arXiv subjects

Ofer Neufeld

Publications and source records attributed to Ofer Neufeld.

51 records · Page 3Linked to original sources

arXiv2022

Attosecond magnetization dynamics in non-magnetic materials driven by intense femtosecond lasers

Irradiating solids with ultrashort laser pulses is known to initiate femtosecond timescale magnetization dynamics. However, sub-femtosecond spin dynamics have not yet been observed or predicted. Here, we explore ultrafast light-driven spin dynamics in a highly non-resonant strong-field regime. Through state-of-the-art ab-initio calculations, we predict that a non-magnetic material can be transiently transformed into a magnetic one via dynamical extremely nonlinear spin-flipping processes, which occur on attosecond timescales and are mediated by a combination of multi-photon and spin-orbit interactions. These are non-perturbative non-resonant analogues to the inverse Faraday effect that build up from cycle-to-cycle as electrons gain angular momentum. Remarkably, we show that even for linearly polarized driving, where one does not intuitively expect any magnetic response, the magnetization transiently oscillates as the system interacts with light. This oscillating response is enabled by transverse anomalous light-driven currents in the solid, and typically occurs on timescales of ~500 attoseconds. We further demonstrate that the speed of magnetization can be controlled by tuning the laser wavelength and intensity. An experimental set-up capable of measuring these dynamics through pump-probe transient absorption spectroscopy is outlined and simulated. Our results pave the way for new regimes of ultrafast manipulation of magnetism.

cond-mat.mes-hall↗

arXiv2022

Time- and angle-resolved photoelectron spectroscopy of strong-field light-dressed solids: prevalence of the adiabatic band picture

In recent years, strong-field physics in condensed-matter was pioneered as a novel approach for controlling material properties through laser-dressing, as well as for ultrafast spectroscopy via nonlinear light-matter interactions (e.g. harmonic generation). A potential controversy arising from these advancements is that it is sometimes vague which band-picture should be used to interpret strong-field experiments: the field-free bands, the adiabatic (instantaneous) field-dressed bands, Floquet bands, or some other intermediate picture. We here try to resolve this issue by performing 'theoretical experiments' of time- and angle-resolved photoelectron spectroscopy (Tr-ARPES) for a strong-field laser-pumped solid, which should give access to the actual observable bands of the irradiated material. To our surprise, we find that the adiabatic band-picture survives quite well, up to high field intensities (~10^12 W/cm^2), and in a wide frequency range (driving wavelengths of 4000 to 800nm, with Keldysh parameters ranging up to ~7). We conclude that to first order, the adiabatic instantaneous bands should be the standard blueprint for interpreting ultrafast electron dynamics in solids when the field is highly off-resonant with characteristic energy scales of the material. We then discuss weaker effects of modifications of the bands beyond this picture that are non-adiabatic, showing that by using bi-chromatic fields the deviations from the standard picture can be probed with enhanced sensitivity. Our work outlines a clear band picture for the physics of strong-field interactions in solids, which should be useful for designing and analyzing strong-field experimental observables and also to formulate simpler semi-empirical models.

cond-mat.mtrl-sci↗

arXiv2022

Ab-initio cluster approach for high-harmonic generation in liquids

High harmonic generation (HHG) takes place in all phases of matter. In gaseous atomic and molecular media, it has been extensively studied and is very well-understood. In solids research is ongoing, but a consensus is forming for the dominant microscopic HHG mechanisms. In liquids on the other hand, no established theory yet exit and approaches developed for gases and solids are generally inapplicable, hindering our current understanding. We develop here a powerful and reliable ab-initio cluster-based approach for describing the nonlinear interactions between isotropic bulk liquids and intense laser pulses. The scheme is based on time-dependent density functional theory and utilizes several approximations that make it feasible yet accurate in realistic systems. We demonstrate our approach with HHG calculations in water, ammonia, and methane liquids, and compare the characteristic response of polar and non-polar liquids. We identify unique features in the HHG spectra of liquid methane that could be utilized for ultrafast spectroscopy of its chemical and physical properties: (i) a structural minima at 15-17eV, and (ii) a well-like shape in the perturbative region that is reminiscent of a shape resonance. Our results pave the way to accessible calculations of HHG in liquids and illustrate the unique nonlinear nature of liquid systems.

physics.chem-ph↗

arXiv2022

Probing phonon dynamics with multi-dimensional high harmonic carrier envelope phase spectroscopy

We explore pump-probe high harmonic generation (HHG) from monolayer hexagonal-Boron-Nitride, where a terahertz pump excites coherent optical phonons that are subsequently probed by an intense infrared pulse that drives HHG. We find, through state-of-the-art ab-initio calculations, that the structure of the emission spectrum is attenuated by the presence of coherent phonons, and is no longer comprised of discrete harmonic orders, but rather of a continuous emission in the plateau region. The HHG yield strongly oscillates as a function of the pump-probe delay, corresponding to ultrafast changes in the lattice such as bond compression or stretching. We further show that in the regime where the excited phonon period and the pulse duration are of the same order of magnitude, the HHG process becomes sensitive to the carrier-envelope-phase (CEP) of the driving field, even though the pulse duration is so long that no such sensitivity is observed in the absence of coherent phonons. The degree of CEP sensitivity vs. pump-probe delay is shown to be a highly selective measure for instantaneous structural changes in the lattice, providing a new approach for ultrafast multi-dimensional HHG-spectroscopy. Remarkably, the obtained temporal resolution for phonon dynamics is ~1 femtosecond, which is much shorter than the probe pulse duration because of the inherent sub-cycle contrast mechanism. Our work paves the way towards novel routes of probing phonons and ultrafast material structural changes and provides a mechanism for controlling the high harmonic response.

cond-mat.mtrl-sci↗

arXiv2021

Unambiguous definition of handedness for locally-chiral light

Synthetic chiral light fields were recently introduced as a novel source of chirality [Ayuso et al. Nat. Phot. 13, 866 (2019)]. This locally-chiral light spans a three-dimensional polarization that plots a chiral trajectory in space-time, leading to huge nonlinear chiral signals upon interactions with chiral media. The degree of chirality of this new form of light was defined, characterized, and shown to be proportional to the chiral signal conversion efficiency. However, the sign of the light's chirality - its 'handedness' - has not yet been defined. Standard definitions of helicity are inapplicable for locally-chiral light due to its complex three-dimensional structure. Here, we define an unambiguous handedness for locally-chiral fields and employ it in practical calculations.

physics.optics↗

arXiv2021

Detecting multiple chirality centers in chiral molecules with high harmonic generation

Characterizing chirality is highly important for applications in the pharmaceutical industry, as well as in the study of dynamical chemical and biological systems. However, this task has remained challenging, especially due to the ongoing increasing complexity and size of the molecular structure of drugs and active compounds. In particular, large molecules with many active chirality centers are today ubiquitous, but remain difficult to structurally analyze due to their high number of stereoisomers. Here we theoretically explore the sensitivity of high harmonic generation (HHG) to the chirality of molecules with a varying number of active chiral centers. We find that HHG driven by bi-chromatic non-collinear lasers is a sensitive probe for the stereo-configuration of a chiral molecule. We first show through calculations (from benchmark chiral molecules with up to three chirality centers) that the HHG spectrum is imprinted with information about the handedness of each chirality center in the driven molecule. Next, we show that using both classical- and deep-learning-based reconstruction algorithms, the composition of an unknown mixture of stereoisomers can be reconstructed with high fidelity by a single-shot HHG measurement. Our work illustrates how the combination of non-linear optics and machine learning might open routes for ultra-sensitive sensing in chiral systems.

physics.chem-ph↗

arXiv2021

Multi-scale dynamical symmetries and selection rules in nonlinear optics

Symmetries and their associated selection rules are extremely useful in all fields of science. In particular, for system that include electromagnetic (EM) fields interacting with matter, it has been shown that both of symmetries of matter and EM field's time-dependent polarization play a crucial role in determining the properties of linear and nonlinear responses. The relationship between the system's symmetry and the properties of its excitations facilitate precise control over light emission and enable ultrafast symmetry-breaking spectroscopy of variety of properties. Here. we formulate the first general theory that describes the macroscopic dynamical symmetries (including quasicrystal-like symmetries) of an EM vector field, revealing many new symmetries and selection rules in light-matter interactions. We demonstrate an example of multi-scale selection rules experimentally in the framework of high harmonic generation (HHG). This work waves the way for novel spectroscopic techniques in multi-scale system as well as for imprinting complex structures in EUV-X-ray beams, attosecond pulses, or the interacting medium itself.

physics.optics↗

arXiv2021

Selection rules in symmetry-broken systems by symmetries in synthetic dimensions

Selection rules are often considered a hallmark of symmetry. When a symmetry is broken, e.g., by an external perturbation, the system exhibits selection rule deviations which are often analyzed by perturbation theory. Here, we employ symmetry-breaking degrees of freedom as synthetic dimensions, to demonstrate that symmetry-broken systems systematically exhibit a new class of symmetries and selection rules. These selection rules determine the scaling of a system's observables (to all orders in the strength of the symmetry-breaking perturbation) as it transitions from symmetric to symmetry-broken. We specifically analyze periodically driven (Floquet) systems subject to two driving fields, where the first field imposes a spatio-temporal symmetry, and the second field breaks it, imposing a symmetry in synthetic dimensions. We tabulate the resulting synthetic symmetries for (2+1)D Floquet group symmetries and derive the corresponding selection rules for high harmonic generation (HHG) and above-threshold ionization (ATI). Finally, we observe experimentally HHG selection rules imposed by symmetries in synthetic dimensions. The new class of symmetries & selection rules extends the scope of existing symmetry breaking spectroscopy techniques, opening new routes for ultrafast spectroscopy of phonon-polarization, spin-orbit coupling, and more.

physics.optics↗

arXiv2021

Terahertz driven extremely nonlinear bulk photogalvanic currents in non-resonant conditions

We report on the generation of bulk photocurrents in materials driven by non-resonant bi-chromatic fields that are circularly polarized and co-rotating. The nonlinear photocurrents have a fully controllable directionality and amplitude without requiring carrier-envelope-phase stabilization or few-cycle pulses, and are generated with photon energies much smaller than the band gap (reducing heating in the photo-conversion process). We demonstrate with ab-initio calculations that the photocurrent generation mechanism is universal and arises in gaped materials (Si, diamond, MgO, hBN), in semi-metals (graphene), and in two- and three-dimensional systems. Photocurrents are shown to rely on sub-laser-cycle asymmetries in the nonlinear response that build-up coherently from cycle-to-cycle as the conduction band is populated. Importantly, the photocurrents are always transverse to the major axis of the co-circular lasers regardless of the material's structure and orientation (analogously to a Hall current), which we find originates from a generalized time-reversal symmetry in the driven system. At high laser powers (~10^13 W/cm^2) this symmetry can be spontaneously broken by vast electronic excitations, which is accompanied by an onset of carrier-envelope-phase sensitivity and ultrafast many-body effects. Our results are directly applicable for efficient light-driven control of electronics, and for enhancing sub-band-gap bulk photovoltaic effects.

cond-mat.mtrl-sci↗

arXiv2020

Strong chiral dichroism in above threshold ionization and ionization rates from locally-chiral light

We derive here a new highly selective photoelectron-based chirality-sensing technique that utilizes 'locally-chiral' laser pulses. We show that this approach results in strong chiral discrimination, where the standard forwards/backwards asymmetry of photoelectron circular dichroism (PECD) is lifted. The resulting dichroism is much larger and more robust than conventional PECD, is found in all hemispheres, and is not symmetric or antisymmetric with respect to any symmetry operator. Remarkably, a CD of up to 10% survives in the angularly-integrated above-threshold ionization (ATI) spectra, and of up to 5% in the total ionization rates. We demonstrate these results through ab-initio calculations in the chiral molecules Bromochlorofluoromethane, Limonene, Fenchone, and Camphor. We also explore the parameter-space of the locally-chiral field and show that the observed CD is strongly correlated to the degree of chirality of the light, validating it as a measure for chiral-interaction strengths. Our results pave the way for highly selective probing of ultrafast chirality in ATI, can potentially lead to all-optical enantio-separation, and motivate the use of locally-chiral light for enhancing ultrafast spectroscopies.

physics.chem-ph↗

arXiv2019

On the Quantum-Optical Nature of High Harmonic Generation

High harmonic generation (HHG) is an extremely nonlinear effect, where a medium is driven by a strong laser field, generating coherent broadband radiation with photon energies ranging up to the X-ray and pulse durations reaching attosecond timescales. Conventional models of HHG treat the medium quantum mechanically, while the driving and emitted fields are treated classically. Such models are usually very successful, but inherently cannot capture the quantum-optical nature of the process. Despite prior works considering quantum HHG, it is still not known in what circumstances the spectral and statistical properties of the radiation considerably depart from the known phenomenology of HHG. Finding such regimes in HHG could lead to novel sources of attosecond light with intrinsically quantum statistics such as squeezing and entanglement. In this work, we present a fully quantum electrodynamical theory of extreme nonlinear optics with which we predict new quantum effects that alter both spectral and statistical properties of HHG. We predict the emission of shifted frequency combs resulting from transitions between perturbed states of the driven atom, and identify new spectral features that arise from the breakdown of the dipole approximation for the emission. Moreover, we find that each HHG emitted photon is a superposition of all frequencies in the spectrum - e.g., HHG creates single photon combs. We also describe how the HHG process changes in the single atom regime, and discuss how our various predictions can be tested experimentally. Our approach is also applicable to a wide range of nonlinear optical processes, paving the way toward novel quantum information techniques in the EUV and X-ray, and in ultrafast quantum optics.

physics.optics↗

arXiv2019

Locally and globally chiral fields for ultimate control of chiral light matter interaction

Light is one of the most powerful and precise tools allowing us to control, shape and create new phases of matter. In this task, the magnetic component of a light wave has so far played a unique role in defining the wave's helicity, but its influence on the optical response of matter is weak. Chiral molecules offer a typical example where the weakness of magnetic interactions hampers our ability to control the strength of their chiral optical response. It is limited several orders of magnitude below the full potential. Here we introduce freely propagating locally and globally chiral electric fields, which interact with chiral quantum systems extremely efficiently. To demonstrate the degree of control enabled by such fields, we focus on the nonlinear optical response of randomly oriented chiral molecules. We show full control over intensity, polarization and propagation direction of the chiral optical response, enabling its background-free detection. This response can be fully suppressed or enhanced at will depending on the molecular handedness, achieving the ultimate limit in chiral discrimination. Our findings open a way to extremely efficient control of chiral matter and to ultrafast imaging of chiral structure and dynamics in gases, liquids and solids.

physics.optics↗

arXiv2018

Symmetries and selection rules in Floquet systems: application to harmonic generation in nonlinear optics

Symmetry is one of the most generic and useful concepts in physics and chemistry, often leading to conservation laws and selection rules. For example, symmetry considerations have been used to predict selection rules for transitions in atoms, molecules, and solids. Floquet systems also demonstrate a variety of symmetries which are spatiotemporal (i.e. dynamical symmetries (DSs)). However, the derivation of selection rules from DSs has so far been limited to several ad hoc cases. A general theory for deducing the impact of DSs in physical systems has not been formulated yet. Here we explore symmetries exhibited in Floquet systems using group theory, and discover novel DSs and selection rules. We derive the constraints on a general system's temporal evolution, and selection rules that are imposed by the DSs. As an example, we apply the theory to harmonic generation, and derive tables linking (2+1)D and (3+1)D DSs of the driving laser and medium to allowed harmonic emission and its polarization. We identify several new symmetries and selection rules, including an elliptical DS that leads to production of elliptically polarized harmonics where all the harmonics have the same ellipticity, and selection rules that have no explanation based on currently known conservation laws. We expect the theory to be useful for manipulating the harmonic spectrum, and for ultrafast spectroscopy. Furthermore, the presented Floquet group theory should be useful in various other systems, e.g., Floquet topological insulators and photonic lattices, possibly yielding formal and general classification of symmetry and topological properties.

physics.optics↗

arXiv2018

Highly selective chiral discrimination in high harmonic generation by dynamical symmetry breaking spectroscopy

We propose and numerically demonstrate a new very robust and highly selective method for femtosecond time-resolved chiral spectroscopy using high harmonic generation (HHG). The method is based on dynamical symmetry breaking from chiral media, and relies only on intense electric-dipole transitions, and not on the interplay of electric and magnetic dipoles. The symmetry breaking results in the emission of a strong chiral signal in the form of otherwise 'forbidden' harmonics (i.e., that are not emitted from achiral media). The intensity of these symmetry-forbidden harmonics is directly correlated to the media's enantiomeric excess, yielding chiral selectivity. On the contrary, the strength of the 'allowed' harmonics is chiral-independent, hence they can be used as a reference to provide chiral selectivity from a single measurement, unlike previous time-resolved schemes that require multiple measurements. We demonstrate numerically 96% discrimination level from microscopic gas phase emission, outperforming by far previous time-resolved methods (the selectivity should be further enhanced when the HHG process is phase matched). We expect the new method to give rise to precise table-top characterization of chiral media in the gas-phase, and for highly sensitive time-resolved ultrafast probing of dynamical chiral processes.

physics.optics↗

arXiv2017

Optical chirality in high harmonic generation

Optical chirality (OC) - one of the fundamental quantities of electromagnetic fields - corresponds to the instantaneous chirality of light. It has been utilized for exploring chiral light-matter interactions in linear optics, but has not yet been applied to nonlinear processes. Motivated to explore the role of OC in the generation of helically polarized high-order harmonics and attosecond pulses, we first separate the OC of transversal and paraxial beams to polarization and orbital terms. We find that the polarization-associated OC of attosecond pulses corresponds to that of the pump in the quasi-monochromatic case, but not in multi-chromatic pump cases. We associate this discrepancy to the fact that the polarization OC of multi-chromatic pumps vary rapidly in time along the optical cycle. Thus, we propose new quantities, non-instantaneous polarization-associated OC, and timescale-weighted polarization-associated OC, that link the chirality of multi-chromatic pumps and their generated attosecond pulses. The presented extension to OC theory should be useful for exploring various nonlinear chiral light-matter interactions. For example, it stimulates us to propose a tri-circular pump for generation of highly elliptical attosecond pulses with a tunable ellipticity.

physics.optics↗