Femtosecond

About: Femtosecond is a research topic. Over the lifetime, 35106 publications have been published within this topic receiving 691405 citations. The topic is also known as: 1 E-15 s & fs.

Femtosecond laser written stress-induced Nd:Y3Al5O12 (Nd:YAG) channel waveguide laser

Abstract: Single tracks and pairs of tracks were written into undoped and Nd-doped YAG crystals using a commercial femtosecond laser system delivering pulses with pulse duration of 140 fs and pulse energies up to 10 μJ. The pulses were focused by a 50× microscope objective below the surface of the crystals. Due to the elasto-optical effect, stress-induced birefringence was observed in domains surrounding the single tracks and between the pairs of tracks. Waveguiding was demonstrated in certain channels in these domains. To investigate the underlying guiding mechanism highly selective chemical etching of the modified material was performed with etching rates up to 5 μm/h. Pumped at 808 nm, laser operation at a wavelength of 1064 nm was achieved. The maximum output power was 25.5 mW at 261 mW of launched pump power with a slope efficiency of 23%.

Femtosecond laser induced nanostructure formation: self-organization control parameters

Abstract: In self-organized nanostructure formation upon femtosecond laser ablation, the laser polarization is an important control parameter. Experiments on fluoride crystals, using circular and elliptical polarization, study this influence in more detail. For circular polarization, spherical nanoparticles of about 100 nm diameter are formed. With increasing ellipticity, longer and longer ordered chains and linear structures are generated, oriented perpendicular to the long axis of the polarization ellipse. A similar effect occurs when, for circular polarization, the angle of incidence is varied from normal to 45°: the s-component of the incident field, not attenuated by the projection, determines length and orientation of the ordered ripples. However, surface defects like scratches exert an even stronger influence on the ripples orientation than the polarization, resulting in curved structures bending from polarization-controlled to defect-controlled orientation. Since the structure formation takes place only long after the end of the laser pulse, a certain electrical field memorizer is required to account for this polarization dependence. A promising approach assumes directional atomic surface diffusion anisotropies, arising, e.g. from plasmon-coupled metal–colloid arrays.

Vacuum Squeezing of Solids: Macroscopic Quantum States Driven by Light Pulses

Abstract: Femtosecond laser pulses and coherent two-phonon Raman scattering were used to excite KTaO3 into a squeezed state, nearly periodic in time, in which the variance of the atomic displacements dips below the standard quantum limit for half of a cycle. This nonclassical state involves a continuum of transverse acoustic modes that leads to oscillations in the refractive index associated with the frequency of a van Hove singularity in the phonon density of states.

Surface-Enhanced Femtosecond Stimulated Raman Spectroscopy.

Abstract: Surface-enhanced Raman spectroscopy (SERS) and femtosecond stimulated Raman spectroscopy (FSRS) have revolutionized the Raman spectroscopy field. SERS provides spectroscopicdetectionofsinglemolecules,andFSRSenablestheacquisitionofRamanspectraon the ultrafast time scale of molecular motion. Here, we present the first successful combination of these two techniques, demonstrating surface-enhanced femtosecond stimulated Raman spectros- copy(SE-FSRS)usinggoldnanoantennaswithembeddedreportermolecules.Usingapicosecond Raman and femtosecond probe pulse, the time- and ensemble-averaged enhancement factor is estimated to be in the range of 10 4 10 6 . We report the line shapes, power dependence, and magnitude of the SE-FSRS signal and discuss contributions to sample degradation on the minute time scale. With these first successful proof-of-principle experiments, time-resolved SE-FSRS techniques can now be rationally attempted with the goals of investigating the dynamics of plasmonic materials as well as examining the contributions of environmental heterogeneities by probing more homogeneous molecular subsets. SECTION: Nanoparticles and Nanostructures

Femtosecond Real-Time Probing of Reactions. 19. Nonlinear (DFWM) Techniques for Probing Transition States of Uni- and Bimolecular Reactions

Abstract: Degenerate four-wave mixing (DFWM), using ∼60 femtosecond (fs) laser pulses, is introduced to study transition-state dynamics of chemical reactions in the gas phase. The ultrafast techniques are applied to a range of systems, atomic, unimolecular, and bimolecular. It is shown how fs DFWM can be incorporated in different temporal pulse schemes to extract the dynamics. The DFWM beams are configured in a folded boxcar geometry, producing a spatially separated, background-free, femtosecond signal pulse. Aspects of the technique, such as absorption, are investigated. We have taken advantage of the relatively broad spectral width of the fs pulses and extended the techniques to two-color grating experiments in the gas phase. The unimolecular system, NaI, provided a means of testing this new approach. Our experimental observations of the wave packet motion are in excellent agreement with results obtained using laser-induced fluorescence (LIF). A control experiment was also performed on this system, demonstrating ...