Search results for "attosecond"

Attosecond Soft-X-Ray Spectroscopy in a Transition Metal Dichalcogenide

2019

Information about the real-time response of carriers to optical fields is paramount to advance information processing or to understand the bottlenecks of light-matter interaction and energy harvesting. Transition-metal dichalcogenide (TMDC) compounds are an emerging class of materials with attractive structural and electronic properties that can be thinned to the 2D limit and TiS 2 is a paradigmatic example for a semi-metallic TMDC, since its electron mobility ranges between that of a metal and a semiconductor.

Bremsstrahlung from a repulsive potential: attosecond pulse generation

2008

The collision of an electron against a repulsive potential in the presence of a laser field is investigated. It is found that a sufficiently strong laser field forces the electron to remain in the neighbourhood of the repulsive potential causing bremsstrahlung. By appropriately filtering the emitted signal, an electron in the presence of a repulsive potential is capable of generating attosecond pulses.

Efficient attosecond pulse generation from HHG spectra

2015

Ab Initio Simulation of Attosecond Transient Absorption Spectroscopy in Two-Dimensional Materials

2018

We extend the first-principles analysis of attosecond transient absorption spectroscopy to two-dimensional materials. As an example of two-dimensional materials, we apply the analysis to monolayer hexagonal boron nitride (h-BN) and compute its transient optical properties under intense few-cycle infrared laser pulses. Nonadiabatic features are observed in the computed transient absorption spectra. To elucidate the microscopic origin of these features, we analyze the electronic structure of h-BN with density functional theory and investigate the dynamics of specific energy bands with a simple two-band model. Finally, we find that laser-induced intraband transitions play a significant role in…

Attosecond state-resolved carrier motion in quantum materials probed by soft x-ray XANES

2021

Recent developments in attosecond technology led to tabletop X-ray spectroscopy in the soft X-ray range, thus uniting the element- and state-specificity of core-level x-ray absorption spectroscopy with the time resolution to follow electronic dynamics in real time. We describe recent work in attosecond technology and investigations into materials such as Si, SiO2, GaN, Al2O3, Ti, TiO2, enabled by the convergence of these two capabilities. We showcase the state-of-the-art on isolated attosecond soft x-ray pulses for x-ray absorption near edge spectroscopy (XANES) to observe the 3d-state dynamics of the semi-metal TiS2 with attosecond resolution at the Ti L-edge (460 eV). We describe how the …

Tailored pump-probe transient spectroscopy with time-dependent density-functional theory: controlling absorption spectra

2016

Recent advances in laser technology allow us to follow electronic motion at its natural time-scale with ultra-fast time resolution, leading the way towards attosecond physics experiments of extreme precision. In this work, we assess the use of tailored pumps in order to enhance (or reduce) some given features of the probe absorption (for example, absorption in the visible range of otherwise transparent samples). This type of manipulation of the system response could be helpful for its full characterization, since it would allow us to visualize transitions that are dark when using unshaped pulses. In order to investigate these possibilities, we perform first a theoretical analysis of the non…

Attosecond control of dissociative ionization of O2molecules

2011

We demonstrate that dissociative ionization of O(2) can be controlled by the relative delay between an attosecond pulse train (APT) and a copropagating infrared (IR) field. Our experiments reveal a dependence of both the branching ratios between a range of electronic states and the fragment angular distributions on the extreme ultraviolet (XUV) to IR time delay. The observations go beyond adiabatic propagation of dissociative wave packets on IR-induced quasistatic potential energy curves and are understood in terms of an IR-induced coupling between electronic states in the molecular ion.

Time- and energy resolved photoemission electron microscopy-imaging of photoelectron time-of-flight analysis by means of pulsed excitations

2010

Abstract The present work enlightens the developments in time- and energy resolved photoemission electron microscopy over the past few years. We describe basic principles of the technique and demonstrate different applications. An energy- and time-filtering photoemission electron microscopy (PEEM) for real-time spectroscopic imaging can be realized either by a retarding field or hemispherical energy analyzer or by using time-of-flight optics with a delay line detector. The latter method has the advantage of no data loss at all as all randomly incoming particles are measured not only by position but also by time. This is of particular interest for pump–probe experiments in the femtosecond an…

A three-colour scheme to generate isolated attosecond pulses

2009

We propose a new scheme to produce isolated attosecond pulses, involving the use of three laser pulses: a fundamental laser field of intensity I = 3.5 × 1014 W cm−2 and of wavelength λ = 820 nm, and two properly chosen weak lasers with wavelengths 1.5λ and 0.5λ. The three lasers have a Gaussian envelope of 36 fs full width at half maximum. The resulting total field is an asymmetric electric field with an isolated peak. We show that a model atom, interacting with the above-defined total field, generates an isolated attosecond pulse as short as 1/10 of a laser period, i.e. approximately 270 as.

Generation of isolated attosecond pulses using unipolar and laser fields

2009

A new scheme to generate isolated attosecond pulses is presented that involves the use of a laser field and of a unipolar field. The laser field has a pulse of intensity I = 1.5×1014 W cm−2 and wavelength λ = 820 nm. The unipolar pulse is an asymmetric pulse consisting of a sharp peak, lasting approximately half a laser period, i.e. nearly 1.4 fs, followed by a long and shallow tail. We show that on combining these two fields, it is possible to generate isolated attosecond pulses as short as 1/10 of a laser period, i.e. approximately 270 as. Moreover, it is argued that this scheme is robust either against small variations of the laser envelope, or against small changes in the delay between …