arXiv subjects

Zhao-Han Zhang

Publications and source records attributed to Zhao-Han Zhang.

6 recordsLinked to original sources

arXiv2025

Coherent Control of Ion-Photoelectron Dynamics through Rabi Oscillations: An ab initio study

We present first-principles numerical simulations of photoionization in neon induced by bichromatic extreme ultraviolet pulses with frequencies $\omega$ and $2\omega$, specially chosen to make $\omega$ equal to the energy difference between the $2s$ and $2p$ subshells. This allows for the production of photoelectrons from the $2s$ shell by $2\omega$ pulse and from the $2p$ shell by $\omega$ pulse with the same energy. Using the multi-configurational time-dependent Hartree-Fock method, we explore how Rabi coupling between subshells generates coherence between the corresponding photoelectron wave packets. Our \textit{ab initio} calculations confirm the analytical results derived from the essential-states approach in [K. L. Ishikawa, K. C. Prince, and K. Ueda, J. Phys. Chem. A 127, 10638 (2023)], validating the theoretical predictions. Although we focus on the Ne $2p$ and $2s$ subshells, our approach is applicable to a broad range of systems exhibiting photoionization from multiple subshells. The laser parameters employed in our simulations are available in modern Free Electron Lasers (FELs), and we anticipate that this work could stimulate experimental investigations using FELs to study ion-photoelectron coherence and entanglement.

physics.atom-ph↗

arXiv2025

Time-dependent Hole States in Multiconfigurational Time-Dependent Hartree-Fock Approaches: A Time-Domain Generalization of Extended Koopmans' Theorem

We introduce a framework for resolving electron-hole dynamics within wavefunction-based multiconfigurational time-dependent Hartree-Fock (MCTDHF) theory. Central to this framework is a time-domain generalization of the extended Koopmans' theorem, which rigorously defines time-dependent hole states through single-electron removal. From this foundation, we prove the existence of exact equations of motion for time-dependent Dyson orbitals, enabling instantaneous construction of photofragments' reduced density matrices. The formalism further yields a systematic procedure to extract hole-resolved observables, such as channel-resolved photoelectron momentum distributions, directly from time-dependent \textit{ab initio} wavefunctions. As a demonstration, we employ an attosecond $\omega-2\omega$ laser strategy to control hole dynamics, thereby resolving a long-standing challenge in MCTDHF simulations. This advance opens a pathway for exploring correlated multielectron dynamics in atoms and molecules under ultrafast laser fields.

physics.atom-ph↗

arXiv2025

Time-dependent Hole States in Multiconfigurational Time-Dependent Hartree-Fock Approaches: Applications in Photoionization of Water Molecule

By simulating the real-time multielectron wavefunction with the multi-configurational time-dependent Hartree-Fock (MCTDHF) approach, we conduct an \textit{ab initio} study of the single-photon ionization process of a body-fixed water molecule ($\mathrm{H_2O}$) driven by attosecond pulses. To this end, we present a full-dimensional implementation of the MCTDHF method based on one-center expansions, allowing for the simulation of arbitrarily polarized lasers and multi-center polyatomic potentials. With a rigorous definition of the time-dependent hole state (TDHS) using the time-domain generalization of extended Koopmans' theorem (TD-EKT), we derive the reduced ion density matrix within the MCTDHF framework, which inherently encodes the total and channel-resolved photoionization cross sections of $\mathrm{H_2O}$. The cross sections obtained are benchmarked against existing experimental and theoretical results, validating the TDHS formalism. Furthermore, by adjusting the phase delay and intensity ratio of a pair of orthogonally polarized attosecond pulses, we explore the ultrafast control of attosecond coherence between electronic states of $\mathrm{H_2O^+}$.

physics.atom-ph↗

arXiv2024

Photoelectron Polarization Vortexes in Strong-Field Ionization

The spin polarization of photoelectrons induced by an intense linearly polarized laser field is investigated using numerical solutions of the time-dependent Schrödinger equation in companion with our analytic treatment via the spin-resolved strong-field approximation and classical trajectory Monte Carlo simulations. We demonstrate that, even though the total polarization vanishes upon averaging over the photoelectron momentum, momentum-resolved spin polarization is significant, typically exhibiting a vortex structure relative to the laser polarization axis. The polarization arises from the transfer of spin-orbital coupling in the bound state to the spin-correlated quantum orbits in the continuum. The rescattering of photoelectrons at the atomic core plays an important role in forming the polarization vortex structure, while there is no significant effect of the spin-orbit coupling during the continuum dynamics. Furthermore, spin-polarized electron holography is demonstrated, feasible for extracting fine structural information about the atom.

physics.atom-ph↗

arXiv2022

Ultrafast Two-electron Orbital Swap in Li Initiated by Attosecond pulses

A universal mechanism of ultrafast two-electron orbital swap is discovered through two-photon sequential double ionization of Li. After a $1s$ electron in Li is ionized by absorbing an EUV photon, the other two bound electrons located on two different shells have either parallel or antiparallel spin orientations. In the latter case, these two electrons are in the superposition of the singlet and triplet states with different energies, forming a quantum beat and giving rise to the two-electron orbital swap with a period of several hundred attoseconds. The orbital swap mechanism can be used to manipulate the spin polarization of photoelectron pairs by conceiving the attosecond-pump attosecond-probe strategy, and thus serves as a knob to control spin-resolved multielectron ultrafast dynamics.

physics.atom-ph↗

arXiv2019

Robust Strategies for Affirming Kramers-Henneberger Atoms

Atoms exposed to high-frequency strong laser fields experience the ionization suppression due to the deformation of Kramers-Henneberger (KH) wave functions, which has not been confirmed yet in experiment. We propose a bichromatic pump-probe strategy to affirm the existence of KH states, which is formed by the pump pulse and ionized by the probe pulse. In the case of the single-photon ionization triggered by a vacuum ultra-violet probe pulse, the double-slit structure of KH atom is mapped to the photoelectron momentum distribution. In the case of the tunneling ionization induced by an infrared probe pulse, streaking in anisotropic Coulomb potential produces a characteristic momentum drift. Apart from bichromatic schemes, the non-Abelian geometric phase provides an alternative route to affirm the existence of KH states. Following specific loops in laser parameter space, a complete spin flipping transition could be achieved. Our proposal has advantages of being robust against focal-intensity average as well as ionization depletion, and is accessible with current laser facilities.

physics.atom-ph↗