The essential role of O affinity in the directed assembly of size-selected Au and Fe nanoparticles (NPs) on a TiOx/Pt(111) ultrathin oxide phase, an effective template for size selected metal NP growth, is revealed through scanning tunneling microscopy and density-functional calculations. A weakly interacting element (Au) diffuses rapidly and gets trapped in the vacancy defects (picoholes) located inside parallel rows (troughs, spaced 1.44 nm apart) peculiar to the film structure, producing size-selected NPs arranged in regular linear arrays aligned along the troughs. In contrast, an element with greater O affinity (Fe) experiences higher diffusion barriers, and the growth is dominated by kinetic effects, with a less effective preferential nucleation and the appearance of irregular NP morphologies.

Directed assembly of Au and Fe nanoparticles on a TiOx/Pt(111) ultrathin template: the role of oxygen affinity

SEDONA, FRANCESCO;AGNOLI, STEFANO;GRANOZZI, GAETANO;
2009

Abstract

The essential role of O affinity in the directed assembly of size-selected Au and Fe nanoparticles (NPs) on a TiOx/Pt(111) ultrathin oxide phase, an effective template for size selected metal NP growth, is revealed through scanning tunneling microscopy and density-functional calculations. A weakly interacting element (Au) diffuses rapidly and gets trapped in the vacancy defects (picoholes) located inside parallel rows (troughs, spaced 1.44 nm apart) peculiar to the film structure, producing size-selected NPs arranged in regular linear arrays aligned along the troughs. In contrast, an element with greater O affinity (Fe) experiences higher diffusion barriers, and the growth is dominated by kinetic effects, with a less effective preferential nucleation and the appearance of irregular NP morphologies.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2445624
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