arXiv subjects

G. G. Xin

Publications and source records attributed to G. G. Xin.

9 recordsLinked to original sources

arXiv2023

Two-Color Attosecond Chronoscope

We study ionization of atoms in strong orthogonal two-color ($ω,2ω$) (OTC) laser fields numerically and analytically. The calculated photoelectron momentum distribution shows two typical structures: a rectangular-like structure and a shoulder-like structure, the positions of which depend on the laser parameters. Using a strong-field model which allows us to quantitatively evaluate the Coulomb effect, we show that these two structures arise from attosecond response of electron inside an atom to light in OTC-induced photoemission. Some simple mappings between the locations of these structures and response time are derived, with which we are able to establish two-color attosecond chronoscope with high resolution for timing electron emission in OTC-based precise manipulation.

physics.atom-ph↗

arXiv2023

Response time of electron inside a molecule to light in strong-field ionization

We study ionization of aligned H$_2^+$ in strong elliptically-polarized laser fields numerically and analytically. The calculated offset angle in photoelectron momentum distribution is several degrees larger for the molecule than a model atom with similar ionization potential at diverse laser parameters. Using a strong-field model that considers the properties of multi-center and single-center Coulomb potentials, we are able to quantitatively reproduce this angle difference between the molecule and the atom. Further analyses based on this model show that the response time of electron to light which is encoded in the offset angle and is manifested as the time spent in tunneling ionization, is about 15 attoseconds longer for the molecule than the atom. This time difference is further enlarged when increasing the internuclear distance of the molecule.

physics.atom-ph↗

arXiv2022

Response time of photoemission at quantum-classic boundary

The response time of the electron to light in photoemission is difficult to define and measure. Tunneling ionization of atoms, a strong-laser-induced photoemission process, provides a semiclassical case for visiting the problem. Here, we show that the response time can be determined at the boundary between quantum and classic. Specifically, tunneling is instantaneous but a finite response time (about 100 attoseconds) is needed for the state of the tunneling electron to evolve into the ionized state around tunnel exit. This time can be well described with a compact expression related to some basic laser and atomic parameters. Moreover, it can be directly mapped to and easily decoded from photoelectron momentum with a simple mapping, allowing an unambiguous measurement. These results shed light on definition and measurement of the response time of photoemission.

physics.atom-ph↗

arXiv2022

Roles of laser ellipticity in attoclock

We study ionization of atoms in strong elliptically-polarized laser fields numerically and analytically. We focus on effects of laser ellipticity on the offset angle in photoelectron momentum distribution. This angle is considered to encode time information of tunneling ionization in attoclock experiments. The calculated offset angle increases with the decrease of ellipticity but the momentum along the major axis of laser polarization related to this angle changes slowly, in agreement with experiments. With a Coulomb-included strong-field model, the scaling laws for ellipticity dependence of this angle and relevant momentum components are obtained, and the ellipticity dependence of Coulomb-induced ionization time lag encoded in this angle is also addressed.

physics.atom-ph↗

arXiv2022

Coulomb scattering inducing time lag in strong-field tunneling ionization

We study ionization of atoms in strong elliptically-polarized laser fields. We focus on the physical origin of the offset angle in the photoelectron momentum distribution and its possible relation to a specific time. By developing a model which is based on strong-field approximation and considers the classical Coulomb scattering, we are able to quantitatively explain recent attoclock experiments in a wide region of laser and atomic parameters. The offset angle can be understood as arising from the scattering of the electron by the ionic potential when the electron exits the laser-Coulomb-formed barrier through tunneling. The scattering time is manifested as the Coulomb-induced ionization time lag and is encoded in the offset angle.

physics.atom-ph↗

arXiv2021

Measuring Coulomb-Induced Ionization Time Lag with a Calibrated Attoclock

Electrons in atoms and molecules can not react immediately to the action of intense laser field. A time lag (about 100 attoseconds) between instants of the field maximum and the ionization-rate maximum emerges. This lag characterizes the response time of the electronic wave function to the strong-field ionization event and has important effects on subsequent ultrafast dynamics of the ionized electron. The absolute time lag is not accessible in experiments. Here, a calibrated attoclock procedure, which is related to a simple Coulomb-induced temporal correction to electron trajectories, is proposed to measure the relative lag of two different ionization events. Using this procedure,the difference (i.e., the relative lag) between the ionization time lags of polar molecules in two consecutive half laser cycles can be probed with a high accuracy.

physics.atom-ph↗

arXiv2020

Tracing origins of asymmetric momentum distribution for polar molecules in strong linearly-polarized laser fields

We study the ionization dynamics of oriented HeH$^+$ in strong linearly-polarized laser fields by numerically solving the time-dependent Schrödinger equation. The calculated photoelectron momentum distributions for parallel orientation show a striking asymmetric structure. With a developed model pertinent to polar molecules, we trace the electron motion in real time. We show that this asymmetric structure arises from the interplay of the Coulomb effect and the permanent dipole in strong laser fields. This structure can be used to probe the degree of orientation which is important in ultrafast experiments for polar molecules. we also check our results for other polar molecules such as CO and BF.

physics.atom-ph↗

arXiv2019

Strong-field double ionization dynamics of vibrating HeH$^+$ versus HeT$^+$

We study double ionization (DI) dynamics of vibrating HeH$^+$ versus its isotopic variant HeT$^+$ in strong laser fields numerically. Our simulations show that for both cases, these two electrons in DI prefer to release together along the H(T) side. At the same time, however, the single ionization (SI) is preferred when the first electron escapes along the He side. This potential mechanism is attributed to the interplay of the rescattering of the first electron and the Coulomb induced large ionization time lag. On the other hand, the nuclear motion increases the contributions of these two electrons releasing together along the He side. This effect differentiates DI of HeH$^+$ from HeT$^+$.

physics.atom-ph↗

arXiv2019

Coulomb-induced ionization time lag after electrons tunnel out of a barrier

After electrons tunnel out of a laser-Coulomb-formed barrier, %formed by the strong laser field and the atomic Coulomb potential, the movement of the tunneling electron can be affected by the Coulomb tail. We show that this Coulomb effect induces a large time difference (longer than a hundred attoseconds) between the exiting time at which the electron exits the barrier and the ionization time at which the electron is free. This large time difference has important influences on strong-field processes such as above-threshold ionization and high-harmonic generation, with remarkably changing time-frequency properties of electron trajectories. Some semi-quantitative evaluations on these influences are addressed, which provide new insight into strong-field physics and give important suggestions on attosecond measurements.

physics.atom-ph↗