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Testing Electronic Friction Models: Vibrational De-excitation in Scattering of H 2 and D 2 from Cu(111).
Journal of Physical Chemistry Letters 2018 April 6
At present, molecular dynamics with electronic friction (MDEF) is the workhorse model to go beyond the Born-Oppenheimer approximation in modeling dynamics of molecules at metal surfaces. Concomitant friction coefficients can be calculated with either the local density friction approximation (LDFA) or orbital-dependent friction (ODF), which, unlike LDFA, accounts for anisotropy while relying on other approximations. Due to the computational cost of ODF, extensive high-dimensional MDEF trajectory calculations of experimentally measurable observables have hitherto only been performed based on LDFA. We overcome this limitation with a continuous neural-network-based representation. In our first application to the scattering of vibrationally excited H2 and D2 from Cu(111), we predict up to three times higher vibrational de-excitation probabilities with ODF than with LDFA. These results indicate that anisotropic electronic friction can be important for specific molecular observables. Future experiments can test for this "fingerprint" of different approximations underlying state-of-the-art MDEF.
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