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Nature Communications

Odd electron wave packets from cycloidal ultrashort laser fields

Stefanie Kerbstadt, Kevin Eickhoff, Tim Bayer, M. Wollenhaupt

Published Feb 8, 2019• 57 citations
Publisher

Abstract

Polarization-tailored bichromatic femtosecond laser fields with cycloidal polarization profiles have emerged as a powerful tool for coherent control of quantum processes. We present an optical scheme to create and manipulate three-dimensional free electron wave packets with arbitrary rotational symmetry by combining advanced supercontinuum pulse shaping with high resolution photoelectron tomography. Here we use carrier-envelope phase-stable polarization-tailored bichromatic (3ω:4ω) counter- and corotating femtosecond laser pulses to generate 7-fold rotational symmetric and asymmetric photoelectron momentum distributions by multiphoton ionization of sodium atoms. To elucidate the physical mechanisms, we investigate the interplay between the symmetry properties of the driving field and the resulting electron wave packets by varying the optical field parameters. Our results show that the symmetry properties of electron wave packets are not fully determined by the field symmetry, but completely described by multipath quantum interference of states with different angular momenta.

DOI
10.1038/s41467-019-08601-7

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Polarization-tailored bichromatic femtosecond laser fields with cycloidal polarization profiles have emerged as a powerful tool for coherent control of quantum processes. We present an optical scheme to create and manipulate three-dimensional free electron wave packets with arbitrary rotational symmetry by combining advanced supercontinuum pulse shaping with high resolution photoelectron tomography. Here we use carrier-envelope phase-stable polarization-tailored bichromatic (3ω:4ω) counter- and corotating femtosecond laser pulses to generate 7-fold rotational symmetric and asymmetric photoelectron momentum distributions by multiphoton ionization of sodium atoms. To elucidate the physical mechanisms, we investigate the interplay between the symmetry properties of the driving field and the resulting electron wave packets by varying the optical field parameters. Our results show that the symmetry properties of electron wave packets are not fully determined by the field symmetry, but completely described by multipath quantum interference of states with different angular momenta.
Abstract We present a three-dimensional (3D) photoelectron wave packet holography scheme based on polarization-tailored trichromatic femtosecond laser pulses for the determination of quantum phases in atomic multiphoton ionization (MPI). Experimentally, we combine supercontinuum polarization pulse shaping with photoelectron tomography for the reconstruction of the 3D photoelectron momentum distribution (PMD). To demonstrate the 3D photoelectron holography scheme, we superimpose a sculptured wave packet encoding a relative continuum phase with a reference wave packet. In particular, we create a sculptured angular momentum superposition wave packet by (2 + 1) resonance-enhanced MPI of potassium atoms using a counter-rotating circularly polarized bichromatic pulse sequence. The sculptured wave packet, consisting of states with different orbital angular momentum quantum numbers, interferes with the reference wave packet generated by direct three-photon ionization with a circularly polarized pulse of the third color. Depending on the circularity of the reference pulse, interference of both wave packets gives rise to 3D photoelectron holograms with c 2 or c 4 rotational symmetry in the laser polarization plane, i.e., in the azimuthal direction. In the polar direction, the azimuthal interference pattern undergoes a phase-shift revealing the relative quantum phase between the p- and f-type continuum partial waves in the sculptured wave packet. We determine the relative continuum phase by fitting the parameters of an analytical model of the hologram to the measured 3D PMD and confirm the result by direct extraction of the continuum phase difference from the polar-angle-dependent azimuthal phase-shift of the photoelectron angular distribution.
We combine bichromatic polarization pulse shaping with photoelectron imaging tomography for time-resolved spatial imaging of ultrafast spin–orbit wave packet (SOWP) dynamics in atoms. Polarization-shaped two-color pump-probe sequences are generated by spectral amplitude and phase modulation of a femtosecond input pulse and used to excite SOWPs in the potassium fine-structure doublet. By selecting different spectral bands for pump and probe pulse, we achieve interference-free detection of the spatiotemporal SOWP dynamics. Using tomographic techniques, we reconstruct the three-dimensional photoelectron momentum distribution (3D-ED) created by the probe pulse. Time-resolved measurement of the 3D-ED reveals the orbital realignment dynamics induced by spin–orbit interaction in the neutral atom.
Atomic and molecular free electron vortices (FEVs), characterized by their spiral-shaped momentum distribution, have recently attracted a great deal of attention due to their varied shapes and their unusual topological properties. Shortly after their theoretical prediction by the single-photon ionization (SPI) of He atoms using pairs of counterrotating circularly polarized attosecond pulses, FEVs have been demonstrated experimentally by the multiphoton ionization (MPI) of alkali atoms using single-color and bichromatic circularly polarized femtosecond pulse sequences. Recently, we reported on the analysis of the experimental results employing a numerical model based on the ab initio solution of the time-dependent Schrödinger equation (TDSE) for a two-dimensional (2D) atom interacting with a polarization-shaped ultrashort laser field. Here, we apply the 2D TDSE model to study molecular FEVs created by SPI and MPI of a diatomic molecule using polarization-tailored single-color and bichromatic femtosecond pulse sequences. We investigate the influence of the coupled electron-nuclear dynamics on the vortex formation dynamics and discuss the effect of CEP- and rotational averaging on the photoelectron momentum distribution. By analyzing how the molecular structure and dynamics is imprinted in the photoelectron spirals, we explore the potential of molecular FEVs for ultrafast spectroscopy.
Phase-shift differences and amplitude ratios of the outgoing sss and ddd continuum wave packets generated by two-photon ionization of helium atoms are determined from the photoelectron angular distributions obtained using velocity map imaging. Helium atoms are ionized with ultrashort extreme-ultraviolet free-electron laser pulses with a photon energy of 20.3, 21.3, 23.0, and 24.3 eV, produced by the SPring-8 Compact SASE Source test accelerator. The measured values of the phase-shift differences are distinct from scattering phase-shift differences when the photon energy is tuned to an excited level or Rydberg manifold. The difference stems from the competition between resonant and non-resonant paths in two-photon ionization by ultrashort pulses. Since the competition can be controlled in principle by the pulse shape, the present results illustrate a new way to tailor the continuum wave packet.
Summary form only given. Angstrom and attosecond control of free electron wave packets is one of the pinnacles of attosecond science. Orthogonally polarized two-color (OTC) laser fields allow to control the motion of field-ionizing electronic wave packets both in time and space[1]. In OTC pulses time and space are connected and thus an attosecond time scale is established in the polarization plane for both the emitted and the re-colliding wave packets[2,3].In this submission, we report on experiments that use OTC pulses for studying atomic single and double ionization. The three-dimensional momentum vector of electrons and ions created by single and double ionization of neon atoms was measured with the COLTRIMS technique as a function of the sub-cycle shape of the OTC pulses. We introduce a concept similar to attosecond streaking that allows reading sub-cycle timing information from the momentum vector of emitted electrons. The concept is then applied to gaining information about the influence of the long-range Coulomb potential on the trajectories of tunneling electrons.Fig.1 (a) shows the measured momentum distributions of electrons correlated with singly ionized neon in the polarization plane of the OTC field with relative phase Δφ between the two color components. The spectra show that the electron emission direction is sensitive to Δφ. Furthermore, the spectra feature a prominent x-shaped central structure and weaker fine-scale modulations due to wave packet interferences. To compare with simulated spectra with strong field approximation (SFA) and solving two-dimensional time-dependent Schrödinger equation (TDSE) with single active electron approximation, we conclude that Coulomb effect plays important role on the spatial distribution of released electron wave packets. In the conference, we will furthermore demonstrate control over the correlation between the two electrons emitted during double ionization upon electron recollision by tuning the shape of the electric field of the OTC pulses on the sub-cycle scale. The results of these experiments are in agreement with theoretical predictions [4].
We propose a scheme to control the shape of the Autler-Townes (AT) doublet in the photoelectron spectrum from atomic resonance-enhanced multiphoton ionization (REMPI). The scheme is based on the interference of two AT doublets created by ionization of the strongly driven atom from the ground and the resonantly excited state using tailored bichromatic femtosecond laser pulses. In this scheme, the quantum phase of the photoelectrons is crucial for the manipulation of the AT doublet. The laser polarization state and the relative optical phase between the two colors are used to manipulate the interference pattern. We develop an analytical model to describe the bichromatic REMPI process and provide a physical picture of the control mechanism. To validate the model, the results are compared to an ab initio calculation based on the solution of the two-dimensional time-dependent Schr\"odinger equation for the nonperturbative interaction of an atom with intense polarization-shaped bichromatic femtosecond-laser pulses. Our results indicate that the control mechanism is robust with respect to the laser intensity, facilitating its experimental observation.