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  • 1985-1989  (28)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 1519-1525 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Elastic differential cross sections in atomic crossed beam experiments contain detailed information about the underlying interatomic potentials. The functional sensitivity density of the cross sections with respect to the potential δσ(θ)/δV(R) reveals such information and has been implemented in an iterative inversion procedure, analogous to that of the Newton–Raphson technique. The stability of the inversion is achieved with the use of the regularization method of Tikhonov and Miller. It is shown that given a set of well resolved and noise-free differential cross section data within a limited angular range and given a reasonable starting reference potential, the recovered potential accurately resembles the desired one in the important region, i.e., the region to which the scattering data are sensitive. The region of importance depends upon the collision energy relative to the well depth of the potential under study; usually a higher collision energy penetrates deeper into the repulsive part of the potential and thus accordingly yields a more accurate potential in that part. The inversion procedure produces also a quality function indicating the well determined radial region. Moreover, the extracted potential is quite independent of the functional form of the reference potential in contrast to curve fitting approaches. As illustrations, the model inert gas systems He–Ne and Ne–Ar have been considered. For collision energies within an order of magnitude of the associated potential well depth, the attractive part of the potential can be determined to high precision provided that scattering data at small enough angles are available. On the other hand, the repulsive part of the potential must be scrutinized by high collision energy data.
    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 90 (1989), S. 1701-1710 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new method of scaling inelastic cross sections is presented which uses an intermediate-level parametrization of the collision dynamics. By expressing the scattering matrix as exp[−iB] and approximating B with a parametrized functional form, this procedure yields a unitary scaled S matrix and incorporates infinite-order rotational coupling into the scaled results. The inclusion of high order collision dynamics enables the scaled cross sections to exhibit physical behavior which is substantially more realistic and flexible than that allowed by traditional fitting methods. The intermediate level scaling procedure accurately produces complete matrices of rotationally inelastic cross sections for He–HD scattering generated from subsets of input cross sections.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Novel modeling and sensitivity analysis techniques are used with experimental data obtained from discharge flow–resonance fluorescence experiments to evaluate the product branching ratio of OH+H2CO. Two channels are considered: the H-atom abstraction reaction (R2) to form HCO and H2O; and the addition reaction (R17) followed by rearrangement and decomposition to form HCOOH and H. The rate constant values obtained at 298 K are kR2 =(7.75±1.24)×10−12 cm3/molecule s and kR17=(0.2+0.8−0.2) ×10−12 cm3/molecule s. The results demonstrate that the reaction proceeds almost exclusively via the H-atom abstraction pathway.
    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 91 (1989), S. 2333-2342 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present a procedure that numerically evaluates the scattering wave function. The solution to the time-independent Schrödinger equation is calculated by a novel combination of: (a) the Møller operator of scattering theory, (b) time-dependent wave packets whose shape is unconstrained, and (c) efficient wave packet propagation on a dynamically-adapted grid. The superposition of packets appropriate to the scattering boundary conditions yields the full wave function, from which scattering amplitudes are then obtained. Since the procedure does not make use of basis-set expansions, its computational cost is independent of the number of open channels. It explicitly calculates the wave function not only in the asymptotic region but also within the interaction region, so it allows one to evaluate additional information beyond the scattering amplitude, as well as the functional sensitivity of transition probabilities with respect to changes in the potential. Applications here are illustrated by two simple examples: one-dimensional tunneling through a potential barrier, and elastic scattering from a one-dimensional periodic surface (i.e., a two-dimensional scattering problem). Extensive applications to imperfect surfaces including sensitivity analysis are separately presented in another article.
    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 90 (1989), S. 1711-1719 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: This paper examines the mass dependences of vibrationally inelastic integral state-to-state cross sections for the helium-hydrogenic scattering system. The cross sections are calculated within the coupled states-exponential distorted wave (CS-EDW) approximation, and are analyzed along with the conceptually simpler distorted wave (CS-DW) cross sections. Quantitative links between the EDW and DW results are made by means of component (or channel coupling) sensitivity coefficients, which measure the sensitivity of a given EDW cross section to the potential matrix elements coupling any two states.
    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 91 (1989), S. 1051-1061 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: This paper examines the effect of infinitesimal functional variations in a rigid rotor He–H2 potential surface on several different levels of observables: inelastic cross sections, rate constants, and energy level populations. Equations are derived for the functional derivatives of these observables with respect to a variation in the potential surface. Sensitivities are presented with respect to the entire potential surface, as well as the individual Legendre components Vn(r). The dynamical and kinetic observables studied were found to be most sensitive to the V2(r) term in the potential with the region of highest sensitivity dependent upon the energy or temperature as well as the states related by the individual observable. Sensitivity to the entire surface tends to show more structure due to interference among sensitivities to the individual components. While the main information on the underlying potential is retained, some information loss has been observed in the transition from the microscopic observables to the macroscopic ones.
    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 91 (1989), S. 7590-7605 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new iterative inversion scheme of atomic scattering data within the framework of functional sensitivity analysis is presented. The inversion scheme is based on the first order Fredholm integral equation δσ(θ)=∫∞0K(θ,R)δV(R)R2 dR, K(θ,R)≡δσ(θ)/δV(R), or symbolically, δσ=KδV, which relates infinitesimal functional changes in the elastic differential cross section δσ(θ) and in the underlying interatomic potential δV(R). This equation can be written equivalently, via integration by parts, as δσ(θ)=∫∞0K[n](θ,R) {Rn×δV(n)(R)}R2 dR, or δσ=K[n]{Rn×δV(n)}, under the a priori assumption that {R(2+n)×K[n](θ,R)×δV(n−1) (R)}||∞R=0=0. Here K[n](θ,R)≡−R−(2+n) ×∫R0K[n−1](θ,R') R'(1+n)dR', δV(n)(R) ≡(dn/dRn)δV(R), with n=0,1,2,..., and K[0](θ,R)≡K(θ,R).A choice of n corresponds to a particular level of additional stabilization inverting the scattering data. By invoking a least squares regularization procedure and singular system analysis, the new indirect inversion scheme solves the linear relation δσ=K[n]{Rn×δV(n)} and results in the approximate solution Rn×δV(n)(R), which can in turn be integrated, n times, to yield the potential correction δV(R). The new algorithm not only makes the inversion more stable and more efficient, but also increases the sensitivity of the large angle scattering data to the repulsive part of the potential, in comparison with a previous method that directly solves the relation δσ=KδV.For illustration, the model system He–Ne is considered at both low- and high-collision energies, relative to the well depth of the potential. It is found that the indirect method based on the linear relation δσ=K[2]{R2×δV(2)} can more accurately determine both attractive and repulsive parts, including a large section of classically forbidden region, of the potential than its direct counterpart. Furthermore, the indirect method allows for substantial deviations of the initial reference potential from final result, not only in well depth, but in range parameter and asymptotic behavior. Finally, these observations are not significantly dependent on the magnitude of the collision energy.
    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 89 (1988), S. 5614-5623 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The iterative, perturbative inversion procedure of Mackintosh et al. is modified for the inversion of (noise free) elastic molecular scattering data at fixed energy, in conjunction with singular system analysis and the Tihkonov–Miller-type regularization method. The singular system consisting of the first order functional relation between infinitesimal changes in the phase shifts and the intermolecular potential provides a natural basis for solving the corresponding linear Fredholm integral equation of the first kind. The regularization procedure stabilizes the ill-conditioned inverse problem arising from the above linear integral equation. Furthermore, in regions where the wavelength is small compared to the length scale of the potential, the first order functional derivatives or sensitivity densities of the phase shifts with respect to the potential δηl/δV(R) are approximated by their mean values to facilitate the regularization procedure and, therefore, the convergence of the problem. This semiclassical modification and the adoption of the singular system analysis are necessary for intermolecular potentials possessing a rapidly varying region that cannot be appropriately represented by a small number of spline functions. For illustration, a model of the He–Ne system has been adopted and the applicability of the proposed method at diffrent energies has been examined in detail.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 2273-2280 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 1110-1119 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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