694 research outputs found
Momentum space tomographic imaging of photoelectrons
We apply tomography, a general method for reconstructing 3-D distributions
from multiple projections, to reconstruct the momentum distribution of
electrons produced via strong field photoionization. The projections are
obtained by rotating the electron distribution via the polarization of the
ionizing laser beam and recording a momentum spectrum at each angle with a 2-D
velocity map imaging spectrometer. For linearly polarized light the tomographic
reconstruction agrees with the distribution obtained using an Abel inversion.
Electron tomography, which can be applied to any polarization, will simplify
the technology of electron imaging. The method can be directly generalized to
other charged particles.Comment: Accepted by J. Phys.
Alignment dependent enhancement of the photo-electron cutoff for multi-photon ionization of molecules
The multiphoton ionization rate of molecules depends on the alignment of the
molecular axis with respect to the ionizing laser polarization. By studying
molecular frame photo-electron angular distributions from N, O and
benzene, we illustrate how the angle-dependent ionization rate affects the
photo-electron cutoff energy. We find alignment can enhance the high energy
cutoff of the photo-electron spectrum when probing along a nodal plane or when
ionization is otherwise suppressed. This is supported by calculations using a
tunneling model with a single ion state.Comment: 4 pages, 4 figure
Mechanisms of two-color laser-induced field-free molecular orientation
Two mechanisms of two-color (\omega + 2\omega) laser-induced field-free
molecular orientation, based on the hyperpolarizability and ionization
depletion, are explored and compared. The CO molecule is used as a
computational example. While the hyperpolarizability mechanism generates small
amounts of orientation at intensities below the ionization threshold,
ionization depletion quickly becomes the dominant mechanism as soon as ionizing
intensities are reached. Only the ionization mechanism leads to substantial
orientation (e.g. on the order of || > 0.1). For intensities typical
of laser-induced molecular alignment and orientation experiments, the two
mechanism lead to robust, characteristic timings of the field-free orientation
wave-packet revivals relative to the the alignment revivals and the revival
time. The revival timings can be used to detect the active orientation
mechanism experimentally
Non-dipole recollision-gated double ionization and observable effects
Using a three-dimensional semiclassical model, we study double ionization for
strongly-driven He fully accounting for magnetic field effects. For linearly
and slightly elliptically polarized laser fields, we show that recollisions and
the magnetic field combined act as a gate. This gate favors more transverse -
with respect to the electric field - initial momenta of the tunneling electron
that are opposite to the propagation direction of the laser field. In the
absence of non-dipole effects, the transverse initial momentum is symmetric
with respect to zero. We find that this asymmetry in the transverse initial
momentum gives rise to an asymmetry in a double ionization observable. Finally,
we show that this asymmetry in the transverse initial momentum of the tunneling
electron accounts for a recently-reported unexpectedly large average sum of the
electron momenta parallel to the propagation direction of the laser field.Comment: Amended the focus of the paper and discussion. 9 pages, 7 figure
Effect of electron exchange on atomic ionization in a strong electric field
Hartree-Fock atom in a strong electric static field is considered. It is
demonstrated that exchange between outer and inner electrons, taken into
account by the so-called Fock term affects strongly the long-range behavior of
the inner electron wave function. As a result, it dramatically increases its
probability to be ionized. A simple model is analyzed demonstrating that the
decay probability, compared to the case of a local (Hartree) atomic potential,
increases by many orders of magnitude. As a result of such increase, the ratio
of inner to outer electrons ionization probability became not too small. It is
essential that the effect of exchange upon probability of inner electron
ionization by strong electric field is proportional to the square of the number
of outer electrons. It signals that in clusters the inner electron ionization
by strong field, the very fact of which is manifested by e.g. high energy
quanta emission, has to be essentially increased as compared to this process in
gaseous atomic objects.Comment: 7 pages, 1 figur
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
Double Ionization by Strong Elliptically Polarized Laser Pulses
We join the tribute to Professor N.B. Delone in this memorial issue by
presenting the results of new calculations on the effects of ellipticity on
double ionization by short and strong near-optical laser pulses.Comment: 3 pages, 4 figures, accepted in Professor N.B. Delone's memorial
issu
Partitioning of the linear photon momentum in multiphoton ionization
The balance of the linear photon momentum in multiphoton ionization is
studied experimentally. In the experiment argon and neon atoms are singly
ionized by circularly polarized laser pulses with a wavelength of 800 nm and
1400 nm in the intensity range of 10^{14} - 10^{15} W/cm^2. The photoelectrons
are measured using velocity map imaging. We find that the photoelectrons carry
linear momentum corresponding to the photons absorbed above the field free
ionization threshold. Our finding has implications for concurrent models of the
generation of terahertz radiation in filaments.Comment: 4 pages, 3 figure
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