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
Barcaro G;Fortunelli A
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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
