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  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 1608-1614 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The effect of attractive interactions on the behavior of polymers between surfaces is studied using Monte Carlo simulations. The molecules are modeled as fused sphere freely rotating chains with fixed bond lengths and bond angles; wall–fluid and fluid–fluid site–site interaction potentials are of the hard sphere plus Yukawa form. For athermal chains the density at the surface (relative to the bulk) is depleted at low densities and enhanced at high densities. The introduction of a fluid–fluid attraction causes a reduction of site density at the surface, and an introduction of a wall–fluid attraction causes an enhancement of site density at the surface, compared to when these interactions are absent. When the wall–fluid and fluid–fluid attractions are of comparable strength, however, the depletion mechanism due to the fluid–fluid attraction dominates. The center of mass profiles show the same trends as the site density profiles. Near the surface, the parallel and the perpendicular components of chain dimensions are different, which is explained in terms of a reorientation of chains. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 106 (1997), S. 2762-2770 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The structure of uniform fluids is studied here by using a density functional approach. The key property of interest is the radial distribution function which is essentially the density distribution in the field of a tagged fluid particle. The theory is applied to the neutral fluid mixture as well as ionic fluids. The only inputs used are the first and second order direct correlation functions. For the uniform fluid mixture, the different auto- and cross-distribution functions are found to show density oscillation depending upon the different diameters and the results are quite comparable to the results obtained through Fourier transform. The work is extended to a uniform electrolyte within the restricted primitive model using a correlation function corresponding to the mean spherical approximation. Once again the results are quite good and compare well with the results obtained from the usual Fourier transform technique. © 1997 American Institute of Physics.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 106 (1997), S. 2752-2761 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A density functional approach is developed for inhomogeneous dipolar fluids consisting of dipolar hard spheres in presence of external electric fields. The theory is applied to two systems, viz. a confined fluid between two planar charged walls where the field is uniform, and also a fluid where the dipoles are subjected to a radial field due to a uniformly charged hard sphere ion at the centre. A nonperturbative weighted density approximation is employed to incorporate the effect of short range hard sphere-like correlations while the long-range effects are obtained perturbatively. The nonuniform density is expanded in terms of spherical harmonics and the correlation function used as input corresponds to the mean spherical approximation. In the case of planar geometry, the calculated density and polarization profiles are quite comparable with the available simulation and other results. In the presence of the radial field, the polarization exhibits oscillations showing a clear variation of the effective dielectric constant within the interface. This theory also gives an approximate estimate of the static solvation energy of an ion in a dipolar solvent. © 1997 American Institute of Physics.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 1579-1584 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A density functional theory is presented for the effect of attractions on the structure of polymers at surfaces. The theory treats the ideal gas functional exactly, and uses a weighted density approximation for the hard chain contribution to the excess free energy functional. The attractive interactions are treated using a van der Waals approximation. The theory is in good agreement with computer simulations for the density profiles at surfaces for a wide range of densities and temperatures, except for low polymer densities at low temperatures where it overestimates the depletion of chains from the surface. This deficiency is attributed to the neglect of liquid state correlations in the van der Waals term of the free energy functional. © 2000 American Institute of Physics.
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 9832-9838 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A simple weighted density functional approach is developed for inhomogeneous ionic fluids and applied to the structure of the electric double layer using the restricted primitive model where the ions are considered to be charged hard spheres of equal diameter. The formalism is nonperturbative with both hard-sphere and electrical contributions to the one-particle correlation function evaluated through a suitably averaged weighted density, the only input being the second-order direct correlation functions of the corresponding uniform system. The approach is designed in such a way, that the calculation of the weight function is decoupled from the weighted density. Numerical results on the ionic density profile and the mean electrostatic potential near a hard wall at several surface charge densities are shown to compare well with available simulation results. The corresponding results for the nonprimitive molecular solvent model provide insight into the layering effect and the charge inversion phenomena. © 1999 American Institute of Physics.
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 6573-6578 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The structure of binary hard-sphere mixtures near a hard wall is studied using a density functional theory. The formalism is based on a simple weighted density approach for the one-particle correlation functions of the nonuniform system, and requires as input only the one- and two-particle direct correlation functions of the corresponding uniform system. The approach is designed in a way, where the weight function is decoupled from the weighted density. Numerical results on the density profiles are shown to compare well with available simulation data. © 1999 American Institute of Physics.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 116 (2002), S. 8509-8516 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A simple weighted-density-functional approach is developed for inhomogeneous fluids by approximating the excess free energy density functional by that of the corresponding uniform system evaluated at an effective density. This effective weighted density is obtained by a suitable local averaging procedure of the actual density distribution using a weight function which is evaluated only once at the bulk density, thus being decoupled from the weighted density. This approach does not involve any power series expansion or solution of any nonlinear differential equation at every point and each iteration, as is required in some of the analogous schemes. The new theory is applied to predict the structure of simple classical fluids, interacting with hard sphere, Coulombic as well as Yukawa potentials, under confinement in several geometries. The calculated results on the density profiles are shown to compare quite well with available simulation data. © 2002 American Institute of Physics.
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  • 8
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 7314-7330 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: This paper introduces a theory to interpret future experiments to simultaneously observe angular distribution of spin-resolved Auger and photoelectrons from a molecule belonging to one of the 32 point groups. The Auger electrons are emitted in the decay of the vacancy created by photoionization. We show that the desired correlation can be completely characterized by 12 parameters which are coefficients of trigonometric functions of the spherical angles of spin quantization directions of two outgoing electrons. The expressions for the parameters themselves, although reduced to the simplest possible forms by using the symmetry properties of the molecular point group to maximum advantage, depend upon bipolar harmonics involving the propagation directions of the Auger and photoelectrons. The angular and spin correlation function thus obtained is completely general and can be readily specialized to any experimental geometry used to observe the ejected electrons. In particular, it is found that for a linear experimental arrangement with spins oriented longitudinally to the respective propagation vectors of the two electrons moving out in opposite directions, the parameters become geometry independent with their number reducing to three, which are now coefficients of the first three Legendre polynomials. Correlation between the spin-quantization directions of Auger and photoelectrons is, on the other hand, described by six parameters which do not depend upon the experimental arrangement. Directional correlation between the two outgoing electrons has also been studied without observing their spins. These angular and/or spin correlation functions are shown to take particularly simpler forms for Auger and photoelectrons emitted from linear molecules. We have applied the procedures developed in this paper to study directional correlation between photoelectrons from 2a1 orbital in a Td molecule and the Auger electrons emitted in the decay of the consequent vacancy.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 5242-5258 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: This paper develops theoretical expressions to study angular distribution and spin polarization of those Auger electrons which are emitted in the decay of a vacancy created by the absorption of a photon in a rotating linear molecule. Identical expressions except, of course, for different decay amplitudes, in both the Hund's coupling schemes (a) and (b), are obtained for the differential Auger current emitted in the transition J→Jf measured by an electron spectrometer sensitive to spin detection. The structure of these angular distributions is exactly the same as that of the spin-resolved photoelectrons from unoriented atoms and molecules. The present paper thus puts the angle- and spin-resolved Auger and photoelectron spectroscopies on the same footing wherein identical geometrical and kinematical analysis is applicable. The four parameters needed to completely characterize such distributions depend, in the present case, on rotational orientation and/or alignment of the photoexcited molecule, in addition to its Auger decay amplitudes. The use of parity-adapted molecular states separates the Auger spectra into even and odd partial wave components of the ejected electron continuum in both of the coupling schemes. Our analysis shows that the integrated Auger current is spin resolved provided it is produced in the decay of oriented vacancies. We further find that Auger electrons which leave the molecular ion in Jf=0 state may have nonzero degree of spin polarization if they follow absorption of only circularly polarized light. In this case, both the angular distribution and spin polarization of emitted electrons become totally independent of Auger dynamics. Thus, angle- and spin-resolved Auger electron spectroscopy can be used to produce polarized electrons, to determine rotational orientation and alignment of linear molecules, to study their structure and dynamics, and to prepare ions of such molecules in selective ro-vibronic states.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 5987-6006 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A recently developed theory for angular distribution of electrons ejected by interaction of light with nonlinear molecules held fixed in space has been used to study ionization in a1 orbital of those systems which transform like the Td point symmetry group. Expressions for photoelectron angular distributions in the dipole approximation with the electric vector in the radiation beam both perpendicular and parallel to the molecular axis are derived. The properties of the two formulas, which are found to have completely different structures, have been studied. These expressions are shown to depend not only on all those quantities [i.e., the partial integrated cross-section σ¯, the asymmetry parameter β¯, and the polar angle θ of the propagation vector k (k,θ,φ) of the ejected electron] which are present in photoionization of an unoriented molecule, but involve in certain cases also the azimuthal angle φ, phase shifts of the continuum waves representing the outgoing electron, and the phase of the dipole transition amplitudes. Such fixed-molecule photoelectron angular distributions will therefore provide more stringent tests of theoretical models and probes of photoionization dynamics than the hitherto performed gas phase experiments on randomly oriented targets. They can also be used to identify the orientation of a molecule and/or geometry of a chemisorption site. The formulation presented here sets a frame work for the analysis of measurements and the calculations of spectra in those Td molecules which are fixed in space. We have applied it, as an example, to ionization in 4a1, 6a1, and 7a1 orbitals of oriented CF4, CCl4, and SiCl4, respectively. Without doing any dynamical calculations, using instead the experimentally measured values of σ¯ and β¯ as a function of the photon wavelength, the variations in the angular distributions with respect to the energy of the ejected electron as well as to the angles (θ,φ) and to the phases (which are treated as parameters) involved have been studied in detail. These distributions are found to have very rich and complicated structures arising from the spectral, angular, and/or phase variations of the angular momentum compositionof the photocurrent.
    Materialart: Digitale Medien
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