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  • 1
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 104-108 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 3522-3525 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 94 (1991), S. 4749-4755 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic spectrum of N+2–Ne has been measured in the region corresponding to the B 2∑+u←X 2∑+g origin and 1–0 transitions of N+2. Spectra were obtained by irradiating a mass selected population of N+2–Ne and monitoring the production of N+2 as a function of wavelength. Low temperature N+2–Ne spectra exhibit several well resolved bands. From the shift of the N+2–Ne origin with respect to that of free N+2 it is apparent that the complex dissociation energy D0 is 146.5 cm−1 greater in the B state than the X state. Pronounced changes in the complex's spectrum occur as the effective temperature is increased. The hottest spectra resemble a broadened and truncated N+2 spectrum. The breaking off at the high energy end of the spectrum at elevated temperatures allows us to establish a rough ground-state dissociation energy of 300 cm−1. Other conclusions resulting from this work are that the equilibrium geometry of the N+2–Ne molecule is probably linear in X and B electronic states, that the ΔG1/2 for the low frequency stretch in the B state is 104 cm−1, and that the N–N stretching motion is affected only very weakly by the presence of the Ne atom.
    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 93 (1990), S. 4477-4478 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The electronic spectrum of N2+–He has been measured in the region corresponding to the N2+ B 2Σ+u←X 2Σ+g origin transition. The spectrum was recorded by photoexciting a mass selected beam of N2+–He ions and detecting N2+ fragments. A likely process for the fragmentation involves fluorescence to a vibrationally excited level of the ground electronic state followed by vibrational predissociation. The observed spectrum exhibits well resolved discrete structure and bears a remarkable resemblance to a cold N2+ spectrum suggesting that the potential between the N2+ ion and helium atom in both the X and B electronic states, has at most only a small barrier to internal rotation. Measurement of the shift of N2+–He transitions with respect to the corresponding N2+ lines indicates that the binding energy of the helium atom to the N2+ ion is almost the same in both the B and X electronic 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 96 (1992), S. 4035-4036 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The B←X spectrum of N+2–He exhibits a hot band which arises from transitions in complexes which have one quantum of the N–N stretching vibration. By measuring the intensity of this peak relative to that of the origin peak as function of the time between ion preparation and laser interrogation we have determined the vibrational predissociation lifetime of the N+2–He complex to be 220±30 μs.
    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. 4645-4650 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Two-photon absorption spectroscopy with a mass-selected beam of CO+2 ions was used to study the predissociative C˜ 2Σ+g state of CO+2. The first photon pumped the A˜ 2Πu←X˜ 2Πg transition and the second photon was used to scan through the C˜ 2Σ+g←A˜ 2Πu transition. A rotational analysis of two bands in this spectrum has been made. The C˜ 2Σ+g state is linear with a C–O bond length of 1.1552(2) A(ring) in the v=0 level.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 86 (1999), S. 5434-5443 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The low-temperature defect chemistry of oxides is considered, characterized by frozen-in interaction with the ambient oxygen and reversibility of internal interactions, in particular the redistribution of electronic carriers. Analytical relations describing ionic and electronic defect concentrations are derived for various conditions. The presence of redox-active, i.e., deep-level, dopants proves to be of special interest in this context. The analytical relations permit the detailed discussion of the dependencies of the charge carrier concentrations on the control parameters. Such analytical relations are useful for understanding and tailoring defect concentrations and thus related properties of electroceramics. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 86 (1999), S. 5422-5433 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Using oxides as examples, the defect chemistry is systematically analyzed for a low-temperature regime, at which the oxygen exchange equilibrium reaction is no longer reversible, while the internal defect equilibrium reactions (in particular, the electronic transfer processes) may still be reversible. For the partially frozen-in states as well as for the complete equilibrium cases, defect concentrations are numerically calculated for idealized model oxides including pure, acceptor-doped, and donor-doped oxides. Foreign ions (major/minor, shallow/deep, acceptor/donor), oxygen vacancies, and oxygen interstitials are taken into account as redox-active defects. The deep-level (redox-active) defects often dominate defect concentrations in the partially frozen-in states, while the major dopants fix the concentrations in complete equilibrium. The temperature and oxygen partial pressure dependencies of defect concentrations in the partially frozen-in states are discussed. The description does not only allow one to extend the defect chemistry to lower temperatures, such as room temperature, but also offers a quantitative basis for manipulation and prediction of defect concentrations in ionic crystals. Thereby, the physical and chemical performance of such materials may be controlled at temperatures lower than those at which the oxygen nonstoichiometry is established. The results are equally relevant for applications in solid state physics (e.g., compound semiconductors) and in solid state chemistry (e.g., solid electrolytes, mixed conductors). © 1999 American Institute of Physics.
    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 96 (1992), S. 7535-7541 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Vibrationally structured electronic transitions of N2O+–Ar have been observed by measuring the wavelength-dependent yields of the photodissociation reactions to yield N2O+ or Ar+. There appear to be four structured overlapping electronic band systems which are distinguished by vibrational spacings and by their propensity towards production of either N2O+ or Ar+. Variations in the Ar+/N2O+ photoproduct ratio with wavelength are explained as due to vibrational predissociation on different potential-energy surfaces correlating with either Ar+ or N2O+ products. The first band system, observed exclusively at the N2O mass, has its origin close to 445 nm, corresponding approximately to the difference in the energies of N2O+[X 2Π3/2]+Ar[1S0] and N2O[1Σ+]+Ar+[2P3/2] and is assigned as an intracluster charge-transfer transition. Two strong band systems situated to higher energy are assigned as transitions to the two additional electronic states which are expected to correlate with 2P3/2 and 2P1/2 Ar+ and N2O[1Σ+] products. While excitation of these two bands results almost exclusively in Ar+ production, a fourth weaker band near 342 nm leads to N2O+ and appears likely to be a transition to a state correlating with an excited vibronic state of N2O+[A 2Σ+(1,0,0)]+Ar[1S0]. The different band systems exhibit extensive vibrational progressions involving the deformation of the bond between the N2O and the Ar. The shift in the onset of the first charge transfer from the difference in the Ar and N2O ionization potentials combined with the appearance energy for Ar+ production allow tentative estimates of 690 and 1340 cm−1 to be made for the dissociation energies of the lowest and first excited states of N2O+–Ar.
    Type of Medium: Electronic Resource
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