Photoelectron angular distributions from strong-field ionization of oriented molecules
Lotte Holmegaard, Jonas L. Hansen, Line Kalhøj, Sofie Louise Kragh, Henrik Stapelfeldt, Frank Filsinger, Jochen Küpper, Gerard Meijer, Darko Dimitrovski, Mahmou… 展开作者
Lotte Holmegaard, Jonas L. Hansen, Line Kalhøj, Sofie Louise Kragh, Henrik Stapelfeldt, Frank Filsinger, Jochen Küpper, Gerard Meijer, Darko Dimitrovski, Mahmoud Abu-samha, Christian P. J. Martiny, Lars Bojer Madsen
The combination of photoelectron spectroscopy and ultrafast light sources is on track to set new standards for detailed interrogation of dynamics and reactivity of molecules. A crucial prerequisite for further progress is the ability to not only detect the electron kinetic energy, as done in traditional photoelectron spectroscopy, but also the photoelectron angular distributions (PADs) in the molecular frame. Here carbonylsulfide (OCS) and benzonitrile molecules, fixed in space by combined laser and electrostatic fields, are ionized with intense, circularly polarized, 30 femtosecond laser pulses. For 1-dimensionally oriented OCS the molecular frame PADs exhibit pronounced anisotropies, perpendicular to the fixed permanent dipole moment, that are absent in PADs from randomly oriented molecules. For 3-dimensionally oriented benzonitrile additional striking structures appear due to suppression of electron emission in nodal planes of the fixed electronic orbitals. Our theoretical analysis, relying on tunneling ionization theory, shows that the PADs reflect nodal planes, permanent dipole moments and polarizabilities of both the neutral molecule and its cation. The calculated results are exponentially sensitive to changes in these molecular properties thereby pointing to exciting opportunities for time-resolved probing of valence electrons dynamics by intense circularly polarized pulses. Molecular frame PADs from oriented molecules will prove important in other contexts notably in emerging free-electron-laser studies where localized inner shell electrons are knocked off by x-ray pulses.
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…
Multiphoton ionization of sodium by laser pulses of 800 nm wavelength and 57 fs duration is studied in the range of laser peak intensities belonging to over-the-barrier ionization regime. Photoelectron momentum distributions (PMD) and the energy spectra are determined numerically by solving the time dependent Schrödinger equation. The calculated spectra agree well with the spectra obtained experimentally by Hart et al. [Phys. Rev. A 93, 063426 (2016)]. The contributions of photoelectrons with different values of the orbital quantum number in the PMD are determined by expanding the photoelectro…
We report measurements on the H$^{+}$ + H$^{+}$ fragmentation channel following direct single-photon double ionization of neutral NH$_{3}$ at 61.5 eV, where the two photoelectrons and two protons are measured in coincidence using 3-D momentum imaging. We identify four dication electronic states that contribute to H$^{+}$ + H$^{+}$ dissociation, based on our multireference configuration-interaction calculations of the dication potential energy surfaces. The extracted branching ratios between these four dication electronic states are presented. Of the four dication electronic states, three disso…
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…
Photoelectron angular distributions of the two-photon ionization of neutral atoms are theoretically investigated. Numerical calculations of two-photon ionization cross sections and asymmetry parameters are carried out within the independent-particle approximation and relativistic second-order perturbation theory. The dependence of the asymmetry parameters on the polarization and energy of the incident light as well as on the angular momentum properties of the ionized electron are investigated. While dynamic variations of the angular distributions at photon energies near intermediate level reso…
We investigate the strong-field ionization of atomic hydrogen in a few-cycle elliptically polarized infrared pulse by solving the time-dependent Schrödinger equation. The dependence of the photoelectron momentum distribution on the pulse intensity, ellipticity, length, envelope, and carrier envelope phase is analyzed. In particular, we explain the variation of the electron offset angle with asymptotic electron energy through the combined action of the field and the Coulomb potential, and demonstrate that low-ellipticity pulses make it possible to access the electron release time.
We consider atomic strong-field ionization in the long-pulse limit for linearly polarized infrared laser fields. We show how nondipole effects in the plane formed by the propagation and polarization directions lead to (i) a shift of the origin of the rings describing the energetically allowed final electron momenta for individual above-threshold ionization channels and (ii) a redistribution in the continuum population on each ring.
We calculate two-dimensional photoelectron momentum distributions and energy spectra after multiphoton ionization of Li atoms subject to intense laser fields in one-photon Rabi-flopping regime. The time-dependent Schrödinger equation is solved within the single-active-electron approximation using a model potential which reproduces accurately the binding energies and dipole matrix elements of the Li atom. Interaction with the external electromagnetic field is treated within the dipole approximation. We show that the Rabi oscillations of the population between the ground $2s$ state and the excit…
Vortex photoelectron holography in strong-field tunneling ionization
School of Physics and Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology（华中科技大学物理科学与技术学院与武汉光电国家研究中心）；Moscow Institute of Physics and Technology（莫斯科物理技术学院）；Institute for Advanced Science, The University of Electro-Communications（电波大学高级科学研究所）；Hubei Fundamental Research Center for Physics（湖北物理基础研究中心）
Recently, in a strong Coulomb field regime of tunneling ionization an unexpected large enhancement of photoelectron spectra due to the Coulomb field of the atomic core has been identified by numerical solution of time-dependent Schrödinger equation [Phys. Rev. Lett. \textbf{117}, 243003 (2016)] in the upper energy range of the tunnel-ionized direct electrons. We investigate the origin of the enhancement employing a classical theory with Monte Carlo simulations of trajectories, and a quantum theory of Coulomb-corrected strong field approximation based on the generalized eikonal approximation fo…
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…
The $\mathrm{X}^+\ ^2Σ_u^+$ ground electronic state of the Mg$_2^+$ ion has been studied by pulsed-field-ionization zero-kinetic-energy (PFI-ZEKE) photoelectron spectroscopy. Rotationally cold Mg$_2$ molecules produced in a laser-ablation supersonic-expansion source were ionized by resonant two-photon absorption from the $\mathrm{X}\ ^1Σ_g^+(v"=0)$ ground vibronic state. The photoelectron spectra of the $v^+=3-14$ vibrational levels of the $\mathrm{X}^+$ state were recorded with rotational resolution and their analysis led to the determination of accurate term values and rotational constants f…
Momentum Distribution of Near-Zero-Energy Photoelectrons in the Strong-Field Tunneling Ionization in the Long Wavelength Limit
研究了波长为3100 nm的超短强激光辐照下氩原子的电离动力学，得到了能量为零的光电子的动量分布。我们发现了一个令人惊讶的积累动量分布对应meV的能量和\textquotedblleft V "状结构在稍大的横动量。半经典模拟表明逃逸电子和剩余离子之间的库仑吸引力在非常大的距离上起着至关重要的作用。通过对经典轨道的追溯，我们发现在一定的场相位和横向速度窗口中产生的隧穿电子是产生显著积累的原因。我们的理论结果与最近的meV分辨的高精度测量是一致的。
Wave-particle duality is an inherent peculiarity of the quantum world. The double-slit experiment has been frequently used for understanding different aspects of this fundamental concept. The occurrence of interference rests on the lack of which-way information and on the absence of decoherence mechanisms, which could scramble the wave fronts. In this letter, we report on the observation of two-center interference in the molecular frame photoelectron momentum distribution upon ionization of the neon dimer by a strong laser field. Postselection of ions, which were measured in coincidence with e…
Time-resolving the birth of photoelectrons in strong-filed ionization with an isolated attosecond pulse
School of Physical Sciences, Great Bay University（大湾大学物理科学学院）；School of Physics and Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology（华中科技大学物理学院与武汉光电国家研究中心）；Research Center for Advanced Optics and Photoelectronics, Department of Physics, College of Science, Shantou University（汕头大学理学院物理系先进光学与光电子学研究中心）
The photoelectric effect describes the ejection of an electron upon absorption of one or several photons. The kinetic energy of this electron is determined by the photon energy reduced by the binding energy of the electron and, if strong laser fields are involved, by the ponderomotive potential in addition. It has therefore been widely taken for granted that for atoms and molecules the photoelectron energy does not depend on the electron's emission direction but theoretical studies have questioned this since 1990. Here we provide experimental evidence, that the energies of photoelectrons emitt…
We show that the combination of two achiral components - atomic or molecular target plus a circularly polarized photon - can yield chirally structured photoelectron angular distributions. For photoionization of CO, the angular distribution of carbon K-shell photoelectrons is chiral when the molecular axis is neither perpendicular nor (anti-)parallel to the light propagation axis. In photo-double-ionization of He, the distribution of one electron is chiral, if the other electron is oriented like the molecular axis in the former case and if the electrons are distinguishable by their energy. In b…
We report two schemes to generate perfect anisotropy in the photoelectron angular distribution of a randomly oriented ensemble of polyatomic molecules. In order to exert full control over the anisotropy of photoelectron emission, we exploit interferences between single-photon pathways and a manifold of resonantly-enhanced two-photon pathways. These are shown to outperform non-sequential $(ω,2ω)$ bichromatic phase control for the example of CHFClBr molecules. We are able to optimize pulses that yield anisotropic photoelectron emission thanks to a very efficient calculation of photoelectron mome…
Strong-field photoelectron momentum imaging of the prototypical biomolecule indole was disentangled in a combined experimental and computational approach. Experimentally, strong control over the molecules enabled the acquisition of photoelectron momentum distributions in the molecular frame for a well-defined, narrow range of incident intensities. A novel, highly efficient semiclassical simulation setup based on the adiabatic tunneling theory quantitatively reproduced these results. Jointly, experiment and computations revealed holographic structures in the asymptotic momentum distributions, w…
We present an experimental and theoretical energy- and angle-resolved study on the photoionization dynamics of non-resonant one-color two-photon single valence ionization of neutral N$_2$ molecules. Using 9.3 eV photons produced via high harmonic generation and a 3-D momentum imaging spectrometer, we detect the photoelectrons and ions produced from one-color two-photon ionization in coincidence. Photoionization of N$_2$ populates the X $^2Σ^+_g$, A $^2Π_u$, and B $^2Σ^+_u$ ionic states of N$_2^+$, where the photoelectron angular distributions associated with the X $^2Σ^+_g$ and A $^2Π_u$ state…
Photoelectron momentum distributions from strong-field ionization of carbonyl sulfide with 800 nm central-wavelength laser pulses at various peak intensities from $4.6$ to $13\times10^{13}$ W/cm$^2$ were recorded and analyzed regarding resonant Rydberg states and photoelectron orbital angular momentum. The evaluation of the differentials of the momentum distributions with respect to the peak intensity highly suppressed the impact of focal volume averaging and allowed for the unambiguous recognition of Freeman resonances. As a result, previously made assignments of photoelectron lines could be …
Wavefunction-splitting or mask method, widely used in the non-relativistic calculations of the photoelectron angular distributions, is extended to the relativistic domain within the dipole approximation. Since the closed-form expressions for the relativistic Volkov states are not available within the dipole approximation, we build such states numerically solving a single second-order differential equation. We calculate the photoelectron energy spectra and angular distributions for highly charged ions under different ionization regimes with both the direct and the relativistic mask methods. We …
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…
High-order above-threshold ionization (HATI) spectrum in IR+XUV two-color laser fields has been investigated. We found that the quantum features corresponding to the absorption of the XUV photon is well illustrated by a peculiar dip structure in the second plateau of the HATI spectrum. By the channel analysis, we show that the angular distribution of the spectrum is attributed to the coherent summation over contributions of different channels, and the dip structure in the spectrum is directly related to the absorption of one XUV photon of the ionized electron during the laser-assisted collisio…
During multi-photon ionization of an atom it is well understood how the involved photons transfer their energy to the ion and the photoelectron. However, the transfer of the photon linear momentum is still not fully understood. Here, we present a time-resolved measurement of linear momentum transfer along the laser pulse propagation direction. Beyond the limit of the electric dipole approximation we observe a time-dependent momentum transfer. We can show that the time-averaged photon radiation pressure picture is not generally applicable and the linear momentum transfer to the photoelectron de…
Photoelectrons, the fast electrons produced in the photoionization of planetary atmospheres, drive transformations in the atmospheric gas that are often inhibited by energy considerations for thermal electrons. The transformations include excitation and ionization of atoms and molecules, which affect the detectability of these gases and constrain the fraction of incident stellar radiation that transforms into heat. To gain insight into these important questions, we build a Monte Carlo model that solves the slowing down of photoelectrons in a gas with arbitrary amounts of H and He atoms and the…
