Structural Stability of Ruthenium Nanoparticles: A Density Functional Theory Study

We
have analyzed the crucial factors that stabilize face-centered
cubic (fcc) ruthenium nanoparticles (Ru-NPs) using the density functional
theory method. We calculated the cohesive energy of the decahedral
fcc, icosahedral fcc, truncated octahedral fcc, and hexagonal close-packed
(hcp) Ru-NPs with between 55 and 1557 atoms. The cohesive energy of
the icosahedral fcc Ru-NPs became closer to that of the hcp Ru-NPs
with decreasing number of atoms, i.e., particle size. This characteristic
is mainly caused by the high coordination number of the icosahedral
fcc Ru-NP and the negative twin boundary energy for fcc {111}. On
the other hand, the d-band center of Ru atoms in
the surface layer of icosahedral fcc Ru-NPs is less negative than
those of the other structures. This characteristic is caused by the
longer interatomic distance between Ru atoms in the surface layer
of the icosahedral fcc Ru-NP. Together with the structural stability,
the icosahedral fcc structure shows a unique electronic structure
compared with the other structures. Our results are expected to be
helpful for controlling and designing the properties, such as stability
and catalytic activity, of Ru-NPs from the shape of the NP.