Surface-segregation-induced phase separation in epitaxial Au/Co nanoparticles: Formation and stability of core-shell structures
Author(s) -
Kazuhisa Sato,
Yuta Matsushima,
Toyohiko J. Konno
Publication year - 2017
Publication title -
aip advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.421
H-Index - 58
ISSN - 2158-3226
DOI - 10.1063/1.4986905
Subject(s) - nanoparticle , metastability , shell (structure) , materials science , transmission electron microscopy , chemical physics , annealing (glass) , surface energy , epitaxy , phase (matter) , high resolution transmission electron microscopy , particle (ecology) , crystallography , nanotechnology , chemical engineering , chemistry , composite material , organic chemistry , layer (electronics) , engineering , oceanography , geology
We have studied formation and stability of core-shell structures in epitaxial Au/Co nanoparticles (NPs) by using atomic-resolution scanning transmission electron microscopy. As the particle size reduces, number of NPs having Au-shell increases and their frequency of occurrence reached 65%. Au segregation proceeds during particle growth at 520 K. The core-shell structure formation is particle size-dependent; the critical diameter dividing the Au-shell and the Co-shell structures is about 11 nm, below which the Au-shell is stable. After annealing at 800 K for 3.6 ks, Au-shell NPs were conserved while the Co-shell NPs changed to two-phase structures with a planar interface separating Au and Co. There is a local energy minimum where the Co-shell NP is metastable in the as-deposited state. A simple model based on surface and interfacial energies suggests stability of Au-shell structures. Surface-segregation-induced phase separation in small NPs, due to low surface free energy of Au, will be responsible for the Au-shell formation
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