arXiv subjects

Alexander E. Volkov

Publications and source records attributed to Alexander E. Volkov.

5 recordsLinked to original sources

arXiv2026

Effect of radially heterogeneous band gap collapse on formation of swift heavy ion tracks in Al2O3

We estimate the effects of radial heterogeneity in the collapse of the electronic band gap on the damage in Al2O3 after impact of a swift heavy ion decelerated in the electronic stopping regime. The Monte Carlo code TREKIS describes the initial excitation of the electronic and ionic systems following the ion passage, while the density functional theory based molecular dynamics traces changes in the band structure in the ion track. This combination of methods enables us to compute the profile of energy transferred to the lattice by the time of relaxation of the electronic excitation, accounting for the induced spatial inhomogeneity of the band structure around the ion trajectory. We demonstrate that impact of a 700 MeV Bi ion induces a transient metal-semiconductor heterojunction in Al2O3: the metallization (the band gap collapse) occurs within a radius of about 2 nm from the ion trajectory. The band gap shrinks at distances of about 3-5 nm, while it remains almost unaffected at radii larger than 5 nm. Using this data, we estimate the atomic heating depending on the degree of band gap reduction at different radii from the ion trajectory. This approach refines the damage modeling, producing more pronounced discontinuous damage patterns along the ion path for all crystallographic directions compared to the model that assumes all the energy accumulated in the electron-hole ensemble is delivered to the atoms.

cond-mat.mtrl-sci↗

arXiv2024

Multi-temperature atomic ensemble: nonequilibrium evolution after ultrafast electronic excitation

Ultrafast laser radiation or beams of fast charged particles primarily excite the electronic system of a solid driving the target transiently out of thermal equilibrium. Apart from the nonequilibrium between the electrons and atoms, each subsystem may be far from equilibrium. From the first principles, we derive the definition of various atomic temperatures applicable to electronically excited ensembles. It is shown that the definition of the kinetic temperature of atoms in the momentum subspace is unaffected by the excitation of the electronic system. When the electronic temperature differs from the atomic one, an expression for the configurational atomic temperature is proposed, applicable to the electronic-temperature-dependent interatomic potentials (such as ab-initio molecular dynamics simulations). We study how the configurational temperature behaves during nonthermal phase transition, triggered by the evolution of the interatomic potential due to the electronic excitation. It is revealed that upon the ultrafast irradiation, the atomic system of a solid exists temporarily in a multi-temperature state: separate equilibria in the momentum and configurational subspaces. Complete equilibration between the various atomic temperatures takes place at longer timescales, forming the energy equipartition. Based on these results, we propose a formulation of multi-temperature heat transport equations.

cond-mat.other↗

arXiv2022

Metallic water: transient state under ultrafast electronic excitation

The modern means of controlled irradiation by femtosecond lasers or swift heavy ion beams can transiently produce such energy densities in samples that reach collective electronic excitation levels of the warm dense matter state where the potential energy of interaction of the particles is comparable to their kinetic energies (temperatures of a few eV). Such massive electronic excitation severely alters the interatomic potentials, producing unusual nonequilibrium states of matter and different chemistry. We employ density functional theory and tight binding molecular dynamics formalisms to study the response of bulk water to ultrafast excitation of its electrons. After a certain threshold electronic temperature, the water becomes electronically conducting via the collapse of its band gap. At high doses, it is accompanied by nonthermal acceleration of ions to a temperature of a few thousand Kelvins within sub-100 fs timescales. We identify the interplay of this nonthermal mechanism with the electron-ion coupling, enhancing the electron-to-ions energy transfer. Various chemically active fragments are formed from the disintegrating water molecules, depending on the deposited dose.

cond-mat.other↗

arXiv2021

Reconciling anomalously fast heating rate in ion tracks with low electron-phonon coupling

Formation of swift heavy ion tracks requires extremely fast energy transfer between excited electrons and a lattice. However, electron-phonon energy exchange is too slow, as known from laser-irradiation experiments and calculations. We resolve this contradiction noticing that electron-phonon coupling is not the sole mechanism of energy exchange between electrons and ions: heating of electrons also alters potential energy surface of atoms, accelerating them and increasing their kinetic energy.

cond-mat.mtrl-sci↗

arXiv2020

Mechanisms of surface nanostructuring of Al2O3 and MgO by grazing incidence irradiation with swift heavy ions

We experimentally discovered that Al2O3 and MgO exhibit well-pronounced nanometric modifications on the surfaces when irradiated under grazing incidence with 23 MeV I beam, in contrast to normal incidence irradiation with the same ion beam when no damage was found. Moreover, ions in these two materials produce notably different structures: grooves surrounded with nanohillocks on MgO surfaces vs. smoother, roll-like discontinuous structures on the surfaces of Al2O3. To explain these results, detailed numerical simulations were performed. We identified that a presence of the surface inhibits recrystallization process, thereby preventing transient tracks from recovery, and thus forming observable nanopatterns. Furthermore, a difference in the viscosities in molten states in Al2O3 vs. MgO explains the differences in the created nanostructures. Our results thus provide a deeper understanding of the fundamental processes of surface nanostructuring, potentially allowing for controlled production of periodic surface nanopatterns.

cond-mat.mtrl-sci↗