Sub-Nanometer Au Monolayer-Protected Clusters Exhibiting Molecule-like Electronic Behavior: Quantitative High-Angle Annular Dark-Field Scanning Transmission Electron Microscopy and Electrochemical Characterization of Clusters with Precise Atomic Stoichio

نویسندگان

  • Laurent D. Menard
  • Shang-Peng Gao
  • Huiping Xu
  • Ray D. Twesten
  • Amanda S. Harper-Leatherman
  • Yang Song
  • Gangli Wang
  • Alicia D. Douglas
  • Judith C. Yang
  • Anatoly I. Frenkel
  • Ralph G. Nuzzo
  • Royce W. Murray
  • Amanda S. Harper
چکیده

Published Citation Menard , Laurent D.; Gao, Sheng-Peng; Xu, Huiping; Twesten, Ray D.; Harper, Amanda S.; Song, Yang; Wang, Gangli; Douglas, Alicia D.; Yang, Judith C.; Frenkel, Anatoly I.; Nuzzo, Ralph G.; Murray, Royce W. “Sub-Nanometer Au Monolayer-Protected Clusters Exhibiting Molecule-like Electronic Behavior: Quantitative High-Angle Annular Dark-Field Scanning Transmission Electron Microscopy and Electrochemical Characterization of Clusters with Precise Atomic Stoichiometry.” Journal of Physical Chemistry B, 2006, 110 (26), 12874-12883. Repository Citation

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Sub-nanometer Au monolayer-protected clusters exhibiting molecule-like electronic behavior: quantitative high-angle annular dark-field scanning transmission electron microscopy and electrochemical characterization of clusters with precise atomic stoichiometry.

The synthesis and characterization of the clusters Au13[PPh3]4[S(CH2)11CH3]2Cl2 (1) and Au13[PPh3]4[S(CH2)11CH3]4 (2) are described. These mixed-ligand, sub-nanometer clusters, prepared via exchange of dodecanethiol onto phosphine-halide gold clusters, show enhanced stability relative to the parent. The characterization of these clusters features the precise determination of the number of gold ...

متن کامل

Metal core bonding motifs of monodisperse icosahedral Au13 and larger Au monolayer-protected clusters as revealed by X-ray absorption spectroscopy and transmission electron microscopy.

The atomic metal core structures of the subnanometer clusters Au13[PPh3]4[S(CH2)11CH3]2Cl2 (1) and Au13[PPh3]4[S(CH2)11CH3]4 (2) were characterized using advanced methods of electron microscopy and X-ray absorption spectroscopy. The number of gold atoms in the cores of these two clusters was determined quantitatively using high-angle annular dark field scanning transmission electron microscopy....

متن کامل

Synthesis, Surface Assembly, Characterization and Electrochemistry of Gold Nanoparticles

Aalto University, P.O. Box 11000, FI-00076 Aalto www.aalto.fi Author Outi Toikkanen Name of the doctoral dissertation Synthesis, Surface Assembly, Characterization and Electrochemistry of Gold Nanoparticles Publisher School of Chemical Technology Unit Department of Chemistry Series Aalto University publication series DOCTORAL DISSERTATIONS 19/2011 Field of research Physical Chemistry Manuscript...

متن کامل

Size and Shape of Nanoclusters: Single-Shot Imaging Approach

A method of single-shot imaging via aberration-corrected scanning transmission electron microscopy equipped with high angle annular dark-field detector (STEM-HAADF) has been applied to size-selected gold model catalysts (Au(25) and Au(39) ) on hydroxyapatite. Through quantitative intensity analysis, the size, in terms of number of atoms as well as 3D shape of the clusters are obtained.

متن کامل

Metal-graphene interaction studied via atomic resolution scanning transmission electron microscopy.

Distributions and atomic sites of transition metals and gold on suspended graphene were investigated via high-resolution scanning transmission electron microscopy, especially using atomic resolution high angle dark field imaging. All metals, albeit as singular atoms or atom aggregates, reside in the omni-present hydrocarbon surface contamination; they do not form continuous films, but clusters ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013