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  • Electronic Resource  (17)
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  • Electronic Resource  (17)
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 94 (1990), S. 8630-8633 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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. 7068-7078 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High resolution stimulated Raman spectroscopy (SRS) has been used to examine N2 and N2/He free jet expansions and also equilibrium samples of N2 from 15 to 110 K. The jet spectra show the formation of large liquid clusters which supercool and subsequently freeze to form crystalline β-N2 solid and, in He expansions, undergo a further transformation to a partially annealed α-N2 form. CW-SRS frequency and linewidth data obtained for equilibrium samples of the condensed phases of N2 yielded frequency–temperature relations used in deducing internal temperatures for the clusters produced in the expansion experiments. Analysis of the cooling curves indicates a mean cluster diameter of 35 nm and favors a prompt freezing process rather than a gradual conversion of liquid to solid in a single cluster on the microsecond time scale of the experiments. Supercooling limits of 34 to 44 K are deduced for the liquid, far below the triple point temperature of 63.2 K at which equilibrium samples freeze. Some evidence for surface versus bulk contributions to the spectra is seen in the asymmetric line shapes observed for liquid clusters in the condensation region. The results show that the high spectral and spatial resolution of nonlinear Raman methods such as SRS and CARS provide a unique probe of the condensation processes in free jet expansions.
    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 98 (1993), S. 6031-6043 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Microwave and infrared measurements are reported for the van der Waals complex Ar–CH3CCH and its isotopomers. The structure is T shaped with equilibrium center-of-mass separation of 3.73 A(ring) and an angle of 82° between the molecule symmetry axis and the van der Waals bond. The infrared and microwave spectra are complex due to the effects of a slightly hindered internal rotor. Analysis of the spectral data shows that the dipole moment is almost parallel to the dimer b axis. A modified vibration/rotation Hamiltonian that includes an internal rotor potential is used to show that the barrier to internal rotation is near 10.8 cm−1.
    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 98 (1993), S. 7480-7484 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In the impact of a C60+ beam against solid surfaces, a substantial fraction of the beam is neutralized. By means of a pulsed photoionization experiment, we have detected the neutralized scatterers from a silicon (100) surface, and found that they are mainly intact C60, with little or no fragmentation at impact energies to 200 eV. The neutralization probability is found to increase monotonically with increasing impact energy. This reionization method has been used in a time-of-flight scheme to measure the recoil velocity distributions of scattered C60. Collisions at impact energies above 50 eV are found to be highly inelastic, and the normal recoil distribution changes very little with impact energy over the range from 50 to 200 eV. The peak in the velocity distribution is near 1150 m/s (∼5 eV), with a full width at half-maximum (FWHM) of 350 m/s. By comparison with molecular dynamics simulations, an interpretation of this speed is proposed in terms of a limit to reversible deformation of the fullerene cage. A model of the scattering kinematics, based on treating the fullerene cage as a deformable, hollow sphere, with a harmonic deformation limit (15 eV) as found by theory, predicts the observed speed quantitatively.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 66 (1995), S. 4188-4197 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A new tandem time-of-flight mass spectrometer is described which is designed to study the mass-, velocity-, and angle-resolved scattering of cluster ions from solid surfaces. Clusters are produced in a supersonic jet laser desorption/vaporization source, ionized either directly in the formation step or by subsequent photoionization of neutrals, mass selected in a primary time-of-flight region, and decelerated to the impact energy (50–1000 eV) close to the target surface. Cluster–surface collisions take place in a field-free region in order to determine both velocity and angular distributions of the scattered clusters and fragments with an independently pulsed, rotatable secondary time-of-flight mass spectrometer. Several surface targets can be mounted in the UHV scattering chamber (10−10 Torr base pressure) on a five-axis manipulator which, together with the rotatable secondary TOF, allows for independent variation of incident and scattering angles. Target surfaces can be cleaned by direct current heating and sputtering with an argon-ion gun. Surface structure and composition are assessed by low-energy electron diffraction (LEED) and Auger spectroscopy with a four grid reverse view LEED/Auger system. Surface collision experiments of fullerenes (C+60, C+70, C+76, C+84, ...) and metallofullerenes (La@xaC+82) with highly oriented pyrolitic graphite (HOPG) surfaces are described as examples for the performance of the instrument. Effects of surface contamination in the scattering of fullerenes from HOPG are described to demonstrate the need for thorough cleaning procedures in order to obtain reproducible results. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Carbon cluster ion impact induced surface damage (500, 1850, and 4000 eV) of highly oriented pyrolytic graphite (HOPG) was imaged on an atomic scale with scanning tunneling microscopy. Penetration depth was accessed by oxygen etching of ion impact induced defects. Depending on ion energy, etched holes up to 6 monolayers deep were observed. Surface morphologies of HOPG crystals can be tailored by the described method promising many applications for surface science studies and nanostructuring. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 3990-3999 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 102 (1995), S. 540-543 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Laser desorption mass spectra of thin films of pure C60O were recorded in a range of equilibrium sample temperatures from 300 to 1100 K. On heating of the sample above 650 K a new peak corresponding to C−119 is detected in the anion mass spectrum which persists even after the sample is cooled to 300 K. Possible solid state reactions leading to the formation of C119 are discussed based on the mass spectrometric observations as well as temperature programmed decomposition measurements which were carried out for C60 and C60O samples. The results are discussed in connection with recently reported polymerization reactions of fullerene materials. © 1995 American Institute of Physics.
    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 100 (1994), S. 5684-5695 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Neutral and positively charged clusters Mx(C60)z, where M=K/Rb and z=1–3 were prepared in pulsed molecular beams by laser desorption (266 nm) from preformed alkali metal fulleride thin films. Experimental results encompassed mass spectral characterization of beam abundance and in selected cases, determination of rough ionization potential brackets and elucidation of fragmentation pathways upon (i) unimolecular dissociation in gas phase and (ii) surface collision induced dissociation from Si(111). Results are contrasted with electrostatic model calculations as well as ab initio self-consistent field computations.
    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 100 (1994), S. 262-270 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Positively and negatively charged coalescence products of C60 and C70 were characterized following pulsed laser desorption from fullerene thin films. Coalescence occurs by gas-phase reactions. Positive ions are generated by thermoionization of hot neutrals, while negative ions likely form by electron attachment to neutral species in the outermost region of the desorption plume. Thermoionization rate and surface-induced dissociation (SID) measurements are consistent with fullerene-like structures for coalescence products detected as positive ions.
    Type of Medium: Electronic Resource
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