Cluster Nucleation and Growth from a Highly Supersaturated Adatom Phase: Silver on Magnetite
Author(s) -
Roland Bliem,
Rukan Kosak,
Lukas Perneczky,
Zbyněk Novotný,
Oscar Gamba,
David Fobes,
Zhiqiang Mao,
Michael Schmid,
Peter Blaha,
Ulrike Diebold,
Gareth S. Parkinson
Publication year - 2014
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/nn502895s
Subject(s) - nucleation , supersaturation , scanning tunneling microscope , chemical physics , materials science , annealing (glass) , cluster (spacecraft) , adsorption , phase (matter) , magnetite , density functional theory , dissociation (chemistry) , crystallography , nanotechnology , chemistry , computational chemistry , metallurgy , organic chemistry , computer science , programming language
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 occurs only 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 as long as the (√2×√2)R45° reconstruction 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.
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