Abstract
Nonadiabatic molecular dynamics simulations in combination with time-dependent Kohn-Sham density functional theory are used to study the nonradiative relaxation of charge carriers in 4-mercaptobenzonitrile (NCOPE1), 4-(mercaptomethyl) benzonitrile (NC-PT1), 4′-mercapto-[1,1′-biphenyl]-4-carbonitrile (NC-BP0) and 4-((4-mercaptophenyl) ethynyl) benzonitrile (NCOPE2) molecules absorbed on Au(111) surface. The fastest hot electron decay (∼30 fs) is obtained for the NCOPE1 molecule due to strong electron-phonon couplings. However, the relaxation kinetics strongly depends on the properties of the initially populated state (e.g., orbital-overlap/hybridization between the organic molecules and the substrate), on the proximity of neighboring electronic states (i.e., intraband gaps) and on the electron-phonon nonadiabatic couplings. The obtained orbital- and size-dependent relaxation dynamics is in qualitative agreement with the results of core-hole clock experiments, which indicates the possibility of modeling the interfacial electron transfer by the decay process of hot electrons.
Published Version
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