اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدOrigin of Plateau and Species dependence of Laser-Induced High-Energy Photoelectron Spectra
54
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We analyzed the energy and momentum distributions of laser-induced high-energy photoelectrons of alkali and rare gas atoms. For the plateau electrons with energies above $4U_p$, ($U_p$ is the ponderomotive energy), in the tunneling ionization regime, we showed that they originate from the backscattering of laser-induced returning electrons. Using the differential elastic scattering cross sections between the target ion with emph{free} electrons, we explain experimental observations of whether the plateau electron spectra is flat or steeply descending, and their dependence on species and laser intensity. This quantitative rescattering theory can be used to obtain energy and momentum distributions of plateau electrons without the need of solving the time-dependent Schr{o}dinger equation, but with similar accuracy.
قيم البحث
اقرأ أيضاً
A comprehensive quantitative rescattering (QRS) theory for describing the production of high-energy photoelectrons generated by intense laser pulses is presented. According to the QRS, the momentum distributions of these electrons can be expressed as
the product of a returning electron wave packet with the elastic differential cross sections (DCS) between free electrons with the target ion. We show that the returning electron wave packets are determined mostly by the lasers only, and can be obtained from the strong field approximation. The validity of the QRS model is carefully examined by checking against accurate results from the solution of the time-dependent Schrodinger equation for atomic targets within the single active electron approximation. We further show that experimental photoelectron spectra for a wide range of laser intensity and wavelength can be explained by the QRS theory, and that the DCS between electrons and target ions can be extracted from experimental photoelectron spectra. By generalizing the QRS theory to molecular targets, we discuss how few-cycle infrared lasers offer a promising tool for dynamic chemical imaging with temporal resolution of a few femtoseconds.
Recently, in a strong Coulomb field regime of tunneling ionization an unexpected large enhancement of photoelectron spectra due to the Coulomb field of the atomic core has been identified by numerical solution of time-dependent Schrodinger equation [
Phys. Rev. Lett. textbf{117}, 243003 (2016)] in the upper energy range of the tunnel-ionized direct electrons. We investigate the origin of the enhancement employing a classical theory with Monte Carlo simulations of trajectories, and a quantum theory of Coulomb-corrected strong field approximation based on the generalized eikonal approximation for the continuum electron. Although the quantum effects at recollisions with a small impact parameter yield an overall enhancement of the spectrum relative to the classical prediction, the high energy enhancement itself is shown to have a classical nature and is due to momentum space bunching of photoelectrons released not far from the peak of the laser field. The bunching is caused by a large and nonuniform, with respect to the ionization time, Coulomb momentum transfer at the ionization tunnel exit.
By analyzing ``exact theoretical results from solving the time-dependent Schrodinger equation of atoms in few-cycle laser pulses, we established the general conclusion that differential elastic scattering and photo-recombination cross sections of the
target ion with {em free} electrons can be extracted accurately from laser-generated high-energy electron momentum spectra and high-order harmonic spectra, respectively. Since both electron scattering and photoionization (the inverse of photo-recombination) are the conventional means for interrogating the structure of atoms and molecules, this result shows that existing few-cycle infrared lasers can be implemented for ultrafast imaging of transient molecules with temporal resolution of a few femtoseconds.
In this paper, we discuss the possibility of imaging molecular orbitals from photoelectron spectra obtained via Laser Induced Electron Diffraction (LIED) in linear molecules. This is an extension of our work published recently in Physical Review A te
xtbf{94}, 023421 (2016) to the case of the HOMO-1 orbital of the carbon dioxide molecule. We show that such an imaging technique has the potential to image molecular orbitals at different internuclear distances in a sub-femtosecond time scale and with a resolution of a fraction of an Angstrom.
Ubiquitous to most molecular scattering methods is the challenge to retrieve bond distance and angle from the scattering signals since this requires convergence of pattern matching algorithms or fitting methods. This problem is typically exacerbated
when imaging larger molecules or for dynamic systems with little a priori knowledge. Here, we employ laser-induced electron diffraction (LIED) which is a powerful means to determine the precise atomic configuration of an isolated gas-phase molecule with picometre spatial and attosecond temporal precision. We introduce a simple molecular retrieval method, which is based only on the identification of critical points in the oscillating molecular interference scattering signal that is extracted directly from the laboratory-frame photoelectron spectrum. The method is compared with a Fourier-based retrieval method, and we show that both methods correctly retrieve the asymmetrically stretched and bent field-dressed configuration of the asymmetric top molecule carbonyl sulfide (OCS), which is confirmed by our quantum-classical calculations.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
