arXiv subjects

Zohar Amitay

Publications and source records attributed to Zohar Amitay.

At least 19 recordsLinked to original sources

arXiv2025

Cavity-Controlled High Harmonic Generation

Employing non-Hermitian Floquet theory, the strong-field process of high harmonic (HH) generation by a classical continuous-wave field irradiating ground-state atom is discovered to be controllable by placing the irradiated atom inside a single-mode quantum cavity initiated even with a single photon. Judicious cavity coupling of cavity-free photo-induced atomic Floquet states forms polaritonic Floquet states that generate side harmonics around the (standard no-cavity) odd harmonics. The different possible cavity-controlled HH spectra, including also the ones resulting from several cavities in a row, enable attosecond-pulse sequences different from the one produced without a cavity. Moreover, the present study sets the framework and opens the way for further cavity control over the HH generation process as well as over other strong-field processes

quant-ph↗

arXiv2025

Accelerated Hydrogen Exchange Reaction in a Dark Cavity: A Benchmark for Bridging the Gap Between Theory and Experiment

The gas-phase hydrogen exchange reaction (HER) is the most fundamental chemical process for benchmarking quantum reaction dynamics. In this Letter, we focus on controlling HER by means of strong light-matter coupling inside a resonant cavity, an approach often called polariton chemistry. In particular, we focus on the isotopic variation of HER involving collisions between molecular hydrogen H$_2$ and deuterium atom D, i.e., H$_2$+D$\to$HD+H. We find that the asymmetry introduced by the different isotopes, despite being small, enables strong cavity-induced modifications of reaction rates. Outside of the cavity the reaction is as usual D+H${_2}$$\to$DH+H. However, inside the cavity another type of reactions take place where D+H$_2$$\to$DH+H+E$_{photon}$, where E$_{photon}$=$\hbarω_{cav}$. Our results show that HER is an ideal platform to make a significant step toward closing the gap between theory and experiment in polariton chemistry.

physics.chem-ph↗

arXiv2023

Weak-Field Coherent Control of Ultrafast Molecule Making

Coherent control of ultrafast molecule making from colliding reactants is crucial for realizing coherent control of binary photoreactions (CCBP). To handle diverse excitation scenarios, feasibility with both weak and strong fields is essential. We experimentally demonstrate here the weak-field feasibility, achieving it even under thermally hot conditions typical of chemical reactions. The making of KAr molecules from hot pairs of colliding K and Ar atoms via resonance-mediated two-photon excitation is controlled by weak linearly-chirped femtosecond pulses. Negative chirps enhance the yield. Our experimental and ab initio results are in excellent agreement. New routes to CCBP are opened.

physics.chem-ph↗

arXiv2021

Coherent Control of Ultrafast Bond Making and Subsequent Molecular Dynamics: Demonstration of Final-State Branching Ratio Control

Quantum coherent control of ultrafast bond making and the subsequent molecular dynamics is crucial for the realization of a new photochemistry, where a shaped laser field is actively driving the chemical system in a coherent way from the thermal initial state of the reactants to the final state of the desired products. We demonstrate here coherent control over the relative yields of Mg$_2$ molecules that are generated via photoassociation and subsequently photodriven into different groups of final states. The strong-field process involves non-resonant multiphoton femtosecond photoassociation of a pair of thermally hot magnesium atoms into a bound Mg$_{2}$ molecule and subsequent molecular dynamics on electronically excited states. The branching-ratio control is achieved with linearly chirped laser pulses, utilizing the different chirp dependence that various groups of final molecular states display for their post-pulse population. Our study establishes the feasibility of high degree coherent control over quantum molecular dynamics that is initiated by femtosecond photoassociation of thermal atoms.

physics.atom-ph↗

arXiv2015

Coherent control of bond making: The performance of rationally phase-shaped femtosecond laser pulses

The first step in the coherent control of a photoinduced binary reaction is bond making or photoassociation. We have recently demonstrated coherent control of bond making in multi-photon femtosecond photoassociation of hot magnesium atoms, using linearly chirped pulses [Levin et al., arXiv:1411.1542]. The detected yield of photoassociated magnesium dimers was enhanced by positively chirped pulses which is explained theoretically by a combination of purification and chirp-dependent Raman transitions. The yield could be further enhanced by pulse optimization resulting in pulses with an effective linear chirp and a sub-pulse structure, where the latter allows for exploiting vibrational coherences. Here, we systematically explore the efficiency of phase-shaped pulses for the coherent control of bond making, employing a parametrization of the spectral phases in the form of cosine functions. We find up to an order of magnitude enhancement of the yield compared to the unshaped transform-limited pulse. The highly performing pulses all display an overall temporally increasing instantaneous frequency and are composed of several overlapping sub-pulses. The time delay between the first two sub-pulses almost perfectly fits the vibrational frequency of the generated intermediate wavepacket.These findings are in agreement with chirp-dependent Raman transitions and exploitation of vibrational dynamics as underlying control mechanisms.

physics.atom-ph↗

arXiv2014

Coherent Control of Bond Making

We demonstrate for the first time coherent control of bond making, a milestone on the way to coherent control of photo-induced bimolecular chemical reactions. In strong-field multiphoton femtosecond photoassociation experiments, we find the yield of detected magnesium dimer molecules to be enhanced for positively chirped pulses and suppressed for negatively chirped pulses. Our ab initio model shows that control is achieved by purification via Franck-Condon filtering combined with chirp-dependent Raman transitions. Experimental closed-loop phase optimization using a learning algorithm yields an improved pulse that utilizes vibrational coherent dynamics in addition to chirp-dependent Raman transitions. Our results show that coherent control of binary photo-reactions is feasible even under thermal conditions.

physics.atom-ph↗

arXiv2013

Femtosecond two-photon photoassociation of hot magnesium atoms: A quantum dynamical study using thermal random phase wavefunctions

Two-photon photoassociation of hot magnesium atoms by femtosecond laser pulses, creating electronically excited magnesium dimer molecules, is studied from first principles, combining \textit{ab initio} quantum chemistry and molecular quantum dynamics. This theoretical framework allows for rationalizing the generation of molecular rovibrational coherence from thermally hot atoms [L. Rybak \textit{et al.}, Phys. Rev. Lett. {\bf 107}, 273001 (2011)]. Random phase thermal wave functions are employed to model the thermal ensemble of hot colliding atoms. Comparing two different choices of basis functions, random phase wavefunctions built from eigenstates are found to have the fastest convergence for the photoassociation yield. The interaction of the colliding atoms with a femtosecond laser pulse is modeled non-perturbatively to account for strong-field effects.

quant-ph↗

arXiv2011

Generating Molecular Rovibrational Coherence by Two-Photon Femtosecond Photoassociation of Thermally Hot Atoms

The formation of diatomic molecules with rotational and vibrational coherence is demonstrated experimentally in free-to-bound two-photon femtosecond photoassociation of hot atoms. In a thermal gas at a temperature of 1000 K, pairs of magnesium atoms, colliding in their electronic ground state, are excited into coherent superpositions of bound rovibrational levels in an electronically excited state. The rovibrational coherence is probed by a time-delayed third photon, resulting in quantum beats in the UV fluorescence. A comprehensive theoretical model based on ab initio calculations rationalizes the generation of coherence by Franck-Condon filtering of collision energies and partial waves, quantifying it in terms of an increase in quantum purity of the thermal ensemble. Our results open the way to coherent control of a binary reaction.

quant-ph↗

arXiv2009

Studies of collisional dephasing of two-photon excited atomic sodium

Coherence relaxation in Na vapor was studied utilizing a pump-probe method with femtosecond pulses. The coherence was created by the pump pulse, which excited the Na atoms to the 4S state. The atoms were further excited to the 7P state by the probe pulse. As a result a coherent UV radiation was emitted by the atoms. This emission was used to study the relaxation of both the 4S-3S and 7P-3S coherent superpositions. The relaxation is mainly due to collisions with the Ar atoms serving as a buffer gas. Coherence relaxation times and collisional cross-sections for the Na-Ar collision pairs were extracted experimentally.

physics.atom-ph↗

arXiv2009

Symmetry-Based Selective Femtosecond Coherent Control of Transient Two-Photon Absorption

We present and implement a new scheme for independent control of both the final and the transient population utilizing the symmetry properties of the system. By proper pulse shaping, utilizing the invariance of the two-photon absorption to specific phase transformations of the pulse, different time evolutions of the transient population are photo-induced for a given (fixed) final state population. The model system is the Na atom. The work is conducted in the weak-field regime for which the transient two-photon excitation is described by second-order perturbation theory. One most attractive case is the extended family of third-order chirp pulses which control the population build-up duration independently of the final population.

physics.atom-ph↗

arXiv2009

Multiphoton Femtosecond Coherent Control in the Single-Cycle Regime

Coherent control of the atomic two-photon absorption with shaped single-cycle pulses is examined theoretically in the weak-field regime. The control over the stabilized carrier-envelope phase (CEP) of the pulses is determined as a key parameter allowing the full utilization of the ultrabroad pulse spectrum. This bandwidth is sufficient to provide besides the sequential two-photon pathways, additional Raman-type pathways coupling between the ground and the excited states. The interference between the different pathways is efficiently controlled via the control over the CEP. Simplified two-level model is analyzed in the frequency domain where the rational pulse shaping is applied. The developed intuition is applied to atomic Cs and verified by the exact numerical solution of time-dependent Schrodinger equation.

physics.atom-ph↗

arXiv2009

Femtosecond Photo-Induced Multiphoton Analog Computation for Symmetry-Based Pattern Classification

Multiphoton femtosecond coherent control of is used for implementing innovative photo-induced analog coherent computation that generally might be a basis for future "smart hardware". The specific implemented computational task the classification of an unknown sequence into one of the three groups: (i) a constant sequence that is composed of identical numbers, (ii) a sequence that is antisymmetric around a given point, or (iii) neither. The input sequence is encoded into the spectral phases of a broadband femtosecond pulse and the computational task is being carried out by the multiphoton nonlinear response of the irradiated physical system. Here, it is the simultaneous coherent two- and three-photon absorption in atomic sodium (Na). The corresponding computational resources are the manifold of initial-to-final multiphoton excitation pathways photo-induced by the broad spectrum of the irradiating femtosecond pulse. The answer is obtained by measuring only two observables, which are two state-populations excited via the two- and three-photon absorption processes. Hence, the computational task is accomplished in a constant number of operations irrespective of the sequence length. As such, the presented scheme, where the femtosecond pulse serves as a query and the irradiated physical system serves as an oracle, provides a sufficient gain in the computational complexity.

physics.atom-ph↗

arXiv2009

Intermediate-field two-photon absorption enhancement by shaped femtosecond pulses with spectral phases of antisymmetric nature

We demonstrate and study the enhancement of intermediate-field two-photon absorption by shaped femtosecond pulses having spectral phases of antisymmetric nature. The intermediate-field regime corresponds to pulse intensities, where the two-photon absorption is coherently induced by the weak-field nonresonant two-photon transitions as well as by additional resonance-mediated four-photon transitions. It is a regime of significant excitation yields, exceeding the weak-field yields by two orders of magnitudes, reaching about 10-20% population transfer. The considered antisymmetric nature is with respect to one-half of the (initial-to-final) two-photon transition frequency. The corresponding pulse spectrum is detuned from this frequency (the detuning direction is according to the system). We study in detail the coherent interference mechanism leading to the observed enhancement using forth-order frequency-domain perturbative analysis. We also show that, even though the maximal enhancement is achieved with phase patterns of perfect antisymmetry, at high enough intermediate-field intensities absorption enhancement beyond the transform-limited level is still achievable even with patterns having some degree of deviation from perfect antisymmetry. The degree of tolerance to deviations from perfect antisymmetry increases as the pulse intensity increases. The theoretical and experimental model system of the study is atomic sodium. These findings are of particular importance for coherent control scenarios that simultaneously involve multiple excitation channels.

physics.atom-ph↗

arXiv2009

All-optical periodic code matching by a single-shot frequency-domain cross-correlation measurement

Optical single-short measurement of the cross-correlation function between periodic sequences is demonstrated. The sequences are encoded into the broadband ultrashort phase-shaped pulses which are mixed in the nonlinear medium with additional amplitude-shaped narrowband pulse. The spectrum of the resulted four wave mixing signal is measured to provide the cross-correlation function. The high contrast between the values of cross-correlation and auto-correlation (the latter includes also the information of the sequence period) has potential to be employed in the optical implementation of CDMA communication protocol.

physics.atom-ph↗

arXiv2009

Multiphoton Femtosecond Control of Resonance-Mediated Generation of Short-Wavelength Coherent Broadband Radiation

We introduce a new scheme for generating short-wavelength coherent broadband radiation with well-controlled spectral characteristics. It is based on shaping long-wavelength femtosecond pulse to coherently control atomic resonance-mediated (2+1) three-photon excitation to a broad far-from-resonance continuum. Here, the spectrum (central frequency and bandwidth) of deep-ultraviolet coherent broadband radiation generated in Na vapor is experimentally controlled by tuning the linear chirp we apply to the driving phase-shaped near-infrared femtosecond pulse. This is a first step in implementing the full scheme for producing shaped femtosecond pulses at wavelengths down-to the vacuum-ultraviolet range.

physics.atom-ph↗

arXiv2007

NIR Femtosecond Control of Resonance-Mediated Generation of Coherent Broadband UV Emission

We use shaped near-infrared (NIR) pulses to control the generation of coherent broadband ultraviolet (UV) radiation in an atomic resonance-mediated (2+1) three-photon excitation. Experimental and theoretical results are presented for phase controlling the total emitted UV yield in atomic sodium (Na). Based on our confirmed understanding, we present a new simple scheme for producing shaped femtosecond pulses in the UV/VUV spectral range using the control over atomic resonance-mediated generation of third (or higher order) harmonic.

physics.atom-ph↗

arXiv2007

Multi-Channel Selective Femtosecond Coherent Control Based on Symmetry Properties

We present and implement a new scheme for extended multi-channel selective femtosecond coherent control based on symmetry properties of the excitation channels. Here, an atomic non-resonant two-photon absorption channel is coherently incorporated in a resonance-mediated (2+1) three-photon absorption channel. By proper pulse shaping, utilizing the invariance of the two-photon absorption to specific phase transformations of the pulse, the three-photon absorption is tuned independently over order-of-magnitude yield range for any possible two-photon absorption yield. Noticeable is a set of two-photon dark pulses inducing widely-tunable three-photon absorption.

physics.atom-ph↗

arXiv2007

Frequency-Domain Coherent Control of Femtosecond Two-Photon Absorption: Intermediate-Field vs. Weak-Field Regime

Coherent control of femtosecond two-photon absorption in the intermediate-field regime is analyzed in detail in the powerful frequency domain using an extended 4th-order perturbative description. The corresponding absorption is coherently induced by the weak-field non-resonant two-photon transitions as well as by four-photon transitions involving three absorbed photons and one emitted photons. The interferences between these two groups of transitions lead to a difference between the intermediate-field and weak-field absorption dynamics. The corresponding interference nature (constructive or destructive) strongly depends on the detuning direction of the pulse spectrum from half the two-photon transition frequency. The model system of the study is atomic sodium, for which both experimental and theoretical results are obtained. The detailed understanding obtained here serves as a basis for coherent control with rationally-shaped femtosecond pulses in a regime of sizable absorption yields.

physics.atom-ph↗