Pt 3Zr(0001): A substrate for growing well-ordered ultrathin zirconia films by oxidation

44Citations
Citations of this article
34Readers
Mendeley users who have this article in their library.

Abstract

We have studied the surface of pure and oxidized Pt 3Zr(0001) by scanning tunneling microscopy (STM), Auger electron microscopy, and density functional theory (DFT). The well-annealed alloy surface shows perfect long-range chemical order. Occasional domain boundaries are probably caused by nonstoichiometry. Pt 3Zr exhibits ABAC stacking along [0001]; only the A-terminated surfaces are seen by STM, in agreement with DFT results showing a lower surface energy for the A termination. DFT further predicts a stronger inward relaxation of the surface Zr than for Pt, in spite of the larger atomic size of Zr. A closed ZrO 2 film is obtained by oxidation in 10 -7 mbar O 2 at 400 -C and post-annealing at ∼800 -C. The oxide consists of an O-Zr-O trilayer, equivalent to a (111) trilayer of the fluorite structure of cubic ZrO 2, but contracted laterally. The oxide forms a (√19×√19)R23 - superstructure. The first monolayer of the substrate consists of Pt and contracts, similar to the metastable reconstruction of pure Pt(111). DFT calculations show that the oxide trilayer binds rather weakly to the substrate. In spite of the O-terminated oxide, bonding to the substrate mainly occurs via the Zr atoms in the oxide, which strongly buckle down toward the Pt substrate atoms if near a Pt position. According to DFT, the oxide has a band gap; STM indicates that the conduction band minimum lies ∼2.3 eV above E F. © 2012 American Physical Society.

Cite

CITATION STYLE

APA

Antlanger, M., Mayr-Schmölzer, W., Pavelec, J., Mittendorfer, F., Redinger, J., Varga, P., … Schmid, M. (2012). Pt 3Zr(0001): A substrate for growing well-ordered ultrathin zirconia films by oxidation. Physical Review B - Condensed Matter and Materials Physics, 86(3). https://doi.org/10.1103/PhysRevB.86.035451

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free