Enhancement of upconversion luminescence of YAlO3：Er^3＋ by Gd^3＋ doping

Two series of Yb3+-doped silica glasses (YA and YAP) are fabricated using the sol-gel method, and their spectroscopic properties are investigated. The longest fluorescence lifetime of 0.96 ms is obtained in YAP2 and YAP3 glasses. The emission cross-section (σemi) and σemi ×τ of Yb3+ in the YAP1 glass are 1.00 pm2 and 0.94 pm2·ms, respectively. Co-doping with Al and P decreases the hydroxyl group content in the glasses because of the reduction in non-bridging oxygen content. The lowest OH content in the YAP3 glass is 9.6 ppm.     

Optimization of calcination temperature of lead-free BiFeO3–BaTiO3 high-temperature piezoceramics

0.7BiFeO₃-0.3BaTiO₃+1mol% MnO₂(0.7BFO-0.3BTO) ceramics were synthesized by conventional solid-state powder method under different calcination temperatures (T_cal) between 770 and 830 °C. The phase structure, microstructure, and ferroelectric and piezoelectric properties changed greatly depending on the applied T_cal. Benefitting from the formation of low defect levels and large grain size and an appropriate morphotropic phase boundary (MPB) with the rhombohedral-to-pseudocubic phase ratio = 49.1 : 50.9, BFO-BTO ceramics calcined at 785 °C showed the best ferroelectric, piezoelectric, and insulating properties (P_r = 23.1 μC/cm², E_C = 25.8 kV/cm, d₃₃ = 167.8 pC/N, k_p = 0.342%). Above T_cal = 800 °C, however, the ferroelectric and piezoelectric properties deteriorated because volatilization of Bi and reduction of Fe caused a poor insulating property and high degree of chemical inhomogeneity. Moreover, the ceramics calcined at 785 °C showed a high Curie temperature (T_C) of 509.2 °C and excellent thermal aging resistance of d₃₃ up to 450 °C, demonstrating great potential for use in high-temperature applications.     

The first-principles study of ferroelectric behaviours of PbTiO3/SrTiO3 and BaTiOn/SrTiO3 superlattices

We have performed the first-principles calculation to investigate the origins of ferroelectricities and different po- larization behaviours of superlattices BaTiO3/SrTiO3 and PbTiO3/SrTiO3. The density of state （DOS） and electronic charge profiles show that there are strong hybridizations between atoms Ti and O and between atoms Pb and O which play very important roles in producing the ferroelectricities of superlattices BaTiO3/SrTiO3 and PbTiO3/SrTiO3. Ow- ing to the decline of internal electric field in SrTiO3 （ST） layer, the tetragonality and polarizations of superlattices decrease with increasing the fraction of SrTiO3 in the superlattices. We find that the polarization of PbTiO3/SrTiO3 is largerthan that of BaTiO3/SrTiO3 at the same ratio of components, because the polarization mismatch between PbTiO3 and SrTiO3 is larger than that between BaTiO3 and SrTiO3. The polarization and tetragonality are en- hanced with respect to those of bulk tetragonal BaTiO3 in the superlattices BaTiO3/SrTiO3, while the polarization and tetragonality are reduced with respect to those of bulk tetragonal PbTiO3 in superlattices PbTiO3/SrTiO3.     

Magneto-optical trapping of bosonic and fermionic neon isotopes and their mixtures: isotope shift of the 3P2 ↔ 3D3 transition and hyperfine constants of the 3D3 state of 21Ne

We have magneto-optically trapped all three stable neon isotopes, including the rare ²¹Ne, and all two-isotope combinations. The atoms are prepared in the metastable ³P₂ state and manipulated via laser interaction on the ³P₂ ? ³D₃ transition at 640.2?nm. These cold (T ≈ 1?mK) and environmentally decoupled atom samples present ideal objects for precision measurements and the investigation of interactions between cold and ultracold metastable atoms. In this work, we present accurate measurements of the isotope shift of the ³P₂ ? ³D₃ transition and the hyperfine interaction constants of the ³D₃ state of ²¹Ne. The determined isotope shifts are (1625.9 ± 0.15)?MHz for ²⁰Ne ? ²²Ne, (855.7 ± 1.0)?MHz for ²⁰Ne ? ²¹Ne, and (770.3 ± 1.0)?MHz for ²¹Ne ? ²²Ne. The obtained magnetic dipole and electric quadrupole hyperfine interaction constants are A(³D₃) = (?142.4 ± 0.2)?MHz and B(³D₃) = (?107.7 ± 1.1)?MHz, respectively. All measurements give a reduction of uncertainty by about one order of magnitude over previous measurements.     

First-principles study of the （001） surface of cubic PbHfO3 and BaHfO3

Using first-principles techniques,we investigate the(001) surfaces of cubic PbHfO3(PHO) and BaHfO3(BHO) terminated with both AO(A=Pb and Ba) and HfO2.Surface structure,partial density of states,band structure,and surface energy are obtained.The BaO surface is found to be similar to its counterpart in BHO.For the HfO2-terminated surface of cubic PHO,the largest relaxation appears on the second-layer atoms but not on the first-layer ones.The analysis of the structure relaxation parameters reveals that the rumpling of the(001) surface for PHO is stronger than that for BHO.The surface thermodynamic stability is explored,and it is found that both the PbO-and the BaO-terminated surfaces are more stable than the HfO2-terminated surfaces for PHO and BHO,respectively.The surface energy calculations show that the(001) surface of PHO is more easily constructed than that of BHO.     

Simulation of 3D moving sound

lIntroductionVirtualauditory3Dspace,orequivalentlythesimulationoffree-fieldsoundsisawidelyneededtechniqueinbothexperimentalandcommercialapplicationsI'].OurlaboratoryhasdevelopedanimplementationofvirtualacousticspaceusingaheadphonedeliverysystemthatissuitableforNeurophysiologicstudiesofdirectionalhearing[2'4l1o].Inthispaper,wereportonanextensionofthisworkthatprovidesforveridicalsimulationofthecomplexacousticsresultingfrommovingsoundsources.Controlledmovementofasoundsourceinthefreefieldisdiffi…     

Characterization of structural transitions and lattice dynamics of hybrid organic–inorganic perovskite CH_3NH_3PbI_3

By combining temperature-dependent x-ray diffraction(XRD) with temperature-dependent Raman scattering, we have characterized the structural transitions and lattice dynamics of the hybrid organic–inorganic perovskite CH_3NH_3PbI_3.The XRD measurements cover distinct phases between 15 K and 370 K and demonstrate a general positive thermal expansion.Clear anomalies are found around the transition temperatures.The temperature evolution of the lattice constants reveals that the transition at 160 K/330 K is of the first-/second-order type.Raman measurements uncover three strong lowfrequency modes, which can be ascribed to the vibration of the Pb/I atoms.The temperature evolution of the modes clearly catches these transitions at 160 K and 330 K, and confirms the transition types, which are exactly consistent with the XRD results.The present study may set an experimental basis to understand the high conversion efficiency in methylammonium lead iodide.     

Investigation of emission properties of Tm3＋：Y2O3 transparent ceramic

A transparent and emitting ceramic of Y 2 O 3 doped with 6% Tm 3+ ions is fabricated by vacuum sintering with ZrO 2 . Absorption, photoluminescence (PL), and PL excitation (PLE) spectra are investigated in a spectral range of 200 to 2 100 nm at various temperatures between 296 and 12 K. Intense emission band appears at 450 to 465 nm in the visible range. Near-infrared emission bands are observed at 1 200 to 1 300 nm and 1 400 to 1 550 nm, with intense peaks at 1 270, 1 450, and 1 523 nm. The luminescence mechanisms and potential applications of the emissions are discussed with the help of Judd-Ofelt theory and PLE spectra.     

Temperature dependence of nitrogen and oxygen broadening of the 16O3 ν 3 band

High-resolution Fourier transform absorption spectra of ozone broadened by N₂ and O₂ have been recorded at room temperature and at 225 K. Nitrogen- and oxygen-broadened half-widths and their temperature dependence for respectively 160 ro-vibrational transitions on the ¹⁶O₃ ν ₃ band with a wide range of rotational quantum numbers J (2–48) and K_a (0–8) have been determined.     

Effect of Al^3＋ on Photoluminescence Properties of Eu^3＋-Doped BaZr（BO3）2 Phosphors

We discuss the influence of Al^3＋ on the charge transfer state （CTS） and the photoluminescence properties of BaZr（BO3）2：Eu. The results reveal that there is a red shift which is about 20nm for the charge transfer state when doping with Al^3＋ and indicate the formation of ‘free＇ electrons due to the change of microstructures. In addition, the influence or Al^3＋ doping on the PPR is analysed and a new explanation is raised based on the photo luminescent mechanism. It is the CTS intensity rather than the CTS energy that influences the peak-peak ratio.     

Diode laser spectroscopic measurement of line shape of (ν1+3ν3) band transitions of acetylene

A near-infrared diode laser spectrometer is set up to study the absorption line shape of acetylene in the 782 nm region. The second-derivative spectra recorded by source modulation technique have enhanced sensitivity. Careful choice of operating current and diode temperature leads to distortion-free line shape for six rotational components of the (ν₁+3ν₃) overtone-combination mode of acetylene. Self- and nitrogen-broadening coefficients and line-strength parameters have been extracted by fitting the observed line shape with Voigt profiles. There is no evidence of the effect of velocity changing collisions on the line shape in this near-infrared band. Received: 6 July 1998 / Revised version: 2 November 1998 / Published online: 10 March 1999     

Effects of Li＋ on photoluminescence of Sr3SiOs： Sm3＋ red phosphor

The structure and photoluminescence （PL） properties of Sr3 SiO5： Sm3＋ and Li＋-doped Sr3SiOs： Sm3＋ red-emitting phosphors were investigated. Samples were prepared by the high-temperature solid-state method. PL spectra show that the concentration quenching occurs when the Sm3＋ concentration is beyond 1.3 mol% in Sr3SiOs： Sm3＋ phosphor without doping Li＋ ions. The concentration-quenching mechanism can be explained by the electric dipole-dipole interaction of Sm3＋ ions. The incorporation of Li＋ ions into Sr3SiOs： Sm3＋ phosphors, as a charge compensator, improves the PL properties. The lithium ions also suppress the concentration quenching in Sm3＋ with concentration increased from 1.3 tool% to 1.7 tool%.     

Composition Dependence of Spectroscopic Properties of Er^3＋ Doped TeO2-WO3-ZnO Glasses

Er^3 -doped TeO2-WO3-ZnO glasses were prepared and the absorption spectra, emission spectra and fluorescence lifetimes were measured. With more Te02 content in the glasses, the emission full width at half maximum (FWHM) increases while the lifetime of the ^4I13/2 level of Er^3 decreases. The stimulated emission cross-sectionof Er^3 calculated by the McCumber theory is as large as 0.86pm^2. The product of the FWHM and the emissioncross-section σe of Er^3 in TeO2-WO3-ZnO glass is larger than those in other glasses, which indicates that the glasses are promising candidates for Er^3 -doped broadband amplifiers. The Judd-Otfelt parameter Ω6 shows close composition dependence of the 1.5μm emission bandwidth. The more the TeO2 content is, the larger thevalues of Ω6 and FWHM.     

Using of sonochemically prepared components for vapor phase growing of SbI3·3S8

The using of sonochemically prepared components for growth of SbI₃·3S₈ single crystals from the vapor phase is presented for the first time. The good optical quality of the obtained crystals is important because this material is valuable for optoelectronics due to its non-linear optical properties. The products were characterized by using techniques such as X-ray crystallography, powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray analysis, high-resolution transmission electron microscopy, selected area electron diffraction, optical diffuse reflection spectroscopy and optical transmittance spectroscopy. The direct and indirect forbidden energy gaps of SbI₃·3S₈ illuminated with plane polarized light with electric field parallel and perpendicular to the c-axis of the crystal have been determined. The second harmonic generation of light in the grown crystals was observed.     

Measurements of air and noble-gas broadening and shift coefficients of the methane R3 triplet of the 2ν3 band

By using a tunable diode laser spectrometer with one absorption White cell for low pressure and one photoacoustic cell for high pressure, line shape parameters of the R3 triplet of the 2ν₃ band of methane at 1.65 μm were measured. The absorption line was recorded by using the wavelength modulation spectroscopy technique with first harmonic detection. The broadening and shift coefficients were obtained by fitting the first harmonic absorption signal while varying the pressure of different perturbing gases: air and noble gases (helium, neon, argon, krypton and xenon). We present here the results for the R3 triplet. The observed shift and broadening coefficients behaviors are discussed. Received: 17 November 2000 / Revised version: 19 February 2001 / Published online: 27 April 2001     

Theoretical calculations of N2-broadened half-widths of ν5 transitions of HNO3

A number of satellite instruments are measuring nitric acid, HNO₃, in the Earth's atmosphere. In order to do retrievals of temperature and concentration profiles, the spectral parameters for many thousands of HNO₃ transitions must be known. Currently the HITRAN database uses a constant estimated value for the air-broadened half-width of HNO₃. To help improve the line shape parameters, complex Robert–Bonamy calculations were made to determine N₂-broadened half-widths for some 5000 transitions of HNO₃ in the ν₅ band. The intermolecular potential is a sum of electrostatic terms (dipole–quadrupole and quadrupole–quadrupole) and the atom–atom potential expanded to eighth order. The trajectory parameters were adjusted to yield better agreement with measurement. Velocity integrated calculations were made at seven temperatures in order to determine the temperature dependence of the half-widths. The half-width data are compared with available rotation band measurements. The average percent difference between the measured and calculated half-widths is ?2.38 for N₂-broadening and ?0.65 for air-broadening. The temperature, vibrational, and rotational state dependence of the half-width are investigated.     

A nonlinear instability for 3×3 systems of conservation laws

The phenomenon of nonlinear resonance provides a mechanism for the unbounded amplification of small solutions of systems of conservation laws. We construct spatially 2-periodic solutionsu ^N C ([0,t _N ] × witht _N bounded, satisfying

Excited state absorption of Ti3+:YAlO 3 ⋆

Spectroscopic properties and excited-state absorption (ESA) of Ti³⁺ doped YAlO₃ are investigated in detail. The fluorescence band is centered at 623 nm with a room-temperature lifetime of 11.4 s and a quantum efficiency nearby one. Till now laser action could not be detected because of strong excited-state absorption into a charge transfer band located 45 500 cm^–1 above the Ti³⁺ ground state. At the Ar-laser pump wavelength the ESA cross-section is determined to be _ESA=1×10^–18 cm². This value is a factor of 44 higher than the ground-state absorption cross-section. Consequently the pumping efficiency is decreased by one or two orders of magnitude. The Ti:YAlO₃ results are compared with the spectroscopic data of Ti:Al₂O₃.Dedicated to Prof. Dr. Herbert Welling on the occasion of his 60th birthday