Strong Differential Photoion Circular Dichroism in Strong-Field Ionization of Chiral Molecules
K. Fehre, S. Eckart, M. Kunitski, C. Janke, D. Trabert, M. Hofmann, J. Rist, M. Weller, A. Hartung, L. Ph. H. Schmidt, T. Jahnke, H. Braun, T. Baumert, J. Stohn… 展开作者
K. Fehre, S. Eckart, M. Kunitski, C. Janke, D. Trabert, M. Hofmann, J. Rist, M. Weller, A. Hartung, L. Ph. H. Schmidt, T. Jahnke, H. Braun, T. Baumert, J. Stohner, Ph. V. Demekhin, M. S. Schöffler, R. Dörner
We investigate the differential ionization probability of chiral molecules in the strong field regime as a function of the helicity of the incident light. To this end, we analyze the fourfold ionization of bromochlorofluoromethane (CHBrClF) with subsequent fragmentation into four charged fragments and different dissociation channels of the singly ionized methyloxirane. We observe a variation of the differential ionization probability in a range of several percent. Accordingly, we conclude that the helicity of light is a quantity that should be considered for the theoretical description of the strong field ionization rate of chiral molecules.
Elliptical dichroism is known in atomic photoionization as the difference in the photoelectron angular distributions produced in nonlinear ionization of atoms by left- and right-handed elliptically polarized light. We theoretically demonstrate that the maximum dichroism |Δ_{ED}|=1 always appears in two-photon ionization of any atom if the photon energy is tuned in so that the electron emission is dominantly determined by two intermediate resonances. We propose the two-photon ionization of atomic helium in order to demonstrate this remarkable phenomenon. The maximum elliptical dichroism could b…
Chiral molecules ionized by circularly polarized fields produce a photoelectron current orthogonal to the polarization plane. This current has opposite directions for opposite enantiomers and provides an extremely sensitive probe of molecular handedness. Recently, such photoelectron currents have been measured in the strong-field ionization regime, where they may serve as an ultrafast probe of molecular chirality. Here we provide a mechanism for the emergence of such strong-field photoelectron currents in terms of two propensity rules that link the properties of the initial electronic chiral s…
We consider few-photon ionization of atomic lithium by linearly polarized femtosecond laser pulses, and demonstrate that asymmetries of the electron angular distribution can occur for initially polarized (2p, m=+1) target atoms. The dependence of the photoelectron emission angle relative to the electric field direction is investigated at different laser intensities and wavelengths. The experimental spectra show excellent agreement with numerical solutions of the time-dependent Schroedinger equation. In the perturbative picture, the angular shift is traced back to interferences between partial …
We investigate few-photon ionization of lithium atoms prepared in the polarized 2$p$($m_\ell=\!+1$) state when subjected to femtosecond light pulses with left- or right-handed circular polarization at wavelengths between 665 nm and 920 nm. We consider whether ionization proceeds more favorably for the electric field co- or counter-rotating with the initial electronic current density. Strong asymmetries are found and quantitatively analyzed in terms of "circular dichroism" ($CD$). While the intensity dependence of the measured $CD$ values is rather weak throughout the investigated regime, a ver…
Chirality causes symmetry breaks in a large variety of natural phenomena ranging from particle physics to biochemistry. We investigate one of the simplest conceivable chiral systems, a laser-excited, oriented, effective one-electron Li target. Prepared in a polarized p state with |m|=1 in an optical trap, the atoms are exposed to co- and counter-rotating circularly polarized femtosecond laser pulses. For a field frequency near the excitation energy of the oriented initial state, a strong circular dichroism is observed and the photoelectron energies are significantly affected by the helicity-de…
The two-color above-threshold ionization (ATI) of atoms and ions is investigated for a vortex Bessel beam in the presence of a strong near-infrared (NIR) light field. While the photoionization is caused by the photons from the weak but extreme ultra-violet (XUV) vortex Bessel beam, the energy and angular distribution of the photoelectrons and their sideband structure are affected by the plane-wave NIR field. We here explore the energy spectra and angular emission of the photoelectrons in such two-color fields as a function of the size and location of the target (atoms) with regard to the beam …
Angular distribution of photoelectrons released by the ionization of randomly-oriented molecules with two laser fields of carrier frequencies $ω$ and $2ω$, which are linearly polarized in two mutually-orthogonal directions, is analyzed in the perturbation limit for the case of one- vs two-photon ionization process. In particular, we focus on the recently predicted [Ph.V. Demekhin {\it et al.}, Phys. Rev. Lett. \textbf{121}, 253201 (2018)] forward-backward asymmetry in the photoelectron emission, which is induced by the interference of two fields and depends on the external relative phase betwe…
We experimentally investigate the effects of the linear photon momentum on the momentum distributions of photoions and photoelectrons generated in one-photon ionization in an energy range of 300 eV $\leq~E_γ~\leq$ 40 keV. Our results show that for each ionization event the photon momentum is imparted onto the photoion, which is essentially the system's center of mass. Nevertheless, the mean value of the ion momentum distribution along the light propagation direction is backward-directed by $-3/5$ times the photon momentum. These results experimentally confirm a 90 year old prediction.
In the semiclassical picture of photoionization process in intense laser fields, the ionization rate solely depends on the amplitude of the electric field and the final photoelectron momentum corresponds to the instant of ionization of the photoelectron, however, this picture has never been checked rigorously. Recently an attosecond angular streaking technique based on this semiclassical perspective has been widely applied to temporal measurement of the atomic and molecular dynamics in intense laser fields. We use a Wigner-distribution-like function to calculate the time-emission angle distrib…
We give examples showing that two well-known versions of the S-matrix theory, which describes a nonresonant multiphoton ionization of atoms and ions in intense laser fields, lead to qualitatively different results. The latter refer not only to total ionization rates, but also to energy distributions of photoelectrons, for instance in a polarization plane of the laser field. It should be possible to make an experiment testing predictions of both theories in the near future.
Nonlinear relativistic ionization phenomena induced by a strong linearly polarized laser field are considered. The starting point is the classical relativistic action for a free electron moving in the electromagnetic field created by a strong laser beam. This action has been used to calculate semiclassical transition rates. Simple analytical expressions for the ionization rate, the photoelectron emission velocity and for the drift momentum distribution of the photoelectron have been found. The analytical formulas apply to nonrelativistic bound systems as well as to initial states with an energ…
Photoelectron circular dichroism (PECD) is a fascinating phenomenon both from a fundamental science aspect but also due to its emerging role as a highly sensitive analytic tool for chiral recognition in the gas phase. PECD has been studied with single-photon as well as multi-photon ionization. The latter has been investigated in the short pulse limit with femtosecond laser pulses, where ionization can be thought of as an instantaneous process. In this contribution, we demonstrate that multiphoton PECD still can be observed when using an ultra-violet nanosecond pulse to ionize chiral showcase f…
We demonstrate coherent control over the photoelectron circular dichroism in randomly oriented chiral molecules, based on quantum interference between multiple photoionization pathways. To significantly enhance the chiral signature, we use a finite manifold of indistinguishable $(1+1^\prime)$ REMPI pathways interfering at a common photoelectron energy but probing different intermediate states. We show that this coherent control mechanism maximizes the number of molecular states that constructively contribute to the dichroism at an optimal photoelectron energy and thus outperforms other schemes…
Photoionization of an atom $A$ by a strong laser field in the presence of a spatially well-separated neighboring atom $B$ is considered. The laser field frequency is assumed to lie below the ionization potential of atom $A$ and be resonant with a dipole-allowed transition in atom $B$. In this situation, the ionization may occur either directly by multiphoton absorption from the laser field at the first atomic center. Or via an indirect pathway involving two-center electron-electron correlations, where the neighbor atom $B$ is first photoexcited and, afterwards, transfers its energy upon deexci…
Propylene oxide, a favorite target of experimental and theoretical studies of circular dichroism, was recently discovered in interstellar space, further amplifying the attention to its role in the current debate on protobiological homochirality. In the present work, a photoelectron-photoion-photoion coincidence technique, using an ion-imaging detector and tunable synchrotron radiation in the 18.0-37.0 eV energy range, permits: (i)-to observe six double-ionization fragmentation channels, their relative yields being accounted for about two-thirds by the couple (C2H4+, CH2O+), one-fifth by (C2H3+…
We propose an attosecond XUV-pump IR-probe photoionization protocol that employs pairs of counter-rotating consecutive harmonics and angularly resolved photoelectron detection, thereby providing direct measurement of ionization phases. The present method, which we call circular holographic ionization-phase meter (CHIP), gives also access to the phase of photoemission amplitudes of even-parity continuum states from a single time-delay measurement, since the relative phase of one- and two-photon ionization pathways is imprinted in the photoemission anisotropy. The method is illustrated with \emp…
We photoionize nitrogen molecules with a train of extreme ultraviolet attosecond pulses together with a weak infrared field. We measure the phase of the two-color two-photon ionization transition (molecular phase) for different states of the ion. We observe a 0.76 $π$ shift for the electrons produced in the ionization channels leading to the X$^2 Σ_g^+$, $v'=1$ and $v'=2$ states. We relate this phase shift to the presence of a complex resonance in the continuum. By providing both a high spectral and temporal resolution, this general approach gives access to the evolution of extremely short liv…
Time-delays in the photoionization of molecules are investigated. As compared to atomic ionization, the time-delays expected from molecular ionization present a much richer phenomenon, with a strong spatial dependence due to the anisotropic nature of the molecular scattering potential. We investigate this from a scattering theory perspective, and make use of molecular photoionization calculations to examine this effect in representative homonuclear and hetronuclear diatomic molecules, nitrogen and carbon monoxide. We present energy and angle-resolved maps of the Wigner delay time for single-ph…
Using $He@C_{60}$ as an example, we demonstrate that static potential of the fullerene core essentially alters the cross section of the two-electron ionization differential in one-electron energy $dσ^{++}(ω)/dε$. We found that at high photon energy prominent oscillations appear in it due to reflection of the second, slow electron wave on the $% C_{60}$ shell, which "dies out" at relatively high $ε$ values, of about 2$÷$3 two-electron ionization potentials. The results were presented for ratios $R_{C_{60}}(ω,ε)\equiv dσ^{++}(ω,ε)/dσ^{a++}(ω,ε)$, where $dσ^{a++}(ω,ε)/dε$ is the two-electron diff…
A review of some recently developed methods of calculating multiple differential cross-sections of photoionization and electron impactionization of atoms and molecules having two active electrons is presented. The methods imply original approaches to calculating three-particle Coulomb wave functions. The external complex scaling method and the formalism of the Schroedinger equation with a source in the right-hand side are considered. Efficiency of the time-dependent approaches to the scattering problem, such as the paraxial approximation and the time-dependent scaling, is demonstrated. An orig…
Photoelectron circular dichroism results from one-photon ionization of chiral molecules by circularly polarized light and manifests itself in forward-backward asymmetry of electron emission in the direction orthogonal to the light polarization plane. What is the physical mechanism underlying asymmetric electron ejection? How "which way" information builds up in a chiral molecule and maps into forward-backward asymmetry? We introduce instances of bound chiral wave functions resulting from stationary superpositions of states in a hydrogen atom and use them to show that the chiral response in one…
Nonlinear relativistic ionization phenomena induced by a strong laser radiation with elliptically polarization are considered. The starting point is the classical relativistic action for a free electron moving in the electromagnetic field created by a strong laser beam. The application of the relativistic action to the classical barrier-suppression ionization is briefly discussed. Further the relativistic version of the Landau-Dykhne formula is employed to consider the semiclassical sub-barrier ionization. Simple analytical expressions have been found for: (i) the rates of the strong-field non…
Most large molecules are chiral in their structure: they exist as two enantiomers, which are mirror images of each other. Whereas the rovibronic sublevels of two enantiomers are almost identical, it turns out that the photoelectric effect is sensitive to the absolute configuration of the ionized enantiomer - an effect termed Photoelectron Circular Dichroism (PECD). Our comprehensive study demonstrates that the origin of PECD can be found in the molecular frame electron emission pattern connecting PECD to other fundamental photophysical effects as the circular dichroism in angular distributions…
We continue our studies of the high energy nonrelativistic asymptotics for the photoionization cross section of the systems bound by a central field $V(r)$. We consider the bound states with the orbital momentum $\ell=1$. We show, that as well as for the $s$ states the asymptotics can be obtained without solving of the wave equations for the bound and outgoing electrons. The asymptotics of the cross sections is expressed in terms of the asymptotics of the Fourier transform $V(p)$ of the field and its derivative $V'(p)$ by employing the Lippmann--Schwinger equation. The shape of the energy depe…
Measuring and controlling the ionization dynamics by intense laser fields has recently led to important breakthroughs, from the investigation of tunneling time delays to attosecond molecular imaging by electron holography. In these experiments, extracting the subtle influence of the ionic potential on the departing electrons is of capital importance, and often challenging. Here we show that molecular chirality naturally provides a solution to this issue by breaking the symmetry of the photoionization process along the laser propagation direction. Using counter-rotating bicircular bichromatic l…
The newly developed method of time-of-flight (ToF) momentum microscopy was used to analyse the cold electron emission from a Cs 3D magneto-optical trap (MOT). Three-step resonant photoionization was implemented via two intermediate states (6P3/2 pumped with 852 nm laser and 7S1/2 with 1470 nm) and a tuneable femtosecond Ti:sapphire laser for the final ionization step. The magnetic field of the MOT is switched off during the photoionization step. The natural bandwidth of the fs-laser is reduced to 4 meV using optical spectral filters. Precise tuning of the photon energy makes it possible to obs…
Bichromatic extreme-ultraviolet pulses from a seeded free-electron laser enable us to measure photoelectron angular distribution (PAD) as a function of the relative phase between the different wavelength components. The time-dependent multiconfiguration self-consistent-field (TD-MCSCF) methods are powerful multielectron computation methods to accurately simulate such photoionization dynamics from the first principles. Here we propose a method to evaluate the amplitude and phase of each ionization path, which completely determines the photoionization processes, using TD-MCSCF simulation results…
Understanding the chirality of molecular reaction pathways is essential for a broad range of fundamental and applied sciences. However, the current ability to probe chirality on the time scale of chemical reactions remains very limited. Here, we demonstrate time-resolved photoelectron circular dichroism (TRPECD) with ultrashort circularly polarized vacuum-ultraviolet (VUV) pulses from a table-top source. We demonstrate the capabilities of VUV-TRPECD by resolving the chirality changes in time during the photodissociation of atomic iodine from two chiral molecules. We identify several general ke…
Spin-current correlations in photoionization of chiral molecules
Max-Born-Institut（马克斯·伯恩研究所）；Humboldt University zu Berlin（柏林洪堡大学）；Technion - Israel Institute of Technology（以色列理工学院）；Imperial College London（伦敦帝国理工学院）；Freie Universität Berlin（柏林自由大学）；Technische Universität Berlin（柏林工业大学）
