N. L. Manakov

Bio: N. L. Manakov is an academic researcher from Voronezh State University. The author has contributed to research in topics: Electron & Ionization. The author has an hindex of 27, co-authored 122 publications receiving 2408 citations.

Electron Vortices in Photoionization by Circularly Polarized Attosecond Pulses

Abstract: Single ionization of He by two oppositely circularly polarized, time-delayed attosecond pulses is shown to produce photoelectron momentum distributions in the polarization plane having helical vortex structures sensitive to the time delay between the pulses, their relative phase, and their handedness Results are obtained by both ab initio numerical solution of the two-electron time-dependent Schrodinger equation and by a lowest-order perturbation theory analysis The energy, bandwidth, and temporal duration of attosecond pulses are ideal for observing these vortex patterns

Wavelength Scaling of High-Harmonic Yield: Threshold Phenomena and Bound State Symmetry Dependence

Abstract: Describing harmonic generation (HG) in terms of a system's complex quasienergy, the harmonic power P_{DeltaE}(lambda) (over a fixed interval, DeltaE, of harmonic energies) is shown to reproduce the wavelength scaling predicted recently by two groups of authors based on solutions of the time-dependent Schrödinger equation: P_{DeltaE}(lambda) approximately lambda;{-x}, where x approximately 5-6. Oscillations of P_{DeltaE}(lambda) on a fine lambda scale are then shown to have a quantum origin, involving threshold phenomena within a system of interacting ionization and HG channels, and to be sensitive to the bound state wave function's symmetry.

Analytic Description of the High-Energy Plateau in Harmonic Generation by Atoms: Can the Harmonic Power Increase with Increasing Laser Wavelengths?

Abstract: A closed-form analytic formula for high-order harmonic generation (HHG) rates for atoms (that generalizes an HHG formula for negative ions [M. V. Frolov, J. Phys. B 42, 035601 (2009)10.1088/0953-4075/42/3/035601]) is used to study laser wavelength scaling of the HHG yield for harmonic energies in the cutoff region of the HHG plateau. We predict increases of the harmonic power for HHG by Ar, Kr, and Xe with increasing wavelength lambda over atom-specific intervals of lambda in the infrared region, lambda approximately (0.8-2.0) microm.

Wavelength Scaling of High-Harmonic Yield: Threshold Phenomena and Bound State Symmetry Dependence

Abstract: Describing harmonic generation (HG) in terms of a system's complex quasienergy, the harmonic power P{sub {delta}}{sub E}({lambda}) (over a fixed interval, {delta}E, of harmonic energies) is shown to reproduce the wavelength scaling predicted recently by two groups of authors based on solutions of the time-dependent Schroedinger equation: P{sub {delta}}{sub E}({lambda}){approx}{lambda}{sup -x}, where x{approx_equal}5-6. Oscillations of P{sub {delta}}{sub E}({lambda}) on a fine {lambda} scale are then shown to have a quantum origin, involving threshold phenomena within a system of interacting ionization and HG channels, and to be sensitive to the bound state wave function's symmetry.

Attosecond Physics

Abstract: Summary form only given. Fundamental processes in atoms, molecules, as well as condensed matter are triggered or mediated by the motion of electrons inside or between atoms. Electronic dynamics on atomic length scales tends to unfold within tens to thousands of attoseconds (1 attosecond [as] = 10-18 s). Recent breakthroughs in laser science are now opening the door to watching and controlling these hitherto inaccessible microscopic dynamics. The key to accessing the attosecond time domain is the control of the electric field of (visible) light, which varies its strength and direction within less than a femtosecond (1 femtosecond = 1000 attoseconds). Atoms exposed to a few oscillations cycles of intense laser light are able to emit a single extreme ultraviolet (XUV) burst lasting less than one femtosecond. Full control of the evolution of the electromagnetic field in laser pulses comprising a few wave cycles have recently allowed the reproducible generation and measurement of isolated sub-femtosecond XUV pulses, demonstrating the control of microscopic processes (electron motion and photon emission) on an attosecond time scale. These tools have enabled us to visualize the oscillating electric field of visible light with an attosecond "oscilloscope", to control single-electron and probe multi-electron dynamics in atoms, molecules and solids. Recent experiments hold promise for the development of an attosecond X-ray source, which may pave the way towards 4D electron imaging with sub-atomic resolution in space and time.

Bright Coherent Ultrahigh Harmonics in the keV X-ray Regime from Mid-Infrared Femtosecond Lasers

Abstract: High-harmonic generation (HHG) traditionally combines ~100 near-infrared laser photons to generate bright, phase-matched, extreme ultraviolet beams when the emission from many atoms adds constructively. Here, we show that by guiding a mid-infrared femtosecond laser in a high-pressure gas, ultrahigh harmonics can be generated, up to orders greater than 5000, that emerge as a bright supercontinuum that spans the entire electromagnetic spectrum from the ultraviolet to more than 1.6 kilo-electron volts, allowing, in principle, the generation of pulses as short as 2.5 attoseconds. The multiatmosphere gas pressures required for bright, phase-matched emission also support laser beam self-confinement, further enhancing the x-ray yield. Finally, the x-ray beam exhibits high spatial coherence, even though at high gas density the recolliding electrons responsible for HHG encounter other atoms during the emission process.

Attosecond real-time observation of electron tunnelling in atoms

Abstract: Atoms exposed to intense light lose one or more electrons and become ions. In strong fields, the process is predicted to occur via tunnelling through the binding potential that is suppressed by the light field near the peaks of its oscillations. Here we report the real-time observation of this most elementary step in strong-field interactions: light-induced electron tunnelling. The process is found to deplete atomic bound states in sharp steps lasting several hundred attoseconds. This suggests a new technique, attosecond tunnelling, for probing short-lived, transient states of atoms or molecules with high temporal resolution. The utility of attosecond tunnelling is demonstrated by capturing multi-electron excitation (shake-up) and relaxation (cascaded Auger decay) processes with subfemtosecond resolution.