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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 95 (1991), S. 8393-8402 
    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 97 (1992), S. 307-319 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The periodically perturbed oscillations in the isothermal CO oxidation on a Pt(110) surface at low pressure were modeled using the recently developed reconstruction model of kinetic oscillations, in which the usual Langmuir–Hinshelwood mechanism is coupled with the CO-driven 1×2(arrow-right-and-left)1×1 phase transition of the surface. The experimental findings (entrainment bands, quasiperiodicity, critical slowing down) could be well reproduced with this model. The calculations revealed a complicated bifurcation fine structure of the Arnol'd tongues. While the skeleton structure turned out to be the same as in other studies, some additional features were found, and several details (mainly in the p/2 tongues) were different from forced systems examined previously. A co-dimension-3 bifurcation (in which a second-order resonance coincides with a degenerate period doubling) is discussed in this context.
    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 96 (1992), S. 9161-9172 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The parameters entering the kinetics for the mechanism of catalytic CO oxidation have been adapted for a Pt(110) surface, giving rise to a two-variable model correctly predicting bistability. Oscillations are obtained when, in addition, the adsorbate-driven 1×2–1×1 structural phase transition of Pt(110) is taken into account. Mixed-mode oscillations can be qualitatively explained by including the faceting of the surface as a fourth variable. The limitations of the model essentially stem from the fact that only ordinary differential equations have been analyzed so far neglecting spatial pattern formation. It is discussed which dynamic phenomena observed experimentally in the CO oxidation on Pt(110) will probably not be adequately describable without taking spatial effects into account.
    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 96 (1992), S. 1582-1589 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The NO+CO reaction, which has been shown to exhibit damped kinetic oscillations on a Pt(100) surface after initial excitation, has been subjected to periodic and random forcing of the temperature and of the CO partial pressure. The experiments were conducted in the 10−7 mbar range and measurements of the CO2 production rate and of the work function were used to follow the response of the system. The response behavior is characterized by strong resonance effects and by the absence of quasiperiodic oscillations. The system is highly sensitive to temperature modulation, but rather insensitive to modulation of pCO with the latter requiring an amplitude of more than 5% of pCO for producing sustained oscillations. Random forcing experiments demonstrate that the response of the system can be described as a bandpass filter since only frequencies close to the natural frequency of the system are amplified. The results of the experiments led to the conclusion that the damping effect is due to the absence of an efficient synchronization mode under isothermal conditions at low pressures.
    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 95 (1991), S. 6162-6170 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Under isothermal conditions at low pressure (10−4 Torr), the catalytic oxidation of CO on a Pt(210) surface exhibits kinetic oscillations which have been investigated using Video-LEED, measurement of the CO2 production rate and the variation of work function. An induction period of ∼30 to 60 min, which has been shown to be due to a facetting of the surface exists before the appearance of kinetic oscillations. If reaction conditions are chosen which correspond to the high rate branch of Langmuir Hinshelwood kinetics, the Pt(210) surface facets into (310) and (110) orientations. The facetting process is associated with a decrease in catalytic activity caused by a lowering of the oxygen sticking coefficient. In situ LEED experiments demonstrated that the oscillations in the reaction rate are associated with periodic intensity variations of the half-order LEED beams belonging to (110) facets. Thus, the oscillations appear to be driven by the CO-induced 1×1(arrow-right-and-left)1×2 phase transition on (110) facets in the same way as has been verified for the system Pt(110)/CO+O2. The involvement of a facetting process explains the characteristic properties of kinetic oscillations on Pt(210) such as the relatively low high-temperature limit of ≈500 K, the existence of an induction period and the period length which is on the order of minutes.
    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. 4942-4948 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The rate of catalytic carbon monoxide oxidation on a Pt(100) single crystal surface under isothermal, low-pressure conditions exhibits for certain ranges of parameters (O2 and CO partial pressures, temperature) sustained temporal oscillations whose mechanism had been explored in previous work. Coupling between reaction and diffusion leads to spatial pattern formation as manifested by patches with different work function on the intrinsically homogeneous surface. Imaging is performed by means of the novel technique of scanning photoemission microscopy. Typically, nuclei with dimensions of a few microns, as determined by the instrumental resolution, are formed spontaneously and expand with sharp fronts and velocities of about 0.5 mm/min (at 480 K) up to sizes ≥1 mm. Waves with even more extended fronts propagating with somewhat higher velocities across the sample surface are responsible for the occurrence of large amplitude temporal oscillations of the integral reaction rate.
    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 90 (1989), S. 510-521 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The rate of catalytic CO oxidation on Pt(100) and (110) surfaces at low pressures (≤10−4 Torr) and under isothermal conditions may exhibit sustained temporal oscillations which are coupled with periodic transformations of the surface structures between reconstructed and nonreconstructed phases, the latter exhibiting higher oxygen sticking coefficients and hence higher reactivity. With Pt(100) the two surface phases exhibit a much larger difference in reactivity (=oxygen sticking coefficient) than with Pt(110), which effect accounts for the qualitative differences in the oscillatory behavior: if two of the control parameters (say pO2, T) are kept fixed, the third (pCO) may be varied with Pt(100) over a fairly wide range without leaving the oscillatory region. Minor (〈1%) fluctuations of the partial pressures associated with the varying reaction rate are hence without any noticeable effect. Coupling between surface reaction and diffusion causes wave propagation of the surface phase transformations and therefore spatial self-organization, as demonstrated by scanning LEED experiments. With Pt(110), on the other hand, the oscillatory region is very narrow. In this case mass transport through the gas phase as caused by the small pressure variations associated with the reaction lead to synchronization between different parts of the surface. Computer simulations with the cellular automaton technique confirm qualitatively the experimental findings and support the conclusions reached.
    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 97 (1992), S. 5193-5204 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A Pt single crystal of cylindrical shape (axis II [001]) whose surface exhibits all orientations of the [001] zone has been used to study coupling effects between orientations which exhibit kinetic oscillations in catalytic CO oxidation. On the clean surface, one can distinguish between an orientational range in between (110) and (320) which exhibits a 1×2 reconstruction, a nonreconstructed surface range around (210) and a hex reconstructed surface range around (100). Structural transitions proceed continuously via atomic steps between (110) and (210), while the orientational range extending from (210) to (100) is faceted. With a rotatable Kelvin probe, the orientational dependence of the work function could be followed. The results revealed that the variation of the oxygen sticking coefficient sO2 displays a mirror-like behavior with respect to the work function variation of the clean surface such that the orientation with the lowest work function (210) exhibits the highest sO2. Kinetic oscillations were studied in the 10−5 and 10−4 Torr range. By means of two Kelvin probes, the Δφ oscillations could be followed simultaneously at two different orientations, while the integral behavior of the cylinder surface was monitored via the CO2 production rate. A strong broadening of the oscillatory region in parameter space, as compared to a flat surface, was detected for the oscillatory range around (100). In the vicinity of this orientation, spatial coupling is provided via reaction fronts which propagate from (210) toward (110). Gas-phase coupling is only observed with the (110) orientations. Prolonged oscillation experiments cause faceting resulting in an increase of catalytic activity around (100), while the orientations around (210) lose catalytic activity by faceting.
    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 96 (1992), S. 8595-8604 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A two-variable Langmuir–Hinshelwood mechanism for isothermal CO oxidation on a catalytically active surface is presented. It shows bistability stemming from 2 cusp bifurcations, which can be obtained analytically for low pressure. Inclusion of CO diffusion on the surface leads to a system of partial differential equations, which exhibits nucleation and front propagation phenomena in the bistable region. While the line of equistability could with good accuracy be solved for analytically, the front velocities and critical radii for nucleation had to be determined numerically (using the method of heteroclinic orbits). Throughout the calculations the kinetics and rate constants for the CO oxidation on Pt(111) are used. Here the model can be reduced by adiabatic elimination of one variable (namely oxygen coverage) allowing a comparison to the exactly solved one-variable Schlögl model. Possible implications for future experimental work are briefly discussed.
    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 93 (1990), S. 5327-5336 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ultraviolet-photochemistry of molecularly adsorbed oxygen on Pd(111) has been studied using pulsed laser light with 6.4 eV photon energy. Three processes occur upon irradiation: desorption of molecular oxygen, conversion between adsorption states, and dissociation to form adsorbed atomic oxygen. By using time-of-flight spectroscopy to detect the desorbing molecular oxygen and post-irradiation thermal desorption spectroscopy (TDS) to characterize the adsorbate state, a detailed picture of the photochemical processes is obtained. The data indicate that the O2 molecules desorbing with low translational energies from the saturated surface as well as the conversion of adsorbed molecules between binding states are induced by the photoinduced build-up of atomic oxygen on the surface. Analysis of a proposed reaction model reproduces the observed data and yields detailed rates. Polarization analysis indicates that the photochemical processes are initiated by electronic excitations of the substrate.
    Type of Medium: Electronic Resource
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