Assessment of Real-Time Time-Dependent Density Functional Theory (RT-TDDFT) in Radiation Chemistry: Ionized Water Dimer

0500249 - ÚFCH JH 2019 RIV US eng J - Článek v odborném periodiku
Chalabala, J. - Uhlig, F. - Slavíček, Petr
Assessment of Real-Time Time-Dependent Density Functional Theory (RT-TDDFT) in Radiation Chemistry: Ionized Water Dimer.
Journal of Physical Chemistry A. Roč. 122, č. 12 (2018), s. 3227-3237. ISSN 1089-5639. E-ISSN 1520-5215
Grant ostatní: GA ČR(CZ) GA13-34168S; Ga MŠk(CZ) LM2015070
Institucionální podpora: RVO:61388955
Klíčová slova: MOLECULAR-DYNAMICS SIMULATIONS * IRRADIATED LIQUID WATER * ELECTRON DYNAMICS
Obor OECD: Physical chemistry
Impakt faktor: 2.641, rok: 2018

Ionization in the condensed phase and molecular clusters leads to a complicated chain of processes with coupled electron–nuclear dynamics. It is difficult to describe such dynamics with conventional nonadiabatic molecular dynamics schemes since the number of states swiftly increases as the molecular system grows. It is therefore attractive to use a direct electron and nuclear propagation such as the real-time time-dependent density functional theory (RT-TDDFT). Here we report a RT-TDDFT benchmark study on simulations of singly and doubly ionized states of a water monomer and dimer as a prototype for more complex processes in a condensed phase. We employed the RT-TDDFT based Ehrenfest molecular dynamics with a generalized gradient approximate (GGA) functional and compared it with wave-function-based surface hopping (SH) simulations. We found that the initial dynamics of a singly HOMO ionized water dimer is similar for both the RT-TDDFT/GGA and the SH simulations but leads to completely different reaction channels on a longer time scale. This failure is attributed to the self-interaction error in the GGA functionals and it can be avoided by using hybrid functionals with large fraction of exact exchange (represented here by the BHandHLYP functional). The simulations of doubly ionized states are reasonably described already at the GGA level. This suggests that the RT-TDDFT/GGA method could describe processes following the autoionization processes such as Auger emission, while its applicability to more complex processes such as intermolecular Coulombic decay remains limited.
Trvalý link: http://hdl.handle.net/11104/0292350