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  • 1
    Publication Date: 2015-06-16
    Description: Langmuir DOI: 10.1021/acs.langmuir.5b01410
    Print ISSN: 0743-7463
    Electronic ISSN: 1520-5827
    Topics: Chemistry and Pharmacology
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  • 2
    Publication Date: 2015-09-23
    Description: Article Hot electrons—electrons with very high kinetic energies—are important in many processes but difficult to observe due to their short lifetimes. Here, the authors analyse STM based nonlocal manipulation of organic molecules on a surface, showing that the measurements probe hot electron dynamics in real space. Nature Communications doi: 10.1038/ncomms9365 Authors: D. Lock, K. R. Rusimova, T. L. Pan, R. E. Palmer, P. A. Sloan
    Electronic ISSN: 2041-1723
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General , Physics
    Published by Springer Nature
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  • 3
    Publication Date: 2012-06-14
    Description: Author(s): Z. W. Wang and R. E. Palmer The equilibrium ground state atomic structures of nanoparticles are critical to understanding the relationship between their structure and functionality, e.g., in catalysis, and are the standard output of first principles and semiempirical theoretical treatments. We demonstrate a method of obtaining... [Phys. Rev. Lett. 108, 245502] Published Wed Jun 13, 2012
    Keywords: Condensed Matter: Structure, etc.
    Print ISSN: 0031-9007
    Electronic ISSN: 1079-7114
    Topics: Physics
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  • 4
    Publication Date: 2011-08-27
    Description: Author(s): Z. W. Wang, Z. Y. Li, S. J. Park, A. Abdela, D. Tang, and R. E. Palmer This paper describes a new approach of quantification of annular-dark-field or Z -contrast image intensity as a function of inner acceptance angle of the detector in a scanning transmission electron microscope. By using size-selected nanoclusters of Pd ( Z = 46) and Au ( Z = 79), it is shown experiment... [Phys. Rev. B 84, 073408] Published Fri Aug 26, 2011
    Keywords: Surface physics, nanoscale physics, low-dimensional systems
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
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  • 5
    Publication Date: 2007
    Description: An unambiguous determination of the three-dimensional structure of nanoparticles is challenging. Electron tomography requires a series of images taken for many different specimen orientations. This approach is ideal for stable and stationary structures. But ultrasmall nanoparticles are intrinsically structurally unstable and may interact with the incident electron beam, constraining the electron beam density that can be used and the duration of the observation. Here we use aberration-corrected scanning transmission electron microscopy, coupled with simple imaging simulation, to determine with atomic resolution the size, three-dimensional shape, orientation and atomic arrangement of size-selected gold nanoclusters that are preformed in the gas phase and soft-landed on an amorphous carbon substrate. The structures of gold nanoclusters containing 3096 atoms can be identified with either Ino-decahedral, cuboctahedral or icosahedral geometries. Comparison with theoretical modelling of the system suggests that the structures are consistent with energetic considerations. The discovery that nanoscale gold particles function as active and selective catalysts for a variety of important chemical reactions has provoked much research interest in recent years. We believe that the detailed structure information we provide will help to unravel the role of these nanoclusters in size- and structure-specific catalytic reactions. We note that the technique will be of use in investigations of other supported ultrasmall metal cluster systems.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, Z Y -- Young, N P -- Di Vece, M -- Palomba, S -- Palmer, R E -- Bleloch, A L -- Curley, B C -- Johnston, R L -- Jiang, J -- Yuan, J -- England -- Nature. 2008 Jan 3;451(7174):46-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Nanoscale Physics Research Laboratory, School of Physics and Astronomy, University of Birmingham, Birmingham B15 2TT, UK. ziyouli@nprl.ph.bham.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18066049" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2016-04-21
    Description: We introduce a new type of cluster beam source based on the assembly of (metal) clusters within a condensed (rare gas) matrix. The “Matrix Assembly Cluster Source” employs an ion beam to enhance collisions between metal atoms in the matrix and to sputter out clusters to form a beam. We demonstrate the formation and deposition of gold and silver nanoclusters with mean size tunable from a few atoms to a few thousand atoms. The cluster flux is equivalent to a current nanoAmp regime but potentially scalable to milliAmps, which would open up a number of interesting experiments and applications.
    Print ISSN: 0034-6748
    Electronic ISSN: 1089-7623
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
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  • 7
    Publication Date: 2016-10-25
    Description: One of the main limitations to the application of clusters on applied areas is the limited production; therefore, it is of great interest to up scale cluster production while keeping good size control. The Matrix-Assembly Cluster Source is a new high flux cluster source, which exploits cluster formation inside a solid rare gas matrix that is sputtered by an ion beam. Clusters are formed and ejected in this process. Here we report the production of Ag clusters when the rare gas is replaced by CO 2 for the matrix formation at 20 K. Size distributions were determined from scanning transmission electron microscopy analysis of samples with four different metal loadings, 4%, 8%, 14%, and 23% of Ag atoms to CO 2 molecules, and two ion beam energies, 1 keV and 2 keV. Cluster mean size showed weak dependence on metal loading, being ≈80 atoms for the first three concentrations, whereas the change in ion beam energy has caused cluster mean size to shift from 86 to 160 atoms. The results are interpreted in terms of bonding energy between Ag and CO 2 and compared to the rare gas (Ar) matrix.
    Print ISSN: 0021-9606
    Electronic ISSN: 1089-7690
    Topics: Chemistry and Pharmacology , Physics
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-11-09
    Description: A discrete, calcareous layer that binds the foliated calcite of the oyster's shell to the organic ligament in the hinge is reported, apparently for the first time. This layer is ultrastructurally, and generally mineralogically, different from the underlying foliated calcite, and is named the ligostracum.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carriker, M R -- Palmer, R E -- New York, N.Y. -- Science. 1979 Nov 9;206(4419):691-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17796935" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 4059-4068 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The J and temperature dependence of the self-broadening coefficients for the Raman Q-branch lines of pure CO have been experimentally determined for Q(J) transitions with J=0–38 and for temperatures in the range 400–1500 K. It is shown that a fitting law, based on a modified exponential energy-gap model for the rates of state-to-state rotationally inelastic collisions, can account for the observed J dependence. The two parameters that determine the J dependence are found to be essentially independent of temperature. A temperature scaling function, recently proposed for N2, is added to the basic rate law, and accurate predictions of both the J and the T dependence of these coefficients and those previously reported at 298 K are obtained. This rate law model, used in conjunction with a relaxation matrix description of the Q-branch spectrum, is shown to give good agreement with the observed, partially collapsed spectrum at 2.8 atm and 295 K.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 8736-8747 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In this paper, we explore the connections between resonance electron scattering by isolated and physisorbed molecules. The multiple scattering Xα method is used to calculate cross sections for electron scattering via the σ shape resonances of O2, N2, and CO, near 9, 22, and 20 eV, respectively. Special emphasis is placed on the O2 resonance, for which no previous theoretical work has been reported. In all three cases, quantitative agreement is obtained with experimental gas phase scattering results. Angular distributions are then calculated for the isolated, oriented molecules, and compared with the angular distributions recently observed in resonance scattering by O2, N2, and CO molecules oriented by physisorption on graphite. Characteristic nodes observed in each of the angular distributions are related to the calculated angular profiles, together with a previously proposed selection rule which we now formalize. This scheme allows the orientation of the molecules on the surface to be determined.
    Type of Medium: Electronic Resource
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