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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 3813-3826 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A procedure is described for the determination of metal cluster ionization potentials (IPs) using available excimer laser lines that gives error limits substantially smaller than traditional bracketing experiments. It is based on the observation that the adsorption of ammonia on cluster surfaces lowers cluster IPs, and that the IP lowering is linear in the number of adsorbed NH3 molecules. By determining the minimum number of NH3 molecules needed for ionization by the various excimer lasers, an approximation to the dependence of IP on coverage can be deduced. Extrapolation of this dependence to zero coverage gives the bare cluster IPs. Results are presented for clusters of iron, cobalt, and nickel having from 4 to 100 atoms. The effect of molecular adsorption on cluster IPs is analyzed theoretically, and the comparison with experimental results used to estimate the effective dipole moment of NH3 molecules adsorbed on these clusters. Comparison of the bare cluster IPs with the simple spherical drop model suggests that for transition metal clusters the Fermi level can be a significant function of cluster size.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 2110-2111 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The equilibrium adsorption of H2O on hydrogenated cobalt clusters is used to estimate the cluster–H2O binding energy. Magic numbers, corresponding to clusters with enhanced binding energy, are found for clusters having one more metal atom than closed shells or subshells of the third Mackay icosahedron. It is argued that a lone metal atom outside a closed (sub)shell should have enhanced ability to bind H2O, and that such chemical probes can be used to provide useful information about metal cluster structure.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 4714-4727 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The reactions of neutral iron clusters Fe7–27 with water are studied in a laser-vaporization cluster source coupled to a continuous-flow reactor. Reaction products are detected via laser ionization and time-of-flight mass spectrometry. The reactions of room-temperature clusters with H2O show adsorbate decomposition and hydrogen desorption, as do the reactions with D2O at elevated temperatures. The room-temperature reaction with D2O appears not to involve any decomposition, and is at equilibrium under the conditions of these experiments. The dependence of reaction extent on D2O pressure yields equilibrium constants for the addition of the first and second D2O molecules. The analysis is complicated by the presence of two-photon ionization processes that are treated quantitatively with a rate-equation model. This treatment also yields estimates for cluster photoabsorption cross sections, which are found to be approximately linear in cluster size, having a magnitude of 2.3×10−17 cm2 per iron atom. From the derived equilibrium constants and estimated adsorption entropies, approximate D2O–cluster binding energies are determined. They range from 0.42 to 0.59 eV, and their dependence on cluster size shows a remarkable similarity to the dependence of the rate constants for reaction of iron clusters with H2. The implications of this similarity are discussed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 1526-1534 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Studies of two-reagent reactions of iron clusters with ammonia and deuterium are described. The compositions of clusters saturated with both ammonia and deuterium have been determined, and indicate that the ammonia binds nondissociatively to iron clusters and to different sites than the deuterium. Rate constants for the reaction of the first deuterium molecule with ammoniated clusters have been measured. In general, low ammonia coverage (one to three molecules) has either little effect on cluster reactivity, or in the case of unreactive bare clusters, increases reactivity dramatically. Clusters saturated with ammonia show general reactivity decreases, although again the least reactive bare clusters show dramatic increases in reactivity when covered with ammonia molecules. Interesting cluster activation and deactivation effects are seen. Possible mechanisms for these reactions are discussed.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 1622-1632 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Evidence is presented for structural changes in iron clusters in the Fe13 to Fe23 size range. Abrupt changes with cluster size are found for several chemical properties, including reactivity with hydrogen and binding energies of ammonia and water. These changes often come at the same cluster sizes, pointing to a common origin—fundamental changes in the structure of the bare iron clusters. In addition, changes in structure as a consequence of adsorbate binding are suggested. The experimental observations leading to these conclusions are detailed, and possible structures for clusters in this size range are proposed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 1066-1067 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new procedure is described for the study of chemical reactions of metal clusters with simple gas phase molecules. It consists of determining the average number of reagent molecules taken up by the clusters as a function of reagent pressure over a very wide range of pressures. When the results of such experiments are appropriately analyzed, they provide information on cluster reaction kinetics, thermodynamics, and the composition of reaction products. An illustration of this procedure for the reaction of iron clusters with ammonia is presented.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 1882-1902 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The reactions of nickel clusters with ammonia and with water are used to probe cluster geometrical structure. Ammonia uptake experiments allow the determination of the number of preferred binding sites on cluster surfaces. This number shows pronounced minima in the 50- to 116- atom size range for many of the cluster sizes that appear as magic numbers in mass spectra of rare gas clusters. Since these magic numbers arise from closings of shells and subshells of the Mackay icosahedra, the correlation suggests that ammoniated nickel clusters in this size region also have icosahedral structure. Similar structure is found for ammoniated clusters smaller than ∼30 atoms, but is not seen for room temperature clusters in the vicinity of the third shell closing at 147 atoms. Icosahedral features do appear for the larger clusters at elevated temperatures. For many clusters above 50 atoms, prolonged exposure to ammonia causes a conversion from the icosahedral structure to some other structure that binds more ammonia molecules, and often the two structures are seen together. The equilibrium reaction of a single water molecule with the bare clusters probes the strength of the cluster–water bond. Enhanced water adsorption is often seen for clusters one atom larger than those showing minima in ammonia uptake, suggesting that these bare clusters likewise have icosahedral structure. The reasons for minima in ammonia uptake and maxima in water binding are discussed.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 8618-8621 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Copper clusters in the 50- to 100-atom size range are found to exhibit electronic shell structure as well as icosahedral geometry. Clusters corresponding to filled shells have minimum intensity in near-threshold photoionization mass spectra, implying that they have locally higher ionization potentials than other cluster sizes. The chemical stability of these clusters is illustrated by a reduced reactivity towards O2. Cluster geometry is probed via the equilibrium reactions with H2O: Clusters having one copper atom more than closed icosahedral subshells show an enhanced binding of water. The relative importance of electronic and geometrical structure in determining cluster chemical properties is discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 6260-6272 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Studies are described of the chemisorption of ammonia on isolated neutral iron clusters Fen for 2≤n≤165. Clusters are generated by laser vaporization in a continuous-flow-tube reactor, and reaction products are detected by laser-ionization time-of-flight mass spectrometry. Ammonia is found to chemisorb nondissociatively on cluster surfaces on the 1 ms time scale of these experiments. Measurements of ammonia uptake provide information on adsorption kinetics and on the number and nature of the binding sites. The ammonia binding energy is found to decrease with increasing cluster coverage. For chemically saturated clusters, the ratio of adsorbed NH3 molecules to surface iron atoms is found to decrease with increasing cluster size, going from 〉1/3 for small clusters to 〈1/3 for n〉100. Ammonia chemisorption is accompanied by a large decrease in cluster ionization potentials, as much as 2 eV for saturated clusters. At sufficiently high exposure the beginning of the formation of a second, physisorbed layer of molecules is seen. Detailed measurements of product composition under different exposure conditions give evidence for numerous changes in cluster structure throughout the growth sequence from small to large clusters. Often these structural changes involve particularly stable reaction products. Evidence for the existence of metastable structures is presented. Several possibilities for cluster structure are suggested.
    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 115 (2001), S. 4125-4131 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Two-reagent reactions of Ni19 and Ni23 with hydrogen/deuterium and ammonia are studied to probe adsorbate-induced cluster structural changes. H/D and NH3 bind to the clusters noncompetitively, i.e., to different sites, so simultaneous saturation by the two reagents can be achieved. It is found that H/D adsorption causes a change in Ni19 from the double icosahedral structure to a face-centered cubic (fcc) or hexagonal close-packed (hcp) one, but that subsequent saturation with NH3 converts the cluster back to the double icosahedron. No such structural changes are seen for the triple icosahedral Ni23. The results for Ni19 are interpreted in terms of the electron withdrawing or donating character of the ligands and the consequent effect on the extent of d-orbital bonding in the cluster. Possible configurations of the H/D atom binding sites on the icosahedral Ni19 and Ni23 clusters and on the fcc/hcp Ni19 cluster are presented. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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