Search results for "attosecond"
showing 10 items of 22 documents
Use of three detuned lasers to generate isolated attosecond pulses
2010
The dynamics of a one-dimensional atom driven by three-laser fields is investigated. The total electric field is made up of a fundamental laser field of intensity W cm−2 and wavelength λ = 820 nm and two weak lasers with larger wavelengths. The intensity of the two weak fields is with k = 0.25. The frequencies of the weak fields are and , with and . The three lasers have a Gaussian envelope of 72 fs FWHM. It is shown, by numerical computation and using the semiclassical theory of high-harmonic generation, that the atom interacting with this combined field is able to emit an isolated attosecond burst of radiation.
Publisher's Note: “Attosecond state-resolved carrier motion in quantum materials probed by soft x-ray XANES” [Appl. Phys Rev. 8, 011408 (2021)]
2021
Recent developments in attosecond technology led to table-top 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, and 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 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 ele…
First-principles simulations for attosecond photoelectron spectroscopy based on time-dependent density functional theory
2018
We develop a first-principles simulation method for attosecond time-resolved photoelectron spectroscopy. This method enables us to directly simulate the whole experimental processes, including excitation, emission and detection on equal footing. To examine the performance of the method, we use it to compute the reconstruction of attosecond beating by interference of two-photon transitions (RABBITT) experiments of gas-phase Argon. The computed RABBITT photoionization delay is in very good agreement with recent experimental results from [Klünder et al., Phys. Rev. Lett. 106, 143002 (2011)] and [Guénot et al., Phys. Rev. A 85, 053424 (2012)]. This indicates the significance of a fully-consiste…
Piecewise static Hamiltonian for an atom in strong laser field
2009
We show that it is possible to use a piecewise constant Hamiltonian to describe the main features of the dynamics of an atom interacting with a laser field. In particular we show that using this approximation we are able to give a good description of the ionization signal, of the HHG spectra and of the attosecond pulses generated by the radiating electron. Finally, we give an explicit formula to evaluate the ionization rate in the time dependent laser field. This formula, which is a generalization of the Landau formula for the ionization rate of an atom in a static electric field, fairly well reproduces the numerical ionization rates for a broad range of laser frequency and intensity. The m…
Angular harmonic dependence from a 3D-H2+ Molecular Ion
2012
The time-dependent Schroedinger equation of a H2+ molecular ion in the presence of a linearly polarized laser field is numerically solved by means of a split-operator parallel code. The electron, driven by the laser electric field, emits electromagnetic radiation whose HHG spectrum (shown in Figure 1) can be finely controlled by changing the angle between the laser electric field and the molecular axis. The numerical results confirm that the structure of the spectra strongly depends on this angle. In particular the correlation between the laser orientation (with respect to the molecular axis) and the intensity of various harmonic peaks are displayed in Figure 2.
Laser induced ultrafast H2+ dinamic and attosecond generation
2012
We examine the possibility that a H2+ molecular ion driven by a linearly polarized laser field can be considered as a source of attosecond pulses. The emisseion is investigated taking into account the role of the internuclear distance and by changing the angle between the laser field and the molecular axis. We find that the attosecond pulses emission happens when the electron cloud is over one nucleus; on the contrary, when the elctron is travelling between the two nuclei the attosecond emission do not take place.
Attosecond soft-X-ray spectroscopy of a transition metal dichalcogenide material
2019
We use attosecond soft X-ray pulses between 284 eV to 543 eV for orbital-selective and real-time probing of the opto-electronic response of semi metallic TiS2.
Simulating pump-probe photo-electron and absorption spectroscopy on the attosecond time-scale with time-dependent density-functional theory
2013
Molecular absorption and photoelectron spectra can be efficiently predicted with real-time time-dependent density functional theory. We show herein how these techniques can be easily extended to study time-resolved pump-probe experiments, in which a system response (absorption or electron emission) to a probe pulse is measured in an excited state. This simulation tool helps with the interpretation of fast-evolving attosecond time-resolved spectroscopic experiments, in which electronic motion must be followed at its natural timescale. We show how the extra degrees of freedom (pump-pulse duration, intensity, frequency, and time delay), which are absent in a conventional steady-state experimen…
Transient attosecond soft-X-ray spectroscopy in layered semi-metals (Conference Presentation)
2020
X-ray absorption fine-structure (XAFS) spectroscopy is a well-established technique capable of extracting information about a material’s electronic and lattice structure with atomic resolution. While the near-edge region (XANES) of a XAFS spectrum provides information about the electronic configuration, structural information is extracted from the extended XAFS (EXAFS) spectrum, consisting of several hundreds of eV above the absorption edge. With the advent of high harmonic sources, reaching photon energies in soft x-ray (SXR) region, it now becomes possible to connect the spectroscopic capabilities of XAFS to the unprecedented attosecond temporal resolution of a high harmonic source allowi…
Modelling the effect of nuclear motion on the attosecond time-resolved photoelectron spectra of ethylene
2014
arXiv:1403.5408