ABSTRACT
In recent years, the stacking and twisting of atom-thin structures with matching crystal symmetry has provided a unique way to create new superlattice structures in which new properties emerge1,2. In parallel, control over the temporal characteristics of strong light fields has allowed researchers to manipulate coherent electron transport in such atom-thin structures on sublaser-cycle timescales3,4. Here we demonstrate a tailored light-wave-driven analogue to twisted layer stacking. Tailoring the spatial symmetry of the light waveform to that of the lattice of a hexagonal boron nitride monolayer and then twisting this waveform result in optical control of time-reversal symmetry breaking5 and the realization of the topological Haldane model6 in a laser-dressed two-dimensional insulating crystal. Further, the parameters of the effective Haldane-type Hamiltonian can be controlled by rotating the light waveform, thus enabling ultrafast switching between band structure configurations and allowing unprecedented control over the magnitude, location and curvature of the bandgap. This results in an asymmetric population between complementary quantum valleys that leads to a measurable valley Hall current7, which can be detected by optical harmonic polarimetry. The universality and robustness of our scheme paves the way to valley-selective bandgap engineering on the fly and unlocks the possibility of creating few-femtosecond switches with quantum degrees of freedom.
ABSTRACT
The development of a recoil ion momentum spectrometer (RIMS) along with a post-collision projectile charge state analyzer (CSA) and its performance for carrying out studies of molecular fragmentation following direct ionization, electron-capture, and capture-ionization have been demonstrated here. This is a two-stage Wiley-McLaren type spectrometer with slight modification introduced by adding a lens to achieve higher momentum resolution as well as larger angular acceptance. Along with the time and position sensitive detector, it can measure all the three momentum components of singly charged recoil ions of energy up to 10 eV emitted in all directions. The CSA assembly is designed for separating out any neutral or singly or doubly charged post-collision projectiles typically of keV energy. The RIMS with initial trigger ("start") from CSA or an ionized electron can uniquely determine the dynamics of molecular fragmentation following different electron-capture or direct ionization events, respectively. To check the performance of the setup, we carried out an experimental study of the fragmentation of N2 molecules under the impact of 250 keV protons. Apart from the single-electron-capture channel, we could clearly identify three more capture-ionization channels, which lead to fragmentation. The essential features of the momentum distributions and the kinetic energy release distributions of all three fragmentation channels are discussed in detail. These results are compared with the findings from the ionization induced fragmentation experiments and with the available results from theoretical calculations as well as high resolution experiments. The branching ratios of these fragmentation channels are determined.
ABSTRACT
A correction to this article has been published and is linked from the HTML version of this paper. The error has been fixed in the paper.
ABSTRACT
Interaction between polycyclic aromatic hydrocarbon (PAH) molecule and energetic ion is a subject of interest in different areas of modern physics. Here, we present measurements of energy and angular distributions of absolute double differential electron emission cross section for coronene (C24H12) and fluorene (C13H10) molecules under fast bare oxygen ion impact. For coronene, the angular distributions of the low energy electrons are quite different from that of simpler targets like Ne or CH4, which is not the case for fluorene. The behaviour of the higher electron energy distributions for both the targets are similar to that for simple targets. In case of coronene, a clear signature of plasmon resonance is observed in the analysis of forward-backward angular asymmetry of low energy electron emission. For fluorene, such signature is not identified probably due to lower oscillator strength of plasmon compared to the coronene. The theoretical calculation based on the first-order Born approximation with correct boundary conditions (CB1), in general, reproduced the experimental observations qualitatively, for both the molecules, except in the low energy region for coronene, which again indicates the role of collective excitation. Single differential and total cross sections are also deduced. An overall comparative study is presented.
