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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 4641-4646 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: ICl chemisorbs onto Si(111)–7×7 by two mechanisms: dissociative chemisorption and abstractive chemisorption. Abstractive chemisorption, in which one halogen atom of ICl bonds to the silicon surface while the other is ejected into the gas phase, is the dominant chemisorption mechanism for ICl/Si(111)–7×7. Multiphoton ionization (205 nm MPI) spectroscopy and time-of-flight (TOF) mass spectrometry were used to determine that the ratio of iodine-selective abstraction to chlorine-selective abstraction is at least 34±4: 1. The ICl and Si(111)–7×7 reaction can be compared to the ICl and atomic hydrogen (deuterium) reaction which has been studied extensively by others. The chemical selectivity of ICl+Si(111) is greater than the chemical selectivity of the gas phase reaction of H+ICl where the ratio of formation of HI to HCl is only 4:1. In both reactions, the iodine atom of ICl molecules is more reactive than the chlorine atom because the πx,y* antibonding orbital (the orbital that covalently reacts with other species) consists primarily of atomic iodine orbitals. The difference in the chemical selectivities of the silicon surface and gaseous hydrogen reactions with ICl is due to the ability of the silicon surface to rotationally steer ICl molecules, and the inability of silicon to migrate between the iodine and chlorine atoms. The median translational energies of ejected halogen atoms were determined to be 0.18±0.04 eV for chlorine atoms and 0.53±0.27 eV for iodine atoms which are a small fraction (14% for ejected iodine atoms and 9% for ejected chlorine atoms) of the total reaction exothermicities. The low translational energies of ejected atoms is due to the fact that the iodine–chlorine bond of ICl lengthens as the Si–I bond contracts; thus, there is little repulsion energy attributed to the Si–I–Cl transition state. © 1999 American Institute of 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 102 (1995), S. 9096-9108 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Polarized ultraviolet light from an excimer laser (193 nm) was used to photodesorb and photodissociate N2O adsorbed on a cold (80 K) Pt(111) surface. The photodesorbed species and their time of flight (TOF) were monitored by resonantly enhanced multiphoton ionization (REMPI) spectroscopy. We have identified three major channels. The photodesorption of molecular N2 is observed only in the slowest channel where N2 produced by fragmenting the N2O is thermalized on the surface before desorbing. Evidence for this behavior includes both low (∼90 K) rotational and translational temperatures of the N2 fragments as well as a lack of correlation between rotational and translational energy. In the next fastest channel, hyperthermal N2O with a kinetic energy of 0.4±0.1 eV is seen to photodesorb. The photodesorbed hyperthermal N2O also has a substantial degree of internal vibrational excitation. The angular distribution of the N2O channel is peaked toward the surface normal. In the fastest channel, the release of ballistic oxygen atoms, a prompt axial recoil with no collisions with neighboring adsorbates, is seen along the tilted N2O molecular bond axis. The ballistic oxygen atoms leave the surface either in the ground state O(3P) or in the first electronically excited state O(1D). The kinetic energy of the O(3P) and of the O(1D) photoproducts is similar (0.5 eV) suggesting a common dissociative intermediate. In all of the channels observed, the dependence of the photoproducts yield on the polarization of the photodesorption laser indicates a hot carrier mediated mechanism at the surface. We propose a dissociative electron attachment model to explain the photochemistry of N2O/Pt(111) with 193 nm light. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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