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Density functional theory study of clean, hydrated, and defective alumina (1 1Ì„ 02 ) surfaces
Journal article   Peer reviewed

Density functional theory study of clean, hydrated, and defective alumina (1 1Ì„ 02 ) surfaces

Sara E Mason, Christopher R Iceman, Thomas P Trainor and Anne M Chaka
Physical review. B, Condensed matter and materials physics, Vol.81(12), 125423
2010
DOI: 10.1103/PhysRevB.81.125423

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Abstract

We report an ab initio thermodynamic analysis of the a-Al2O3 (1-102) surface aimed at understanding the experimentally observed terminations over a range of surface preparation conditions, as well as a novel stoichiometric model for the (2x1) surface reconstruction observed after high temperature annealing. As temperature is increased under both ultra-high vacuum and ambient hydrated conditions, the predicted minimum energy structural model goes through the same series of changes: from the hydroxylated ``missing-Al'' surface model (or half layer model in which the topmost Al site of the stoichiometric surface has zero occupancy), to the hydroxylated stoichiometric model, to another hydroxylated missing-Al surface model with tetrahedral coordinated surface Al, and finally to the clean (1x1) stoichiometric model. These results are in agreement with observations of both missing-Al and bulk-like stoichiometries under wet conditions and in agreement with similar trends reported for isostructural hematite. However, we observe that the models with excess oxygen have a relatively higher surface free energy and distinct surface relaxations in the case of alumina as compared to hematite. At very high temperatures where oxygen defects are generated, we find that a novel stoichiometric, charge-neutral (2x1) structure becomes the most thermodynamically stable. This is consistent with the observation of a (2x1) electron diffraction pattern when the surface is annealed at 2000 K, while a (1x1) pattern persists at lower annealing temperatures. A general rule that emerges from our modeling results is that while the full phase space of hydrated and defective surfaces is expansive, model stoichiometries that can be made charge-neutral through either hydration or defects offer the greatest thermodynamic stability.

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