Facile and rapid synthesis of highly luminescent nanoparticles via Pulsed Laser Ablation in Liquid

This paper demonstrates the usefulness of pulsed laser ablation in liquids as a fast screening synthesis method able to prepare even complex compositions at the nanoscale. Nanoparticles of Y2O3:Eu3+, Lu2O2S: Eu3+, Gd2SiO5:Ce3+ and Lu3TaO7:Gd3+,Tb3+ are successfully synthesized by pulsed laser ablation in liquids. The phase and stoichiometries of the original materials are preserved while the sizes are reduced down to 5-10 nm. The optical properties of the materials are also preserved but show some small variations and some additional structures which are attributed to the specificities of the nanoscale (internal pressure, inhomogeneous broadening, surface states...

Shells of crystal field symmetries evidenced in oxide nano-crystals

By the use of a point charge model based on the Judd-Ofelt transition theory, the luminescence from Eu3+ ions embedded in Gd2O3 clusters is calculated and compared to the experimental data. The main result of the numerical study is that without invoking any other mechanisms such as crystal disorder, the pure geometrical argument of the symmetry breaking induced by the particle surface has influence on the energy level splitting. The modifications are also predicted to be observable in realistic conditions where unavoidable size dispersion has to be taken into account. The emission spectrum results from the contribution of three distinct regions, a cluster core, a cluster shell and a very surface, the latter being almost completely quenched in realistic conditions. Eventually, by detailing the spectra of the ions embedded at different positions in the cluster we get an estimate of about 0.5 nm for the extent of the crystal field induced Stark effect. Due to the similarity between Y2O3 and Gd2O3, these results apply also to Eu3+ doped Y2O3 nanoparticles

Scintillation of Sol-Gel derived Lutetium orthophosphate doped with rare earth ions.

In this paper, the synthesis, the characterization and the scintillation properties of LuPO4 doped, with several concentrations of Ce3+, Eu3+ and Tb3+ ions, are presented. These materials have been synthesized by sol-gel process. The purity of powders has been verified by X-Ray diffraction and the results confirm the xenotime structure of all the materials. A thermogravimetric analysis allows the obtention of informations on the crystallisation of LuPO4 and the study of its evolution from the amorphous to crystalline form. The morphology of the powders has been studied by Scanning Electron Microscopy and shows that the powders are constituted of small particles with narrow size distribution. Optical properties have been studied in order to determine the scintillation performances of these materials. The optima are obtained for Ce3+, Eu3+ and Tb3+ concentration of respectively 0.1%, 10% and 5% with high scintillation yields. This study thus confirms the potentialities of these materials as scintillators

Concentration effect on the scintillation properties of Sol-Gel derived LuBO3 doped with Eu3+ and Tb3+.

International audienceLu1-xEuxBO3 and Lu1-xTbxBO3 powders have been prepared by a sol-gel process with 0 < x < 0.15 for Eu3+ and 0 < x < 0.05 for Tb3+. The purity of powders has been verified by X-Ray diffraction and the results confirm that all the materials have the vaterite type even if the calcination has been performed at 800°C. Furthermore, the solid solution for LuBO3 vaterite is observed up to x=0.15 and x=0.05 for europium and terbium ions respectively. So doping with Eu3+ or Tb3+ ions does not affect the structure. These materials have also been analyzed by Fourier Transform Infra Red Spectroscopy. The morphology of the powders has been studied by Scanning Electron Microscopy and shows a very nice morphology with small spherical particles with narrow size distribution. Optical properties have then been studied to confirm the effective substitution of Eu3+ or Tb3+ for Lu3+ ions and to determine the materials scintillation performances. The optima, in term of scintillation yield, are obtained for Eu3+ and Tb3+ concentration of x=0.05 in both cases. The afterglows have also been measured and confirm the potentiality of these materials as scintillators

Characterization and Scintillation properties of Sol-Gel derived Lu2SiO5:Ln3+ (Ln = Ce, Eu, Tb) powders

International audienceIn this paper, we report the synthesis, the characterization and the scintillation properties of sol-gel derived Lu2SiO5 (LSO) powders. Ce3+, Eu3+ and Tb3+ doped LSO powders have been synthesized by an original sol-gel process. The purity of the materials has been checked by X-Ray diffraction, confirming the elaboration of monophasic powders even for doped samples. Finally, the scintillation properties of the rare earth doped materials have been studied, the substitution of Ln3+ (Ln: Ce, Eu or Tb) for Lu3+ is confirmed, the scintillation yields have been calculated and the afterglow have also been measured, confirming the potentiality of the sol-gel derived LSO

YAG nano-light sources with high Ce concentration

We investigate the luminescence properties of 10 nm YAG nanoparticles doped with Ce ions at 0.2%, 4% and 13% that are designed as active probes for Scanning Near field Optical Microscopy. They are produced by a physical method without any subsequent treatment, which is imposed by the desired application. The structural analysis reveals the amorphous nature of the particles, which we relate to some compositional defect as indicated by the elemental analysis. The optimum emission is obtained with a doping level of 4%. The emission of the YAG nanoparticles doped at 0.2% is strongly perturbed by the crystalline disorder whereas the 13% doped particles hardly exhibit any luminescence. In the latter case, the presence of Ce4+ ions is confirmed, indicating that the Ce concentration is too high to be incorporated efficiently in YAG nanoparticles in the trivalent state. By a unique procedure combining cathodoluminescence and Rutherford backscattering spectrometry, we demonstrate that the enhancement of the particles luminescence yield is not proportional to the doping concentration, the emission enhancement being larger than the Ce concentration increase. Time-resolved photoluminescence reveals the presence of quenching centres likely related to the crystalline disorder as well as the presence of two distinct Ce ions populations. Eventually, nano-cathodoluminescence indicates that the emission and therefore the distribution of the doping Ce ions and of the defects are homogeneous

Inorganic, Organic, and Perovskite Halides with Nanotechnology for High-Light Yield X- and γ-Ray Scintillators

Trends in scintillators that are used in many applications, such as medical imaging, security, oil-logging, high energy physics and non-destructive inspections are reviewed. First, we address traditional inorganic and organic scintillators with respect of limitation in the scintillation light yields and lifetimes. The combination of high–light yield and fast response can be found in Ce 3+ , Pr 3+ and Nd 3+ lanthanide-doped scintillators while the maximum light yield conversion of 100,000 photons/MeV can be found in Eu 3+ doped SrI 2 . However, the fabrication of those lanthanide-doped scintillators is inefficient and expensive as it requires high-temperature furnaces. A self-grown single crystal using solution processes is already introduced in perovskite photovoltaic technology and it can be the key for low-cost scintillators. A novel class of materials in scintillation includes lead halide perovskites. These materials were explored decades ago due to the large X-ray absorption cross section. However, lately lead halide perovskites have become a focus of interest due to recently reported very high photoluminescence quantum yield and light yield conversion at low temperatures. In principle, 150,000–300,000 photons/MeV light yields can be proportional to the small energy bandgap of these materials, which is below 2 eV. Finally, we discuss the extraction efficiency improvements through the fabrication of the nanostructure in scintillators, which can be implemented in perovskite materials. The recent technology involving quantum dots and nanocrystals may also improve light conversion in perovskite scintillators