Extreme ultraviolet attosecond pulses, generated by a process known as laser-induced electron recollision, are a key ingredient for attosecond metrology, providing a tool to precisely initiate and probe subfemtosecond dynamics in atoms, molecules, and solids. However, extending attosecond metrology to scrutinize the dynamics of the inner-shell electrons is a challenge, that is because of the lower efficiency in generating the required soft x-ray (ℏω>300 eV) attosecond bursts. A way around this problem is to use the recolliding electron to directly initiate the desired inner-shell process, instead of using the currently low flux x-ray attosecond sources. Such an excitation process occurs in a subfemtosecond time scale, and may provide the necessary “pump” step in a pump-probe experiment. Here we used a few cycle infrared (λ0≈1800 nm) source and observed direct evidence for inner-shell excitations through the laser-induced electron recollision process. It is the first step toward time-resolved core-hole studies in the keV energy range with subfemtosecond time resolution.

Extreme ultraviolet (XUV) attosecond pulses, generated by a process known as laser-induced electron recollision, are a key ingredient for attosecond metrology, providing a tool to precisely initiate and probe sub-femtosecond dynamics in the microcosms of atoms, molecules and solids[1]. However, with the current technology, extending attosecond metrology to scrutinize the dynamics of the inner-shell electrons is a challenge, that is because of the lower efficiency in generating the required soft x-ray \hbar\omega>300 eV attosecond bursts and the lower absorption cross-sections in this spectral range. A way around this problem is to use the recolliding electron to directly initiate the desired inner-shell process, instead of using the currently low flux x-ray attosecond sources.Such an excitation process occurs in a sub-femtosecond timescale, and may provide the necessary "pump" step in a pump-probe experiment[2]. Here we used a few cycle infrared \lambda_0 1800nm source[3] and observed direct evidences for inner-shell excitations through the laser-induced electron recollision process. It is the first step toward time-resolved core-hole studies in the keV energy range with sub-femtosecond time resolution.

Resonance enhancement of high-order harmonic generation has recently been found in the interaction of intense ultra-short laser pulses with laser ablated plasma plumes. It is a promising route towards the production of an intense and coherent extreme ultraviolet radiation source. However, the mechanism of this resonance enhancement is still not clear. There are two possible explanations; one relies on a better recombination cross-section through an auto-ionization state in the single-atom response. The other, relies on improved phase matchingconditions around the resonance. Here we try to discriminate between these two conjectures by measuring coherence lengths of the harmonics, both on resonance and off resonance. Our findings support the single-atom response hypothesis.

A passively Q-switched diode-pumped Tm:YLF laser with polycrystalline Cr:ZnSe as the saturable absorber is demonstrated for the first time, to the best of our knowledge. By using saturable absorbers with different initial transmission, the maximum pulse energy reached 4.22 mJ with peak power of 162.3 kW for a pulse duration of 26 ns. The maximum output average power amounted to 2.2 W. These results constitute significant improvement from the highest average power, pulse energy and peak power results for the PQS Tm:YLF laser to date.

We produce 1.5 cycle (10.5 fs), 1.2 mJ, 3 kHz carrier-envelope-phase-stable pulses at 2.1 μm carrier wavelength, from a three-stage optical parametric chirped-pulse amplifier system, pumped by an optically synchronized 1.6 ps Yb:YAG thin disk laser. A chirped periodically poled lithium niobate crystal is used to generate the ultrabroad spectrum needed for a 1.5 cycle pulse through difference frequency mixing of spectrally broadened pulse from a Ti:sapphire amplifier. It will be an ideal tool for producing isolated attosecond pulses with high photon energies.

The steering of electron motion in molecules is accessible with waveform-controlled few-cycle laser light and may control the outcome of light-induced chemical reactions. An optical cycle of light, however, is much shorter than the duration of the fastest dissociation reactions, severely limiting the degree of control that can be achieved. To overcome this limitation, we extended the control metrology to the midinfrared studying the prototypical dissociative ionization of D2 at 2.1 μm. Pronounced subcycle control of the directional D+ ion emission from the fragmentation of D2+ is observed, demonstrating unprecedented charge-directed reactivity. Two reaction pathways, showing directional ion emission, could be observed and controlled simultaneously for the first time. Quantum-dynamical calculations elucidate the dissociation channels, their observed phase relation, and the control mechanisms.

Subfemtosecond bursts of extreme ultraviolet radiation, facilitated by a process known as high-order harmonic generation, are a key ingredient for attosecond metrology, providing a tool to precisely initiate and probe ultrafast dynamics in the microcosms of atoms, molecules, and solids. These ultrashort pulses are always, and as a by-product of the way they are generated, accompanied by laser-induced recollisions of electrons with their parent ions. By using a few-cycle infrared (λ0=2.1 μm) driving laser, we were able to directly excite high-energy (\~870 eV) inner-shell electrons through laser-induced electron recollision, opening the door to time-resolved studies of core-level and concomitant multielectron dynamics.

We report the design, implementation, and characterization of a grism-pair stretcher in a near-infrared noncollinear optical parametric chirped-pulse amplifier (OPCPA) that is capable of controlling a bandwidth of 440 nm. Our dynamic dispersion control scheme relies on the grism stretcher working in conjunction with an acousto-optic programmable dispersive filter (Dazzler) to jointly compensate large amount of material dispersion. A spectral interference technique is used to characterize the spectral phase of the grism stretcher. This ultra-broadband device opens up the way to generate sub-2-cycle laser pulses.

We produce carrier-envelope-phase-stable 15.7-fs (2-cycle) 740-μJ pulses at the 2.1-μm carrier wavelength, from a three-stage optical parametric chirped-pulse amplifier system, pumped by an optically synchronized 49-ps 11-mJ Nd:YLF laser. A novel seed pulse spectral shaping method is used to ascertain the true amplified seed energy and the parametric superfluorescence levels.

Spatially uniform electric fields have been used to induce instabilities in liquids and polymers, and to orient and deform ordered phases of block-copolymers. Here we discuss the demixing phase transition occurring in liquid mixtures when they are subject to spatially nonuniform fields. Above the critical value of potential, a phase-separation transition occurs, and two coexisting phases appear separated by a sharp interface. Analytical and numerical composition profiles are given, and the interface location as a function of charge or voltage is found. The possible influence of demixing on the stability of suspensions and on inter-colloid interaction is discussed. ©2009 The Physical Society of Japan

In this paper we demonstrate the use of NIR femtosecond filament for improving the generation of second harmonic using a type I BBO crystal. Using this method the beam propagation factor (M2) of the second harmonic was improved significantly; which led to enhancement of the attainable SH intensity by up to two orders of magnitude. This method can be beneficial for applications demanding high intensities, small spot size or long interaction lengths.

We study the thermodynamic behavior of nonpolar liquid mixtures in the vicinity of curved charged objects, such as electrodes or charged colloids. There is a critical value of charge (or potential), above which a phase-separation transition occurs, and the interface between high- and low-dielectric constant components becomes sharp. Analytical and numerical composition profiles are given, and the equilibrium front location as a function of charge or voltage is found. We further employ a simple Cahn–Hilliard type equation to study the dynamics of phase separation in spatially nonuniform electric fields. We find an exponential temporal relaxation of the demixing front location. We give the dependence of the steady-state location and characteristic time on the charge, mixture composition and ambient temperature. [ABSTRACT FROM AUTHOR]