arXiv subjects

XuanYang Lai

Publications and source records attributed to XuanYang Lai.

8 recordsLinked to original sources

arXiv2024

Attosecond pulse synthesis from high-order harmonic generation in intense squeezed light

High-order harmonic generation (HHG) provides a broad spectral bandwidth for synthesizing attosecond pulses. However, in the current HHG schemes, only part of the harmonics can be phase-locked, which limits the ability to achieve shorter attosecond pulses. Here, we study attosecond pulse synthesis from HHG of an atom driven by an intense quantum light, i.e., squeezed light. It is interestingly found that the harmonics in the whole spectrum can be phase-locked and, by using these harmonics, the width of the synthesized attosecond pulse is greatly reduced. By developing strong-field approximation theory in squeezed light, the physics of the phase-locked harmonic generation throughout the HHG spectrum is revealed and is found to be independent of the target system. Furthermore, we uncover the dependence of the synthesized attosecond pulse width on the squeezing parameter of the squeezed light. Our findings provide a robust tool for obtaining phase-locked harmonics throughout the HHG spectrum for synthesizing short attosecond pulses.

physics.optics↗

arXiv2023

Imaging molecular orbitals with laser-induced electron tunneling spectroscopy

Photoelectron spectroscopy in intense laser fields has proven to be a powerful tool for providing detailed insights into molecular structure. The ionizing molecular orbital, however, has not been reconstructed from the photoelectron spectra, mainly due to the fact that its phase information can be hardly extracted. In this work, we propose a method to retrieve the phase information of the ionizing molecular orbital with laser-induced electron tunneling spectroscopy. By analyzing the interference pattern in the photoelectron spectrum, the weighted coefficients and the relative phases of the constituent atomic orbitals for a molecular orbital can be extracted. With this information we reconstruct the highest occupied molecular orbital of N$_2$. Our work provides a reliable and general approach for imaging of molecular orbitals with the photoelectron spectroscopy.

physics.atom-ph↗

arXiv2020

Holographic detection of parity in atomic and molecular orbitals

We introduce a novel and concise methodology to detect the parity of atomic and molecular orbitals based on photoelectron holography, which is more general than the existing schemes. It fully accounts for the Coulomb distortions of electron trajectories, does not require sculpted fields to retrieve phase information and, in principle, is applicable to a broad range of electron momenta. By comparatively measuring the differential photoelectron spectra from strong-field ionization of N$_{2}$ molecules and their companion atoms of Ar, some photoelectron holography patterns are found to be dephased for both targets. This is well reproduced by the full-dimensional time-dependent Schrödinger equation and the Coulomb quantum-orbit strong-field approximation (CQSFA) simulation. Using the CQSFA, we trace back our observations to different parities of the 3$p$ orbital of Ar and the highest-occupied molecular orbital of N$_{2}$ via interfering Coulomb-distorted quantum orbits carrying different initial phases. This method could in principle be used to extract bound-state phases from any holographic structure, with a wide range of potential applications in recollision physics and spectroscopy.

physics.atom-ph↗

arXiv2020

Laser-induced Electron-Transfer in the Dissociative Multiple Ionization of Argon Dimers

We report on an experimental and theoretical study of the ionization-fragmentation dynamics of argon dimers in intense few-cycle laser pulses with a tagged carrier-envelope phase. We find that a field-driven electron transfer process from one argon atom across the system boundary to the other argon atom triggers sub-cycle electron-electron interaction dynamics in the neighboring atom. This attosecond electron-transfer process between distant entities and its implications manifest themselves as a distinct phase-shift between the measured asymmetry of electron emission curves of the $\text{Ar}^{+}+\text{Ar}^{2+}$ and $\text{Ar}^{2+}+\text{Ar}^{2+}$ fragmentation channels. Our work discloses a strong-field route to controlling the dynamics in molecular compounds through the excitation of electronic dynamics on a distant molecule by driving inter-molecular electron-transfer processes.

physics.atm-clus↗

arXiv2020

Spiral-like Holographic Structures: Unwinding Interference Carpets of Coulomb-Distorted Orbits in Strong-Field Ionization

We unambiguously identify, in experiment and theory, a previously overlooked holographic interference pattern in strong-field ionization, dubbed "the spiral", stemming from two trajectories for which the binding potential and the laser field are equally critical. We show that, due to strong interaction with the core, these trajectories are optimal tools for probing the target \textbf{after} ionization and for revealing obfuscated phases in the initial bound states. The spiral is shown to be responsible for interference carpets, formerly attributed to direct above-threshold ionization trajectories, and we show the carpet-interference condition is a general property due to the field symmetry.

physics.atom-ph↗

arXiv2017

Disentangling intra-cycle interferences in photoelectron momentum distributions using orthogonal two-colour laser fields

We use orthogonally polarized two-colour (OTC) laser pulses to separate quantum paths in multiphoton ionization of Ar atoms. Our OTC pulses consist of 400~nm and 800~nm light at a relative intensity ratio of 10:1. We find a hitherto unobserved interference in the photoelectron momentum distribution, which exhibits a strong dependence on the relative phase of the OTC pulse. Analysis of model calculations reveal that the interference is caused by quantum pathways from non-adjacent quarter cycles.

physics.atom-ph↗

arXiv2017

Near-threshold photoelectron holography beyond the strong-field approximation

We study photoelectron angular distributions (PADs) near the ionization threshold with a newly developed Coulomb quantum-orbit strong-field approximation (CQSFA) theory. The CQSFA simulations present an excellent agreement with the result from time-dependent Schrödinger equation method. We show that the low-energy fan-shaped structure in the PADs corresponds to a subcycle time-resolved holographic structure and stems from the significant influence of the Coulomb potential on the phase of the forward-scattering electron trajectories, which affects different momenta and scattering angles unequally. For the first time, our work provides a direct explanation of how the fan-shaped structure is formed, based on the quantum interference of direct and forward-scattered orbits.

physics.atom-ph↗

arXiv2013

Temporal and spatial interference in molecular above-threshold ionization with elliptically polarized fields

We investigate direct above-threshold ionization in diatomic molecules, with particular emphasis on how quantum interference is altered by a driving field of non-vanishing ellipticity. This interference may be either temporal, i.e., related to ionization events occurring at different times, or spatial, i.e., related to the electron emission at different centers in the molecule. Employing the strong-field approximation and saddle-point methods, we find that, in general, for non-vanishing ellipticity, there will be a blurring of the temporal and spatial interference patterns. The former blurring is caused by the electron velocity component perpendicular to the major polarization axis, while spatial interference is washed out as a consequence either of s-p mixing, or of the temporal dependence of the ionization prefactor. Both types of interference are analyzed in detail in terms of electron trajectories, and specific conditions for which sharp fringes occur are provided.

physics.atom-ph↗