Citation: QIAN Huifeng, BARRY Ellen, ZHU Yan, JIN Rongchao. Doping 25-Atom and 38-Atom ld Nanoclusters with Palladium[J]. Acta Physico-Chimica Sinica, ;2011, 27(03): 513-519. doi: 10.3866/PKU.WHXB20110304 shu

Doping 25-Atom and 38-Atom ld Nanoclusters with Palladium

  • Received Date: 4 November 2010
    Available Online: 21 January 2011

    Fund Project: The project was supported by Carnegie Mellon University (CMU) (CMU) the Air Force Office of Scientific Research (AFOSR) (AFOSR)the National Institute for ccupational Safety and Health (NIOSH) (NIOSH) USA. BARRY Ellen was supported by the National Science Foundation-Research Experiences for Undergraduates, USA (NSF grant DMR #1005076). (NSF grant DMR #1005076)

  • In this work, we describe two synthetic procedures for preparing palladium doped 25-atom nanoclusters (referred to as Pd1Au24(SR)18, where ―SR represents thiolate, R=C2H4Ph). Pure Pd1Au24(SC2H4Ph)18 nanoclusters are isolated by solvent extraction and size exclusion chromatography. Mass spectrometry and optical spectroscopy analyses demonstrate that the Pd1Au24(SC2H4Ph)18 nanocluster adopts the same core-shell structure as that of the homo ld Au25(SC2H4Ph)18 nanocluster, that is, a Pd- or Au-centered icosahedron surrounded by six Au2(SR)3 “staple”-like motifs. Similar doping behavior has also been observed in 38-atom M38(SR)24 (M: metal) nanoclusters, indicating the unique behavior of Pd dopant being preferentially located in the icosahedral center. The catalytic activity of Pd1Au24(SC2H4Ph)18 has also been evaluated for the selective hydrogenation of α,β-unsaturated ketone (e.g., benzalacetone) to α,β- unsaturated alcohol, and a 42% conversion of benzalacetone is attained.

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