Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

An accurate full-dimensional potential energy surface for H–Au(111): Importance of nonadiabatic electronic excitation in energy transfer and adsorption

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4931669· OSTI ID:22489656
; ;  [1];  [1]
  1. Institute for Physical Chemistry, Göttingen University, Tammannstr. 6, 37077 Göttingen (Germany)

We have constructed a potential energy surface (PES) for H-atoms interacting with fcc Au(111) based on fitting the analytic form of the energy from Effective Medium Theory (EMT) to ab initio energy values calculated with density functional theory. The fit used input from configurations of the H–Au system with Au atoms at their lattice positions as well as configurations with the Au atoms displaced from their lattice positions. It reproduces the energy, in full dimension, not only for the configurations used as input but also for a large number of additional configurations derived from ab initio molecular dynamics (AIMD) trajectories at finite temperature. Adiabatic molecular dynamics simulations on this PES reproduce the energy loss behavior of AIMD. EMT also provides expressions for the embedding electron density, which enabled us to develop a self-consistent approach to simulate nonadiabatic electron-hole pair excitation and their effect on the motion of the incident H-atoms. For H atoms with an energy of 2.7 eV colliding with Au, electron-hole pair excitation is by far the most important energy loss pathway, giving an average energy loss ≈3 times that of the adiabatic case. This increased energy loss enhances the probability of the H-atom remaining on or in the Au slab by a factor of 2. The most likely outcome for H-atoms that are not scattered also depends prodigiously on the energy transfer mechanism; for the nonadiabatic case, more than 50% of the H-atoms which do not scatter are adsorbed on the surface, while for the adiabatic case more than 50% pass entirely through the 4 layer simulation slab.

OSTI ID:
22489656
Journal Information:
Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 12 Vol. 143; ISSN JCPSA6; ISSN 0021-9606
Country of Publication:
United States
Language:
English

Similar Records

Ab initio molecular dynamics calculations on scattering of hyperthermal H atoms from Cu(111) and Au(111)
Journal Article · Thu Aug 07 00:00:00 EDT 2014 · Journal of Chemical Physics · OSTI ID:22420002

Ab initio (HeH sub 2 ) sup + energy surfaces and nonadiabatic couplings between them
Journal Article · Wed Oct 31 23:00:00 EST 1990 · Journal of Chemical Physics; (USA) · OSTI ID:6162488

High-Dimensional Atomistic Neural Network Potentials for Molecule–Surface Interactions: HCl Scattering from Au(111)
Journal Article · Thu Jan 19 23:00:00 EST 2017 · Journal of Physical Chemistry Letters · OSTI ID:1483849