Spin Controlled Surface Chemistry: Alkyl Desorption from Si(100)-2x1 by Nonadiabatic Hydrogen Elimination

23 March 2020, Version 1
This content is a preprint and has not undergone peer review at the time of posting.


An understanding of the role that spin states play in semiconductor surface chemical reactions is currently limited. Herein, we provide evidence of a nonadiabatic reaction involving a localized singlet to triplet thermal excitation of the Si(100) surface dimer dangling bond. By comparing the β-hydrogen elimination kinetics of ethyl adsorbates probed by thermal desorption experiments to electronic structure calculation results, we determined that a coverage-dependent change in mechanism occurs. At low coverage, a nonadiabatic, inter-dimer mechanism is dominant, while adiabatic mechanisms become dominant at higher coverage. Computational results indicate that the spin flip is rapid near room temperature and the nonadiabatic path is accelerated by a barrier that is 40 kJ/mol less than the adiabatic path. Simulated thermal desorption reactions using nonadiabatic transition state theory (NA-TST) for the surface dimer electron spin flip are in close agreement with experimental observations.


surface chemistry
spin crossover
density functional calculations

Supplementary materials

NA ethyl desorption ChemRxiv SI Final2


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