Mode-locking of neodymium lasers by glasses doped with PbS nanocrystals

Nonlinear optical absorption properties of silicate glasses doped by the PbS nanocrystals were investigated by means of the picosecond pump-probe absorption spectroscopy and absorption bleaching technique. The glass samples were used as saturable absorbers for passive mode-locking of Nd:YAG and Nd:glass lasers. Application of the PbS doped glass together with the active mode-locking and laser cavity quality control enabled the stable of generation of 28 ps and 5 ps duration pulses in Nd:YAG and Nd:glass lasers respectively. PACS 42.60.Fc; 42.70.Hj; 78.47.+p     

Generalized Transvectants-Rankin–Cohen Brackets

We introduce o(p+1q+1)-invariant bilinear differential operators on the space of tensor densities on Rⁿ generalizing the well-known bilinear sl₂-invariant differential operators in the one-dimensional case, called Transvectants or Rankin–Cohen brackets. We also consider already known linear o(p+1q+1)-invariant differential operators given by powers of the Laplacian.     

The Q-switched Nd : YAG and Yb : YAG microchip lasers optimization and comparative analysis

The microchip lasers based on the neodymium or the ytterbium doped yttrium-aluminium garnet crystal and Q-sw itched by the Cr⁴⁺:YAG film are considered. The optimal (maximizing of energy) values of the pumping beam radius, the absorber parameters (the thickness and tetravalent chromium ion concentration), and the output mirror reflectivity are determined. The possibility of higher values of energy in the Yb:YAG laser pulse, in comparison with a more traditional Nd:YAG laser, is also substantiated. PACS 42.60.Gd     

Electroless deposition of Ag on Pd-activated TiN/p-Si(100) substrate

Nano-thick Ag films were electrolessly deposited on TiN/p-Si(100) substrates. The substrates were prepared by sputtering TiN on p-Si(100) wafers. An activation process of the substrates was performed by immersing the substrates in a solution of 0.0019 moLL^-1PdCl₂+0.45 moLL^-1HF+8.7 moLL^-1aceticacid+0.036 moLL^-1 HCl so as to obtain the Pd seed layer. The general composition of the electroless Ag bath was 0.0032 moLL^-1AgNO₃+2.24 moLL^-1NH₃+0.56 moLL^-1aceticacid+0.1 moLL^-1 NH₂NH₂ at pH 10.2. The morphologies of the Pd seed layer and the Ag films were characterized by atomic force microscopy (AFM). The effect of the Pd activation on electroless Ag deposition was tested by open circuit potential with time technology (OCP-t). For comparison, the morphology of the films deposited by electrochemical deposition on the substrates was also studied by AFM. PACS 82.45.Mp; 81.15.Pq; 81.10.Dn     

Optimizing non-resonant frequency conversion in periodically poled media

Non-resonant frequency conversion into the blue, green, orange, and red spectral regions is reported. Fundamental light sources were continuous-wave non-planar monolithic single-mode ring Nd:YAG lasers as well as a standing-wave multi-mode Nd:YAG laser. Periodically poled KTiOPO₄ was employed as the nonlinear medium, but the considerations could also be applied to other periodically poled materials. A multi-pass scheme resulted in a normalized conversion efficiency as high as 27.2 %W^-1 for frequency doubling in the small-signal regime at 1064 nm. PACS 42.65.Ky; 42.79.Nv; 42.70.Mp     

Influence of Hydrothermal Temperature on Structures and Photovoltaic Properties of SnO2 Nanoparticles

Two SnO₂ nanoparticles were synthesized by hydrothermal method at 170°C and 180°C, respectively. Transmission electron microscope observations reveal that the diameters of both the nanoparticles are around 6nm. At the same time, surface photovoltage spectroscopy measurements show that the nanoparticle synthesized at 180°C has more surface electronic states at 0.3eV below the conduction band than the one synthesized at 170°C. This means that the temperatures chosen in hydrothermal synthesis have significant influence on the surface electronic characteristics of resultant SnO² nanoparticles but the effect on their sizes is not obvious. However, after being calcined at 500°C for 2h, the diameter of the nanoparticle synthesized at 180°C increased to 23nm and that of the nanoparticle synthesized at 170°C increased to 32nm as calculated from X-ray diffraction pattern.     

The early oxynitridation stages of hydrogen-terminated (100) silicon after exposure to N2:N2O. II. Silicon and oxygen bonding states

The early oxidation stages of hydrogen-terminated single-crystalline (100) silicon have been studied by X-ray photoemission spectroscopy, following the evolution of the Si2p and O1s signals after exposure to N₂:N₂O ambient at 850 °C for different durations. Evidence is given that the usual analysis of the film in terms of the Si2p peak leads to inconsistencies, related to the presence in the film of non-siloxanic bridges, as oxygen-rich defects (like hydroxyl terminations or peroxo bridges) or oxygen-deficient defects (like amino bridges). Information on the film structure is obtained by combining the analysis of the Si2p peak with that of the O1s peak. PACS 82.65.+r; 68.35.Fx; 68.35.Dv; 79.60.Jv     

Noncommutative Ricci Curvature and Dirac Operator on C q [SL2] at Roots of Unity

We find a unique torsion free Riemannian spin connection for the natural Killing metric on the quantum group C _q [ SL₂], using a recent frame bundle formulation. We find that its covariant Ricci curvature is essentially proportional to the metric (i.e. an Einstein space). We compute the Dirac operator and find for q an odd rth root of unity that its eigenvalues are given by q-integers [m] _q for m=0,1...,r–1 offset by the constant background curvature. We fully solve the Dirac equation for r=3.     

Q-switching of a diode cladding-pumped Erbium Fibrelaser at 2.7 μm

Reliable Q-switched operation of a cladding-pumped 2.7m ZBLAN fibre laser in the range of the power limit of self-destruction is shown for the first time. The laser is pumped by a multimode diode. Q-switching is achieved by two different techniques: a rotating mirror and an acousto-optical modulator. Pulse widths of 500ns with the rotating mirror and 300ns (FWHM) with the acousto-optical modulator and pulse energies in the J range are achieved.     

Luminescent CdS Nanoparticles Embedded in Polyethylene Glycol (PEG 300) Matrix Thin Film

A simple method for synthesis of well dispersed cadmium sulphide (CdS) nanoparticles embedded in a polyethylene glycol matrix (PEG 300) in thin film form is presented. The molar ratio of PEG and CdS was varied within the range 70:30 to as high as 50:50. Films with controllable sizes (r 3 –8nm) of nanocrystals could be obtained by adjusting post-deposition annealing temperature (T) and time (t). The obtained films showed systematic variation in optical properties with decreasing crystal size due to quantum confinement. Transmission electron micrographs (TEM) indicated well resolved nanoparticles for films annealed at lower temperature (T = 373K) and time (t < 45 min). Photoluminescence (PL) studies indicated blue shift with decreasing particle size. The films did not degrade with aging in a humid atmosphere (relative humidity 40%) for several weeks.     

Tailoring of the functional properties of sol–gel films on Pt/TiO2/SiO2/(100)Si substrates: (Pb,La)TiO3/(Pb,Ca)TiO3 multilayer heterostructures

Preferentially oriented sol–gel (Pb,Ca)TiO₃/(Pb,La)TiO₃/(Pb,Ca)TiO₃ and (Pb,La)TiO₃/(Pb,Ca)TiO₃/(Pb,La)TiO₃ multilayer heterostructure thin films deposited on silicon-based substrates have been studied and compared with identically prepared (Pb,La)TiO₃ (PTL) and (Pb,Ca)TiO₃ (PTC) films. The existence in their texture of two components that contribute to the net polarization in the direction normal to the plane of the film, 001 and 111, results in significant ferroelectric and pyroelectric properties. P_r=26 Ccm^-2 and =28.5×10^-9 Ccm^-2K^-1, and P_r=17 Ccm^-2 and =22.8×10^-9 Ccm^-2K^-1, have been achieved, respectively, in the PTL/PTC/PTL and PTC/PTL/PTC heterostructures. The surface roughness of these films provides a high specific surface that can be interesting for infrared detectivity. An increase of the dielectric permittivity in the whole temperature interval up to the transition temperature has been observed for both heterostructures with respect to the PTL and PTC films. This effect is due to a release of stress in the heterostructures that is revealed by the increase of the tetragonal distortion, c/a, of these films. PACS 68.55.Jk; 77.80.-e; 77.84.Dy     

Reaction-Induced Transformations in Pt–Sn/SiO2 Catalysts: In Situ 119Sn Mössbauer Study

Reaction-induced separation of tin-rich surface layers and tin-depleted inner region was observed in metallic particles of Pt–Sn/SiO₂ catalysts in two reactions: (i) dechlorination of 1,2-dichloroethane at 473 K (modeling catalytic removal of chlorine from hazardous chlorocarbons) and (ii) oxidation of carbon monoxide at room temperature. In the former, a Pt:Sn catalyst (1:2 atomic ratio, 1 wt% metal content), prepared via co-impregnation, showed high selectivity (>80%) toward ethylene (at the expense of ethane), but only after a prolonged (ca. 24 h) period. In situ Mössbauer studies revealed stabilization of a homogeneous Pt–Sn alloy and SnCl₂ after activation in hydrogen; whereas tin-depleted and tin-rich components were separated after a 24-h period. Hence, inhibition of the hydrogenation activity of Pt, by surface tin enrichment and Cl deposition favors high ethylene selectivity. For the oxidation of CO at room temperature, a catalyst with a Pt:Sn atomic ratio of 3:2 (3 wt% Pt) was prepared by an organometallic (CSR) method using ¹¹⁹Sn(CH₃)₄. Platinum-rich PtSn(1) and tin-rich PtSn(2) components were separated in the Mössbauer spectra of catalyst activated at 570 K. The PtSn(2) component is primarily involved in surface reactions. Both in CO oxidation and the subsequent re-activation in hydrogen at room temperature a reversible PtSn(2) Sn⁴⁺ interconversion occurred. d ln(A ₇₇/A ₃₀₀)/dT data indicate the surface location of the involved components.     

Microstructure and Chemical States of Hydroxyapatite/silk Fibroin Nanocomposites Synthesized via A Wet-mechanochemical Route

Hydroxyapaptite (HAp)/silk fibroin (SF) nanocomposites were prepared via a wet-mechanochemical route at room temperature. The results reveal that the inorganic phase in the composites is carbonate-substituted HAp containing 2.9–3.1 wt% of carbonate ions. The primary HAp crystals are rod-like in shape with a typical size of 20–30nm in length and 8–10nm in width, and lattice parameters a = 9.423, c = 6.888. The self-assembled HAp crystals along their c-axes aggregate into bundles, which are connected with SF fibrils. Consequently, a three-dimensional porous network is formed in the composite, which is beneficial to inducing new bone formation in practical implantation.     

Dispersion of Singularities of Solutions for Schrödinger Equations

We consider the singularities of solutions for the Schrödinger evolution equation associated with where Q is a d×d real symmetric matrix with the eigenvalues ₁,,_d, and WC(R^d,R) satisfies W(x)=o(|x|²) as |x|. Under additional conditions, we show the dispersion of microlocal singularities of solutions due to the principal symbol in all directions at time and in the nondegenerate directions at t. We also show the weaker dispersion of microlocal singularities of solutions due to the subprincipal symbol W in the degenerate directions at t if W satisfies W(x)=O(|x|¹⁺) as |x| for some 0<<1 and additional conditions. In particular, we prove the dispersion of microlocal singularities of solutions at resonant times when H is a perturbed harmonic oscillator.Partly supported by Grand-in-Aid for Young Scientists (B) 14740110, Japan Society of the Promotion of Science; and Mathematical Sciences Research Institute in BerkeleyDedicated to Professor Mitsuru Ikawa on his sixtieth birthday     

A sensitive non-destructive method for measuring the Nd doping concentration in Nd : YAG with high spatial resolution

This paper reports on an experimental method for measuring in Nd:YAG the Nd doping concentration (C) with high sensitivity (0.01 at.%Nd) and high spatial resolution (50 m). The method is based on the measurement of the fluorescence lifetime _f of the upper Nd laser level. Additional parameters required to determine C are the intrinsic fluorescence lifetime ₀ and the quenching parameter Q. The measured values of _f, ₀ (256.47±0.14 s) and Q (4.45±0.40×10²⁰ cm^-3) allow us to calculate the Nd concentration C with an absolute accuracy of 0.1 at.%Nd. By using this method C is measured at the outer surfaces of standard laser rods and at the faces of boule slices (with diameters of up to 50 mm). The obtained results demonstrate a detection sensitivity of 0.01 at.%Nd. PACS 42.70.Hj; 81.70.Fy     

Low-resistivity indium tantalum oxide films by magnetron sputtering

Low-resistivity Ta-doped In₂O₃ (InTaO) films from ceramic targets of In₂O₃ doped with 2, 5, and 10 wt% Ta₂O₅ were deposited on Corning glass # 1737 substrates by magnetron sputtering. The electrical and optical properties of these films were studied. The carrier type of InTaO films was found to be n-type. The resistivity, carrier density, and Hall mobility of InTaO films were in the range of 0.28–200.2×10^-4 cm, 0.2–7.4×10²⁰ cm^-3, and 3–31 cm²V^-1s^-1, respectively. A minimum resistivity of 2.8×10^-4 cm with a mobility of 31 cm²V^-1s^-1 and a high transparency of 85% in the visible were achieved for the InTaO thin films doped with 5 wt% Ta₂O₅. PACS 81.15.Cd; 81.40.Rs; 73.90.+f     

Bethe-Salpeter Meson Masses Beyond Ladder Approximation

The effect of quark-gluon vertex dressing on the ground-state masses of the u/d-quark pseudoscalar, vector and axialvector mesons is considered with the Dyson-Schwinger equations. This extends the ladder-rainbow Bethe-Salpeter kernel to two-loops. To render the calculations feasible for this exploratory study, we employ a simple infrared dominant model for the gluon exchange that implements the vertex dressing. The resulting model, involving two distinct representations of the effective gluon exchange kernel, preserves both the axial-vector Ward-Takahashi identity and charge conjugation symmetry. Numerical results confirm that the pseudoscalar meson retains its Goldstone boson character. The vector meson mass, already at a very acceptable value at ladder level, receives only 30MeV of attraction from this vertex dressing. For the axial-vector states, which are about 300MeV too low in ladder approximation, the results are mixed: The 1^+– state receives 290MeV of repulsion, but the 1⁺⁺ state is lowered further by 30MeV. The exotic channels 0^–– and 1^–+ are found to have no states below 1.5GeV in this model.     

Investigation of β–ν Angular Correlation in the β+ Decay of 18Ne and 14O

The – angular correlation in the ⁺ decay of ¹⁸Ne and ¹⁴O has been investigated using a new experimental technique. The technique is based on the precise measurement of the energy Doppler shift of a -quantum following the ^± decay. The measurement with the ¹⁸Ne isotope gives the – angular correlation coefficient = +1.06 ±0.19 which corresponds to a constraint on the scalar interaction of {|C_S|²+|C'_S|²} 0.29|C _V|. An inter-atomic interaction between the ¹⁴O daughter atom (¹⁴N) and a CO complex has been studied in a measurement with the ¹⁴O isotope.     

Experimental demonstration of a photonic-crystal-fiber optical diode

Two cascaded hollow-core photonic-crystal fibers with slightly shifted, but still overlapping, transmission peaks are shown to function as an optical diode for ultra-short laser pulses. Submicrojoule 100-fs Ti:sapphire laser pulses with a spectrum falling within the passband of one of the fibers, but outside the passband of the second fiber, experience spectral broadening due to self-phase modulation in the first fiber. A part of this self-phase-modulation-broadened spectrum is then transmitted through the second fiber. Identical short pulses propagating in the opposite direction are blocked by the second fiber with a shifted passband. A forward-to-backward signal ratio exceeding 40 is achieved with the created photonic-crystal fiber diode for 0.9-J, 100-fs pulses of 800-nm Ti:sapphire laser radiation. PACS 42.65.Wi; 42.81.Qb     

Unusual Behavior of Nanocrystalline Strontium Oxide Toward Hydrogen Sulfide

The thermodynamically favored reaction of solid strontium oxide with gaseous hydrogen sulfide is kinetically enhanced to a large degree by the use of higher surface area nanocrystalline SrO in the form of brush-like collections of metal oxide fibers. An unusual feature is that the reaction SrO + H₂S SrS + H₂O proceeds stoichiometrically at room temperature, but at higher temperatures the reaction efficiency goes down, apparently due to rapid temperature induced crystal growth of the nanocrystalline SrO. The samples studied vary in crystallite size from 20 to 27nm, while average particle size (nanocrystal aggregates) varies in the following order; aerogel prepared SrO (100nm) 相似文献