Pulse Propagation through Different Materials User-Friendly Simulation Software

High-intensity ultrashort laser pulses are affected by many different effects pass-ing through materials. There is often a need to estimate these effects, especially the impact on the pulse duration and the spectrum. This estimation is not a trivial problem and needs to be simulated numerically. In this report a user-friendly simulation program that simulates the propagation of pulses through several different materials is presented

Phase metrology with multi-cycle two-colour pulses

Strong-field phenomena driven by an intense infrared (IR) laser depend on during what part of the field cycle they are initiated. By changing the sub-cycle character of the laser electric field it is possible to control such phenomena. For long pulses, sub-cycle shaping of the field can be done by adding a relatively weak, second harmonic of the driving field to the pulse. Through constructive and destructive interference, the combination of strong and weak fields can be used to change the probability of a strong-field process being initiated at any given part of the cycle. In order to control sub-cycle phenomena with optimal accuracy, it is necessary to know the phase difference of the strong and the weak fields precisely. If the weaker field is an even harmonic of the driving field, electrons ionized by the field will be asymmetrically distributed between the positive and negative directions of the combined fields. Information about the asymmetry can yield information about the phase difference. A technique to measure asymmetry for few-cycle pulses, called Stereo-ATI (Above Threshold Ionization), has been developed by [Paulus G G, et al 2003 Phys. Rev. Lett. 91]. This paper outlines an extension of this method to measure the phase difference between a strong IR and its second harmonic

Accessing properties of electron wave packets generated by attosecond pulse trains through time-dependent calculations

We present a time-dependent method for calculating the energy-dependent atomic dipole phase that an electron acquires when it is ionized by the absorption of a single ultraviolet photon. Our approach exactly mirrors the method used to experimentally characterize a train of attosecond pulses. In both methods the total electron phase is measured (calculated) via a two-photon interference involving the absorption or emission of an additional infrared photon in the continuum. In our calculation we use a perfect (zero spectral phase) light field and so extract the atomic dipole phase directly from the electron wave packet. We calculate the atomic phase for argon, neon, and helium at low infrared intensities and compare them to previous perturbative calculations. At moderate infrared probe intensities, we find that that the dipole phase can still be reliably determined using two-photon interference, even when higher-order processes are non-negligible. We also show that a continuum structure, in this case a Cooper minimum in argon, significantly affects the probability for infrared absorption and emission over a range of energies around the minimum, even at low infrared intensities. We conclude that well-characterized attosecond pulse trains can be used to examine continuum structures in atoms and molecules. © 2005 The American Physical Society

High-order harmonic generation using a high-repetition-rate turnkey laser

We generate high-order harmonics at high pulse repetition rates using a turnkey laser. High-order harmonics at 400 kHz are observed when argon is used as target gas. In neon we achieve generation of photons with energies exceeding 90 eV ($\sim$13 nm) at 20 kHz. We measure a photon flux of 4.4$\cdot10^{10}$ photons per second per harmonic in argon at 100 kHz. Many experiments employing high-order harmonics would benefit from higher repetition rates, and the user-friendly operation opens up for applications of coherent extreme ultra-violet pulses in new research areas

Ponderomotive shearing for spectral interferometry of extreme-ultraviolet pulses

We propose a novel method for completely characterizing ultrashort pulses at extreme-ultraviolet (XUV) wavelengths by adapting the technique of spectral phase interferometry for direct electric-field reconstruction to this spectral region. Two-electron wave packets are coherently produced by photoionizing atoms with two time-delayed replicas of the XUV pulse. For one of the XUV pulses, photoionization occurs in the presence of a strong infrared pulse that ponderomotively shifts the binding energy, thereby providing the spectral shear needed for reconstruction of the spectral phase of the XUV pulse. © 2003 Optical Society of America

Spatial control of extreme ultraviolet light with opto-optical phase modulation

Extreme-ultraviolet (XUV) light is notoriously difficult to control due to its strong interaction cross-section with media. We demonstrate a method to overcome this problem by using Opto-Optical Modulation guided by a geometrical model to shape XUV light. A bell-shaped infrared light pulse is shown to imprint a trace of its intensity profile onto the XUV light in the far-field, such that a change in the intensity profile of the infrared pulse leads to a change in the shape of the far-field XUV light. The geometrical model assists the user in predicting the effect of a specific intensity profile of the infrared pulse, thus enabling a deterministic process

Macroscopic effects in noncollinear high-order harmonic generation.

We study two-color high-order harmonic generation using an intense driving field and its weak second harmonic, crossed under a small angle in the focus. Employing sum- and difference-frequency generation processes, such a noncollinear scheme can be used to measure and control macroscopic phase matching effects by utilizing a geometrical phase mismatch component, which depends on the noncollinear angle. We further show how spatial phase effects in the generation volume are mapped out into the far field allowing a direct analogy with temporal carrier envelope effects in attosecond pulse generation

Attosecond pulse trains generated using two color laser fields

We investigate the spectral and temporal structure of high harmonic emission from argon exposed to an infrared laser field and its second harmonic. For a wide range of generating conditions, trains of attosecond pulses with only one pulse per infrared cycle are generated. The synchronization necessary for producing such trains ensures that they have a stable pulse-to-pulse carrier envelope phase, unlike trains generated from one color fields, which have two pulses per cycle and a pi phase shift between consecutive pulses. Our experiment extends the generation of phase stabilized few cycle pulses to the extreme ultraviolet regime

Laserteknik berättar elektronernas dramatik

Attofysik handlar om att öppna ögonen för en värld som vi länge vetat fanns men fram till nu inte har kunnat se – elektronernas värld. En värld av ofattbart små och snabba förlopp och fenomen. Utvecklingen av lasertekniken har kommit så långt att vi faktiskt har möjlighet att studera den världen