arXiv subjects

M. Telmini

Publications and source records attributed to M. Telmini.

4 recordsLinked to original sources

arXiv2026

Electron-impact cross sections for dissociation processes of vibrationally excited CH radical

This paper presents a theoretical investigation of the cross sections for dissociative electron attachment and dissociative excitation processes in vibrationally excited CH radicals induced by electron impact. Resonant electron-CH collisions are analyzed using the ab-initio R-matrix method, while nuclear dynamics are explored within the Local Complex Potential framework. A comprehensive set of vibrationally resolved cross sections and rate coefficients is provided for both the ground and first excited electronic states of the CH molecule. These findings contribute to a better understanding of the kinetics of non-equilibrium systems containing CH molecules with applications in plasma technologies for CO2 reduction, combustion processes and various astrophysical contexts.

physics.atom-ph↗

arXiv2024

Rotational transitions induced by collisions of HD$^{+}$ ions with low energy electrons

A series of Multichannel Quantum Defect Theory-based computations have been performed, in order to produce the cross sections of rotational transitions (excitations $N_{i}^{+}-2 \rightarrow$ $N_{i}^{+}$, de-excitations $N_{i}^{+}$ $\rightarrow$ $N_{i}^{+}-2$, with $N_{i}^{+}=2$ to $10$) and of their competitive process, the dissociative recombination, induced by collisions of HD$^+$ ions with electrons in the energy range $10^{-5}$ to 0.3 eV. Maxwell anisotropic rate coefficients, obtained from these cross sections in the conditions of the Heidelberg Test Storage Ring (TSR) experiments ($k_{B}T_{t}=2.8$ meV and $k_{B}T_{l}=45$ $\mu$eV), have been reported for those processes in the same electronic energy range. Maxwell isotropic rate coefficients have been as well presented for electronic temperatures up to a few hundreds of Kelvins. Very good overall agreement is found between our results for rotational transitions and the former theoretical computations as well as with experiment. Furthermore, owing to the full rotational computations performed, the accuracy of the resulting dissociative recombination cross sections is considerably improved.

astro-ph.IM↗

arXiv2019

Anisotropy Control in Photoelectron Spectra: A Coherent Two-Pulse Interference Strategy

Coherence among rotational ion channels during photoionization is exploited to control the anisotropy of the resulting photoelectron angular distributions at specific photoelectron energies. The strategy refers to a robust and single parameter control using two ultra-short light pulses delayed in time. The first pulse prepares a superposition of a few ion rotational states, whereas the second pulse serves as a probe that gives access to a control of the molecular asymmetry parameter $\beta$ for individual rotational channels. This is achieved by tuning the time delay between the pulses leading to channel interferences that can be turned from constructive to destructive. The illustrative example is the ionization of the $E(1\Sigma_{g}^{+})$ state of Li$_{2}$. Quantum wave packet evolutions are conducted including both electronic and nuclear degrees of freedom to reach angle-resolved photoelectron spectra. A simple interference model based on coherent phase accumulation during the field-free dynamics between the two pulses is precisely exploited to control the photoelectron angular distributions from almost isotropic, to marked anisotropic.

physics.chem-ph↗

arXiv2017

Extracting spectroscopic molecular parameters from short pulse photo-electron angular distributions

Using a quantum wave packet simulation including the nuclear and electronic degrees of freedom, we investigate the femtosecond and picosecond energy- and angle-resolved photoelectron spectra of the E($^1\Sigma_g^+$) electronic state of Li$_2$. We find that the angular distributions of the emitted photoelectrons depend strongly on the pulse duration in the regime of ultrashort laser pulses. This effect is illustrated by the extraction of a time-dependent asymmetry parameter whose variation with pulse duration can be explained by an incoherent average over different ion rotational quantum numbers. We then derive for the variation of the asymmetry parameter a simple analytical formula, which can be used to extract the asymptotic CW asymmetry parameters of individual transitions from measurements performed with ultra-short pulses.

physics.chem-ph↗