Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2016Switching a Nanocluster Core from Hollow to Non-hollow89citations
  • 2016[Ag67(SPhMe2)32(PPh3)8]3+: Synthesis, Total Structure, and Optical Properties of a Large Box-Shaped Silver Nanocluster179citations

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Joshi, Chakra Prasad
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Malola, Sami
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Juarez-Mosqueda, Rosalba
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Hakkinen, Hannu
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Kaappa, Sami
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Emwas, Abdul-Hamid M.
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Adil, Karim
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2016

Co-Authors (by relevance)

  • Joshi, Chakra Prasad
  • Malola, Sami
  • Juarez-Mosqueda, Rosalba
  • Hakkinen, Hannu
  • Kaappa, Sami
  • Emwas, Abdul-Hamid M.
  • Adil, Karim
OrganizationsLocationPeople

article

[Ag67(SPhMe2)32(PPh3)8]3+: Synthesis, Total Structure, and Optical Properties of a Large Box-Shaped Silver Nanocluster

  • Malola, Sami
  • Alhilaly, Mohammad J.
  • Juarez-Mosqueda, Rosalba
  • Hakkinen, Hannu
  • Kaappa, Sami
  • Emwas, Abdul-Hamid M.
  • Joshi, Chakra Prasad
  • Adil, Karim
Abstract

Engineering the surface ligands of metal nanoparticles is critical in designing unique arrangements of metal atoms. Here, we report the synthesis and total structure determination of a large box-shaped Ag-67 nanocluster (NC) protected by a mixed shell of thiolate (2,4-dimethylbenzenethiolate, SPhMe2) and phosphine (triphenylphosphine, PPh3) ligands. Single crystal X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revealed the cluster formula to be [Ag-67(SPhMe2)(32)(PPh3)(8)](3+). The crystal structure shows an Ag-23 metal core covered by a layer of Ag44S32P8 arranged in the shape of a box. The Ag-13, core was formed through an unprecedented centered cuboctahedron, i.e., Ag-13, unlike the common centered Ag-13 icosahedron geometry. Two types of ligand motifs, eight AgS3P and eight bridging thiols, were found to stabilize the whole cluster. The optical spectrum of this NC displayed highly structured multiple absorption peaks. The electronic structure and optical spectrum of Ag-67 were computed using time-dependent density functional theory (TDDFT) for both the full cluster [Ag-67(SPhMe2)(32)(PPh3)(8)](3+) and a reduced model [Ag-67(SH)(32)(PH3)(8)](3+). The lowest metal-to-metal transitions in the range 500-800 nm could be explained by considering the reduced model that shows almost identical electronic states to 32 free electrons in a jellium box. The successful synthesis of the large box-shaped Ag-67 NC facilitated by the combined use of phosphine and thiol paves the way for synthesizing other metal clusters with unprecedented shapes by judicious choice of thiols and phosphines.

Topics
  • nanoparticle
  • density
  • impedance spectroscopy
  • surface
  • single crystal X-ray diffraction
  • cluster
  • single crystal
  • silver
  • theory
  • density functional theory
  • spectrometry
  • electrospray ionisation
  • electrospray ionisation mass spectrometry