arXiv subjects

Ilya Sh. Averbukh

Publications and source records attributed to Ilya Sh. Averbukh.

At least 19 recordsLinked to original sources

arXiv2026

Direct imaging of enantiomer-specific orientation dynamics in unidirectionally rotating chiral molecules

Selectively controlling the dynamics of molecular enantiomers underlies advances across chemistry, biology, and physics, yet direct imaging of enantiomer-specific motion has so far remained elusive. Here, we image ultrafast enantioselective orientation dynamics in isolated chiral molecules. Unidirectional coherent rotation induced by a femtosecond laser-pulse pair generates equal and opposite out-of-plane orientations of the two enantiomers. Applying this scheme to 2-methyloxirane, we follow the rotational wave packets by time-resolved Coulomb explosion imaging with two orthogonally arranged detectors. The measured angular distributions reveal that the unidirectional rotation is identical for both enantiomers, while the out-of-plane orientations are mirror images that persist through both early-time quasi-classical and quantum dynamics regimes, in quantitative agreement with simulations. We demonstrate that full angular distributions provide richer dynamical information, with some qualitatively different distributions yielding similar orientation factors upon integration. Our approach opens a route to real-time observation and control of chiral dynamics in the gas phase.

physics.chem-ph↗

arXiv2025

Echoes in a parametrically perturbed Kerr-nonlinear oscillator

We study classical and quantum echoes in a Kerr oscillator driven by a frequency-controlling pulsed perturbation. We consider dynamical response to the perturbation for a single coherent state and for Schrödinger cat states constructed as both balanced and imbalanced superpositions of two coherent states. For individual coherent states, we demonstrate that a weak parametric drive yields a long-lived sequence of classical echoes. Cat states are found to exhibit distinct quantum echoes that are sensitive to the initial relative phase and weights of the coherent states in superposition. We examine the effect of dissipation on quantum echoes and quantum revivals of cat states. We demonstrate that, even when dissipation suppresses quantum revivals, quantum echoes can be recovered by properly tuning the timing and strength of the perturbation. These results may be useful for characterizing and mitigating errors of cat qubits.

quant-ph↗

arXiv2023

Enhanced Persistent Orientation of Asymmetric-Top Molecules Induced by Cross-Polarized Terahertz Pulses

We investigate the persistent orientation of asymmetric-top molecules induced by time-delayed THz pulses that are either collinearly or cross polarized. Our theoretical and numerical results demonstrate that the orthogonal configuration outperforms the collinear one, and a significant degree of persistent orientation - approximately 10% at 5 K and nearly 3% at room temperature - may be achieved through parameter optimization. The dependence of the persistent orientation factor on temperature and field parameters is studied in detail. The proposed application of two orthogonally polarized THz pulses is both practical and efficient. Its applicability under standard laboratory conditions lays a solid foundation for future experimental realization of THz-induced persistent molecular orientation.

physics.chem-ph↗

arXiv2022

Ionization-induced Long-lasting Orientation of Symmetric-top Molecules

We theoretically consider the phenomenon of field-free long-lasting orientation of symmetric-top molecules ionized by two-color laser pulses. The anisotropic ionization produces a significant long-lasting orientation of the surviving neutral molecules. The degree of orientation increases with both the pulse intensity and, counterintuitively, with the rotational temperature. The orientation may be enhanced even further by using multiple delayed two-color pulses. The long-lasting orientation may be probed by even harmonic generation or by Coulomb-explosion-based methods. The effect may enable the study of relaxation processes in dense molecular gases, and may be useful for molecular guiding and trapping by inhomogeneous fields.

physics.chem-ph↗

arXiv2022

Echo-enhanced molecular orientation at high temperatures

Ultrashort laser pulses are widely used for transient field-free molecular orientation -- a phenomenon important in chemical reaction dynamics, ultrafast molecular imaging, high harmonics generation, and attosecond science. However, significant molecular orientation usually requires rotationally cold molecules, like in rarified molecular beams, because chaotic thermal motion is detrimental to the orientation process. Here we propose to use the mechanism of the echo phenomenon previously observed in hadron accelerators, free-electron lasers, and laser-excited molecules to overcome the destructive thermal effects and achieve efficient field-free molecular orientation at high temperatures. In our scheme, a linearly polarized short laser pulse transforms a broad thermal distribution in the molecular rotational phase space into many separated narrow filaments due to the nonlinear phase mixing during the post-pulse free evolution. Molecular subgroups belonging to individual filaments have much-reduced dispersion of angular velocities. They are rotationally cold, and a subsequent moderate terahertz (THz) pulse can easily orient them. The overall enhanced orientation of the molecular gas is achieved with some delay, in the course of the echo process combining the contributions of different filaments. Our results demonstrate that the echo-enhanced orientation is an order of magnitude higher than that of the THz pulse alone. The mechanism is robust -- it applies to different types of molecules, and the degree of orientation is relatively insensitive to the temperature. The laser and THz pulses used in the scheme are readily available, allowing quick experimental demonstration and testing in various applications. Breaking the phase space to individual filaments to overcome hindering thermal conditions may find a wide range of applications beyond molecular orientation.

physics.chem-ph↗

arXiv2022

Gradient-based reconstruction of molecular Hamiltonians and density matrices from time-dependent quantum observables

We consider a quantum system with a time-independent Hamiltonian parametrized by a set of unknown parameters $α$. The system is prepared in a general quantum state by an evolution operator that depends on a set of unknown parameters $P$. After the preparation, the system evolves in time, and it is characterized by a time-dependent observable ${\cal O}(t)$. We show that it is possible to obtain closed-form expressions for the gradients of the distance between ${\cal O}(t)$ and a calculated observable with respect to $α$, $P$ and all elements of the system density matrix, whether for pure or mixed states. These gradients can be used in projected gradient descent to infer $α$, $P$ and the relevant density matrix from dynamical observables. We combine this approach with random phase wave function approximation to obtain closed-form expressions for gradients that can be used to infer population distributions from averaged time-dependent observables in problems with a large number of quantum states participating in dynamics. The approach is illustrated by determining the temperature of molecular gas (initially, in thermal equilibrium at room temperature) from the laser-induced time-dependent molecular alignment.

quant-ph↗

arXiv2022

Optimal Selective Orientation of Chiral Molecules Using Femtosecond Laser Pulses

We present a comprehensive study of enantioselective orientation of chiral molecules excited by a pair of delayed cross-polarized femtosecond laser pulses. We show that by optimizing the pulses' parameters, a significant (~ 10%) degree of enantioselective orientation can be achieved at zero and at five kelvin rotational temperatures. This study suggests a set of reasonable experimental conditions for inducing and measuring strong enantioselective orientation. The strong enantioselective orientation and the wide availability of the femtosecond laser systems required for the proposed experiments may open new avenues for discriminating and separating molecular enantiomers.

physics.optics↗

arXiv2022

Femtosecond rotational dynamics of D$_2$ molecules in superfluid helium nanodroplets

Rotational dynamics of D$_2$ molecules inside helium nanodroplets is induced by a moderately intense femtosecond (fs) pump pulse and measured as a function of time by recording the yield of HeD$^+$ ions, created through strong-field dissociative ionization with a delayed fs probe pulse. The yield oscillates with a period of 185 fs, reflecting field-free rotational wave packet dynamics, and the oscillation persists for more than 500 periods. Within the experimental uncertainty, the rotational constant BHe of the in-droplet D$_2$ molecule, determined by Fourier analysis, is the same as Bgas for an isolated D$_2$ molecule. Our observations show that the D$_2$ molecules inside helium nanodroplets essentially rotate as free D$_2$ molecules.

physics.atm-clus↗

arXiv2021

Rotation of polarization of light propagating through a gas of molecular super-rotors

We present a detailed theoretical and experimental study of the rotation of the plane of polarization of light traveling through a gas of fast-spinning molecules. This effect is similar to the polarization drag phenomenon predicted by Fermi a century ago and it is a mechanical analog of the Faraday effect. In our experiments, molecules were spun up by an optical centrifuge and brought to the super-rotor state that retains its rotation for a relatively long time. Polarizability properties of fast-rotating molecules were analyzed considering the rotational Doppler effect and Coriolis forces. We used molecular dynamics simulations to account for intermolecular collisions. We found, both experimentally and theoretically, a nontrivial nonmonotonic time dependence of the polarization rotation angle. This time dependence reflects transfer of the angular momentum from rotating molecules to the macroscopic gas flow, which may lead to the birth of gas vortices. Moreover, we show that the long-term behavior of the polarization rotation is sensitive to the details of the intermolecular potential. Thus, the polarization drag effect appears as a novel diagnostic tool for the characterization of intermolecular interaction potentials and studies of collisional processes in gases.

physics.optics↗

arXiv2021

Visualizing coherent molecular rotation in a gaseous medium

Inducing and controlling the ultrafast molecular rotational dynamics using shaped laser fields is essential in numerous applications. Several approaches exist that allow following the coherent molecular motion in real-time, including Coulomb explosion-based techniques and recovering molecular orientation from the angular distribution of high harmonics. We theoretically consider a non-intrusive optical scheme for visualizing the rotational dynamics in an anisotropic molecular gas. The proposed method allows determining the instantaneous orientation of the principal optical axes of the gas. The method is based on probing the sample using ultra-short circularly polarized laser pulses and recording the transmission image through a vortex wave plate. We consider two example excitations: molecular alignment induced by an intense linearly polarized laser pulse and unidirectional molecular rotation induced by a polarization-shaped pulse. The proposed optical method is promising for visualizing the dynamics of complex symmetric- and asymmetric-top molecules.

physics.optics↗

arXiv2021

Three Dimensional Orientation of Complex Molecules Excited by Two-Color Femtosecond Pulses

We study the excitation of asymmetric-top (including chiral) molecules by two-color femtosecond laser pulses. In the cases of non-chiral asymmetric-top molecules excited by an orthogonally polarized two-color pulse, we demonstrate, classically and quantum mechanically, three-dimensional orientation. For chiral molecules, we show that the orientation induced by a cross-polarized two-color pulse is enantioselective along the laser propagation direction, namely, the two enantiomers are oriented in opposite directions. On the short time scale, the classical and quantum simulations give results that are in excellent agreement, whereas on the longer time scale, the enantioselective orientation exhibits quantum beats. These observations are qualitatively explained by analyzing the interaction potential between the two-color pulse and molecular (hyper-)polarizability. The prospects for utilizing the long-lasting orientation for measuring and using the enantioselective orientation for separating the individual enantiomers are discussed.

physics.optics↗

arXiv2021

Long-Lasting Orientation of Symmetric-top Molecules Excited by Two-Color Femtosecond Pulses

Impulsive orientation of symmetric-top molecules excited by two-color femtosecond pulses is considered. In addition to the well-known transient orientation appearing immediately after the pulse and then reemerging periodically due to quantum revivals, we report the phenomenon of field-free long-lasting orientation. Long-lasting means that the time averaged orientation remains non-zero until destroyed by other physical effects, e.g. intermolecular collisions. The effect is caused by the combined action of the field-polarizability and field-hyperpolarizability interactions. The dependence of degree of long-lasting orientation on temperature and pulse's parameters is considered. The effect can be measured by means of second (or higher-order) harmonic generation, and may be used to control the deflection of molecules traveling through inhomogeneous electrostatic fields.

physics.optics↗

arXiv2021

Observation of mechanical Faraday effect in gas media

We report the experimental observation of the rotation of the polarization plane of light propagating in a gas of fast-spinning molecules (molecular super-rotors). In the observed effect, related to Fermi's prediction of "polarization drag" by a rotating medium, the vector of linear polarization tilts in the direction of molecular rotation due to the rotation-induced difference in the refractive indices for the left and right circularly polarized components. We use an optical centrifuge to bring the molecules in a gas sample to ultrafast unidirectional rotation and measure the polarization drag angles of the order of 0.2 milliradians in a number of gases under ambient conditions. We demonstrate an all-optical control of the drag magnitude and direction, and investigate the robustness of the mechanical Faraday effect with respect to molecular collisions.

physics.atom-ph↗

arXiv2020

Enantioselective Orientation of Chiral Molecules Induced by Terahertz Pulses with Twisted Polarization

Chirality and chiral molecules are key elements in modern chemical and biochemical industries. Individual addressing, and the eventual separation of chiral enantiomers has been and still is an important elusive task in molecular physics and chemistry, and a variety of methods has been introduced over the years to achieve this goal. Here, we theoretically demonstrate that a pair of cross-polarized THz pulses interacting with chiral molecules through their permanent dipole moments induces an enantioselective orientation of these molecules. This orientation persists for a long time, exceeding the duration of the THz pulses by several orders of magnitude, and its dependency on temperature and pulses' parameters is investigated. The persistent orientation may enhance the deflection of the molecules in inhomogeneous electromagnetic fields, potentially leading to viable separation techniques.

physics.optics↗

arXiv2020

Echoes in Unidirectionally Rotating Molecules

Abstract We report the experimental observation of molecular unidirectional rotation (UDR) echoes, and analyze their origin and behavior both classically and quantum mechanically. The molecules are excited by two time-delayed polarization-twisted ultrashort laser pulses and the echoes are measured by exploding the molecules and reconstructing their spatial orientation from the detected recoil ions momenta. Unlike alignment echoes which are induced by linearly polarized pulses, here the axial symmetry is broken by the twisted polarization, giving rise to molecular unidirectional rotation. We find that the rotation sense of the echo is governed by the twisting sense of the second pulse even when its intensity is much weaker than the intensity of the first pulse. In our theoretical study, we rely on classical phase space analysis and on three-dimensional quantum simulations of the laser-driven molecular dynamics. Both approaches nicely reproduce the experimental results. Echoes in general, and the unique UDR echoes in particular, provide new tools for studies of relaxation processes in dense molecular gases.

physics.optics↗

arXiv2020

Long-lasting Molecular Orientation Induced by a Single Terahertz Pulse

Control of molecular rotations by laser fields is an active area of research focusing on the alignment/orientation of otherwise isotropic molecular samples. Oriented molecules are useful in many applications, such as molecular orbital tomography, femtosecond imaging of molecular structure, dynamics and chemical reaction control. In this work, we present a novel, previously unreported phenomenon appearing in thermal ensembles of non-linear polar molecules excited by a single THz pulse. We find that the induced orientation lasts long after the excitation pulse is over. In the case of symmetric-top molecules, the ensemble averaged orientation remains indefinitely constant after the pulse, whereas in the case of asymmetric-top molecules the orientation persists for a long time after the end of the pulse. We discuss the underlying mechanism, study its non-monotonous temperature dependence, and show that there exists an optimal temperature for the maximal residual orientation. The persistent orientation implies long lasting macroscopic dipole moment, which may be probed by second (or higher order) harmonic generation.

physics.chem-ph↗

arXiv2019

Optical imaging of coherent molecular rotors

Short laser pulses are widely used for controlling molecular rotational degrees of freedom and inducing molecular alignment, orientation, unidirectional rotation and other types of coherent rotational motion. To follow the ultra-fast rotational dynamics in real time, several techniques for producing molecular movies have been proposed based on the Coulomb explosion of rotating molecules, or recovering molecular orientation from the angular distribution of high-harmonics. The present work offers and demonstrates a novel non-destructive optical method for direct visualization and recording of movies of coherent rotational dynamics in a molecular gas. The technique is based on imaging the time-dependent polarization dynamics of a probe light propagating through a gas of coherently rotating molecules. The probe pulse continues through a radial polarizer, and is then recorded by a camera. We illustrate the technique by implementing it with two examples of time-resolved rotational dynamics: alignment-antialignment cycles in a molecular gas excited by a single linearly polarized laser pulse, and unidirectional molecular rotation induced by a pulse with twisted polarization. This method may open new avenues in studies on fast chemical transformation phenomena and ultrafast molecular dynamics caused by strong laser fields of various complexities.

physics.optics↗

arXiv2019

Giant Polarization Drag in a Gas of Molecular Superrotors

Experiments on light dragging in a moving medium laid the cornerstones of modern physics more than a century ago, and they still are in the focus of current research. When linearly polarized light is transmitted through a rotating dielectric, the polarization plane is slightly rotated -- a phenomenon first studied by Fermi in 1923. For typical non-resonant dielectric materials, the measured polarization drag angle does not surpass several microradians. Here we show that this effect may be dramatically enhanced if the light is sent to a gas of fast unidirectionally spinning molecular superrotors. Several femtosecond-laser labs have already succeeded in optically creating such a medium. We show that the specific rotation power of the superrotor medium exceeds the values previously observed in mechanically rotated bulk optical specimens by many orders of magnitude. This nonreciprocal opto-mechanical phenomenon may open new avenues for ultra-fast control of the polarization state of light.

physics.optics↗