Nanoparticle Formation by Laser Ablation

The properties of nanoparticle aerosols of size ranging from 4.9nm to 13nm, generated by laser ablation of solid surfaces are described. The experimental system consisted of a pulsed excimer laser, which irradiated a rotating target mounted in a cylindrical chamber 4cm in diameter and 18-cm long. Aerosols of oxides of aluminum, titanium, iron, niobium, tungsten and silicon were generated in an oxygen carrier gas as a result of a reactive laser ablation process. Gold and carbon aerosols were generated in nitrogen by non-reactive laser ablation. The aerosols were produced in the form of aggregates of primary particles in the nanometer size range. The aggregates were characterized using a differential mobility analyzer and electron microscopy. Aggregate mass and number concentration, electrical mobility size distribution, primary particle size distribution and fractal dimension were measured. System operating parameters including laser power (100mJ/pulse) and frequency (2Hz), and carrier gas flow rate (1l/min) were held constant.A striking result was the similarity in the properties of the aerosols. Primary particle size ranged between 4.9 and 13nm for the eight substances studied. The previous studies with flame reactors produced a wider spread in primary particle size, but the order of increasing primary particle size follows the same trend. While the solid-state diffusion coefficient probably influences the size of the aerosol in flame reactors, its effect is reduced for aerosols generated by laser ablation. It is hypothesized that the reduced effect can be explained by the collision-coalescence mechanism and the very fast quenching of the laser generated aerosol.     

Silver Nanoparticles Synthesized by Vapor Deposition onto an Ice Matrix

As a strategy for synthesizing metal nanoparticles, thermally evaporated Ag was deposited onto a thin (1.2nm) crystalline ice layer on hafnia (HfO₂) at 100K. The Ag atoms penetrate into the ice matrix but do not reach the underlying HfO₂ substrate. After controlled thermal desorption of water by heating to 300K, atomic force microscopy reveals Ag particle formation. Their lateral dimensions are between 5 and 20nm and, in many cases, their heights exceed the thickness of the original water layer. Fewer, higher and more regular Ag particles are formed in the presence, as compared to the absence, of ice. This is discussed in terms of two factors – Ag atoms reaching HfO₂ are thermally colder when they arrive from the ice matrix and desorption of water involves formation of liquid droplets, a process that concentrates Ag into the volumes occupied by the water droplets.     

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     

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.     

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.     

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     

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     

Diode-pumped passively Q-switched Nd : YAG laser at 1123 nm

A diode-pumped Nd:YAG laser at 1123 nm is passively Q-switched by using a low doping concentration Cr⁴⁺:YAG crystal as a saturable absorber. When pumped by a 1.5-W laser diode, the laser produces pulses of 50-ns duration with a pulse energy of as much as 15 J and a peak power of 300 W at a pulse-repetition rate of 10 kHz. PACS 42.60.Gd; 42.55.Rz; 42.55.Xi     

Iron Nanoparticles in Severe-plastic-deformed Copper

Superparamagnetic iron nanoparticles with a size of a few nanometers were produced in copper by severe plastic deformation. In a isochronal annealing experiment near a temperature of 450K, which corresponds to the temperature of structural relaxation and the first step of grain growth (from 128 to 150nm) of submicrocrystalline copper, an abrupt increase in the magnetic susceptibility is detected. This increase is shown to be due to iron nanoparticles increasing in size from 2.8 to 3.3nm. The vanishing of the ferromagnetic contribution by iron nanoparticles observed at 850K, well below the Curie temperature of iron, is due to the dissolution of nanoparticles in plastically deformed copper.     

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.     

Publisher's Note

When the article 'Modification of the finite difference scheme for efficient analysis of thin lossy metal layers in optical devices' by O. Conradi, S. Helfert, and R. Pregla was first published in the Optical Waveguide special issue of Optical and Quantum Electronics (volume 30, nos. 5–6, pages 369–373) the authors' affiliation given was incorrect. The article is printed again in full with the original pagination and credit lines. A misprint in the Results section has been corrected as well: the refractive index of both silver layers is 0.14–j11.0 at a wavelength of = 1523 nm, and not 0.41–j11.0.     

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   

Compact efficient intracavity optical parametric oscillator with a passively Q-switched Nd : YVO<Subscript>4</Subscript>/Cr<Superscript>4+</Superscript> : YAG laser in a hemispherical cavity

A compact eye-safe optical parametric oscillator (OPO) using a noncritically phase-matched KTP crystal intracavity pumped by a passively Q-switched Nd:YVO₄ laser is experimentally demonstrated. To enhance the performance of passive Q-switching, a Cr⁴⁺:YAG saturable absorber crystal is coated as an OPO output coupler in a nearly hemispherical cavity. With an incident pump power of 2.5 W, the compact intracavity OPO cavity, operating at 62.5 kHz, produces average powers at 1573 nm up to 255 mW and peak powers higher than 1 kW. PACS 42.60.Gd; 42.65.Yj; 42.55.Xi     

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     

Electroless gold deposition on silicon(100) wafer based on a seed layer of silver

This article describes a method of electroless gold deposition on a Si(100) wafer having a silver surface as seed layer. The seed layer was firstly deposited onto the surface of an etched wafer in an acidic solution of 0.005 mol/L AgNO₃+0.06 mol/LHF. The electroless gold deposition is performed by immersing the Ag-activated wafer in an electroless bath with a composition of 1.27×10^-3 mol/L[AuCl₄]^-+2.00×10^-2 mol/LNaH₂PO₂+8.32×10^-2 mol/L NH₂CH₂CH₂NH₂ (pH = 9.0–9.5). The bath temperature is 50–70 °C. The morphology of the seed layer and the gold film were characterized by atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS).PACS 82.45.Mp; 81.15.Pq; 81.10.Dn     

Model for the hydrogen adsorption on carbon nanostructures

The hydrogen sorption capacity of carbon nanostructures was for several years a very controversial subject. Theoretical models have been published demonstrating a great potential for a large hydrogen sorption capacity of carbon nanostructures. Here we present a simple empirical model where condensation of hydrogen as a monolayer at the surface of nanotubes as well as bulk condensation in the cavity of the tube is assumed. The maximum potential amount of hydrogen absorbed according to the model was calculated to be 2.28×10^-3 mass%S[m²g^-1]=3.0 mass% for the adsorption of a monolayer hydrogen at the surface. The condensation of hydrogen in the cavity of the tube leads to a potential absorption for single wall nanotubes starting at 1.5 mass% and increasing with the diameter of the tubes. The experimentally measured hydrogen capacity of the nanotube samples correlates with the B.E.T. specific surface area. The slope of the linear relationship is 1.5×10^-3 mass%/m²g^-1. Therefore, the extrapolated maximum discharge capacity of a carbon sample is 2 mass%. Furthermore, it can be concluded, that the hydrogen sorption mechanism is related to the surface of the sample, i.e. a surface adsorption process. PACS 81.05.Uw; 81.07.De; 82.33.Pt     

Nanometer Calibration Particles: What is Available and What is Needed?

Information on available polystyrene calibration spheres is presented regarding the particle diameter, uncertainty in the size, and the width of the size distribution for particles in a size range between 20 and 100nm. The use of differential mobility analysis for measuring the single primary calibration standard in this size range, 100nm NIST Standard Reference Material®1963, is described along with the key factors in the uncertainty assessment. The issues of differences between international standards and traceability to the NIST Standard are presented. The lack of suitable polystyrene spheres in the 20–40nm size range will be discussed in terms of measurement uncertainty and width of the size distributions. Results on characterizing a new class of molecular particles known as dendrimers will be described and the possibilities of using these as size calibration standards for the size range from 3 to 15nm will be discussed.     

The Formation of Porous Membranes by Filtration of Aerosol Nanoparticles

Flame-generated aerosol particles of Al₂O₃ were deposited by gas filtration on two types of porous and ceramic tubes of -Al₂O₃ with mean pore diameters of 450 and 2700nm, respectively. The particles were aggregates with average mobility diameters in the range of 30–100nm and primary particle diameters of 4–8nm. The particles are characterized by differential mobility analysis, transmission electron microscopy, and by their specific surface area. The deposited membranes are characterized by gas permeability measurements, scanning electron microscopy, and by their pore size distribution from nitrogen capillary condensation. The particles form a distinct, homogeneous membrane layer with a porosity of 90% on top of the substrate surface and only penetrate slightly into the substrate structure. The mean pore sizes of the deposited membranes determined by nitrogen condensation agree approximately with those determined by gas permeation and the specific surface area. The mean pore diameter varies in the range of 30–70nm. The gas permeability of the deposited membranes is related to the specific surface area but influenced by the high porosity. The mean pore size and the permeability of the membranes are almost independent of the substrate structure.The development of a membrane with uniform properties is preceded by a short initial period in which the deposited particles, with an equivalent membrane thickness of roughly 2m, have a significantly lower permeability than the ultimately developed uniform membrane layer. This effect is particularly significant for the aerosol particles with the lowest mean size, probably due to particles deposited in the pore mouths of the substrate.The particles and the deposited membranes are X-ray amorphous but retain their specific surface area on heating to even high temperatures. When the membranes are heated to 1473K for 10h, X-ray diffraction shows a mixture of - and -alumina, accompanied by a partial disintegration of the membrane and a considerable loss of surface area.     

Laser direct write of planar alkaline microbatteries

We are developing a laser engineering approach to fabricate and optimize alkaline microbatteries in planar geometries. The laser direct-write technique enables multicapability for adding, removing and processing material and provides the ability to pattern complicated structures needed for fabricating complete microbattery assemblies. In this paper, we demonstrate the production of planar zinc–silver oxide alkaline cells under ambient conditions. The microbattery cells exhibit 1.55-V open-circuit potentials, as expected for the battery chemistry, and show a flat discharge behavior under constant-current loads. High capacities of over 450 Ahcm^-2 are obtained for 5-mm² microbatteries. PACS 82.47.Cb; 81.16.Mk; 82.45.Fk