arXiv subjects

Daniil Kartashov

Publications and source records attributed to Daniil Kartashov.

16 recordsLinked to original sources

arXiv2025

Long Living Hot and Dense Plasma from Relativistic Laser-Nanowire Array Interaction

Long-living, hot and dense plasmas generated by ultra-intense laser beams are of critical importance for laser-driven nuclear physics, bright hard X-ray sources, and laboratory astrophysics. We report the experimental observation of plasmas with nanosecond-scale lifetimes, near-solid density, and keV-level temperatures, produced by irradiating periodic arrays of composite nanowires with ultra-high contrast, relativistically intense femtosecond laser pulses. Jet-like plasma structures extending up to 1~mm from the nanowire surface were observed, emitting K-shell radiation from He-like Ti$^{20+}$ ions. High-resolution X-ray spectra were analyzed using 3D Particle-in-Cell (PIC) simulations of the laser-plasma interaction combined with collisional--radiative modeling (FLYCHK). The results indicate that the jets consist of plasma with densities of $10^{20}$-$10^{22}$ cm$^{-3}$ and keV-scale temperatures, persisting for several nanoseconds. We attribute the formation of these jets to the generation of kiloTesla-scale global magnetic fields during the laser interaction, as predicted by PIC simulations. These fields may drive long-timescale current instabilities that sustain magnetic fields of several hundred tesla, sufficient to confine hot, dense plasma over nanosecond durations.

physics.plasm-ph↗

arXiv2025

Ultrafast Coherent Bandgap Modulation Probed by Parametric Nonlinear Optics

Light-matter interactions in crystals are powerful tools that seamlessly allow both functionalities of sizeable bandgap modulation and non-invasive spectroscopy. While we often assume that the border between the two regimes of modulation and detection is sharp and well-defined, there are experiments where the boundaries fade. The study of these transition regions allows us to identify the real potentials and inherent limitations of the most commonly used optical spectroscopy techniques. Here, we measure and explain the co-existence between bandgap modulation and non-invasive spectroscopy in the case of resonant perturbative nonlinear optics in an atomically thin direct gap semiconductor. We report a clear deviation from the typical quadratic power scaling of second-harmonic generation near an exciton resonance, and we explain this unusual result based on all-optical modulation driven by the intensity-dependent optical Stark and Bloch-Siegert shifts in the $\pm$K valleys of the Brillouin zone. Our experimental results are corroborated by analytical and numerical analysis based on the semiconductor Bloch equations, from which we extract the resonant transition dipole moments and dephasing times of the used sample. These findings redefine the meaning of perturbative nonlinear optics by revealing how coherent light-matter interactions can modify the band structure of a crystal, even in the weak-field regime. Furthermore, our results strengthen the understanding of ultrafast all-optical control of electronic states in two-dimensional materials, with potential applications in valleytronics, Floquet engineering, and light-wave electronics.

physics.optics↗

arXiv2024

Unveiling the Role of Electron-Phonon Scattering in Dephasing High-Order Harmonics in Solids

High-order harmonic generation (HHG) in solids is profoundly influenced by the dephasing of the coherent electron-hole motion driven by an external laser field. The exact physical mechanisms underlying this dephasing, crucial for accurately understanding and modelling HHG spectra, have remained elusive and controversial, often regarded more as an empirical observation than a firmly established principle. In this work, we present comprehensive experimental findings on the wavelength-dependency of HHG in both single-atomic-layer and bulk semiconductors. These findings are further corroborated by rigorous numerical simulations, employing ab initio real-time, real-space time-dependent density functional theory and semiconductor Bloch equations. Our experimental observations necessitate the introduction of a novel concept: a momentum-dependent dephasing time in HHG. Through detailed analysis, we pinpoint momentum-dependent electron-phonon scattering as the predominant mechanism driving dephasing. This insight significantly advances the understanding of dephasing phenomena in solids, addressing a long-standing debate in the field. Furthermore, our findings pave the way for a novel, all-optical measurement technique to determine electron-phonon scattering rates and establish fundamental limits to the efficiency of HHG in condensed matter.

physics.optics↗

arXiv2023

Valley Polarization-Electric Dipole Interference and Nonlinear Chiral Selection Rules in Monolayer WSe$_2$

In monolayer transition metal dichalcogenides time-reversal symmetry, combined with space-inversion symmetry, defines the spin-valley degree of freedom. As such, engineering and control of time-reversal symmetry by optical or magnetic fields constitutes the foundation of valleytronics. Here, we propose a new approach for the detection of broken time-reversal symmetry and valley polarization in monolayer WSe$_2$ based on second harmonic generation. Our method can selectively and simultaneously generate and detect a valley polarization at the $\pm K$ valleys of transition metal dichalcogenides at room temperature. Furthermore, it allows to measure the interference between the real and imaginary parts of the intrinsic (electric dipole) and valley terms of the second order nonlinear susceptibility. This work demonstrates the potential and unique capabilities of nonlinear optics as a probe of broken time-reversal symmetry and as a tool for ultrafast and non-destructive valleytronic operations.

physics.optics↗

arXiv2022

Nonclassical light generation and control from laser-driven semiconductor intraband excitations

We investigate the generation of higher-order harmonics from a quantum optics perspective via the interaction of a semiconductor with a coherent pump field focusing on the regime where strong-field intraband excitations dominate. The related Schrödinger equation for the system is solved approximately and the classical and quantum characteristics of the fundamental light mode as well as the higher frequency modes are analyzed. We find intricate but sufficiently mild modifications of the fundamental mode and coherent displacements depending on the position quadrature component of the driving laser field for the harmonic modes within our approximations due to the intricate induced nonlinear interactions. Similar to high-harmonic generation in atoms, all radiation field modes are entangled, allowing for potential novel protocols for quantum information processing with high photon numbers over a large range of frequencies.

quant-ph↗

arXiv2022

High-Harmonic Spectroscopy of Coherent Lattice Dynamics in Graphene

High-harmonic spectroscopy of solids is a powerful tool, which provides access to both electronic structure and ultrafast electronic response of solids, from their band structure and density of states, to phase transitions, including the emergence of the topological edge states, to the PetaHertz electronic response. However, in spite of these successes, high harmonic spectroscopy has hardly been applied to analyse the role of coherent femtosecond lattice vibrations in the attosecond electronic response. Here we study coherent phonon excitations in monolayer graphene to show how high-harmonic spectroscopy can be used to detect the influence of coherent lattice dynamics, particularly longitudinal and transverse optical phonon modes, on the electronic response. Coherent excitation of the in-plane phonon modes results in the appearance of sidebands in the spectrum of the emitted harmonic radiation. We show that the spectral positions and the polarisation of the sideband emission offer a sensitive probe of the dynamical symmetries associated with the excited phonon modes. Our work brings the key advantage of high harmonic spectroscopy -- the combination of sub-femtosecond to tens of femtoseconds temporal resolution -- to the problem of probing phonon-driven electronic response and its dependence on the dynamical symmetries in solids.

physics.optics↗

arXiv2022

Signatures of multi-band effects in high-harmonic generation in monolayer MoS$_2$

High-harmonic generation (HHG) in solids has been touted as a way to probe ultrafast dynamics and crystal symmetries in condensed matter systems. Here, we investigate the polarization properties of high-order harmonics generated in monolayer MoS$_2$, as a function of crystal orientation relative to the mid-infrared laser field polarization. At several different laser wavelengths we experimentally observe a prominent angular shift of the parallel-polarized odd harmonics for energies above approximately 3.5 eV, and our calculations indicate that this shift originates in subtle differences in the recombination dipole strengths involving multiple conduction bands. This observation is material specific and is in addition to the angular dependence imposed by the dynamical symmetry properties of the crystal interacting with the laser field, and may pave the way for probing the vectorial character of multi-band recombination dipoles.

cond-mat.mtrl-sci↗

arXiv2020

High-harmonic generation from metasurfaces empowered by bound states in the continuum

The concept of optical bound states in the continuum (BICs) underpins the existence of strongly localized waves embedded into the radiation spectrum that can enhance the electromagnetic fields in subwavelength photonic structures. Early studies of optical BICs in waveguides and photonic crystals uncovered their topological properties, and the concept of quasi-BIC metasurfaces facilitated applications of strong light-matter interactions to biosensing, lasing, and low-order nonlinear processes. Here we employ BIC-empowered dielectric metasurfaces to generate efficiently high optical harmonics up to the 11th order. We optimize a BIC mode for the first few harmonics and observe a transition between perturbative and nonperturbative nonlinear regimes. We also suggest a general strategy for designing subwavelength structures with strong resonances and nonperturbative nonlinearities. Our work bridges the fields of perturbative and nonperturbative nonlinear optics on the subwavelength scale.

physics.optics↗

arXiv2018

Filamentation of Mid-IR pulses in ambient air in the vicinity of molecular resonances

Properties of filaments ignited by multi-millijoule, 90-fs mid-IR pulses centered at 3.9 μm are examined experimentally by monitoring plasma density and losses as well as spectral dynamics and beam profile evolution at different focusing strengths. By softening the focusing from strong (f=0.25 m) to loose (f=7 m) we observe a shift from plasma assisted filamentation to filaments with low plasma density. In the latter case, filamentation manifests itself by beam self-symmetrization and spatial self-channeling. Spectral dynamics in the case of loose focusing is dominated by the non-linear Raman frequency downshift, which leads to the overlap with the CO2 resonance in the vicinity of 4.2 μm. The dynamic CO2 absorption in the case of 3.9-μm filaments with their low plasma content is the main mechanism of energy losses and either alone or together with other nonlinear processes contributes to the arrest of intensity.

physics.optics↗

arXiv2017

Disentangling intra-cycle interferences in photoelectron momentum distributions using orthogonal two-colour laser fields

We use orthogonally polarized two-colour (OTC) laser pulses to separate quantum paths in multiphoton ionization of Ar atoms. Our OTC pulses consist of 400~nm and 800~nm light at a relative intensity ratio of 10:1. We find a hitherto unobserved interference in the photoelectron momentum distribution, which exhibits a strong dependence on the relative phase of the OTC pulse. Analysis of model calculations reveal that the interference is caused by quantum pathways from non-adjacent quarter cycles.

physics.atom-ph↗

arXiv2017

Localizing High-Lying Rydberg Wave Packets with Two-Color Laser Fields

We demonstrate control over the localization of high-lying Rydberg wave packets in argon atoms with phase-locked orthogonally polarized two-color (OTC) laser fields. With a reaction microscope, we measured ionization signals of high-lying Rydberg states induced by a weak dc field and black-body radiation as a function of the relative phase between the two-color fields. We find that the dc-field ionization yields of high-lying Rydberg argon atoms oscillate with the relative two-color phase with a period of $2π$ while the photoionization signal by black-body radiation shows a period of $π$. These observations are a clear signature of the asymmetric localization of electrons recaptured into high-lying Rydberg states after conclusion of the laser pulse and are supported by a semiclassical simulation of argon-OTC laser interaction. Our findings thus open an effective pathway to control the localization of high-lying Rydberg wave packets.

physics.atom-ph↗

arXiv2017

Soliton explosion driven multi-octave supercontinuum generation by geometry-enforced dispersion design in antiresonant hollow-core fibers

Ultrafast supercontinuum generation in gas-filled waveguides is one enabling technology for many intriguing application ranging from attosecond metrology towards biophotonics, with the amount of spectral broadening crucially depending on the pulse dispersion of the propagating mode. Here we show that the structural resonances in gas-filled anti-resonant hollow core optical fiber provide an additional degree of freedom in dispersion engineering, allowing for the generation of more than three octaves of broadband light ranging deep UV wavelength towards the near infrared.Our observation relies on the introduction of a geometric-induced resonance in the spectral vicinity of the pump laser outperforming the gas dispersion, thus yielding a dispersion being independent of core size, which is highly relevant for scaling input powers.Using a Krypton filled fiber we observe spectral broadening from 200 nm towards 1.7 μm at an output energy of about 23 μJ within a single mode across the entire spectral bandwidth. Simulations show that the efficient frequency generation results from a new physical effect the soliton explosion originating from the strongly non-adiabatic mode dispersion profile.This effect alongside with the dispersion tuning capability of the fiber will enable compact ultrabroadband high energy sources spanning from the UV to the mid-infrared spectral range.

physics.optics↗

arXiv2016

Channel-resolved subcycle interferences of electron wave packets emitted from H$_2$ in two-color laser fields

We report on the observation of subcycle interferences of electron wave packets released during the strong field ionization of H$_2$ with cycle-shaped two-color laser fields. With a reaction microscope, channel-resolved photoelectron momentum distribution are obtained for different final products originating from single ionization of H$_2$. Our results show that the subcycle interference structures of electron wave packet are very sensitive to the cycle-shape of the two-color laser field. The reason is that the ionization time within an optical cycle is determined by the cycle-shape of the laser field. The subcycle interference structures can be further used to get the subcycle dynamics of molecules during strong field interaction.

physics.chem-ph↗

arXiv2016

Fragmentation of long-lived hydrocarbons after strong field ionization

We experimentally and theoretically investigated the deprotonation process on nanosecond to microsecond timescale in ethylene and acetylene molecules, following their double ionization by a strong femtosecond laser field. In our experiments we utilized coincidence detection with the reaction microscope technique, and found that both the lifetime of the long-lived ethylene dication leading to the delayed deprotonation and the relative channel strength of the delayed deprotonation compared to the prompt one have no evident dependence on the laser pulse duration and the laser peak intensity. Quantum chemical simulations suggest that such delayed fragmentation originates from the tunneling of near-dissociation-threshold vibrational states through a dissociation barrier on a dication electronic state along C--H stretching. Such vibrational states can be populated through strong field double ionization induced vibrational excitation on an electronically excited state in the case of ethylene, and through intersystem crossing from electronically excited states to the electronic ground state in the case of acetylene.

physics.chem-ph↗

arXiv2014

Laser-sub-cycle two-dimensional electron momentum mapping using orthogonal two-color fields

The two-dimensional sub-cycle-time to electron momentum mapping provided by orthogonal two-color laser fields is applied to photoelectron spectroscopy. Using neon as the example we gain experimental access to the dynamics of emitted electron wave packets in electron momenta spectra measured by coincidence momentum imaging. We demonstrate the opportunities provided by this time-to-momentum mapping by investigating the influence of the parent ion on the emitted electrons on laser-sub-cycle times. It is found that depending on their sub-cycle birth time the trajectories of photoelectrons are affected differently by the ion's Coulomb field.

physics.atom-ph↗

arXiv2012

Attosecond-recollision-controlled selective fragmentation of polyatomic molecules

Control over various fragmentation reactions of a series of polyatomic molecules (acetylene, ethylene, 1,3-butadiene) by the optical waveform of intense few-cycle laser pulses is demonstrated experimentally. We show both experimentally and theoretically that the responsible mechanism is inelastic ionization from inner-valence molecular orbitals by recolliding electron wavepackets, whose recollision energy in few-cycle ionizing laser pulses strongly depends on the optical waveform. Our work demonstrates an efficient and selective way of pre-determining fragmentation and isomerization reactions in polyatomic molecules on sub-femtosecond time-scales.

physics.chem-ph↗