arXiv subjects

Serguei Patchkovskii

Publications and source records attributed to Serguei Patchkovskii.

At least 37 records · Page 2Linked to original sources

arXiv2023

Isotopic effects in molecular attosecond photoelectron interferometry

Isotopic substitution in molecular systems can affect fundamental molecular properties including the energy position and spacing of electronic, vibrational and rotational levels, thus modifying the dynamics associated to their coherent superposition. In extreme ultraviolet spectroscopy, the photoelectron leaving the molecule after the absorption of a single photon can trigger an ultrafast nuclear motion in the cation, which can lead, eventually, to molecular fragmentation. This dynamics depends on the mass of the constituents of the cation, thus showing, in general, a significant isotopic dependence. In time-resolved attosecond photoelectron interferometry, the absorption of the extreme ultraviolet photon is accompanied by the exchange of an additional quantum of energy (typically in the infrared spectral range) with the photoelectron-photoion system, offering the opportunity to investigate in time the influence of isotopic substitution on the characteristics of the photoionisation dynamics. Here we show that attosecond photoelectron interferometry is sensitive to isotopic substitution by investigating the two-color photoionisation spectra measured in a mixture of methane (CH$_4$) and deuteromethane (CD$_4$). The isotopic dependence manifests itself in the modification of the amplitude and contrast of the oscillations of the photoelectron peaks generated in the two-color field with the two isotopologues. The observed effects are interpreted considering the differences in the time evolution of the nuclear autocorrelation functions in the two molecules.

physics.atom-ph↗

arXiv2022

Imprinting chirality on atoms using synthetic chiral light fields

Atoms are usually thought of as achiral objects. However, one can construct superpositions of atomic states that are chiral [1]. Here we show how to excite such superpositions with tailored light fields both in the weak-field and strong-field regimes, using realistic laser parameters. First, we use time-dependent Schrodinger equation (TDSE) simulations to demonstrate the creation of a time-dependent bound chiral wavepacket in sodium atoms. Second, we show how the time-dependent handedness of this wavepacket can be probed by photoelectron circular dichroism, in spite of the central symmetry of the core potential. Third, we use TDSE simulations to show how chirality can be directly imprinted on a photoelectron wavepacket created by strong-field ionization and introduce an unambigous chiral measure that allows us to characterize its handedness.

physics.atom-ph↗

arXiv2022

Rydberg Atomic Antenna in Strongly Driven Multi-Electron Atoms

We study the role of intermediate excitations of Rydberg states as an example of Kuchiev's "atomic antenna" in above-threshold ionization of xenon, in particular their effect on the coherence between the spin-orbit-split states of the ion. We focus on the case of a laser frequency close to resonant with the spin-orbit splitting, where a symmetry (parity) argument would preclude any coherence being directly generated by strong-field ionization. Using ab initio simulations of coupled multielectron spin-orbit dynamics in strong laser fields, we show how field-driven rescattering of the trapped Rydberg electrons introduces efficient coupling between the spin-orbit-split channels, leading to substantial coherences, exceeding 10 % for some photon energies.

physics.atom-ph↗

arXiv2022

Theory of nuclear motion in RABBITT spectra

Reconstruction of attosecond beating by interference of two-photon transitions (RABBITT) is a powerful photoelectron spectroscopy, offering direct access to internal dynamics of the target. It is being increasingly applied to molecular systems, but a general, computationally tractable theory of RABBITT spectra in molecules has so far been lacking. We show that under quite general assumptions, RABBITT spectra in molecules can be expressed as a convolution of the vibronic cross-correlation functions and two-electron photoionization matrix elements. We specialize the general expressions to the commonly-encountered special cases. We expect our theory to enable accurate modeling and interpretation of molecular RABBITT spectra in most medium-sized molecules.

physics.chem-ph↗

arXiv2022

General Time-Dependent Configuration-Interaction Singles II: The Atomic Case

We present a specialization of the grid-based implementation of the time-dependent configuration-interaction singles described in the preceding paper (arXiv:2204.09966) to the case of spherical symmetry. We describe the intricate time propagator in detail, and conclude with a few example calculations. Among these, of note are high-resolution photoelectron spectra in the vicinity of the Fano resonances in photoionization of neon, and spin-polarized photoelectrons from xenon, in agreement with recent experiments.

physics.atom-ph↗

arXiv2022

General Time-Dependent Configuration-Interaction Singles I: The Molecular Case

We present a grid-based implementation of the time-dependent configuration-interaction singles method suitable for computing the strong-field ionization of small gas-phase molecules. After outlining the general equations of motion used in our treatment of this method, we present example calculations of strong-field ionization of helium, lithium hydride, water, and ethylene that demonstrate the utility of our implementation. The following companion paper specializes to the case of spherical symmetry, which is applied to various atoms.

physics.chem-ph↗

arXiv2022

Highly spin-polarized multi-GeV electron beams generated by single-species plasma photocathodes

High-gradient and high-efficiency acceleration in plasma-based accelerators has been demonstrated, showing its potential as the building block for a future collider operating at the energy frontier of particle physics. However, generating and accelerating the required spin-polarized beams in such a collider using plasma-based accelerators has been a long-standing challenge. Here we show that the passage of a highly relativistic, high-current electron beam through a single-species (ytterbium) vapor excites a nonlinear plasma wake by primarily ionizing the two outer 6s electrons. Further photoionization of the resultant Yb2+ ions by a circularly polarized laser injects the 4f14 electrons into this wake generating a highly spin-polarized beam. Combining time-dependent Schrodinger equation simulations with particle-in-cell simulations, we show that a sub-femtosecond, high-current (4 kA) electron beam with up to 56% net spin polarization can be generated and accelerated to 15 GeV in just 41 cm. This relatively simple scheme solves the perplexing problem of producing spin-polarized relativistic electrons in plasma-based accelerators.

physics.plasm-ph↗

arXiv2022

Evidence of ac-Stark-shifted resonances in intense two-color circularly polarized laser fields

We report on the appearance of a structure at low energies in the photo-electron momentum distribution of the hydrogen atom exposed to two-color counter-rotating bi-circular laser fields. These structures, which arise due to AC-Stark shifted resonances, break the three-fold symmetry, typical for the $ω-2ω$ bi-circular fields. We discuss the physical origin of this structure in terms of partial-wave interference between direct ionization channels and a resonant pathway, that passes through the AC-Stark shifted state and show how the underlying Rydberg state population depend on the field strength and pulse duration.

physics.atom-ph↗

arXiv2021

In Situ Generation of High-Energy Spin-Polarized Electrons in a Beam-Driven Plasma Wakefield Accelerator

In situ generation of a high-energy, high-current, spin-polarized electron beam is an outstanding scientific challenge to the development of plasma-based accelerators for high-energy colliders. In this Letter we show how such a spin-polarized relativistic beam can be produced by ionization injection of electrons of certain atoms with a circularly polarized laser field into a beam-driven plasma wakefield accelerator, providing a much desired one-step solution to this challenge. Using time-dependent Schrödinger equation (TDSE) simulations, we show the propensity rule of spin-dependent ionization of xenon atoms can be reversed in the strong-field multi-photon regime compared with the non-adiabatic tunneling regime, leading to high total spin-polarization. Furthermore, three-dimensional particle-in-cell (PIC) simulations are incorporated with TDSE simulations, providing start-to-end simulations of spin-dependent strong-field ionization of xenon atoms and subsequent trapping, acceleration, and preservation of electron spin-polarization in lithium plasma. We show the generation of a high-current (0.8 kA), ultra-low-normalized-emittance (~37 nm), and high-energy (2.7 GeV) electron beam within just 11 cm distance, with up to ~31% net spin polarization. Higher current, energy, and net spin-polarization beams are possible by optimizing this concept, thus solving a long-standing problem facing the development of plasma accelerators.

physics.plasm-ph↗

arXiv2021

A comparison of partial atomic charges for electronically excited states

Partial atomic charges are a useful and intuitive concept for understanding molecular properties and chemical reaction mechanisms, showing how changes in molecular geometry can affect the flow of electronic charge within a molecule. However, the use of partial atomic charges remains relatively uncommon in the characterization of excited-state electronic structure. Here we show how well-established partial atomic charge methods perform for interatomic, intermolecular and inter-bond electron transfer in electronically excited states. Our results demonstrate the utility of real-space partial atomic charges for interpreting the electronic structures that arise in excited-state processes. Furthermore, we show how this analysis can be used to demonstrate that analogous electronic structures arise near photochemically relevant conical intersection regions for several conjugated polyenes. Based on our analysis, we find that charges computed using the iterative Hirshfeld approach provide results which are consistent with chemical intuition and are transferable between homologous molecular systems.

physics.chem-ph↗

arXiv2021

Enantiosensitive steering of free-induction decay

Chiral discrimination, a problem of vital importance, has recently become an emerging frontier in ultrafast physics, with remarkable progress achieved in multiphoton and strong-field regimes. Rydberg excitations, unavoidable in the strong-field regime and intentional for few-photon processes, arise in all these approaches. Here we show how to harness this ubiquitous feature by introducing a new phenomenon, enantiosensitive free-induction decay, steered by a tricolour chiral field at a gentle intensity, structured in space and time. We demonstrate theoretically that an excited chiral molecule accumulates an enantiosensitive phase due to perturbative interactions with the tricolour chiral field, resulting in a spatial phase gradient steering the free-induction decay in opposite directions for opposite enantiomers. Our work introduces a general, extremely sensitive, all-optical, enantiosensitive detection technique which avoids strong fields and takes full advantage of recent advances in structuring light.

physics.optics↗

arXiv2021

Generation and characterisation of isolated attosecond pulses at 100kHz repetition rate

The generation of coherent light pulses in the extreme ultraviolet (XUV) spectral region with attosecond pulse durations constitutes the foundation of the field of attosecond science. Twenty years after the first demonstration of isolated attosecond pulses, they continue to be a unique tool enabling the observation and control of electron dynamics in atoms, molecules and solids. It has long been identified that an increase in the repetition rate of attosecond light sources is necessary for many applications in atomic and molecular physics, surface science, and imaging. Although high harmonic generation (HHG) at repetition rates exceeding 100 kHz, showing a continuum in the cut-off region of the XUV spectrum was already demonstrated in 2013, the number of photons per pulse was insufficient to perform pulse characterisation via attosecond streaking, let alone to perform a pump-probe experiment. Here we report on the generation and full characterisation of XUV attosecond pulses via HHG driven by near-single-cycle pulses at a repetition rate of 100 kHz. The high number of 10^6 XUV photons per pulse on target enables attosecond electron streaking experiments through which the XUV pulses are determined to consist of a dominant single attosecond pulse. These results open the door for attosecond pump-probe spectroscopy studies at a repetition rate one or two orders of magnitude above current implementations.

physics.optics↗

arXiv2021

Vibrational relaxation of hot ground state cations of naphthalene

Time-resolved XUV-IR photoion mass spectroscopy of naphthalene conducted with broadband, as well as with wavelength-selected narrowband XUV pulses reveals a rising probability of fragmentation characterized by a lifetime of $92\pm4$~fs. This lifetime is independent of the XUV excitation wavelength and is the same for all low appearance energy fragments recorded in the experiment. Analysis of the experimental data in conjunction with a statistical multi-state vibronic model suggests that the experimental signals track vibrational energy redistribution on the potential energy surface of the ground state cation. In particular, populations of the out-of-plane ring twist and the out-of-plane wave bending modes could be responsible for opening new IR absorption channels leading to enhanced fragmentation.

physics.chem-ph↗

arXiv2020

Time-resolving the UV-initiated photodissociation dynamics of OCS

We present a time-resolved study of the photodissociation dynamics of OCS after UV-photoexcitation at $λ=237$ nm. OCS molecules ($X\,^1Σ^+$) were primarily excited to the $1\,^1\!A''$ and the $2\,^1\!A'$ Renner-Teller components of the $^1Σ^{-}$ and $^1\!Δ$ states. Dissociation into CO and S fragments was observed through time-delayed strong-field ionisation and imaging of the kinetic energy of the resulting CO$^+$ and S$^+$ fragments by intense $790$ nm laser pulses. Surprisingly, fast oscillations with a period of $\sim100$ fs were observed in the S$^+$ channel of the UV dissociation. Based on wavepacket-dynamics simulations coupled with a simple electrostatic-interaction model, these oscillations do not correspond to the known highly-excited rotational motion of the leaving CO$(X\,^1Σ^+,J\gg0)$ fragments, which has a timescale of $\sim140$ fs. Instead, we suggest to assign the observed oscillations to the excitation of vibrational wavepackets in the $2\,^3\!A''$ or $2\,^1\!A''$ states of the molecule that predissociate to form S$(^3\!P_{J})$ photoproducts.

physics.chem-ph↗

arXiv2019

Robust transverse structures in rescattered photoelectron wavepackets and their observable consequences

Initial-state symmetry has been underappreciated in strong-field spectroscopies, where laser fields dominate the dynamics. We demonstrate numerically that the transverse photoelectron phase structure, arising from this symmetry, is robust in strong-field rescattering, and manifests in strong-field photoelectron spectra. Interpretation of rescattering experiments need to take these symmetry effects into account. In turn, transverse photoelectron phase structures may enable attosecond super-resolution imaging with structured electron beams.

physics.atom-ph↗

arXiv2019

Partial covariance two-dimensional mass spectrometry for determination of biomolecular primary structure

Mass spectrometry (MS) is used widely in biomolecular structural analysis and is particularly dominant in the study of proteins. Despite its considerable power, state-of-the-art protein MS frequently suffers from limited reliability of spectrum-to-structure assignments. This could not be solved fully by the dramatic increase in mass accuracy and resolution of modern MS instrumentation or by the introduction of new fragmentation methods. Here we present a new kind of two-dimensional mass spectrometry for high fidelity determination of a biomolecular primary structure based on partial covariance mapping. Partial covariance two-dimensional mass spectrometry (pC-2DMS) detects intrinsic statistical correlations between biomolecular fragments originating from the same or consecutive decomposition events. This enables identification of pairs of ions produced along the same fragmentation pathway of a biomolecule across its entire fragment mass spectrum. We demonstrate that the fragment-fragment correlations revealed by pC-2DMS provide much more specific information on the amino acid sequence and its covalent modifications than the individual fragment mass-to-charge ratios on which standard one-dimensional MS is based. We illustrate the power of pC-2DMS by using it to resolve structural isomers of combinatorially modified histone peptides inaccessible to standard MS.

physics.chem-ph↗

arXiv2019

Time-resolved inner-shell photoelectron spectroscopy: from a bound molecule to an isolated atom

Due to its element- and site-specificity, inner-shell photoelectron spectroscopy is a widely used technique to probe the chemical structure of matter. Here we show that time-resolved inner-shell photoelectron spectroscopy can be employed to observe ultrafast chemical reactions and the electronic response to the nuclear motion with high sensitivity. The ultraviolet dissociation of iodomethane (CH$_3$I) is investigated by ionization above the iodine 4d edge, using time-resolved inner-shell photoelectron and photoion spectroscopy. The dynamics observed in the photoelectron spectra appear earlier and are faster than those seen in the iodine fragments. The experimental results are interpreted using crystal field and spin-orbit configuration interaction calculations, and demonstrate that time-resolved inner-shell photoelectron spectroscopy is a powerful tool to directly track ultrafast structural and electronic transformations in gas-phase molecules.

physics.chem-ph↗

arXiv2018

Electron correlations and pre-collision in the re-collision picture of high harmonic generation

We discuss the seminal three-step model and the recollision picture in the context of high harmonic generation in molecules. In particular, we stress the importance of multi-electron correlation during the first and the third of the three steps of the process: (1) the strong field ionization and (3) the recombination. We point out how accurate account for multi-electron correlations during the third, recombination, step allows one to gauge the importance of pre-collision: the term coined by J. H. Eberly to describe unusual pathways during the first, ionization, step.

physics.atom-ph↗