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  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    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 87 (1987), S. 1062-1069 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report center-of-mass kinetic energy distributions for the 193 nm photodissociation of H2S and HBr using the method of velocity–aligned Doppler spectroscopy. Nascent H atoms are detected by sequential two-photon photoionization via Lyman-α (121.6 nm + 364.7 nm), and internal SH(X 2Π) and Br excitations are observed directly in the H-atom kinetic energy distributions. The kinetic energy resolution is much better than in "conventional'' sub-Doppler resolution spectroscopy and results from detecting spatially selected species whose velocities are aligned with the wave vector of the probe radiation, kprobe, thereby providing a kinetic energy distribution for a specific laboratory direction. This improved resolution is achieved in the present experiments by using pulsed, collimated, and overlapped photolysis and probe beams, but the vital aspect of the technique involves increasing the delay between the two lasers in order to discriminate against species having velocity components perpendicular to kprobe. In the case of HBr, we identify the Br(2P3/2) and Br(2P1/2) contributions and find that the Br(2P1/2) channel accounts for approximately 14% of the fragmentation associated with perpendicular electronic transitions. Concerning H2S, SH(X 2Π) vibrational structure is clearly evident in the H-atom kinetic energy distribution, and the SH vibrational distribution shows oscillations, with [v″=0]〉[v″=1], [v″=1]〈[v″=2], [v″=2]〉[v″=3], [v″=3]〈[v″=4], and [v″=4]〉[v″=5]. Such oscillatory behavior was predicted theoretically by Kulander. A simulation of our data places 32% of the SH in v″〉0 (〈Evib(SH)〉∼2700 cm−1, which is approximately 14% of the available energy, hν-D0), while the general features of our H2S data are in accord with the TOF study of van Veen et al. Presently, our measurements appear to be limited by the dye laser resolution (∼0.06 cm−1 at 364.7 nm), but a significant improvement of the laser bandwidth is possible using commercially available sources. The velocity-aligned Doppler spectroscopy technique is not limited to detecting atoms, and species can be monitored using ionization, LIF, and absorption spectroscopy. As a result, this method should find applications in many areas of molecular physics.
    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 86 (1987), S. 6523-6530 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: IRAS (infrared reflection absorption spectroscopy) has been employed to study the isotopic mixing reaction: 13C16O(a)+12C18O(a)→13C18O(a)+12C16O(a) on Ni(111) with preadsorbed K adatoms. Under high temperature conditions (T〉450 K) where the isotopically mixed CO is being desorbed, it has been shown that the isotopic exchange reaction cannot be detected by IRAS on the surface among CO molecules strongly interacting with K adatoms. This result implies that dissociation of CO occurs at K-promoted Ni sites followed by surface diffusion of C(a) and O(a) away from the K promoter site. Statistical recombination of C(a)+O(a) occurs with concomitant CO desorption on Ni(111) sites some distance from K centers. The empty K-promoted sites may be refilled by surface diffusion of CO from outside. Thus, alkali metal promotion of C–O bond scission may act via a "feeder-site'' mechanism connecting promoter atoms to external surface sites via surface diffusion of atomic C and O species.
    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 90 (1989), S. 2692-2702 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The technique of velocity-aligned Doppler spectrosocopy (VADS) is presented and discussed. For photolysis/probe experiments with pulsed initiation, VADS can yield Doppler profiles for nascent photofragments that allow detailed center-of-mass (c.m.) kinetic energy distributions to be extracted. When compared with traditional forms of Doppler spectroscopy, the improvement in kinetic energy resolution is dramatic. Changes in the measured profiles are a consequence of spatial discrimination (i.e., focused and overlapping photolysis and probe beams) and delayed observation. These factors result in the selective detection of species whose velocities are aligned with the wave vector of the probe radiation kpr, thus revealing the speed distribution along kpr rather than the distribution of nascent velocity components projected upon this direction. Mathematical details of the procedure used to model VADS are given, and experimental illustrations for HI, H2S, and NH3 photodissociation are presented. In these examples, pulsed photodissociation produces H atoms that are detected by sequential two-photon, two-frequency ionization via Lyman-α with a pulsed laser (121.6+364.7 nm), and measuring the Lyman-α Doppler profile as a function of probe delay reveals both internal and c.m. kinetic energy distributions for the photofragments. Strengths and weaknesses of VADS as a tool for investigating photofragmentation phenomena are also discussed.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 879-887 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Experimental results involving 193 nm PH3 photodissociation are reported. Detection of the PH2 fragment using laser induced fluorescence suggests that PH2 is formed with appreciable internal excitation, but no quantitative results concerning nascent PH2 could be obtained using this direct method. In related kinetics studies, the reaction of thermalized (300 K) PH2 with O2 yields a rate coefficient of 2.7×10−13 cm3 molecule−1 s−1, while PH2+NO is rather unreactive (k〈10−14 cm3 molecule−1 s−1). In separate experiments, sub-Doppler spectroscopy on the H-atom fragment at Lyman-α (121.6 nm) allowed the center-of-mass kinetic energy distribution to be extracted; the PH2 internal energy distribution was obtained using energy conservation. Most of the available energy (E° (approximately-equal-to)hν−D0=22 000 cm−1) appears as PH2 internal excitation; the mean internal energy is 14 000 cm−1 and the distribution peaks at ∼19 000 cm−1. The experimental distribution compares favorably with a simple statistical (prior) calculation, and the agreement is discussed in terms of possible photodissociation mechanisms.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 5518-5523 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 52 (1988), S. 860-862 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Experiments involving 193 nm AsH3 excitation are described. With ≥25 ns delay between the firing of photolysis and probe lasers, product H atoms are detected by two-frequency, two-photon ionization (121.6 nm+364.7 nm) via Lyman-α. However, temporally overlapping the photolysis and "probe'' beams enables ionization to complete with dissociation. The resulting AsH+x signal displays a marked dependence on the near-UV frequency, and AsH+x peaks are accompanied by dips in the H-atom signal. Delay and near-UV frequency control the competition between the different pathways, and the overall effect is both easily induced and macroscopic. Applications may be found in the photoassisted growth of semiconductor materials.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 452 (1985), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 41 (1985), S. 252-255 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 45 (1989), S. 413-415 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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