Controlled nanoscale morphology on the alpha-Fe2O3 (0001) surface

GEOC 68

Steven T. Christensen, s-christensen@northwestern.edu1, Mark E. Greene1, Ann N. Chiaramonti1, Michael J. Bedzyk2, and Mark C. Hersam, m-hersam@northwestern.edu1. (1) Department of Materials Science and Engineering, Northwestern University, 2220 Campus Drive, Evanston, IL 60208, (2) Center for Catalysis and Surface Science, Department of Materials Science and Engineering, Northwestern University, 2220 Campus Drive, Evanston, IL 60208
The ability to control surface morphology at the nanometer scale may enhance several technological applications for alpha-Fe2O3 (0001) including catalysis, photoelectrochemistry, magnetic data storage, and spintronics. In pursuit of this goal, atomic force microscopy is employed to study the nanoscale morphology of alpha-Fe2O3 following annealing treatments in oxygen-rich atmospheres. The alpha-Fe2O3 (0001) crystals were grown via chemical vapor transport using the equilibrium reaction. [1] [2] [3] Upon annealing the crystals in oxygen rich atmospheres at 900°C for 2 hours, the originally featureless surface was transformed to one with broad (~100 microns wide) atomically flat terraces separated by narrow (~1 microns wide) regions with dense step bunching. The terraces support two-dimensional circular domains with diameters on the order of hundreds of nanometers and depths of 2.2 ± 0.2 Å. The domains extend across >90% of the surface and can locally coalesce to form layered domains that are multiple unit cell lengths deep. The formation of these circular domain structures are consistent with a theoretical model based on relatively long range repulsive dipole interactions among the domains. [4] [5] [6] The generality of this model will be discussed by comparing the case of circular domains in alpha-Fe2O3 with similar domain formation observed in other oxide systems (e.g., SrTiO3 and TiO2).

[1] V.P. Kleinert, Z Anorg Allgem Chem 378 (1970) 71. [2] K.R. Poepplemeier & B.B. Ansell, J Crystal Growth 51 (1981), 587. [3] H. Schäfer, Chemical Transport Reactions, New York, Academic Press, 1964. [4] K.-O. Ng & D. Vanderbilt, 52 (1995) 2177. [5] R. Plass, J.A. Last, N.C. Bartlett, & G.L. Kellogg, Nature, 412 (2001) 875. [6] J.B. Hannon, J. Tersoff, & R.M. Tromp, Science 295 (2002) 299.