Weathering properties of treated southern yellow pine wood examined by X-ray photoelectron spectroscopy, scanning electron microscopy and physical characterization

In this study the weathering behavior of southern yellow pine (SYP) wood samples pretreated in different solutions has been examined using X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and various types of physical characterization regarding material loss and discoloration. The treatment solutions include water as a control, a commercially available water repellent (WR) wood treating additive and polyethylene glycol (PEG) products including PEG PLUS™, PEG 8000 solutions and Compound 20M in varying concentrations. All contained the wood preservative chromated copper arsenate (CCA). One sample was treated with a CCA solution only. The treatments were carried out at 20 °C and 150 psig for 1/2 h after exposure to vacuum (28 mmHg) for 15 min. Simulated weathering was achieved in an Atlas 65-W Weather-Ometer for 2000 h with both light and dark periods and rain. The temperature ranged from 23 °C during the dark cycle to 35 °C during the light cycle. With weathering the XPS O/C ratios increase due to oxidation of the surface. Exposure to UV light results in bond breakage and reaction with oxygen in the presence of air to form organic functional groups such as , , CO and/or O-C-O. These oxidized products can protect the underlying wood from deterioration if they are insoluble in water and remain on the surface as a protective coating. If soluble, rain washes the compounds away and assists in the degradation. Correlated changes are observed in the XPS O/C ratios, the high-resolution XPS C 1s spectra, the SEM micrographs and physical measurements including thickness alteration, weight loss, and discoloration by yellowing or whitening of the weathered wood. The PEG treatments are effective in protecting wood with the 2% PEG PLUS treatment providing the best weathering behavior similar to that of the CCA treatment. The WR and water treatments yield the poorest weathering properties.     

The coherent effect of chirped femtosecond laser pulses on the formation of ultracold molecules in a magneto-optical trap

We have investigated how the formation of ultracold molecules in a rubidium magneto-optical trap is affected by the application of positively-chirped femtosecond laser pulses. The application of femtosecond pulses resulted in a reduction, rather than an increase, in the rate of detection of ⁸⁵Rb₂ and ⁸⁷Rb₂ triplet ground-state molecules, and compared this to the effects of non-chirped pulses, continuous-wave light, and the formation rate when no additional light was applied. A dependence on the amount of chirp of the femtosecond laser pulses suggests that the reduction in the molecular signal is the result of a coherent effect, and provides a promising indication that coherent control could be used to engineer the production of ultracold molecules.     

Widely tunable femtosecond fiber optical parametric oscillator

The phase-matching condition in a fiber is discussed. A balance among the different orders of fiber dispersion can be found to achieve a widely tuning modulation instability gain for pumping around the normal dispersion regime. Three coupled nonlinear wave equations are used to simulate the femtosecond fiber optical parametric oscillator. The numerical results show that, through appropriate choice of dispersion, femtosecond pulses with a 180-nm tunable range can be generated when pump wavelength near a fiber’s zero-dispersion wavelength is tuned only 7 nm. Further tuning is limited by the walk-off between the pump and the signal pulses.     

Hydrogenation of carbon fragments after femtosecond laser ablation of solid C60

We have observed several kinds of hydrocarbon cations after the nanosecond and the femtosecond laser ablation (nsLA and fsLA) of solid C₆₀. The observation indicates that the carbon fragments produced just after laser ablation of the C₆₀ molecule react with the hydrogen atoms and ions coexisting in the ablation plume. In the case of fsLA, clear dependence of the product hydrocarbon species on the ablation laser power has been observed although the dependence is not clearly observed in nsLA. The production of C_nH₅⁺ (n = 8, 10, and 12) is only observed in fsLA suggesting the unique nature of the transient carbon fragments produced by fsLA.     

An asymmetric imidazole derivative as potential fluorescent chemosensor for Fe in aqueous solution

A novel conjugated molecule, L, based on 2,4,5-triphenylimidazole and 6-phenyl-2,2′-bipyridine (HC^∧N^∧N) was synthesized in two steps. The molecule can recognize Fe³⁺ in aqueous solution (THF/H₂O, 1/1, v/v) by the appearance of new emission bands at 416 and 442 nm, which can be attributed to the emission of the newly formed L-Fe³⁺ complex. The binding constant of the complex was calculated to be (6.6±0.39)×10³ M⁻¹, and its formation was also confirmed by the appearance of isosbestic points at 312 and 381 nm in the UV-visible spectral titration experiment. While other transition and rare-earth metal ions, such as Mn²⁺, Fe²⁺, Co²⁺, Ni²⁺, Zn²⁺, Cd²⁺, Hg²⁺, Pb²⁺, Eu³⁺ and Nd³⁺, can only cause some decrease of L's fluorescence, alkali and alkaline earth metal ions, such as Li⁺, Na⁺, K⁺, Mg²⁺ and Ca²⁺, almost have no effect on L's fluorescence. The fluorescence of L can be recovered by the addition of EDTA to the L-Fe³⁺ system just due to EDTA's stronger chelating ability than that of L.     

Control of bond-selective photochemistry in CH BrCl using adaptive femtosecond pulse shaping

Adaptive femtosecond laser pulse shaping is employed to achieve bond selective photodissociation/photoionization of CH₂ClBr in the gas phase. The photoproduct signal measured in a reflectron time-of-flight mass spectrometer is used as feedback to improve iteratively the spectral phases of the laser pulse via an evolutionary algorithm. We observe an increase of the fission of the stronger versus the weaker carbon halogen bond by 100%. Single parameter control schemes proved unable to achieve bond-selectivity. The complexity of the control problem is addressed by mapping it onto the well-known problem of maximizing second-harmonic generation (SHG). Further spectroscopic results indicate that the control involves manipulation of wave-packet dynamics on the neutral surfaces. Received 21 December 2001 / Received in final form 2 April 2002 Published online 28 June 2002     

Multidimensional quantum dynamics and infrared spectroscopy of hydrogen bonds

Hydrogen bonds are of outstanding importance for many processes in Chemistry, Biology, and Physics. From the theoretical perspective the small mass of the proton in a hydrogen bond makes it the primary quantum nucleus and the phenomena one expects to surface in a particular clear way are, for instance, zero-point energy effects, quantum tunneling, or coherent wave packet dynamics. While this is well established in the limit of one-dimensional motion, the details of the multidimensional aspects of the dynamics of hydrogen bonds are just becoming accessible to experiments and numerical simulations.     

Ultra fast melting process in femtosecond laser crystallization of thin a-Si layer

In this paper, we investigated the mechanism of crystallization induced by femtosecond laser irradiation for an amorphous Si (a-Si) thin layer on a crystalline Si (c-Si) substrate. The fundamental, SHG, THG wavelength of a Ti:Sapphire laser was used for the crystallization process. To investigate the processed areas we performed Laser Scanning Microscopy (LSM), Transmission Electron Microscopy (TEM) and Imaging Pump-Probe measurements. Except for 267 nm femtosecond laser irradiation, the crystallization occurred well. The threshold fluences for the crystallization using 800 nm and 400 nm femtosecond laser irradiations were 100 mJ/cm² and 30 mJ/cm², respectively. TEM observation revealed that the crystallization occurred by epitaxial growth from the boundary surface between the a-Si layer and c-Si substrate. The melting depths estimated by Imaging Pump-Probe measurements became shallower when the shorter wavelength was used.     

Comparative study of UV absorption changes induced in germanosilicate glass by high-intensity femtosecond pulses at 267, 400 and 800 nm

We investigated UV absorption changes induced in 3.5 mol% Ge-doped fused silica at high-intensity (∼10¹¹-10¹³ W/cm²) femtosecond (130 fs) irradiation at 267, 400 and 800 nm. We have shown that the induced spectra in the region 190-300 nm are similar in all three cases. At 800 nm irradiation, in addition to the UV absorption changes, we observed small-scale damage due to self-focusing. This damage appears when the incident pulse fluence value of about 1 J/cm² (pulse intensity of about 7.5 × 10¹² W/cm²) is overcome, while the threshold for the induced absorption changes is twice lower.     

Measurement of ultraviolet femtosecond pulses using the optical kerr effect

We demonstrate the optical Kerr shutter technique as a simple and powerful tool for the measurement of femtosecond pulses in the ultraviolet as well as in the visible spectral region. The method provides the third-order intensity correlation function which gives information about pulse asymmetry and pulse structures.     

Studies on widely tunable ultra-short laser pulses using energy transfer distributed feedback dye laser

This paper presents both theoretical and experimental study of the characteristics of Nd: YAG laser pumped energy transfer distributed feedback dye laser (ETDFDL). Using theoretical model proposed, the behavior of ETDFDL such as the characteristics of donor DFDL, the acceptor DFDL, the dependence of their pulse width and output power on donor-acceptor concentrations and pump power are studied for dye mixture Rhodamine 6G and Cresyl Violet in detail. Experimentally using prism-dye cell configuration, the ETDFDL output is obtained and the output energy of DFDL is measured at the emission peaks of donor and acceptor dyes for different pump powers and donor-acceptor concentrations. In addition, the DFDL linewidth measurement has been carried out at the lasing wavelengths of the donor and acceptor dyes using Fabry-Perot etalon and the tunability of DFDL is measured to be in the wavelength range of 545-.     

Preparation and characterization of Cobalt Sulfophthalocyanine/TiO2/fly-ash cenospheres photocatalyst and study on degradation activity under visible light

Cobalt Sulfophthalocyanine (CoSPc) sensitized TiO₂ sol samples were prepared through a Sol-Gel method using Cobalt Sulfophthalocyanine as a sensitizer. Loading and modified floating photocatalyst was prepared by hydrothermal method using fly-ash cenospheres as a carrier. The properties of the samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) and UV-vis diffuse reflectance spectrum (DRS). Photocatalytic activity was studied by degrading wastewater of methylene blue under visible light. The results indicate that the fly-ash cenospheres are covered by modified TiO₂ film which composed of the anatase, brookite and rutile misch crystal phase. CoSPc/TiO₂/fly-ash cenospheres samples have good catalytic activity under visible light, and have strong absorbency during 600-700 nm. The sensitization of CoSPc can enhance visible light catalytic activity of TiO₂/fly-ash cenospheres. The degradation rate of methylene blue reaches 73.36% in 180 min under the visible light illumination. But too much CoSPc can decrease its catalytic activity.     

Nonlinear mixing between the emission of a cw laser and a femtosecond laser

We mix the emission of a femtosecond Ti:sapphire laser with the emission of a continuous wave infrared laser in a beta-barium borate crystal. Green light with a center wavelength of 527 nm and a spectral width of 2.5 nm resulting from sum frequency generation is detected. An intensity study verifies that a nonlinear χ⁽²⁾ process is at the origin of the green light generation. The experimentally obtained conversion efficiency of 7 × 10⁻¹⁰ is in good agreement to simple theoretical considerations.     

Control of wavepacket dynamics in mixed alkali metal clusters by optimally shaped fs pulses

We have performed adaptive feedback optimization of phase-shaped femtosecond laser pulses to control the wavepacket dynamics of small mixed alkali-metal clusters. An optimization algorithm based on Evolutionary Strategies was used to maximize the ion intensities. The optimized pulses for NaK and Na₂K converged to pulse trains consisting of numerous peaks. The timing of the elements of the pulse trains corresponds to integer and half integer numbers of the vibrational periods of the molecules, reflecting the wavepacket dynamics in their excited states. Received 4 December 2001     

Luminescence of undoped β-Ga2O3 single crystals excited by picosecond X-ray and sub-picosecond UV pulses

Undoped β-Ga₂O₃ single crystals were grown using the floating zone technique under a pressure of 2 atm oxygen. Luminescence spectra of the crystals were measured with steady-state X-ray (<15 keV) and UV (258 nm, 4.8 eV) sources. The X-ray excitation produced a spectrum with a peak at 390 nm (3.2 eV) whereas the UV excited spectrum had a peak at 430 nm (2.9 eV). The luminescence rise and decay were also examined by using picosecond X-ray and sub-picosecond UV pulses. It was found that the X-ray pulse excitation gave a slower rise and a faster decay of the luminescence compared with the UV pulse excitation. These results suggest that X-ray excitation generates high energy electrons, building up luminescent states until those electrons lose their kinetic energies, giving rise to the formation of local hot spots in the gallium oxide crystals.     

Structure formation on the surface of alloys irradiated by femtosecond laser pulses

Laser-induced periodic surface structures with different spatial characteristics have been observed after multiple linearly polarized femtosecond laser pulse (120 fs, 800 nm, 1 Hz to 1 kHz pulse repetition frequency) irradiation on alloys. With the increasing number of pulses, nanoripples, classical ripples and modulation ripples with a period close to half of classical ripples have all been induced. The generation of second-harmonic has been supposed to be the main mechanism in the formation of modulation ripples.     

Ultrafast X-ray experiments on structural changes in single crystals of polar molecules

Intramolecular charge transfer in aminobenzonitrile (DIABN) single crystals is studied by a combination of ultrafast techniques. The intramolecular dynamics is probed by time-resolved spectroscopy in the UV/Vis and mid-IR. The intermolecular structural response is investigated by transient X-ray scattering and transmission experiments. A theoretical analysis shows that diffuse scattering and dipole solvation determine the X-ray data. The observed dynamics results from charge transfer reaction leading to strong local changes of molecular dipole moments and related structural rearrangements in the crystal.     

High energy and short pulses generation by Nd:yttrium aluminum garnet laser mode-locked using frequency-doubling nonlinear mirror

The generation of laser pulses with energies of >40 mJ at 25 Hz and durations variable from 15 ps to 45 ps using an Nd:yttrium aluminum garnet laser mode-locked with a Stankov nonlinear mirror is demonstrated. This laser is used to pump an optical parametric generator-amplifier, which is tunable in the visible spectral range.     

Effect of hydrogen on modulation-doped AlGaAs/InGaAs/GaAs heterostructures: a photoluminescence study

The effect of hydrogen on donors and interface defects in silicon modulation doped Al_xGa_1−xAs/In_yGa_1−yAs/GaAs heterostructures has been investigated by photoluminescence (PL). Hydrogenation was carried out on two sets of samples, one set consists of high quality pseudomorphic heterostructures and another set having partially lattice relaxed structures prone to the defects. On exposure of high quality pseudomorphic structures to hydrogen plasma above 150 °C, a significant blue shift in the PL peak positions as well as bandwidth narrowing is observed. This indicates, the reduction in two-dimensional electron gas in the In_yGa_1−yAs quantum well due to hydrogen passivation of silicon donors in the Al_xGa_1−xAs supply layer. The reactivation of the donors is observed upon annealing the hydrogenated sample for 1 h at 250 °C under hydrogen ambient. Another interesting feature is a significant improvement in the PL of lattice-relaxed structures upon hydrogenation of the samples above 250 °C, which is attributed to the hydrogen passivation of interface defects due to the misfit dislocations.