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Regensburg 2016 – scientific programme

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SYES: Symposium Frontiers of Electronic Structure Theory: Focus on Topology and Transport

SYES 4: Frontiers of Electronic Structure Theory: Focus on Topology and Transport II

SYES 4.2: Talk

Wednesday, March 9, 2016, 10:45–11:00, H24

Surface adsorption energetics at the "gold standard": Small molecule binding to TiO2(110) — •Daniel Berger1,2, A. Kubas3, D. Manganas3, H. Oberhofer1, F. Neese3, and K. Reuter11TU München — 2University of California, Los Angeles — 3MPI für chemische Energiekonversion, Mülheim an der Ruhr

Adsorption energies at oxide surfaces are central quantities required for catalysis, energy and a multitude of other application areas. At present, the by far dominant computational method to obtain such energetics is density-functional theory (DFT). Unfortunately, systematic benchmarking of such energetics against accurate reference numbers from correlated wave-function theory as known from molecular systems is scarce, largely owing to the fact that the latter techniques are often not available for standard periodic boundary condition supercell calculations.

We address this situation with a solid-state QM/MM embedded cluster approach, in which the adsorbate and immediate surrounding surface atoms are described quantum mechanically, while the long-range electrostatic interactions are accounted for through a polarizable force field. This yields a numerically highly efficient approach that enables use of the recently developed domain-based local pair natural orbital coupled cluster method with single-, double- and perturbative triple-excitations (DLPNO-CCSD(T)) in the quantum region. We exploit corresponding "gold standard" adsorption energies for a set of prototypical small molecules interacting with the rutile TiO2(110) surface for a systematic benchmark of DFT numbers.

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