posted on 2013-07-03, 00:00authored byHuayan Yang, Yu Wang, Jing Lei, Lei Shi, Xiaohu Wu, Ville Mäkinen, Shuichao Lin, Zichao Tang, Jian He, Hannu Häkkinen, Lansun Zheng, Nanfeng Zheng
Three
novel bimetallic Au-Cu nanoclusters stabilized by a mixed
layer of thiolate and phosphine ligands bearing pyridyl groups are
synthesized and fully characterized by X-ray single crystal analysis
and density functional theory computations. The three clusters have
an icosahedral Au13 core face-capped by two, four, and
eight Cu atoms, respectively. All face-capping Cu atoms in the clusters
are triply coordinated by thiolate or pyridyl groups. The surface
ligands control the exposure of Au sites in the clusters. In the case
of the Au13Cu8 cluster, the presence of 12 2-pyridylthiolate
ligands still leaves open space for catalysis. All the 3 clusters
are 8-electron superatoms displaying optical gaps of 1.8–1.9
eV. The thermal decomposition studies suggest that the selective release
of organic ligands from the clusters is possible.