A simple and versatile method for the preparation of
bimetallic
AuPd nanoclusters (NCs) with controlled atomic gold distributions
and stabilization by poly(vinyl-2-pyrrolidone) is demonstrated. The
dropwise injection of ethanolic HAuCl4 and the strong acidic
reaction environment assist the control of the distribution of gold
atoms on preformed Pd NCs. These bimetallic NCs are highly active
and selective catalysts for the dehydrogenative aromatization of tetralin
into naphthalene. Several AuPd NC catalysts have been tested, and
these results demonstrate that AuPd NCs with the lowest gold content
have higher catalytic activity. Characterization, including extended
X-ray absorption fine structure and X-ray absorption near-edge structure
analyses, reveals that AuPd NCs with the lowest gold content have
more Au–Pd heterobonds, which play a key role in the dehydrogenative
aromatization reaction. In contrast, transmission electron microscopy
and high-resolution TEM analyses show that AuPd NCs with a greater
gold content have island-like morphologies, where nanocrystalline
gold is deposited on the surfaces of the Pd NCs, which reduces the
number of Au–Pd bond active sites on the Pd NC surfaces. Our
study reveals that tuning of the Au–Pd bond on the surface
of the Pd NCs with a very low content of gold results in high synergy
in catalytic activity and may be expected to be applicable to a wide
variety of bimetallic NCs.
The morphology and surface elemental composition of Au-Pd bimetallic nanoclusters are reported to be sensitive to and affected by reduced silicon defect sites and structural corrugation on SiO2/Si(100), generated by argon ion sputtering under ultrahigh vacuum (UHV) conditions. Metastable structures of the bimetallic clusters, where Au atoms are depleted from the top surface upon annealing, are stabilized by the interaction with the reduced silica sites, as indicated from CO temperature programmed desorption (TPD) titration measurements. Acetylene conversion to ethylene and benzene has been studied as a probe reaction, revealing the modification of selectivity and reactivity enhancement in addition to improved thermal stability on substrates rich in reduced-silica sites. These observations suggest that these unique sites play an important role in anchoring thermodynamically metastable conformations of supported Au-Pd bimetallic catalysts and dictate their high-temperature activity.
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