: τavg = (A1τ1 + A2τ2)/(τ1 + τ2), where A1 and A2 are the amplitudes of long and short decay components, respectively.
Table 1

Judd–Ofelt analysis of Eu3+ doped Gd2O3 NPs with different shapes: intensity parameters (Ω2 and Ω4), emission quantum efficiency (η), lifetimes (τ), non-radiative (Anrad), radiative (Arad), and total (Atotal) rates for observed transitions

Samples Gd2O3:x %Eu3+

Ω2 (10−20 cm2)

Ω4 (10−20 cm2)

Arad (s−1)

Anrad (s−1)

Atotal (s−1)

τ (ms)

η (%)

Nanospheres

 0.5 % Eu3+

11.7

5.10

502.4

688.1

1190.5

0.84

42.2

 1 % Eu3+

9.3

4.58

419.9

1095.2

1515.0

0.66

27.7

 2 % Eu3+

12.8

4.92

520.2

714.4

1234.6

0.81

42.1

 3 % Eu3+

12.1

5.26

505.4

484.7

990.1

1.01

51.1

 4 % Eu3+

12.8

5.08

520.5

521.2

1041.8

0.96

50.0

 5 % Eu3+

11.3

5.39

496.2

738.3

1234.6

0.81

40.2

Nanodiscs

 0.5 % Eu3+

13.4

7.65

583.8

1029.0

1612.8

0.62

36.2

 1 % Eu3+

15.0

7.10

623.9

566.6

1190.5

0.84

52.4

 2 % Eu3+

14.7

7.52

622.8

286.3

909.1

1.10

68.5

 3 % Eu3+

13.8

6.55

577.0

443.4

1020.4

0.98

56.6

 4 % Eu3+

14.5

8.52

633.8

80.5

714.3

1.40

88.7

 5 % Eu3+

13.3

7.60

580.6

182.8

763.4

1.31

76.1

Nanotripods

 0.5 % Eu3+

14.6

5.41

603.0

116.4

719.4

1.39

83.8

 1 % Eu3+

15.4

5.57

629.7

100.2

729.9

1.37

86.3

 2 % Eu3+

16.3

5.64

661.6

79.2

740.7

1.35

89.3

 3 % Eu3+

16.1

5.52

582.3

186.9

769.2

1.30

75.7

 4 % Eu3+

16.3

5.50

586.8

188.4

775.2

1.29

75.7

 5 % Eu3+

17.1

5.49

683.1

136.5

819.7

1.22

83.3

Intermediate (Nanotripods → Nanotriangles)

 0.5 % Eu3+

15.1

5.66

623.5

117.3

740.7

1.35

84.2

 1 % Eu3+

16.4

5.38

658.1

56.2

714.3

1.40

92.1

 2 % Eu3+

16.8

5.70

676.6

129.9

806.5

1.24

83.9

 3 % Eu3+

16.7

5.72

672.8

108.5

781.3

1.28

86.1

 4 % Eu3+

17.5

5.46

695.7

137.6

833.3

1.20

83.5

 5 % Eu3+

16.3

5.62

660.8

208.8

869.6

1.15

76.0

Nanotriangles

 0.5 % Eu3+

14.9

5.57

615.3

142.3

757.6

1.32

81.2

 1 % Eu3+

16.7

5.49

668.8

77.5

746.3

1.34

89.6

 2 % Eu3+

15.9

5.53

645.7

160.7

806.5

1.24

80.1

 3 % Eu3+

16.6

5.70

670.4

136.1

806.5

1.24

83.1

 4 % Eu3+

18.2

5.64

720.9

112.4

833.3

1.20

86.5

 5 % Eu3+

16.6

5.47

666.5

203.1

869.6

1.15

76.7

The Ω2 intensity parameter reflects the hypersensitive behavior of the 5D0 → 7F2 transitions, and the observed relatively high Ω2 values, when compared to Eu3+ doped NaYF4 NPs (Bednarkiewicz et al. 2005) result from the presence of highly electronegative O2- ions in the Gd2O3 crystal structure. We have also observed slightly lower Ω2 values for nanosphere and nanodisc-like shaped Gd2O3:Eu3+ NPs in comparison with Gd2O3:Eu3+ NPs of other shapes. It may be due to the fact, that in smaller NPs, the lanthanide ion tends to increase its local symmetry (Malyukin et al. 2003). Additionally, in the synthesis of nanotripods, intermediate form, and nanotriangles, Li+ ions have been used, and since the ionic radius of this alkali metal is different from Gd3+ ions, the crystal lattice is distorted, and therefore, the symmetry around the Eu3+ ions can be disturbed. The observed higher Ω2 values for bigger Gd2O3:Eu3+ NPs can be thus indicative of efficient incorporation of Li+ ions inside the crystal structure of matrix. Additionally, the colloidal character of studied Gd2O3:Eu3+ NPs and influence of organic ligands attached to the NPs surface can influence the values of Ω2. Kumar et al. (Kumar et al. 2013) reported lower Ω2 values for nanosized Gd2O3:Eu3+ NPs; however, those nanophosphors did not have any organic molecules attached to the surface. In the case of Ω4 intensity parameter, no size or shape dependency was observed. Only for nanodiscs the values of Ω4 were slightly higher.

It is also very important to study the influence of both Gd2O3:Eu3+ NPs size and shape on the radiative contribution for the depopulation of the emitting level, and consequently for the emission quantum efficiency. Arad was higher for nanotripods and nanotriangles, when compared to the nanospheres, with simultaneous decrease of non-radiative contribution. This is why the relatively high η values, ranging from ~60 % for nanospheres up to ~90 % for nanotripods, were observed suggesting high efficiencies of energy transfer and efficient Eu3+ luminescence excitation in Gd2O3 matrix of those shapes.

Nonlinear optical properties of Gd2O3:Eu3+ nanocrystals

For complex spectroscopic characterization of the synthesized Gd2O3:Eu3+ NPs, we have also performed measurements of wavelength dispersion of the effective two-photon absorption cross-section (σ2,eff). Based on our previous results (Wawrzynczyk et al. 2013b), which showed that NLO absorption in YVO4 NPs is mainly dominated by NLO absorption through the CT transitions, and the contribution from 4f-4f transitions in Eu3+ ions is negligible, we have selected four representative Gd2O3:Eu3+ NPs shaped as nanospheres, nanodiscs, nanotripods, and nanotriangles for Z-scan measurements. Concentration of the selected samples was estimated through gravimetric analysis after evaporating the solvent from a known amount of the solution. Concentrations of the samples were ~67, 89, 25, and 45 mg/ml for nanospheres, nanodiscs, nanotripods, and nanotriangles, respectively. Density of bulk cubic Gd2O3 and mean sizes estimated based on TEM images of individual Gd2O3:Eu3+ NPs were used to calculate the molar mass (M) of a single Gd2O3:Eu3+ NP. The determined values allowed us to calculate the NLO parameters, and the appropriate merit factors for quantitative comparisons between different types of lanthanide-doped NPs, quantum dots (QDs), and plasmonic NPs. The results of wide-wavelength studies of NLO absorption of the selected Gd2O3:Eu3+ NPs are plotted in Fig. 8, as the effective two-photon absorption cross sections taken per single Gd2O3:Eu3+ NP. The smallest nanosphere-shaped Gd2O3:Eu3+ NPs did not show measurable NLO absorption in the whole spectral range. In general, the strength of the NLO absorption, presented as the σ2,eff value, scales with the NPs size, and since those Gd2O3:Eu3+ NPs had mean sizes smaller than 5 nm, a weak excitation band in comparison with larger investigated NPs (Fig. 4) together with linear absorption spectra dominated by scattering (inset in Fig. 8) could result in lack of observable NLO absorption in nanosphere-shaped Gd2O3:Eu3+ NPs.
Fig. 8

The wavelength dependence of the effective two-photon absorption cross-section σ2,eff for Gd2O3:Eu3+ NPs shaped as nanodiscs (red), nanotripods (green), and nanotriangles (blue). The inset shows linear absorption spectra of the investigated Gd2O3:Eu3+ NPs. (Color figure online)

The nanodisc-, nanotripod-, and nanotriangle-shaped Gd2O3:Eu3+ NPs showed well-defined NLO absorption in the wavelength range between 600 nm and 750 nm (Fig. 8). Additionally, the nanotripod-shaped Gd2O3:Eu3+ NPs exhibited a second band in the σ2,eff vs. λ plot in the range between 800 nm and 950 nm. The actual mechanisms responsible for the non-linear absorption occurring within the observed NLO absorption bands are likely to be quite complicated, possibly involving both two- and three-photon transitions, thus one should treat the values given here as effective ones, referring to intensities of about 100 GW/cm2, with possible more complex intensity dependences. The transitions are likely to have components due to both the host matrix absorption and the CT bands. In order to quantitatively compare the NLO properties of studied Gd2O3:Eu3+ NPs with different inorganic nanostructures, we have collected the calculated peak values of σ2,eff and σ2,eff/M in Table 2.
Table 2

Comparison of NLO parameter σ2,eff and merit factor σ2,eff/M for different types of inorganic nonlinear absorbers

Nanostructure

Wavelength (nm)

σ2,eff (GM)

σ2,eff/M (GM mol/g)

Reference

Nano-disk-shaped Gd2O3:Eu3+ NPs

600

4,700

0.01

This work

Nanotripod-shaped Gd2O3:Eu3+ NPs

700

7,600

0.03

This work

Nanotriangle-shaped Gd2O3:Eu3+ NPs

700

26,700

0.01

This work

NaYF4:2 %Er3+, 20 %Yb3+ NPs

980

8,000,000

0.1

Nyk et al. (2011)

YVO4:Eu3+ NPs

650

720,000

0.09

Wawrzynczyk et al. (2013b)

CdSe quantum dots (4.2 nm)

970

66,000

0.13

Nyk et al. (2012)

CdS quantum dots (5 nm)

750

7,200

0.04

Szeremeta et al. (2013)

10 × 35 nm gold nanorods

850

21,000,000

14

Olesiak-Banska et al. (2012)

For the case of the studied in this work Gd2O3:Eu3+ NPs of different shapes the most significant values of σ2,eff were ~4,700, 7,600, ~26,700 GM for nanodiscs, nanotripods, and nanotriangles at 600, 700, and 700 nm, respectively. For the sake of the comparisons of multiple photon absorption merit, one needs to scale the values of σ2,eff with the Gd2O3:Eu3+ NPs size. The calculated merit factors σ2,eff/M (M being the molecular weight of a particle) were ~0.01, 0.03, 0.01 for nanodiscs, nanotripods, and nanotriangles, respectively. These values are therefore an order of magnitude lower than the corresponding ones for YVO4 (Wawrzynczyk et al. 2013b) and NaYF4 (Nyk et al. 2011) lanthanide-doped NPs, and two orders of magnitude lower than those for some two-photon absorbing chromophores (Schwich et al. 2011). However, the 5 nm large CdS quantum dots exhibited similar value of σ2,eff/M merit factor. In comparison with lanthanide-doped NPs, previously investigated in our group (Nyk et al. 2011; Wawrzynczyk et al. 2013b), as well as quantum dots and metallic NPs (Nyk et al. 2012; Olesiak-Banska et al. 2012; Szeremeta et al. 2013), the Gd2O3:Eu3+ NPs seem to be only moderately efficient multi-photon absorbing luminophores.

Conclusions

We have investigated the correlation between the size and shape of colloidal Gd2O3 NPs and the Eu3+ luminescence. In the case of lanthanide-doped inorganic NPs, the size and shape effect on spectroscopic features is more ambiguous, than for QDs or metallic NPs. Surface to volume ratio, type of surface attached ligands molecules, as well as deliberately introduced defects in the crystal structure of NPs can have great influence of their optical properties. For the purpose of that work, we have obtained Gd2O3:Eu3+ NPs shaped as nanospheres, nanodiscs, nanotripods, and nanotriangles. Narrow size and shape distribution of obtained Gd2O3:Eu3+ NPs allowed us to relate the observed changes in Eu3+ luminescence with morphology of NPs. The initially observed narrowing and splitting of 5D0 → 7FJ transitions for bigger ~40 nm NPs (nanotripods and nanotriangles) could be attributed to the changing homogeneous crystal fields, when compared to the smaller ~5 nm in size Gd2O3 NPs. In such small NPs, the crystal field changes significantly from grain to grain due to the higher dispersion of lattice constants. In addition, a higher number of Eu3+ ions are located close to the surface of the Gd2O3 particle. It is expected that those surface states influence the energies and splitting of 5D0 → 7FJ transitions as well. This effect is more important for a small diameter particle (~ 5 nm) than for a bigger one (~40 nm), due to the higher probability of the Eu3+ ions being close to the surface of Gd2O3 grains, if we consider only random distribution of atoms in the Gd2O3:Eu3+ nanomatrix. Additionally, a high number of Eu3+ ions located near or at the surface of the investigated colloidal nanosized Gd2O3 resulted in emission spectra with shapes similar to those of the monoclinic form of Gd2O3 NPs. Such ions demonstrate a lower coordinating number, and behave as if they were embedded in lower symmetry sites, causing noticeable changes in the shape of emission spectra. Based on emission spectra and kinetics, we have estimated the optimum Eu3+ ions doping level concentration in the host matrix. The higher optimum (3 and 4 %) europium (III) concentrations were found for smaller nanosphere and nanodiscs shaped Gd2O3:Eu3+ NPs in comparison with 0.5 and 1 % for nanotripods and nanotriangles. Those differences were also related to the size of the studied NPs. The spectroscopic properties of the synthesized Gd2O3:Eu3+ NPs were also evaluated in the frame of Judd–Ofelt theory. The intensity parameter Ω2 showed lower hypersensitive behavior of nanospheres and nanodiscs, and also indirectly proved the incorporation of Li+ ions inside the Gd2O3 crystal matrix. The hypersensitive character of Ω2 parameter resulted also from the colloidal character of synthesized Gd2O3:Eu3+ NPs, and interaction between Eu3+ ions situated close to the NP surface and capping ligands molecules. Additionally, both radiative rates and quantum efficiencies were higher for the nanotripods and the nanotriangles. Finally, we have investigated the NLO properties of differently shaped Gd2O3:Eu3+ NPs. The smallest, nanosphere shaped, Gd2O3:Eu3+ NPs did not show any measurable NLO absorption in the whole spectral range. However, we have observed NLO absorption in the bigger Gd2O3:Eu3+ NPs in the spectral range between 600 nm and 750 nm. The strength of the NLO absorption scaled with the Gd2O3:Eu3+ NPs size, and was the highest for the nanotripod-shaped particles. By calculating the σ2,eff/M merit factor, and comparison with other lanthanide-doped NPs, quantum dots, and metallic NPs, we have concluded that the investigated Gd2O3:Eu3+ NPs are from ten to a hundred times less efficient than efficient two-photon absorbing chromophores.

Notes

Acknowledgments

DW, MS, and MN acknowledge financial support from the National Science Centre under Grant No. DEC-2012/05/N/ST5/00601, by a statutory activity subsidy from the Polish Ministry of Science and Higher Education for the Faculty of Chemistry of Wroclaw University of Technology, as well as from the Foundation for Polish Science under START 2014 and WELCOME programmes. A.B. acknowledges financial support from the National Science Centre under Grant No. DEC-2012/05/E/ST5/03901.

References

  1. Andraud C, Maury O (2009) Lanthanide complexes for nonlinear optics: from fundamental aspects to applications. Eur J Inorg Chem 29–30:4357–4371CrossRefGoogle Scholar
  2. Banski M, Podhorodecki A, Misiewicz J, Afzaal M, Abdelhady AL, O’Brien P (2013) Selective excitation of Eu3+ in the core of small β-NaGdF4 nanocrystals. J Mater Chem C 1(4):801–807CrossRefGoogle Scholar
  3. Bednarkiewicz A, Mech A, Karbowiak M, Strek W (2005) Spectral properties of Eu3+ doped NaGdF4 nanocrystals. J Lumin 114(3–4):247–254CrossRefGoogle Scholar
  4. Blasse GGBC (1994) Luminescent materials. Springer-Verlag, BerlinCrossRefGoogle Scholar
  5. Boyer JC, Vetrone F, Capobianco JA, Speghini A, Bettinelli M (2004) Variation of fluorescence lifetimes and Judd-Ofelt parameters between Eu3+ doped bulk and nanocrystalline cubic Lu2O3. J Phys Chem B 108(52):20137–20143CrossRefGoogle Scholar
  6. Bünzli J-C, Eliseeva S (2011) Basics of Lanthanide Photophysics. In: Hänninen P, Härmä H (eds) Lanthanide Luminescence, vol 7., Springer Series on FluorescenceSpringer, Berlin Heidelberg, pp 1–45CrossRefGoogle Scholar
  7. Cao YC (2004) Synthesis of square gadolinium-oxide nanoplates. J Am Chem Soc 126(24):7456–7457CrossRefGoogle Scholar
  8. Chang J, Xiong S, Peng H, Sun L, Lu S, You F, Huang S (2007) Site selective excitation in La2O3:Eu3+ nanoparticles. J Lumin 122–123:844–846CrossRefGoogle Scholar
  9. Chen J, Meng Q, May PS, Berry MT, Lin C (2013) Sensitization of Eu3+ Luminescence in Eu:YPO4 Nanocrystals. J Phys Chem C 117(11):5953–5962CrossRefGoogle Scholar
  10. Du G, Guo W, Khalaf Al-zyadi J, Han Y, Liu P, Liu Z (2013) Effect of Ce3+ dopant ions on the shape and luminescence of YPO4:Eu3+ and YPO4:Tb3+ nanocrystals. J Nanopart Res 15(5):1–8CrossRefGoogle Scholar
  11. Gai SL, Yang PP, Wang D, Li CX, Niu N, He F, Li XB (2011) Monodisperse Gd2O3:Ln (Ln = Eu3+, Tb3+, Dy3+, Sm3+, Yb3+/Er3+, Yb3+/Tm3+, and Yb3+/Ho3+) nanocrystals with tunable size and multicolor luminescent properties. CrystEngComm 13(17):5480–5487CrossRefGoogle Scholar
  12. Grzyb T, Weclawiak M, Rozowska J, Lis S (2013) Structural and spectroscopic properties of YOF:Eu3+ nanocrystals. J Alloys Compd 576:345–349CrossRefGoogle Scholar
  13. Hreniak D, Strek W, Amami J, Guyot Y, Boulon G, Goutaudier C, Pazik R (2004) The size-effect on luminescence properties of BaTiO3:Eu3+ nanocrystallites prepared by the sol-gel method. J Alloys Compd 380(1–2):348–351CrossRefGoogle Scholar
  14. Jia CJ, Sun LD, Yan ZG, Pang YC, Lü SZ, Yan CH (2010) Monazite and Zircon Type LaVO4:Eu Nanocrystals—synthesis, luminescent properties, and spectroscopic identification of the Eu3+ Sites. Eur J Inorg Chem (18):2626–2635Google Scholar
  15. Jiang XC, Yan CH, Sun LD, Wei ZG, Liao CS (2003) Hydrothermal homogeneous urea precipitation of hexagonal YBO3:Eu3+ nanocrystals with improved luminescent properties. J Solid State Chem 175(2):245–251CrossRefGoogle Scholar
  16. Judd BR (1962) Optical absorption intensities of rare-earth ions. Phys Rev 127(3):750–761CrossRefGoogle Scholar
  17. Kaminskii AA (1996) Crystalline lasers : physical processes and operating schemes. CRC Press, Boca RatonGoogle Scholar
  18. Kodaira CA, Brito HF, Malta OL, Serra OA (2003) Luminescence and energy transfer of the europium (III) tungstate obtained via the Pechini method. J Lumin 101(1–2):11–21CrossRefGoogle Scholar
  19. Kumar RGA, Hata S, Gopchandran KG (2013) Diethylene glycol mediated synthesis of Gd2O3:Eu3+ nanophosphor and its Judd-Ofelt analysis. Ceram Int 39(8):9125–9136CrossRefGoogle Scholar
  20. Lakowicz JR, Piszczek G, Maliwal BP, Gryczynski I (2001) Multiphoton excitation of lanthanides. Chemphyschem 2(4):247–252CrossRefGoogle Scholar
  21. Li YH, Hong GY (2007) Synthesis and luminescence properties of nanocrystalline Gd2O3:Eu3+ by combustion process. J Lumin 124(2):297–301CrossRefGoogle Scholar
  22. Liu CX, Liu JY, Dou K (2006) Judd–Ofelt intensity parameters and spectral properties of Gd2O3:Eu3+ nanocrystals. J Phys Chem B 110(41):20277–20281CrossRefGoogle Scholar
  23. Liu LQ, Ma E, Li RF, Liu GK, Chen XY (2007) Effects of phonon confinement on the luminescence dynamics of Eu3+ in Gd2O3 nanotubes. Nanotechnology 18(1):015403Google Scholar
  24. Malyukin YV, Masalov AA, Zhmurin PN (2003) Single-ion fluorescence spectroscopy of a Y2SiO5:Pr3+ nanocluster. Phys Lett A 316(1–2):147–152CrossRefGoogle Scholar
  25. Medenbach O, Dettmar D, Shannon RD, Fischer RX, Yen WM (2001) Refractive index and optical dispersion of rare earth oxides using a small-prism technique. J Opt A: Pure Appl Opt 3(3):174–177CrossRefGoogle Scholar
  26. Meltzer RS, Feofilov SP, Tissue B, Yuan HB (1999) Dependence of fluorescence lifetimes of Y2O3:Eu3+ nanoparticles on the surrounding medium. Phys Rev B 60(20):14012–14015CrossRefGoogle Scholar
  27. Nyk M, Wawrzynczyk D, Parjaszewski K, Samoc M (2011) Spectrally resolved nonlinear optical response of upconversion lanthanide-doped nayf4 nanoparticles. J Phys Chem C 115(34):16849–16855CrossRefGoogle Scholar
  28. Nyk M, Wawrzynczyk D, Szeremeta J, Samoc M (2012) Spectrally resolved size-dependent third-order nonlinear optical properties of colloidal CdSe quantum dots. Appl Phys Lett 100(4):041102Google Scholar
  29. Ofelt GS (1962) intensities of crystal spectra of rare-earth ions. J Chem Phys 37(3):511–520CrossRefGoogle Scholar
  30. Olesiak-Banska J, Gordel M, Kolkowski R, Matczyszyn K, Samoc M (2012) Third-order nonlinear optical properties of colloidal gold nanorods. J Phys Chem C 116(25):13731–13737CrossRefGoogle Scholar
  31. Paik T, Murray CB (2013) Shape-directed binary assembly of anisotropic nanoplates: a nanocrystal puzzle with shape-complementary building blocks. Nano Lett 13(6):2952–2956CrossRefGoogle Scholar
  32. Paik T, Gordon TR, Prantner AM, Yun H, Murray CB (2013) Designing tripodal and triangular gadolinium oxide nanoplates and self-assembled nanofibrils as potential multimodal bioimaging probes. ACS Nano 7(3):2850–2859CrossRefGoogle Scholar
  33. Samoc M, Samoc A, Luther-Davies B, Humphrey MG, Wong M-S (2003) Third-order optical nonlinearities of oligomers, dendrimers and polymers derived from solution Z-scan studies. Opt Mater 21(1–3):485–488CrossRefGoogle Scholar
  34. Schwich T, Cifuentes MP, Gugger PA, Samoc M, Humphrey MG (2011) Electronic, molecular weight, molecular volume, and financial cost-scaling and comparison of two-photon absorption efficiency in disparate molecules (organometallic complexes for nonlinear optics. 48.)—A response to “comment on ‘organometallic complexes for nonlinear optics. 45. Dispersion of the third-order nonlinear optical properties of triphenylamine-cored alkynylruthenium dendrimers.’ Increasing the Nonlinear Response by Two Orders of Magnitude”. Adv Mater 23 (12):1433–1435Google Scholar
  35. Seo S, Yang H, Holloway PH (2009) Controlled shape growth of Eu- or Tb-doped luminescent Gd2O3 colloidal nanocrystals. J Colloid Interface Sci 331:236–242CrossRefGoogle Scholar
  36. Sheikbahae M, Said AA, Wei TH, Hagan DJ, Vanstryland EW (1990) Sensitive measurements of optical nonlinearities using a single beam. IEEE J Quantum Electron 26(4):760–769CrossRefGoogle Scholar
  37. Si R, Zhang YW, You LP, Yan CH (2005) Rare-earth oxide nanopolyhedra, nanoplates, and nanodisks. Angew Chem Int Ed 44:3256–3260CrossRefGoogle Scholar
  38. Singh LR, Ningthoujam RS, Sudarsan V, Singh SD, Kulshreshtha SK (2008) Probing of surface Eu3+ ions present in ZnO:Eu nanoparticles by covering ZnO:Eu core with Y2O3 shell: Luminescence study. J Lumin 128(9):1544–1550CrossRefGoogle Scholar
  39. Szeremeta J, Nyk M, Wawrzynczyk D, Samoc M (2013) Wavelength dependence of nonlinear optical properties of colloidal CdS quantum dots. Nanoscale 5(6):2388–2393CrossRefGoogle Scholar
  40. Sztucki J, Strȩk W (1986) Two-photon absorption in lanthanide complexes. Phys Rev B 34(5):3120–3126CrossRefGoogle Scholar
  41. Wawrzynczyk D, Bednarkiewicz A, Nyk M, Strek W, Samoc M (2013a) Ligand-dependent luminescence of ultra-small Eu3+-doped NaYF4 nanoparticles. J Nanoparticle Res 15(6):1707CrossRefGoogle Scholar
  42. Wawrzynczyk D, Nyk M, Samoc M (2013b) Multiphoton absorption in europium(III) doped YVO4 nanoparticles. J Mater Chem C 1(37):5837–5842CrossRefGoogle Scholar
  43. Wiglusz RJ, Bednarkiewicz A, Lukowiak A, Strek W (2010) Synthesis and optical properties of Eu3+ ion doped nanocrystalline hydroxyapatites. Spectrosc Lett 43(5):333–342CrossRefGoogle Scholar
  44. Xue X, Wang L, Huang L, Zhao D, Qin W (2013) Effect of alkali ions on the formation of rare earth fluoride by hydrothermal synthesis: structure tuning and size controlling. CrystEngComm 15(15):2897–2903CrossRefGoogle Scholar
  45. Yan Z-G, Yan C-H (2008) Controlled synthesis of rare earth nanostructures. J Mater Chem 18(42):5046–5059CrossRefGoogle Scholar
  46. Yang J et al (2008) Self-assembled 3D flowerlike Lu2O3 and Lu2O3:Ln3+ (Ln = Eu, Tb, Dy, Pr, Sm, Er, Ho, Tm) micro architectures: ethylene glycol-mediated hydrothermal synthesis and luminescent properties. J Phys Chem C 112(33):12777–12785CrossRefGoogle Scholar
  47. Zhang F, Li J, Shan J, Xu L, Zhao D (2009) Shape, size, and phase-controlled rare-earth fluoride nanocrystals with optical up-conversion properties. Chem Eur J 15(41):11010–11019CrossRefGoogle Scholar
  48. Zheng KZ, Zhang DS, Zhao D, Liu N, Shi F, Qin WP (2010) Bright white upconversion emission from Yb3+, Er3+, and Tm3+-codoped Gd2O3 nanotubes. Phys Chem Chem Phys 12(27):7620–7625CrossRefGoogle Scholar

Copyright information

© The Author(s) 2014

Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Authors and Affiliations

  • Dominika Wawrzynczyk
    • 1
  • Marcin Nyk
    • 1
  • Artur Bednarkiewicz
    • 2
    • 3
  • Wiesław Strek
    • 2
  • Marek Samoc
    • 1
  1. 1.Institute of Physical and Theoretical ChemistryWroclaw University of TechnologyWroclawPoland
  2. 2.Institute of Low Temperature and Structure ResearchPASWroclawPoland
  3. 3.Wroclaw Research Centre EIT+WroclawPoland

Personalised recommendations