The photoelectron circular dichroism (PECD) of the O 1s-photoelectrons of trifluoromethyloxirane (TFMOx) is studied experimentally and theoretically for different photoelectron kinetic energies. The experiments were performed employing circularly polarized synchrotron...
We have measured the double-differential cross sections (DDCS) for electron emission in ionization of H 2 O molecules under the impact of 4.5-MeV/u O 8+ ions. The data were collected between 1 and 600 eV, in an angular range of 20 • -150 • by using an electrostatic hemispherical analyzer. In the experiment we used the H 2 O vapor in a static gas condition which allowed us to deduce the absolute value of the cross sections. The single-differential cross sections (SDCS) and the total cross sections have also been obtained. The DDCS as well as the SDCS spectra are compared with the continuum-distorted-wave eikonal-initial-state (CDW-EIS) calculations for both the prior as well as the post forms of the scattering matrix. The initial state is represented within the complete neglect of differential overlap approximation, where the molecular orbitals are expressed in terms of atomic orbitals of the atomic constituents. The overall agreement with the CDW-EIS model is quite good as far as the energy dependence is concerned. The prior form of the model is found to provide a better understanding of the
The
simplest molecular dimer, H2-H2, poses
a challenge to both experiment and theory as a system with a multidimensional
energy surface that supports only a single weakly bound quantum state.
Here, we provide a direct experimental image of the structure of hydrogen
dimers [(H2)2, H2-D2,
and (D2)2] obtained via femtosecond laser-induced
Coulomb explosion imaging. Our results indicate that hydrogen dimers
are not restricted to a particular geometry but rather occur as a
mixture of all possible configurations. The measured intermolecular
distance distributions were used to deduce the isotropic intermolecular
potential as well as the binding energies of the dimers.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.