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 bandgap. 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.

Multitemperature 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 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 multitemperature 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 multitemperature heat transport equations.