195 research outputs found
A comparison of the operational models of publicly funded open access nano research infrastructures
Non-sequential double ionization with near-single cycle laser pulses
A three-dimensional semiclassical model is used to study double ionization of Ar when driven by a near-infrared and near-single-cycle laser pulse for intensities ranging from 0.85 x 10(14) W/cm(2) to 5 x 10(14) W/cm(2). Asymmetry parameters, distributions of the sum of the two electron momentum components along the direction of the polarization of the laser field and correlated electron momenta are computed as a function of the intensity and of the carrier envelope phase. A very good agreement is found with recently obtained results in kinematically complete experiments employing near-single-cycle laser pulses. Moreover, the contribution of the direct and delayed pathways of double ionization is investigated for the above observables. Finally, an experimentally obtained anti-correlation momentum pattern at higher intensities is reproduced with the three-dimensional semiclassical model and shown to be due to a transition from strong to soft recollisions with increasing intensity
Ferroelectric vs. structural properties of large-distance sputtered epitaxial LSMO/PZT heterostructures
Carrier-envelope phase control over pathway interference in strong-field dissociation of H
The dissociation of an H molecular-ion beam by linearly polarized,
carrier-envelope-phase-tagged 5 fs pulses at 4W/cm with a
central wavelength of 730 nm was studied using a coincidence 3D momentum
imaging technique. Carrier-envelope-phase-dependent asymmetries in the emission
direction of H fragments relative to the laser polarization were observed.
These asymmetries are caused by interference of odd and even photon number
pathways, where net-zero photon and 1-photon interference predominantly
contributes at H+H kinetic energy releases of 0.2 -- 0.45 eV, and
net-2-photon and 1-photon interference contributes at 1.65 -- 1.9 eV. These
measurements of the benchmark H molecule offer the distinct advantage
that they can be quantitatively compared with \textit{ab initio} theory to
confirm our understanding of strong-field coherent control via the
carrier-envelope phase
Steering proton migration in hydrocarbons using intense few-cycle laser fields
Proton migration is a ubiquitous process in chemical reactions related to
biology, combustion, and catalysis. Thus, the ability to control the movement
of nuclei with tailored light, within a hydrocarbon molecule holds promise for
far-reaching applications. Here, we demonstrate the steering of hydrogen
migration in simple hydrocarbons, namely acetylene and allene, using
waveform-controlled, few-cycle laser pulses. The rearrangement dynamics are
monitored using coincident 3D momentum imaging spectroscopy, and described with
a quantum-dynamical model. Our observations reveal that the underlying control
mechanism is due to the manipulation of the phases in a vibrational wavepacket
by the intense off-resonant laser field.Comment: 5 pages, 4 figure
Spatiotemporal imaging of valence electron motion
Electron motion on the (sub-)femtosecond time scale constitutes the fastest response in many natural phenomena such as light-induced phase transitions and chemical reactions. Whereas static electron densities in single molecules can be imaged in real space using scanning tunnelling and atomic force microscopy, probing real-time electron motion inside molecules requires ultrafast laser pulses. Here, we demonstrate an all-optical approach to imaging an ultrafast valence electron wave packet in real time with a time-resolution of a few femtoseconds. We employ a pump-probe-deflect scheme that allows us to prepare an ultrafast wave packet via strong-field ionization and directly image the resulting charge oscillations in the residual ion. This approach extends and overcomes limitations in laser-induced orbital imaging and may enable the real-time imaging of electron dynamics following photoionization such as charge migration and charge transfer processes
Influence of particle size and fluorination ratio of CFâ‚“ precursor compounds on the electrochemical performance of C-FeFâ‚‚ nanocomposites for reversible lithium storage
Systematical studies of the electrochemical performance of CFx-derived carbon–FeF2 nanocomposites for reversible lithium storage are presented. The conversion cathode materials were synthesized by a simple one-pot synthesis, which enables a reactive intercalation of nanoscale Fe particles in a CFx matrix, and the reaction of these components to an electrically conductive C–FeF2 compound. The pretreatment and the structure of the utilized CFx precursors play a crucial role in the synthesis and influence the electrochemical behavior of the conversion cathode material. The particle size of the CFx precursor particles was varied by ball milling as well as by choosing different C/F ratios. The investigations led to optimized C–FeF2 conversion cathode materials that showed specific capacities of 436 mAh/g at 40 °C after 25 cycles. The composites were characterized by Raman spectroscopy, X-Ray diffraction measurements, electron energy loss spectroscopy and TEM measurements. The electrochemical performances of the materials were tested by galvanostatic measurements
Structural and Electrochemical Insights from the Fluorination of Disordered Mn-Based Rock Salt Cathode Materials
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Signatures of Light-Induced Potential Energy Surfaces in H2+
Using theory and Cold Target Recoil Ion Momentum Spectroscopy we find signatures of light-induced molecular potential energy surfaces in the 3-dimensional proton momentum distributions of dissociating H+2. © 2020 Journal of Physics: Conference Series. All rights reserved
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