X-ray diffuse scattering measurements of nucleation dynamics at femtosecond resolution

Femtosecond time-resolved small and wide angle x-ray diffuse scattering techniques are applied to investigate the ultrafast nucleation processes that occur during the ablation process in semiconducting materials. Following intense optical excitation, a transient liquid state of high compressibility characterized by large-amplitude density fluctuations is observed and the buildup of these fluctuations is measured in real time. Small-angle scattering measurements reveal snapshots of the spontaneous nucleation of nanoscale voids within a metastable liquid and support theoretical predictions of the ablation process.     

Phase-locked, time-delayed harmonic pulses for high spectral resolution in the extreme ultraviolet

We present experiments in the time and frequency domains aimed at confirming the measured mutual phase coherence of time-delayed, collinear harmonic pulses. We show that pairs of phase-locked harmonic pulses of medium order can be generated for peak intensities up to ~1.5 10(14)W/cm(2) in xenon, demonstrating the possibility of performing high-resolution spectroscopy in the extreme ultraviolet with Ramsey-like techniques.     

Generation and propagation of a picosecond acoustic pulse at a buried interface: time-resolved x-ray diffraction measurements

We report on the propagation of coherent acoustic wave packets in (001) surface oriented Al0.3Ga0.7As/GaAs heterostructure, generated through localized femtosecond photoexcitation of the GaAs. Transient structural changes in both the substrate and film are measured with picosecond time-resolved x-ray diffraction. The data indicate an elastic response consisting of unipolar compression pulses of a few hundred picosecond duration traveling along [001] and [001] directions that are produced by predominately impulsive stress. The transmission and reflection of the strain pulses are in agreement with an acoustic mismatch model of the heterostructure and free-space interfaces.     

Adaptive dispersion compensation for remote fiber delivery of near-infrared femtosecond pulses

We report on remote delivery of 25-pJ broadband near-infrared femtosecond light pulses from a Ti:sapphire laser through 150 m of single-mode optical fiber. Pulse distortion caused by dispersion is overcome with precompensation by adaptive pulse shaping techniques, while nonlinearities are mitigated by use of an SF10 glass rod for the final stage of pulse compression. A near-transform-limited pulse duration of 130 fs was measured after the final compression.     

Temporal compression of nanosecond laser pulses using coherent control

We present a study of the temporal compression of nanosecond laser pulses resulting from the coherent control peculiarities of the propagation dynamics in a regime of electromagnetically induced transparency. We describe the general theoretical framework and discuss the crucial conditions required in order to experimentally realize such a temporal compression scheme. A proof-of-concept experimental realization of a scheme of this type in a sample of hot sodium vapors is currently being implemented: we describe in detail the experimental setup designed for this purpose.     

Chitosan loaded with silver nanoparticles,CS‐AgNPs,using thymus syriacus,wild mint,and rosemary essential oil extracts as reducing and capping agents

The present study describes the green method for the preparation of chitosan loaded with silver nanoparticles (CS‐AgNPs) in the presence of 3 different extracted essential oils. The essential oils play dual roles as reductant and capping agents. The reducing power and DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) assay for the 3 essential oils—Thymus syriacus (T), wild mint (M), and rosemary (R)—have been reported. The preparation of CS‐AgNPs was performed by 2 steps. The 3 previously extracted essential oils have been used as reducing and capping agent in the first step, while in the second step, silver nanoparticles were integrated in chitosan. The integration of AgNPs in the structure of chitosan was confirmed by ultraviolet‐visible, Fourier transform infrared spectroscopy, scanning electron microscopy techniques, and energy dispersive X‐ray. Surface plasmon resonance confirmed the formation of CS‐AgNPs with maximum absorbance at λ_max between 405 ‐ 410 and 410 ‐ 430 nm for colloidal and films of CS‐AgNPs, respectively. The intensity of bands at 3408 cm^?1 in the fourier transform infrared spectroscopy measurements was decreased substantially and shifted slightly to lower frequency (?υ = 43 cm^?1). Scanning electron microscopy shows a spherical morphology of AgNPs with size of 62 nm for both colloidal and film samples, and energy dispersive X‐ray analysis shows peaks confirming AgNPs formation.     

Resolvent analysis in unbounded flows: role of free-stream modes

Theoretical and Computational Fluid Dynamics - The problem of finding optimal forcing and response for unbounded base flows, exemplified by the Blasius boundary layer, is assessed by means of a...