Bridgman growth and site occupation in LuAG:Ce scintillator crystals

LuAG:Ce single crystals with various activator concentrations were grown by the vertical Bridgman technique. Characterization of crystals was done in terms of actual doping level, macroscopic defects and degree of non-equivalent substitutions by Lu for Al in octahedral lattice sites. Scintillation measurements were performed using 2×2×8 mm³ shaped samples with Ce concentration in the range 0.05–0.55 at%. Essential improvement of performance was demonstrated in samples containing ≥0.2 at% of Ce; the light yield measured in LuAG:Ce (0.55 at%) was about 26000 ph/MeV, or close to that of LSO.     

Investigating material trends and lattice relaxation effects for understanding electron transfer phenomena in rare-earth-doped optical materials

Rare-earth-doped insulators and semiconductors play an important role in a wide range of modern optical technologies. Knowledge of the relative energies of rare-earth ions’ localized electronic states and the band states of the host crystal is important for understanding the properties of these materials and for determining the potential material performance in specific applications such as lasers, phosphors, and optical signal processing. Current understanding of the systematic variations of electron binding energies in these materials is reviewed with analysis of how lattice relaxation affects the results obtained from different experimental techniques. Detailed examples are presented for rare-earth-doped YAG and LaF₃ material systems. A method for predicting the chemical shift of the 4f electrons of rare-earth impurities from the host crystal’s photoemission spectrum is also demonstrated. Furthermore, a simple model is presented that predicts host-dependent trends in the binding energies of the rare-earth ion states in materials ranging from the elemental metals to the ionic fluorides. By understanding the systematic changes in the relative energies for different states, different ions, and different host materials, insight is gained into electron transfer transitions, valence stability, and luminescence quenching that can accelerate the development of materials for optical applications.     

光纤放大器的半经典分析

本文采用半经典理论分析稀土掺杂光纤中光与介质的相互作用机理,讨论了增益、饱和、光纤归一化频率、泵功率、信号功率及掺杂粒子数浓度等各参数之间的关系.计算与实验结果相符,可用这个理论设计所需特性的光纤放大器或对光纤放大器作进一步的改进.     

Formation and stability of Gd, Y, Yb and Lu disilicates and their solid solutions

The synthesis and the phase stability regions of the disilicates of Y, Lu, Yb and Gd have been investigated at temperatures between 1300 and 1600 °C. The mean ionic radius of the rare-earth element ion including Y turns out to be the key parameter to govern the stabilities of polymorph types of both pure disilicates and their solid solutions. Both are predicted correctly by the phase stability diagram of Felsche [1] [J. Felsche, Struct. Bond. 13 (1973) 99-197]. Furthermore, it correlates with the reactivity, with increasing radius a faster reaction is observed at a given temperature. A fast reactivity is assumed to create difficulties in the densification of disilicates with ionic radius exceeding ∼0.88 Å. In the reaction from oxide powders monosilicates are formed in a first step. Disilicates are formed from those initially in the form of low-temperature modifications, which transform in a sequence to high-temperature modifications.     

Rare-earth-mediated magnetism and magneto-optical Kerr effects in nanocrystalline CoFeMn0.9RE0.1O4 thin films

A series of rare-earth (RE)-doped nanocrystalline CoFeMn_0.9RE_0.1O₄ thin films were prepared on monocrystalline silicon substrate by a sol–gel process, and the influences of the various RE³⁺ ions on the microstructure, magnetism and polar magneto-optical Kerr effects of the as-deposited films were examined. The results revealed that both of the magnetism and Kerr effect of CoFeMn_0.9RE_0.1O₄ films could be mediated by doping with various RE³⁺ ions. The trend of both M_S and H_C of CoFeMn_0.9RE_0.1O₄ films is similar to that of Bohr magneton across the series of rare-earth ions. The position of Kerr rotation peaks was red-shifted and their intensities increased, especially when doping with La³⁺, Tb³⁺, Y³⁺ or Yb³⁺ and so on. The enhanced MOKEs in CoFeMn_0.9RE_0.1O₄ nanocrystalline thin films might promise their applications for magneto-optical recording in the future.     

Spectroscopic investigations and luminescence spectra of Nd and Dy doped different phosphate glasses

Spectral properties of Nd³⁺ and Dy³⁺ ions in different phosphate glasses were studied and several spectroscopic parameters were reported. Covalency of rare-earth-oxygen bond was studied in these phosphate glass matrices with the variation of modifier in host glass matrix. Using Judd-Ofelt intensity parameters (Ω₂, Ω₄ and Ω₆), radiative transition probabilities (A) and radiative lifetimes (τ_R) of certain excited states of Nd³⁺ and Dy³⁺ ions are estimated in these glass matrices. From the magnitudes of branching ratios (β_R) and integrated absorption cross-sections (Σ), certain transitions of both the ions are identified for laser excitation. From the emission spectra, peak stimulated emission cross-sections (σ_P) are evaluated for the emission transitions observed in all these phosphate glass matrices for both Nd³⁺ and Dy³⁺ ions.     

High pressure and emission spectra of Eu3+ in L-EuBO3

Effects of the high pressure on the emission spectra of Eu³⁺-activated L-EuBO₃ were considered at room temperature up to 100 kbar. The position of five 0–2 lines in the ⁵D₀→⁷F₂ transition region was determined. The pressure does not have the same effect on all these lines. In four of them, high pressure induced a red shift with different shift rates:+0.0022,+0.0035,+0.0034 and+0.0027 nm kbar^?1, respectively, whereas in the last one, high pressure induced a blue shift with shift rate?0.0034 nm kbar^?1. Possible reasons for the mentioned pressure effects on the line positions were considered.     

Coadsorption of lanthanum with boron and gadolinium with boron on Mo(1 1 0)

Submonolayer to multilayer coadsorption of lanthanum (La) with boron (B) and gadolinium (Gd) with boron on the surface of Mo(1 1 0) has been studied by means of Auger electron spectroscopy (AES), electron energy loss spectroscopy (EELS) and work function () measurements. The equilibrium state of double adsorbate systems achieved either by adsorption of rare-earth metal (REM) on boron precovered Mo(1 1 0) surface held at room temperature or after moderate annealing of the system with opposite order of adsorption (B on REM films) is the layer which is the inhomogeneous mixture of boron and REM atoms with preferential concentration of boron in the surface area of the mixed film. The work function of such films even at REM to boron concentration ratio much higher than 1/6 are very close to the values of corresponding bulk LaB₆ and GdB₆, favoring assumption of surface rearrangement as the dominant reason of high electron emission efficiency of hexaborides. Almost total similarity of the results for La–B and Gd–B systems can be viewed as the consequence of weak participation of Gd f-electrons in determining the thermionic properties of corresponding double layers.     

Investigation of spin transition in GdCoO3 by measuring the electric field gradient at Co sites

In the present work, the time differential perturbed angular correlation (PAC) technique was used to study the temperature dependence of electric field gradient (efg) in GdCoO₃ perovskite using ¹¹¹Cd and ¹⁸¹Ta nuclear probes. The radioactive parent nuclei ¹¹¹In and ¹⁸¹Hf were introduced in the oxide lattice through chemical process during sample preparation and were found to occupy only the Co sites in GdCoO₃. The efg's at ¹¹¹Cd and ¹⁸¹Ta show temperature dependence with two different fractions each that change with temperature. In the case of ¹¹¹Cd the quadrupole frequency slowly decreases, with corresponding increase of the temperature and shows a peak like structure at around 200 K and a discontinuity at 700 K. These changes have been interpreted as thermally activated spin-state transitions from low-spin ground state configuration to the intermediate-spin state and from intermediate-spin to high-spin state of Co³⁺${\mathrm{Co}}^{3+}$ ion similar to LaCoO₃ compound. Indication of a Jahn–Teller distortion, which stabilizes the intermediate-spin state with orbital ordering, is also pointed out.     

显示用上转换绿色发光材料NaYF4∶Er,Yb及其特性

采用喷射微波燃烧合成法制备了上转换发光显示器中发绿光的上转换发光材料NaYF4∶Er,Yb.测试了该材料的XRD衍射图谱和发光效率.给出了该材料在1 064 nm三种激光功率激发下的发光光谱.分析了该材料的上转换发光机理,得到545 nm和662 nm峰值发光分别是Er3+的4S3/2→4I15/2和4F9/2→4I15/2跃迁产生的.NaYF4∶Er,Yb具有较强的上转换绿光,同时存在的较弱的红光易于用滤色膜滤除,满足显示对三基色中绿色的要求;并且喷射微波燃烧合成法制备的该材料达到了高分辨率显示应用超细粉体的要求.