Comparison of optical properties between ladder and lambda-type EIT medium with Er3+ ion concentration in Er3+:YAG crystal

The effect of Er³⁺ doped ion concentration on optical properties of two type three-level schemes in 35 nm Er³⁺:YAG (yttrium aluminum garnet) crystal is studied. It is found that intensity threshold of optical bistability and multistability can be changed by Er³⁺ doped ion concentration. Moreover, switching from optical multistability to optical bistability can be done differently by Er³⁺ concentration in two types of three-level schemes. The steady-state and transient behaviors of absorption, dispersion and group index of weak probe field in two schemes are also discussed. In this study, we will report an initial study on optical properties in Er³⁺:YAG crystal and propose a basis for selecting the suitable concentration to carry out experimental investigations in the future.     

YAG晶体中Yb~(3+)对Er~(3+)的敏化作用

根据能级跃迁速率方程得出Yb,Er:YAG中各能级布居数与Er3+离子浓度的关系.并与单掺Er:YAG中各能级布居数相比较,讨论共掺Yb3+对Er3+的波长为1.64和2.94μm两荧光的影响.结合作者关于红外光激励Yb,Er:YAG能量上转换为可见光工作,提出将Yb,Er:YAG晶体研制成以半导体激光器为激励源的可见光和1.64μm红外光的双波长全固化激光器的设想.     

The effect of In ion on the optical characteristics of Er in Er/Yb:LiNbO3 crystal

The effect of In³⁺ ion on the optical characteristics of Er³⁺ ion in Er/Yb:LiNbO₃ crystal under 980 nm excitation has been investigated. The Er and Yb contents in the crystals were measured by an inductively coupled plasma atomic emission spectrometer (ICP-AES). A significant enhancement of 1.54 μm emission was observed for Er/Yb:LiNbO₃ crystal doped with 1 mol% In₂O₃. The studies on the UV-vis absorption and the OH⁻ absorption spectra indicate that the threshold concentration of In³⁺ ion decreases with the Er/Yb doping in Er/Yb/In:LiNbO₃ crystal. The 1 mol% In₂O₃ doping results in the reduction of absorption cross section in the UV-vis region, meaning the formation of Er³⁺ cluster sites. The enhancement of 1.54 μm emission is attributed to the larger probabilities of the cross relaxation processes ⁴S_3/2 + ⁴I_15/2 → ⁴I_9/2 + ⁴I_13/2 (Er), ⁴S_3/2 + ⁴I_15/2 → ⁴I_13/2 + ⁴I_9/2 (Er) and ⁴I_9/2 + ⁴I_15/2 → ⁴I_13/2 + ⁴I_13/2 (Er) induced by Er³⁺ cluster sites.     

Eu3+ concentration effect on luminescence properties of YAG:Eu3+ nanoparticles

Nanocrystalline Eu³⁺-doped YAG powders were prepared by modified Pechini method. The structural properties were investigated with XRD, SEM and Raman spectroscopy. XRD pattern indicated that the phase-pure YAG:Eu³⁺ crystallites were obtained without the formation of any other phases. Raman spectrum revealed good homogeneity and crystallinity of synthesized nanopowders. The luminescent properties were studied by measurement of excitation and emission spectra, quantum yields and decay curves. The effect of Eu³⁺ concentration on ⁵D₀ level lifetime was studied. The processes resulting in the relaxation of excited state (⁵D₀ level) were discussed and the probabilities of radiative and nonradiative processes were calculated using the model of f–f transition intensities. It was found that the observed shortening of ⁵D₀ level lifetime with Eu concentration is caused by increase of nonradiative process probability.     

Investigation on the mechanical,thermal properties,and refractive index of Er,Pr:GYSGG laser crystal

Journal of Materials Science: Materials in Electronics - We investigate the mechanical, thermal properties, and refractive index of (Er0.66Gd1.17)(Pr0.003Y1.167)Sc2Ga3O12 (Er,Pr:GYSGG) crystal with...     

Spectral parameters of Nd3+ ion in Nd:KLa(WO4)2 crystal

The spectral parameters of Nd³⁺ ions in Nd:KLa(WO₄)₂ crystal have been investigated based on Judd-Ofelt theory. The spectral parameters were obtained: the parameters of oscillator strengths are Ω₂=3.0887×10^–20 cm², Ω₄=1.0375×10^–20 cm², Ω₆=1.0422×10^–20 cm², the radiative lifetime is 685 μs, the quantum efficiency is 30.7%, and the fluorescence branch ratios were calculated: β₁=0.432, β₂=0.475, β₃=0.089, β₄=0.004. Electronic Publication     

表面效应对YAG:Eu3+纳米晶发光特性的影响研究

分别采用沉淀法和燃烧法制备了YAG:1%Eu3+纳米晶粉末,用XRD和TEM对样品进行了结构分析和形貌表征。室温光谱分析表明,其发射主峰位于590nm,来源于5 D0→7F1跃迁,另外来源于5 D0→7F4跃迁的709nm发射也较强。另外发现,燃烧法制备的样品在不同激发波长激发时,发射光谱峰形有显著变化。对沉淀法制备的纳米微粒经盐酸"浸蚀"表面修饰后,发现395nm激发时,676nm和693nm发光显著增强,而且693nm发射的激发谱中存在两个宽激发带。对表面修饰后样品的变温发光特性研究发现,随着温度的降低,676nm发射显著增强,而693nm发射显著减弱。对于上述现象通过纳米微粒的表面效应和缺陷态进行了分析和解释。     

Optical absorption and fluorescence properties of Er3+ in sodium borate glass

Spectroscopic properties of Er³⁺ ions in sodium borate glass have been studied. The indirect and direct optical band gaps (E_opt) and energy level parameters (RacahE ¹, E² and E³), spin-orbit (ξ_4f) and configurational interaction (α)) are evaluated. Spectral intensities for various absorption bands of Er₃₊ doped sodium borate glass are calculated. Using Judd-Ofelt intensity parametersΩ ₂, Ω₄, Ω₆, radiative transition probabilities (A), branching ratios (β) and integrated absorption cross sections (Σ) are reported for certain transitions. The radiative lifetimes (τ_R) for different excited states are estimated. From the fluorescence spectra, the emission cross section (σ_P) for the transition,⁴I_13/2 → ⁴I_15/2 is reported.     

Polarizability, volume expansion, and stress contributions to the refractive index change of Cu+-Na+ ion exchanged waveguides in glass

The refractive index of optical waveguides formed by electric field assisted Cu(+)-Na(+) ion exchange in two types of glass is measured. Assuming, as in a previously published work, that the observed refractive index increase is solely due to polarizability changes, the difference in electronic polarizability between Cu(+) and Na(+) ions is determined by applying the Lorentz-Lorenz equation to the data. In our work, the concentration of exchanged ions, which is a necessary input to the Lorentz-Lorenz equation, is determined by combining optical data and electrical data obtained during the exchange. Values for the electronic polarizability difference are in agreement with that in the literature. However, when a correction is made, taking into consideration the measured volume expansion and stress in the glass, the calculated electronic polarizability difference is shown to increase by 19%.     

All-optical switching based on the electromagnetically induced transparency effect of an active photonic crystal microcavity

We report a new all-optical switching in a two-dimensional photonic crystal microcavity made of semiconductor multiple quantum wells and realized based on the electromagnetically induced transparency effect with exciton and two-exciton energy levels. We use the quantum coherence effects to achieve small absorption of the probe field, and the absorption of the probe field can be adjusted by controlling the pump field and decay rate. We turn the control field into pulses of light field so that we can regulate the efficiency of the switch. Through selecting the appropriate control light field intensity, we can obtain a switching efficiency of 85% and a switching time is 10 ps. This result can be used for the development of new types of nanoelectronic devices for realizing the switching process.     

Concentration effect of Nd ion on the spectroscopic properties of Er/Nd co-doped LiYF4 single crystal

High quality Er³⁺/Nd³⁺:LiYF₄ single crystals were grown by a Bridgman method. Their spectroscopic properties were studied to understand the Nd³⁺ concentration effect upon excitation of an 800 nm laser diode. The intensest 2.7 μm emission was observed in the LiYF₄ crystal codoped with 0.99 mol% Er³⁺ and 0.62 mol% Nd³⁺. Meanwhile, the emission intensity for the green up-conversion and 1.5 μm downconversion of Er³⁺ decreased with increasing of the Nd³⁺ concentration. The modified Inokuti–Hirayama model was used to analyze the decay curves of the 1.06 (Nd³⁺) and 1.5 (Er³⁺) μm emissions. The results indicated that the energy transfer process (Er³⁺:⁴I_13/2 + Nd³⁺:⁴I_9/2 → Er³⁺:⁴I_15/2 + Nd³⁺:⁴I_15/2) is mainly due to the electric dipole–dipole interaction. The energy transfer efficiencies between Nd³⁺ and Er³⁺ ions were calculated. All results suggested that the Er³⁺/Nd³⁺:LiYF₄ single crystals may have potential applications in mid-infrared lasers.     

Large gradients of refractive index in nanosphere dispersed liquid crystal metamaterial with inhomogeneous anchoring: Monte Carlo study

We study the effect of spatial inhomogeneity of anchoring forces on real part of effective refractive index in nanosphere dispersed liquid crystal (NDLC) metamaterial at infrared frequencies using the approach of Khoo et al. [1] and Monte Carlo modeling proposed recently in Ref. [2]. Local and global characterization is made using 2D maps of spatial distribution of the index, its gradients and its modulation amplitude below and above Freedericksz threshold. We find that NDLC with step-wise modulation of anchoring forces gives rise to much larger gradients and absolute values of the effective index than NDLC with modulated external electric field as well as pure nematic liquid crystal (NLC) with inhomogeneous anchoring. This indicates that the filling factor of coated spheres in NDLC is an important design parameter which tunes the effective refractive index. We find that the results are strongly dependent on wavelength in the infrared interval 2800-2900 nm. Some potential applications to molding the flow of light are briefly mentioned.     

Investigation of the liquid crystal alignment layer: effect on electrical properties

Abstract

We investigate the electrical behavior of a symmetric liquid crystal (LC) cell: elecrode-silane-LC-silane-electrode. The silane (chlorodimethyloctadecyl-silane) layer induces a homeotropic orientation of the nematic liquid crystal (NLC) molecules. The wettability technique is used to detect the change of the surface energy of the electrode upon cleaning and silane layer deposition. We report on the dynamic impedance measurements of the nematic liquid crystal cell. It is found that the silane alignment layer has a blocking effect on the liquid crystal (LC) cell. We also study the relaxation behavior of the cell which is later assimilated as an electrical equivalent circuit.     

Investigation of the liquid crystal alignment layer: effect on electrical properties

We investigate the electrical behavior of a symmetric liquid crystal (LC) cell: elecrode-silane-LC-silane-electrode. The silane (chlorodimethyloctadecyl-silane) layer induces a homeotropic orientation of the nematic liquid crystal (NLC) molecules. The wettability technique is used to detect the change of the surface energy of the electrode upon cleaning and silane layer deposition. We report on the dynamic impedance measurements of the nematic liquid crystal cell. It is found that the silane alignment layer has a blocking effect on the liquid crystal (LC) cell. We also study the relaxation behavior of the cell which is later assimilated as an electrical equivalent circuit.     

晶粒可控BaTiO3-CoFe2O4磁电复合陶瓷制备及生长机制研究

采用全溶液络合法合成了BaTiO3-CoFe2O4混合粉体,用X射线衍射仪对反应产物进行了表征,分析了不同热处理温度对粉体合成的影响.用X射线衍射仪、扫描电镜对由前述预制粉体烧成的磁电陶瓷进行了微观表征,观测到由不同热处理粉体烧成的陶瓷晶粒形貌显著不同,形成了可控晶粒的磁电耦合材料.以全溶液法合成的该磁电陶瓷中,两相晶体各自析出长大,同时CoFe2O4依附于BaTiO3上生长,两种晶体因共格而形成良好的相界面层,对获得较好的磁电耦合性能作用明显.     

H＋离子浓度对WO3粉体化学键及晶体微观结构的影响

分别在不同H＋离子浓度的酸性环境下,采用溶胶-凝胶法制备纳米多孔WO3粉体。利用粉末X射线衍射仪（XRD）、扫描电子显微镜（SEM）、傅立叶变换红外光谱仪（FT-IR）等分析手段对不同条件下制备的粉末样品晶体结构、微观形貌、透射光谱特性及化学健态结构进行对比研究。结果表明,在其它制备条件相同的情况下,强酸环境可以有效增加溶胶-凝胶的反应速度,而且有利于形成WO3材料的非晶化,可得到呈现交联网状的纳米级多孔结构。     

The effect of erbium on the adsorption and photodegradation of orange I in aqueous Er3+-TiO2 suspension

Pure TiO(2) and erbium ion-doped TiO(2) (Er(3+)-TiO(2)) catalysts prepared by the sol-gel method were characterized by means of XRD and diffusive reflectance spectra (DRS). The XRD results showed that erbium ion doping could enhance the thermal stability of TiO(2) and inhibit the increase of the crystallite size, and the DRS results showed that the optical absorption edge slightly shifted to red direction owing to erbium ion doping and the Er(3+)-TiO(2) catalysts had three typical absorption peaks located at 490, 523 and 654 nm owing to the transition of 4f electron from (4)I(15/2) to (4)F(7/2), (2)H(11/2) and (4)F(9/2). With a purpose of azo dyes degradation, orange I was used as a model chemical. And the adsorption isotherm, degradation and mineralization of orange I were investigated in aqueous suspension of pure TiO(2) or Er(3+)-TiO(2) catalysts. The results showed that Er(3+)-TiO(2) catalysts had higher adsorption equilibrium constants and better adsorption capacity than pure TiO(2). The adsorption equilibrium constants (K(a)) of Er(3+)-TiO(2) catalysts were about twice of that of pure TiO(2). The maximum adsorption capacity (Q(max)) of 2.0% Er(3+)-TiO(2) catalyst was 13.08x10(-5)mol/g, which was much higher than that of pure TiO(2) with 9.03x10(-5)mol/g. Among Er(3+)-TiO(2) catalysts, 2.0% Er(3+)-TiO(2) catalyst achieved the highest Q(max) and K(a) values. The kinetics of the orange I degradation using different Er(3+)-TiO(2) catalysts were also studied. The results demonstrated that the degradation and mineralization of orange I under both UV radiation and visible light were more efficient with Er(3+)-TiO(2) catalyst than with pure TiO(2), and an optimal dosage of erbium ion at 1.5% achieved the highest degradation rate. The higher photoactivity under visible light might be attributable to the transitions of 4f electrons of Er(3+) and red shifts of the optical absorption edge of TiO(2) by erbium ion doping.     

Controllable synthesis of Co3O4 from nanosize to microsize with large-scale exposure of active crystal planes and their excellent rate capability in supercapacitors based on the crystal plane effect

Co₃O₄ nanorods, nanobelts, nanosheets and cubic/octahedral nanoparticles have been successfully synthesized with tunable size from the nanoscale to the microscale, accompanied by a variation in the nature of the exposed crystal planes. The products are formed by thermal treatment of Co(CO₃)_0.5(OH)·_0.11H₂O nanorod, nanobelt, nanosheet and nanocubic/nanooctahedral precursors at 250 °C. Detailed characterization, including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photo-electron spectroscopy (XPS), and nitrogen adsorption and desorption isotherms, revealed that the as-prepared nanorods, nanobelts, and nanosheet Co₃O₄ samples are single crystalline and mesoporous in nature with a predominance of exposed high-energy (110) crystal planes. They exhibited excellent electrochemical properties in supercapacitors, showing higher capacitance and better rate capability than conventional cubic/octahedral Co₃O₄ nanoparticles having exposed low-energy (100) and (111) planes. No decay in capacitance was observed when the scan rate was increased from 5 mV/s to 100 mV/s, or from 1 A/g to 10 A/g. The maximum value of the specific capacitance was calculated to be 162.8 F/g and the capacitance retention reached as high as 90%. Their excellent performance in supercapacitors is believed to result from the large-area exposure of active (110) crystal planes. The Co₃O₄ nanosheets showed the best performance due to their larger surface area and ability to provide a better pathway for charge transfer, and are promising electrode materials for application in practical supercapacitors.      

Effect of Ag nanoparticles on the radiative properties of tellurite glasses doped with Er3+, Yb3+ and Tm3+ ions

The present work is devoted to the characterization of the thermal and spectroscopic properties of tellurite glasses, codoped with Er³⁺, Yb³⁺ and Tm³⁺ rare-earth ions and silver nanoparticles (NPs). The techniques used for this investigation were UV–visible and infrared absorption, time-resolved luminescence and thermal lens. Time-resolved luminescence studies indicate efficient Yb³⁺ → Er³⁺ and Yb³⁺ → Tm³⁺ energy transfers and intense Er³⁺ and Tm³⁺ mid-infrared emissions around 1550 nm and 1860 nm, respectively. The presence NPs is found to increase the thermal diffusivity of the materials and to shorten the mid-infrared emission lifetime of both the Er³⁺ and Tm³⁺ ions.     

Hole burning in YSZ:Pr3+ and YSZ:Eu3+ with various Y2O3 concentration

We have measured the hole spectra in YSZ:Pr³⁺ and YSZ:Eu³⁺ with various Y₂O₃ concentrations at low temperature. The temperature dependence of the hole width which obtained from the hole spectra in YSZ:Pr³⁺ and YSZ:Eu³⁺ was similar to that for disordered materials.

However, the Y₂O₃ concentration dependence of the hole width in YSZ:Pr³⁺ was contrary to that for YSZ:Eu³⁺ at low temperature. The hole width was the widest in the case of YSZ:Pr³⁺ at 10 mol% Y₂O₃. On the contrary, it was the narrowest in the case of YSZ:Eu³⁺ at the same concentration of Y₂O₃. It was found that there are two states in YSZ, in which the degree of ordered differs from each other. Additionally, the Y₂O₃ concentration dependence of the hole width at low temperature has reflected the ionic conductivity of YSZ at high temperature. It is suggested that the ordering of local structure is responsible for the ionic conduction in YSZ.

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