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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 95 (1991), S. 8393-8402 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    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 97 (1992), S. 307-319 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: 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.
    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 96 (1992), S. 9161-9172 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: 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.
    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 96 (1992), S. 1582-1589 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: 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.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 6162-6170 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: 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.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 5193-5204 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: 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.
    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 96 (1992), S. 8595-8604 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: 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.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 5327-5336 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: 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.
    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 95 (1991), S. 3756-3766 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: During oxidation of thin Cs films, a nonadiabatic surface reaction manifests itself in the emission of electrons. This effect was investigated in detail by combining measurements of the current and of energy distributions of these exoelectrons with studies on the electronic properties of the surface by means of ultraviolet photoelectron spectroscopy and metastable deexcitation spectroscopy. Exoelectron emission occurs via Auger deexcitation of the empty state derived from the O2 affinity level. This process is confined to the stage Cs2O2→CsO2 in which resonance ionization of the affinity level of the impinging O2 molecule upon crossing the Fermi level EF is efficiently suppressed due to the absence of metallic states near EF. A kinetic model based on the successive steps involved in the oxidation of Cs is developed which describes qualitatively well all the experimental findings.
    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 94 (1991), S. 4609-4619 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: UV-laser irradiation (hν=6.4 eV and 5.0 eV) of the water bilayer adsorbed on a Pd(111) surface leads to molecular desorption and to conversion of the adsorbed state as manifested in thermal desorption spectra. The latter effect is attributed to photodissociation of water on the surface. Time-of-flight measurements show that water molecules desorb with a translational energy of about 600 K for both photon energies indicating a nonthermal process. While desorption is largely suppressed with adsorbed multilayers, conversion within the first layer still proceeds. The dependence of the desorption yield on angle of incidence and polarization of the light reveals substrate excitations as the dominant primary step. A strong variation of cross sections with isotopic substitution is observed. This is interpreted as evidence for the operation of a mechanism involving excitation onto an isotope-independent excited potential energy surface followed by rapid deexcitation to the ground state so that, of the total number of species excited, only a small mass dependent fraction actually fragments or desorbs.
    Materialart: Digitale Medien
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