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  • 2000-2004  (31)
  • 1990-1994  (203)
  • 1955-1959  (34)
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  • 1900-1904  (3)
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Year
  • 11
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 6997-7000 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High-resolution inelastic neutron scattering was used to investigate the rotational tunneling of methane molecules in a (large-closed-square)×(large-closed-square)R45° commensurate, square-lattice–solid monolayer adsorbed on MgO (100) surfaces. Good matches to the observed transition energies were obtained using potential functions with C2v symmetry, suggesting that the preferred orientation of the molecule is the dipod-down configuration with two opposite edges of the H-atom tetrahedron parallel to the surface plane.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 9200-9202 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An experimental method is described that is directed at monitoring the creation and decay of core hole states in molecules from state-to-state. Data in the form of a coincidence map are presented and analyzed for the case of nitrous oxide.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 1304-1311 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A method is presented for numerical integration of the generalized Langevin equation (GLE) based on modeling of the "random force'' as a discrete autoregressive process. This modeling procedure, drawn from digital signal processing and spectral estimation methods which have been used extensively in electrical engineering applications, provides for efficient evaluation of the friction integral in the GLE as well as for generation of a random force process with the desired spectrum. The method is shown, through comparison with molecular dynamics results, to be effective in simulating the force autocorrelation function of an iodine atom dissolved in Lennard-Jones (LJ) xenon. In a companion paper this method is applied in a simulation of the vibrational relaxation of I2 in LJ xenon at two very different densities and found to perform well.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 2169-2175 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Electron energy spectra characterizing the relaxation of molecular oxygen from different core hole excited states are reported. By using monochromatic synchrotron radiation, spectra are obtained with excitation at the π* and σ* resonances and at various energies above the ionization threshold. The spectra obtained with excitation above threshold are very similar and result from Auger decay. The spectra obtained at the σ* resonance result from spectator autoionization, and those for the π* resonance result from both spectator and participator autoionization. The σ* resonance is broadened by spectral congestion, and the autoionization spectra indicate the presence of three components. Configurations and states produced by the electronic decay are identified, and a correlation between spectator screening and term values is documented.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 7936-7945 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The symmetry of excited states reached by photoexcitation of K-shell electrons of N2 and O2 is identified from the fragmentation anisotropy. For each molecule, ion yield excitation spectra were obtained at 90°, 54.7°, and 0° relative to the axis of soft x-ray polarization. The degree of polarization of the synchrotron radiation was determined experimentally. From this determination and the angular dependence of the ion yield, the photoabsorption anisotropy parameter β is obtained as a function of photon energy. Variations in the β spectra are discussed in terms of previously assigned spectral features and are compared with other experimental results. A comparison also is made with theoretical calculations, which are available for the case of N2.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 1312-1319 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A simple classical stochastic model for diatomic vibrational relaxation, based on the generalized Langevin equation, is presented. The memory function in the generalized Langevin equation is determined directly from equilibrium force autocorrelation functions for the individual atoms of the diatomic dissolved in the solvent of interest. A simple autoregressive (AR) procedure, developed in a preceding paper [D. E. Smith and C. B. Harris, J. Chem. Phys. 92, xxx (1990)], is used for modeling the memory functions to arbitrary order. This model is tested on the system of iodine in Lennard–Jones xenon using fourth order AR approximations for the memory functions, and is found to be very effective in reproducing data from molecular dynamics simulations at two very different densities. Results are discussed in terms of the simplifying assumption that the solvent interaction with the diatomic can be characterized by equilibrium dynamics of single atoms in solution.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 1741-1747 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Many vibration–rotation components of the ν2 fundamental of the SiH+3 cation have been measured using diode laser velocity modulation spectroscopy. By comparing the intensities of these components with their nuclear statistical weights, the ion is shown to be planar (D3h). The position of the ν2 band center is 838.0674(7) cm−1 and the ground state rotational constant is B0=5.2153(1) cm−1, r0=0.1462 nm. These results are compared with ab initio calculations.
    Type of Medium: Electronic Resource
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  • 18
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The flowing afterglow technique, coupled with laser induced fluorescence (LIF) and vacuum ultraviolet (vuv) absorption spectroscopy, has been used to determine the fractional H-atom contributions, fH, to the product distributions for the dissociative recombination of a series of protonated ions (N2H+, HCO+, HCO+2, N2OH+, OCSH+, H2CN+, H3O+, H3S+, NH+4, and CH+5 ) with electrons. The measurements were made at 300 K in two separate ways in two laboratories by (i) directly determining the H-atom number density using vuv absorption spectroscopy at the Lα (121.6 nm) wavelength and (ii) converting the H atoms to OH radicals using the reaction H+NO2→OH+NO followed by LIF to determine the OH number density. The agreement between the two techniques is excellent and values of fH varying from ∼0.2 (for OCSH+ ) to 1.2 (for CH+5 ) have been obtained showing that in some of the cases recombination can lead to the ejection of two separate H atoms. Comparison of the oxygen/sulphur analogs, HCO+2/OCSH+ and H3O+/H3S+ showed that the fH values were very different. Possible reasons for these differences are discussed. Comparison is also made with the available theory.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 8660-8666 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A selected ion flow tube study has been carried out at 300 K of the reactions of some atomic and molecular positive and negative halogen ions with Cl2 and Br2 from which the rate coefficients k and ion product distributions have been determined. For the energetic F+ ion reactions, dissociative charge transfer is the dominant process, while for the Cl+ ions, only nondissociative charge transfer occurs. For the less energetic Br+ and I+ reactions, dihalogen molecular ions are important products. All these positive ion reactions proceed quite efficiently, i.e., the k are appreciable fractions of kc, their respective collisional rate coefficients, except for the reactions of Cl2 with the lower energy ions of the spin–orbit triplet of I+, i.e., I+(3P1,0), for which k∼0.07kc, this being due to the endothermicities of the reactions. The molecular ion Cl2+ undergoes rapid nondissociative charge transfer with Br2, a process which is, of course, endothermic for the reaction of Br2+ with Cl2 and so no reaction is observed. The less-energetic atomic negative ion reactions proceed—via atom exchange—in which the atomic negative ion of the reactant molecular species and a dihalogen molecule are produced. For those reactions that are exothermic, the k are, within error, equal to (2/3)kc, implying that they proceed via complexes which separate statistically back to reactants (1/3) and forward to products (2/3). Both the Br−+Cl2 and Cl−+Br2 reactions are somewhat less efficient (i.e., k〈2/3kc), a result of the slight endothermicities of the reactions. Of the molecular negative ion reactions, electron transfer is the major process in the Cl2− reaction with Br2, whereas the reaction of Br2− with Cl2 proceeds relatively slowly producing the triatomic ion BrCl2−.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 87 (2000), S. 1974-1982 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Organic materials that have desirable luminescence properties, such as a favorable emission spectrum and high luminescence efficiency, are not necessarily suitable for single layer organic light-emitting diodes (LEDs) because the material may have unequal carrier mobilities or contact limited injection properties. As a result, single layer LEDs made from such organic materials are inefficient. In this article, we present device model calculations of single layer and bilayer organic LED characteristics that demonstrate the improvements in device performance that can occur in bilayer devices. We first consider an organic material where the mobilities of the electrons and holes are significantly different. The role of the bilayer structure in this case is to move the recombination away from the electrode that injects the low mobility carrier. We then consider an organic material with equal electron and hole mobilities but where it is not possible to make a good contact for one carrier type, say electrons. The role of a bilayer structure in this case is to prevent the holes from traversing the device without recombining. In both cases, single layer device limitations can be overcome by employing a two organic layer structure. The results are discussed using the calculated spatial variation of the carrier densities, electric field, and recombination rate density in the structures. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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