262 research outputs found
Laser-induced interference, focusing, and diffraction of rescattering molecular photoelectrons
We solve the time-dependent Schrodinger equation in three dimensions for H-2(+) in a one-cycle laser pulse of moderate intensity. We consider fixed nuclear positions and Coulomb electron-nuclear interaction potentials. We analyze the field-induced electron interference and diffraction patterns. To extract the ionization dynamics we subtract the excitations to low-lying bound states explicitly. We follow the time evolution of a well-defined wave packet that is formed near the first peak of the laser field. We observe the fragmentation of the wave packet due to molecular focusing. We show how to retrieve a diffraction molecular image by taking the ratio of the momentum distributions in the two lateral directions. The positions of the diffraction peaks are well described by the classical double slit diffraction rule
High-harmonic generation: taking control of polarization
The ability to control the polarization of short-wavelength radiation generated by high-harmonic generation is useful not only for applications but also for testing conservation laws in physics
Attosecond control of electrons emitted from a nanoscale metal tip
Attosecond science is based on steering of electrons with the electric field
of well-controlled femtosecond laser pulses. It has led to, for example, the
generation of XUV light pulses with a duration in the sub-100-attosecond
regime, to the measurement of intra-molecular dynamics by diffraction of an
electron taken from the molecule under scrutiny, and to novel ultrafast
electron holography. All these effects have been observed with atoms or
molecules in the gas phase. Although predicted to occur, a strong light-phase
sensitivity of electrons liberated by few-cycle laser pulses from solids has
hitherto been elusive. Here we show a carrier-envelope (C-E) phase-dependent
current modulation of up to 100% recorded in spectra of electrons laser-emitted
from a nanometric tungsten tip. Controlled by the C-E phase, electrons
originate from either one or two sub-500as long instances within the 6-fs laser
pulse, leading to the presence or absence of spectral interference. We also
show that coherent elastic re-scattering of liberated electrons takes place at
the metal surface. Due to field enhancement at the tip, a simple laser
oscillator suffices to reach the required peak electric field strengths,
allowing attosecond science experiments to be performed at the 100-Megahertz
repetition rate level and rendering complex amplified laser systems
dispensable. Practically, this work represents a simple, exquisitely sensitive
C-E phase sensor device, which can be shrunk in volume down to ~ 1cm3. The
results indicate that the above-mentioned novel attosecond science techniques
developed with and for atoms and molecules can also be employed with solids. In
particular, we foresee sub-femtosecond (sub-) nanometre probing of (collective)
electron dynamics, such as plasmon polaritons, in solid-state systems ranging
in size from mesoscopic solids via clusters to single protruding atoms.Comment: Final manuscript version submitted to Natur
Streaking strong-field double ionization
Double ionization in intense laser fields can comprise electron correlations which manifest in the nonindependent emission of two electrons from an atom or molecule. However, experimental methods that directly access the electron emission times have been scarce. Here we explore the application of an all-optical streaking technique to strong-field double ionization, both theoretically and experimentally. We show that both sequential and nonsequential double-ionization processes lead to streaking delays that are distinct from each other and single ionization. Moreover, coincidence detection of ions and electrons provides access to the emission time difference, which is encoded in the two-electron momentum distributions. The experimental data agree very well with simulations of sequential double ionization. We further test and discuss the application of this method to nonsequential double ionization, which is strongly affected by the presence of the streaking field
Attophysics - Ultrafast control
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/62570/1/421593a.pd
Carrier-envelope phase effects on the strong-field photoemission of electrons from metallic nanostructures
Sharp metallic nanotapers irradiated with few-cycle laser pulses are emerging
as a source of highly confined coherent electron wavepackets with attosecond
duration and strong directivity. The possibility to steer, control or switch
such electron wavepackets by light is expected to pave the way towards direct
visualization of nanoplasmonic field dynamics and real-time probing of electron
motion in solid state nanostructures. Such pulses can be generated by
strong-field induced tunneling and acceleration of electrons in the near-field
of sharp gold tapers within one half-cycle of the driving laser field. Here, we
show the effect of the carrier-envelope phase of the laser field on the
generation and motion of strong-field emitted electrons from such tips. This is
a step forward towards controlling the coherent electron motion in and around
metallic nanostructures on ultrashort length and time scales
Determination of the Carrier-Envelope Phase of Few-Cycle Laser Pulses with Terahertz-Emission Spectroscopy
The availability of few-cycle optical pulses opens a window to physical
phenomena occurring on the attosecond time scale. In order to take full
advantage of such pulses, it is crucial to measure and stabilise their
carrier-envelope (CE) phase, i.e., the phase difference between the carrier
wave and the envelope function. We introduce a novel approach to determine the
CE phase by down-conversion of the laser light to the terahertz (THz) frequency
range via plasma generation in ambient air, an isotropic medium where optical
rectification (down-conversion) in the forward direction is only possible if
the inversion symmetry is broken by electrical or optical means. We show that
few-cycle pulses directly produce a spatial charge asymmetry in the plasma. The
asymmetry, associated with THz emission, depends on the CE phase, which allows
for a determination of the phase by measurement of the amplitude and polarity
of the THz pulse
Lightwave-driven quasiparticle collisions on a subcycle timescale
Ever since Ernest Rutherford scattered alpha-particles from gold foils(1), collision experiments have revealed insights into atoms, nuclei and elementary particles(2). In solids, many-body correlations lead to characteristic resonances(3)-called quasiparticles-such as excitons, dropletons(4), polarons and Cooper pairs. The structure and dynamics of quasiparticles are important because they define macroscopic phenomena such as Mott insulating states, spontaneous spin-and charge-order, and high-temperature superconductivity(5). However, the extremely short lifetimes of these entities(6) make practical implementations of a suitable collider challenging. Here we exploit lightwave-driven charge transport(7-24), the foundation of attosecond science(9-13), to explore ultrafast quasiparticle collisions directly in the time domain: a femtosecond optical pulse creates excitonic electron-hole pairs in the layered dichalcogenide tungsten diselenide while a strong terahertz field accelerates and collides the electrons with the holes. The underlying dynamics of the wave packets, including collision, pair annihilation, quantum interference and dephasing, are detected as light emission in high-order spectral sidebands(17-19) of the optical excitation. A full quantum theory explains our observations microscopically. This approach enables collision experiments with various complex quasiparticles and suggests a promising new way of generating sub-femtosecond pulses
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