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N. R. Arista

Publications and source records attributed to N. R. Arista.

2 recordsLinked to original sources

Deeper-band electron contributions to stopping power of silicon for low-energy ions

This study provides accurate results for the electronic stopping cross-sections of H, He, N, and Ne in silicon in low to intermediate energy ranges using various non-perturbative theoretical methods, including real-time time-dependent density functional theory, transport cross-section, and induced-density approach. Recent experimental findings [Ntemou \textit{et al.}, Phys. Rev. B {\bf 107}, 155145 (2023)] revealed discrepancies between the estimates of density functional theory and observed values. We show that these discrepancies vanish by considering the nonuniform electron density of the silicon deeper bands for ion velocities approaching zero ($v \to 0$). This indicates that mechanisms such as ``elevator'' and ``promotion,'' which can dynamically excite deeper-band electrons, are active, enabling a localized free electron gas to emulate ion energy loss, as pointed out by [Lim \textit{et al.}, Phys. Rev. Lett. {\bf 116}, 043201 (2016)]. The observation and the description of a velocity-proportionality breakdown in electronic stopping cross-sections at very low velocities are considered to be a signature of the deeper-band electrons' contributions.

physics.chem-ph

Computational Design of Chemical Nanosensors: Metal Doped Carbon Nanotubes

We use computational screening to systematically investigate the use of transition metal doped carbon nanotubes for chemical gas sensing. For a set of relevant target molecules (CO, NH3, H2S) and the main components of air (N2, O2, H2O), we calculate the binding energy and change in conductance upon adsorption on a metal atom occupying a vacancy of a (6,6) carbon nanotube. Based on these descriptors, we identify the most promising dopant candidates for detection of a given target molecule. From the fractional coverage of the metal sites in thermal equilibrium with air, we estimate the change in the nanotube resistance per doping site as a function of the target molecule concentration assuming charge transport in the diffusive regime. Our analysis points to Ni-doped nanotubes as candidates for CO sensors working under typical atmospheric conditions.

cond-mat.mes-hall