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Surface Structure of V2O3(0001) Revisited

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Feiten,  Felix E.
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Seifert,  Jan
Chemical Physics, Fritz Haber Institute, Max Planck Society;
Humboldt-Universität zu Berlin, Institut für Physik;

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Kuhlenbeck,  Helmut
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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Freund,  Hans-Joachim
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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PhysRevLett.114.216101.pdf
(Publisher version), 921KB

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Citation

Feiten, F. E., Seifert, J., Paier, J., Kuhlenbeck, H., Winter, H., Sauer, J., et al. (2015). Surface Structure of V2O3(0001) Revisited. Physical Review Letters, 114(21): 216101. doi:10.1103/PhysRevLett.114.216101.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0027-9DF1-7
Abstract
In a recent paper [A. J. Window et al., Phys. Rev. Lett. 107, 016105 (2011)], it was proposed that V2O3(0001) is terminated by the so-called O3 termination, a reconstruction with a terminating distorted hexagonal oxygen layer. We show that the surface is terminated by vanadyl (V═O) groups instead. This conclusion is based on quantitative low-energy electron diffraction combined with scanning tunneling microscopy, fast atom scattering, and density functional theory employing the Heyd-Scuseria-Ernzerhof functional. New insights into the subsurface sensitivity of ion beam triangulation show that results previously interpreted in favor of the O3 termination are reconcilable with vanadyl termination as well.