Vacuum ultraviolet luminescence from a micro-pulling-down method grown Nd:(La0.9,Ba0.1)F2.9

Vacuum ultraviolet (VUV) luminescence from a Nd³⁺:(La_1−x,Ba_x)F_3−x (x=0.1) and a Nd³⁺:LaF₃ single crystal grown by the micro-pulling-down method modified for fluoride crystal growth is discussed. Emission resulting from excitation with 157 nm pulses of a F₂ laser and by 290 nm femtosecond pulses of a Ti:sapphire laser show that the luminescence spectral and temporal characteristics are similar for both excitation cases and that they have good prospects as a VUV laser material.     

UV-VUV-excited photoluminescence of Tm substituted β-rhenanite as a blue-emitting phosphor

Tm³⁺ doped β-rhenanite (β-NaCaPO₄) series were synthesized by solid-state reaction. The crystalline structure of β-rhenanite was simulated and the photoluminescence properties of NaCa_1-xPO₄:xTm³⁺ (0<x≤0.03) were characterized in ultraviolet (UV) and vacuum ultraviolet (VUV) regions for the first time. Under 356 and 172 nm excitation, the emission spectra of the doped series samples exhibited a blue peak centered at 451 nm with the optimum emission intensity at x=0.015. The location of f→d transition was calculated by Dorenbos relationship as well as the possible luminescent mechanisms were discussed via energy levels diagrams derived from our work. Furthermore, the thermal stability and color purity of the optimum sample were both verified. The results indicated that β-NaCaPO₄: Tm³⁺ was a novel blue-emitting phosphor in UV and VUV application.     

Hydrothermal synthesis and luminescent properties of LnPO4:Tb,Bi (Ln=La,Gd) phosphors under UV/VUV excitation

Monoclinic LnPO₄:Tb,Bi (Ln=La,Gd) phosphors were prepared by hydrothermal reaction and their luminescent properties under ultraviolet (UV) and vacuum ultraviolet (VUV) excitation were investigated. LaPO₄:Tb,Bi phosphor and GdPO₄:Tb phosphor showed the strongest emission intensity under 254 and 147 nm excitation, respectively, because of the different energy transfer models. In UV region, Bi³⁺ absorbed most energy then transferred to Tb³⁺, but in VUV region it was the host which absorbed most energy and transferred to Tb³⁺.     

Proton and electron impact on molecular and atomic oxygen: I. High resolution fluorescence spectra in the visible and VUV spectral range and emission cross-sections for dissociative ionisation and excitation of

Molecular oxygen O₂ was dissociated in collisions with protons and electrons in the intermediate velocity range (p⁺-energies: 17-800 keV, e^--energies: 0.2-2 keV). Fluorescence from excited atomic and singly ionised fragments and from singly ionised molecules was detected in the VUV and in the visible and near UV spectral range. Highly resolved spectra are presented for the VUV (46-131 nm) and the near UV/visible (340-605 nm) spectral range. Absolute emission cross-sections have been determined for dissociative ionisation and excitation leading to fluorescence in the VUV. Results are compared with published data. Received 9 September 1999 and Received in final form 15 December 1999     

分子在真空紫外区的相干辐射光谱及转动温度的测量

本文报道的是作者利用分子作为介质,通过非线性光学过程（四波和频,三次谐波）在真空紫外波段产生宽带可调谐相干光的理论和实验研究及其结果,实验产生的宽波段可调谐激光输出为建成完备的小型真空紫外激光光源奠定了基础。此文还报道了作者用该光源在XUV波希成功测量分子转动温度的方法和结果。     

A novel Dy3+-doped Gd(PO3)3 white-light phosphors under VUV excitation for Hg-free lamps application

Novel Dy³⁺-doped Gd(PO₃)₃ white light phosphors each with an orthorhombic system are successfully synthesized by solid-state reaction. The luminescence properties of white-light Gd_1-x(PO₃)₃:xDy³⁺ (0<x≤ 0.25) under vacuum ultraviolet (VUV) excitation are investigated. The strong absorption at around 147 nm in excitation spectrum energy can be transferred to the energy levels of Dy³⁺ ion from the host absorption. Additionally, the white light phosphor is activated by a single Dy³⁺ ion. Therefore, the luminescence of Gd_1-x(PO₃)₃:xDy (0<x≤ 0.25) under VUV excitation is effective, and it has the promise of being applied to mercury-free lamp.     

Mass spectrometric study of photo dissociation of organic molecules by vacuum-ultraviolet irradiation for development of analysis technique

We have observed the photo-chemical reaction process of organic molecules in gas phase induced by vacuum ultraviolet (VUV) radiation. We chose hydrocarbons that contain five carbons in a molecule as samples. To observe the wavelength dependence, three kinds of excimer lamps (Ar₂*-126 nm, Kr₂*-147 nm and Xe₂*-172 nm) were used as light sources of the VUV radiation. Vaporized organic molecular compounds were irradiated by the VUV at a pressure of 12 Pa and detected by means of mass spectrometry. Change of the mass spectra with the irradiation period was measured. As a result, we found that different reaction rates were observed for the different compounds. In particular, 1-pentene and cyclopentane, which have the same molecular weight, have very different decomposition speeds for the irradiation of 172-nm radiation. The facts observed in this work are considered to be very promising for developing a technique to distinguish the targeted compound from others that have similar structures.     

The luminescent properties of CaYBO4:Ln(Ln=Eu, Tb) under UV-VUV range

The luminescent properties of CaYBO₄:Ln(Ln=Eu³⁺, Tb³⁺) were investigated under ultraviolet (UV) and vacuum ultraviolet (VUV) region. The CT band of Eu³⁺ at about 245 nm blue-shifted to 230 nm in VUV excitation spectrum; the band with the maximum at 183 nm was considered as the host lattice absorption. For the sample of CaYBO₄:0.08Tb³⁺, the bands at about 235 and 263 nm were assigned to the f-d transitions of Tb³⁺ and the CT band of Tb³⁺ was calculated according to Jφrgensen's theory. Under UV and VUV excitation, the main emission of Eu³⁺ corresponding to the ⁵D₀-⁷F₂ transition located at about 610 nm and two intense emission of Tb³⁺ from the ⁵D₄-⁷F₅ transition had been observed at about 542 and 552 nm, respectively. With the incorporation of Gd³⁺ into the host lattice of CaYBO₄, the luminescence of Tb³⁺ was enhanced while that of Eu³⁺ was decreased because of their different excitation mechanism.     

Luminescent properties of KGd1−x(WO4)2:Eux and KGd1−x(WO4)2−y(MoO4)y:Eux phosphors in UV-VUV regions

KGd_1−x(WO₄)_2−y(MoO₄)_y:Eu³⁺_x(0.1?x?0.75, y=0 and 0.2) phosphors are synthesized through traditional solid-state reaction and their luminescent properties in ultraviolet (UV) and vacuum ultraviolet (VUV) regions are investigated. Under 147 nm excitation, these phosphors show characteristic red emission with good color purity. In order to improve their emission intensity, the MoO₄²⁻ (20 wt%) is introduced into the anion of KGd_1−x(WO₄):Eu³⁺_x. The Mo⁶⁺ and Eu³⁺ co-doped KGd(WO₄)₂ phosphors show higher emission intensity in comparison with the singly Eu³⁺-doped KGd(WO₄)₂ in VUV region. The chromaticity coordination of KGd_0.45(WO₄):Eu³⁺_0.55 is (x=0.669, y=0.331), while that of KGd_0.45(WO₄)_1.8(MoO₄)_0.2:Eu³⁺_0.55 is (x=0.666, y=0.334) in VUV region.     

Efficient VUV sensitization of Eu3+ emission by Tb3+ in potassium rare‐earth double phosphate

The luminescence properties of K₃Tb(PO₄)₂ activated by Eu³⁺ were studied at excitation over the 120–300 nm wavelength range. It is demonstrated that Tb³⁺ ions, exhibiting a strong absorption band in the vacuum‐ultraviolet (VUV), can provide efficient sensitisation of Eu³⁺ emission in this wave length range, giving rise to intense red luminescence at 150 nm excitation. A proof is given for the concept of VUV sensitisation enabling the engineering of luminescence materials with enhanced conversion efficiency of VUV radiation into visible light. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Vacuum ultraviolet gain measurements in optically pumped LiYF4:Nd3+

 We present measurements of the net-induced gain on the 5d–4f transition at 186 nm in LiYF₄ : Nd³⁺ optically pumped by radiation from a molecular fluorine laser. It is found that for LiYF₄ : Nd³⁺, one of a series of potential continuously tunable VUV lasers, relatively strong excited-state absorption results in net-induced loss. The prospects for VUV laser operation being realised in other rare-earth-doped fluorides is discussed. Received: 4 March 1996/Revised version: 10 July 1996     

A new powerful source for coherent VUV radiation: Demonstration of exponential growth and saturation at the TTF free-electron laser

We present experimental evidence that the free-electron laser at the TESLA Test Facility has reached the maximum power gain of 10⁷ in the vacuum ultraviolet (VUV) region at wavelengths between 80 and 120 nm. At saturation the FEL emits short pulses with GW peak power and a high degree of transverse coherence. The radiation pulse length can be adjusted between 30 fs and 100 fs. Radiation spectra and fluctuation properties agree with the theory of high gain, single-pass free-electron lasers starting from shot noise. Received 26 April 2002 Published online 28 June 2002     

小分子在真空紫外波段从量子态到量子态的光解离动力学

本文主要描述小分子在真空紫外波段(VUV,6-20 eV)光解离动力学的最新实验和理论研究进展.得益于基于商业化激光器的真空紫外光源技术,以及离子速度成像、高分辨氢原子-里德堡态标记-飞行时间测量和VUV-VUV泵浦-探测等方法的发展,研究人员现在可以对很多小分子在真空紫外波段的光解离动力学进行量子态到量子态层面的测量和研究,本文重点综述H_2(D_2,HD),CO,N_2,NO,O_2,H_2O(D_2O,HOD),CO_2,N_2O以及一些多原子分子在真空紫外波段光解离动力学的最新研究进展.这些小分子在真空紫外波段的光解离在天体化学以及大气化学中有着非常重要的应用.分子吸收一个VUV光子以后,通常会被直接激发到比较高的电子激发态,解离过程会涉及到多个电子态势能面之间的复杂非绝热相互作用.在实验上对解离截面等参数进行从量子态到量子态层面的精细测量对于深入了解这些复杂的势能面之间的相互作用有非常重要的意义.最近建成的大连相干光源是目前世界上唯一一台在真空紫外波段工作的自由电子激光,具有脉冲能量高、扫描范围宽(50～150 nm)等优越的性能,它的建成必将会大大促进小分子真空紫外光解离研究的发展.     

Multi-wavelength excimer ultraviolet sources from a mixture of krypton and iodine in a dielectric barrier discharge

New ultraviolet (UV) sources (excimer lamps) have been demonstrated using mixtures of krypton and iodine in a high-pressure dielectric barrier discharge to provide intense multi-wavelength radiation at λ=183 nm (atomic iodine line, ⁴ P _5/2?² P _3/2), 191 nm (KrI^*, B _1/2?X _1/2), 206 nm (atomic iodine line, ² P _3/2?² P _1/2), and 342 nm (I^* ₂, D _1/2?X _1/2). The characteristics of the optical emission spectra of the atomic species and the excited dimers (excimers) formed for different total gas pressures and in the presence of a buffer gas have been investigated. The highest intensity, at 183 nm, is obtained at pressures up to 1 bar while the overall emission spectra can be controlled by adjusting the total pressure. The results show that these strong multi-wavelength lamps offer an interesting alternative to conventional UV sources. Received: 1 March 2000 / Revised version: 5 April 2000 / Published online: 30 June 2000     

Photoluminescence of Eu-doped CaMgSi2xO6+2x (1.00?x?1.20) phosphors in UV-VUV region

Alkaline-earth silicate phosphors CaMgSi_2xO_6+2x:Eu²⁺ (1.00?x?1.20) were prepared by traditional solid-state reaction. The phosphors showed an intense blue emission centered around 453 nm, with both 254 and 147 nm excitations. The host absorption below 200 nm in the excitation spectra consisted of two bands around 160 and 190 nm. The band around 160 nm was ascertained to be associated with the SiO₄-tetrahedra and MgO₆-polyhedra, and that around 190 nm was due to the CaO₈-polyhedra or some impurities. The incorporation of excess Si of less than 15% would not lead to formation of impurities and the results indicated that an appropriate Si excess could improve the Photoluminescence (PL) intensity in both ultraviolet (UV) and vacuum ultraviolet (VUV) regions     

Effect of vacancies and interstitials on the dynamic properties of the La2−x SrxCuO4 superconductor

The effect of vacancies and interstitials in the CuO₂ layer on the vibrational spectrum in the La_2−x Sr_xCuO₄ system has been calculated by molecular dynamics. It is shown that the excitation probability for local ∼0.4-eV high-frequency vibrations of nonphonon origin in the vicinity of Sr impurity atoms decreases if copper vacancies are introduced at a concentration x=0.17, which corresponds to the maximum superconducting transition temperature, this decrease being still more effective (by about ten times) if interstitial atoms are present. The appearance of interstitials makes a considerable region around them (five to six nearest neighbors) quasi-amorphous. A comparison with available experimental data is made. It is concluded that the behavior of the system under irradiation is accounted for primarily by interstitials, which bring about strong perturbation in the lattice (∼1 nm) up to making it completely amorphous. Fiz. Tverd. Tela (St. Petersburg) 40, 984–988 (June 1998)     

Total cross-sections for positron scattering by a series of molecules

The additivity rule is employed to obtain the total (elastic+inelastic) cross-sections for positron scattering from molecules including a number of diatomic, polyatomic molecules (H₂, N₂, HCl, CO₂, NH₃, SF₆, CH₄, C₂H₄ and C₃H₈) over an incident energy range of 10-1000 eV. The total cross-sections (TCS) of the constituent atoms of molecules are obtained by employing a complex optical model potential (composed of static, polarization and absorption potential). The present results are compared with experimental data and other theoretical calculations, good agreement is obtained in intermediate- and high-energy region. Received: 11 November 1997 / Revised: 23 March 1998 / Accepted: 16 June 1998     

Photoluminescence properties of Sr(Y, Gd)2O4:Euunder VUV excitation

Vacuum ultraviolet (VUV) excitation and photoluminescence (PL) properties of Sr(Y, Gd)₂O₄ doped with Eu³⁺ were studied. The excitation spectra of SrY_1.9Eu_0.1O₄ and SrY_1.0Gd_0.9Eu_0.1O₄ had absorption in the VUV region with the absorption band edge at 149 nm, while the absorption of SrGd_1.9Eu_0.1O₄ in the VUV region was weak, which could be due to the narrow host band gap and no efficient energy transfer occurred in the VUV region. The PL spectra of all samples exhibited the characteristic emission of Eu³⁺ with the red ⁵D₀-⁷F₂ transition (611 nm) being the most prominent group.     

Martensitic transformations: first-principles calculations combined with molecular-dynamics simulations

Results are presented of first-principles total-energy calculations and molecular-dynamics simulations of structural transformations in magnetic transition metal alloys like Fe_1-xNi_x. While first-principles calculations allow to identify those structures having the lower total energy, molecular-dynamics simulations can be used to trace out the dependence of the transformation on temperature, composition, concentration of defects etc. We have used the method of the semi-empiric embedded-atom potential in the molecular-dynamics simulations which yields remarkable good results for the structural changes. Received: 3 February 1998 / Revised: 4 May 1998 / Accepted: 24 June 1998     

High luminance of new green emitting phosphor, Mg2SnO4:Mn

Mg₂SnO₄, which has an inverse spinel structure, was adopted as the host material of a new green emitting phosphor. Luminescence properties of the manganese-doped magnesium tin oxide prepared by the solid state reaction were investigated under vacuum ultraviolet (VUV) ray and low-voltage electron excitation. The Mg₂SnO₄:Mn phosphor exhibited green luminescence with the emission spectrum centered at 500 nm due to spin flip transition of the d-orbital electron associated with the Mn²⁺ ion. Optimum Mn concentration of Mg₂SnO₄:Mn under VUV excitation with 147 nm wavelength and electron beam excitation with 800 V excitation voltage are 0.25 and 0.6 mol%, respectively. The emission intensities of Mg₂SnO₄:Mn phosphors under the two excitation sources are higher than those of Zn₂SiO₄:Mn and ZnGa₂O₄:Mn phosphors. At 0.25 mol% of Mn concentration, on the other hand, the decay time is shorter than 10 ms.