AVS 64th International Symposium & Exhibition
    Surface Science Division Wednesday Sessions
       Session SS+HC+NS-WeA

Paper SS+HC+NS-WeA12
Experimental and Theoretical Study of Rotationally Inelastic Diffraction of H2(D2) from Methyl-Terminated Si(111)

Wednesday, November 1, 2017, 6:00 pm, Room 25

Session: Dynamical Processes at Surfaces
Presenter: Kevin Nihill, University of Chicago
Authors: K. Nihill, University of Chicago
Z.M. Hund, University of Chicago
A. Muzas, Universidad Autónoma de Madrid, Spain
C. Diaz, Universidad Autónoma de Madrid, Spain
M. del Cueto, Universidad Autónoma de Madrid, Spain
T. Frankcombe, University of New South Wales, Australia
N. Plymale, California Institute of Technology
N.S. Lewis, California Institute of Technology
F. Martin, Universidad Autónoma de Madrid, Spain
S.J. Sibener, University of Chicago
Correspondent: Click to Email
Fundamental details concerning the interaction between H2 and CH3-Si(111) have been elucidated by the combination of diffractive scattering experiments and electronic structure and scattering calculations. Rotationally inelastic diffraction (RID) of H2 and D2 from this model hydrocarbon-decorated semiconductor interface has been confirmed for the first time via both time-of-flight and diffraction measurements, with modest j = 0 → 2 RID intensities for H2 compared to the strong RID features observed for D2 over a large range of kinematic scattering conditions along two high-symmetry azimuthal directions. The Debye-Waller model was applied to the thermal attenuation of diffraction peaks, allowing for precise determination of the RID probabilities by accounting for incoherent motion of the CH3-Si(111) surface atoms. The probabilities of rotationally inelastic diffraction of H2 and D2 have been quantitatively evaluated as a function of beam energy and scattering angle, and have been compared with complementary electronic structure and scattering calculations to provide insight into the interaction potential between H2 (D2) and hence the surface charge density distribution. Specifically, a six-dimensional potential energy surface (PES), describing the electronic structure of the H2(D2)/CH3-Si(111) system, has been computed based on interpolation of density functional theory (DFT) energies. Quantum and classical dynamics simulations have allowed for an assessment of the accuracy of the PES, and subsequently for identification of the features of the PES that serve as classical turning points. A close scrutiny of the PES reveals the highly anisotropic character of the interaction potential at these turning points. This combination of experiment and theory provides new and important details about the interaction of H2 with a hybrid organic-semiconductor interface, which can be used to further investigate energy flow in technologically relevant systems.