Cluster nucleation and growth from a highly supersaturated adatom phase: silver on magnetite

R. Bliem, R. Kosak, L. Perneczky, Z. Novotny, O. Gamba, D. Fobes, Z. Mao, M. Schmid, P. Blaha , U. Diebold, G. S. Parkinson

Institut für Angewandte Physik, Technische Universität Wien, 1040 Wien, Austria

ACS Nano 8 (2014) 7531-7537

The atomic-scale mechanisms underlying the growth of Ag on the (√2 × √2)R45°-Fe3O4(001) surface were studied using scanning tunneling microscopy and density functional theory based calculations. For coverages up to 0.5 ML, Ag adatoms populate the surface exclusively; agglomeration into nanoparticles only occurs with the lifting of the reconstruction at 720 K. Above 0.5 ML, Ag clusters nucleate spontaneously, and grow at the expense of the surrounding material with mild annealing. This unusual behavior results from a kinetic barrier associated with the (√2×√2)R45° reconstruction, which prevents adatoms from transitioning to the thermodynamically favorable 3D phase. The barrier is identified as the large separation between stable adsorption sites, which prevents homogeneous cluster nucleation, and the instability of the Ag dimer against decay to two adatoms. Since the system is dominated by kinetics so long as the (√2×√2)R45° exists, the growth is not well described by the traditional growth modes. It can be understood, however, as the result of supersaturation within an adsorption template system.

Corresponding author: Gareth S. Parkinson (parkinson at iap_tuwien_ac_at).

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