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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 2995-3003 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Photoion–photoelectron coincidence (PIPECO) spectra for Ar+n (n=2–4) in the wavelength region of 750–875 A(ring) have been measured at different nozzle stagnation pressures. The ionization energies (IE) for the ground Ar+2[I(1/2)u] and Ar+3[I(1/2)u] states are determined to be 14.518±0.017 eV (854±1 A(ring)) and 14.350±0.033 eV (864±2 A(ring)), in agreement with the findings of previous photoionization experiments. The IE for Ar+2[II(1/2)u] is found to be (approximately-less-than)15.83 eV (783 A(ring)). The observation of the Ar+2[II(1/2)u] PIPECO band supports the interpretation that Ar+2[II(1/2)u] is metastable with a lifetime longer than 47 μs, a value in accord with the calculated radiative lifetime of 90.9 μs for the II(1/2)u →I(1/2)g transition. The PIPECO spectrum for Ar+2 is dominated by autoionization structure similar to that resolved in the photoionization efficiency spectrum for Ar+2, indicating that a significant fraction of electrons produced by these autoionizing states are slow electrons with near-zero kinetic energies. Evidence is found that metastable Ar+3 and Ar+4 ions formed by photoionization of Ar3 and Ar4 at energies above the Ar+2[I(1/2)u]+Ar(1S0) and Ar+3[I(1/2)u]+Ar(1S0) dissociation limits may live longer than 58 and 66 μs, respectively. We suggest that the formation of Ar+3 in metastable electronic states may be responsible for the long dissociation lifetimes of Ar+3 observed in this experiment.
    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 90 (1989), S. 6026-6033 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photoion–photoelectron coincidence (PIPECO) spectra for (CO)+2 in the wavelength region of 620–990 A(ring) have been obtained at different nozzle stagnation pressures (P0). The ionization energy for (CO)2 to CO+(X˜)⋅CO is determined to be (approximately-less-than)12.73±0.05 eV (974±4 A(ring)), indicating that CO+(X˜)⋅CO is bound by more than 1.29 eV. The PIPECO measurements also provide evidence that CO+(A˜,B˜)⋅CO are bound with dissociation energies 〉0.3 eV. At P0≤200 Torr and a nozzle temperature (T) of 120 K, nozzle expansion conditions which minimize the formation of (CO)n (n≥3), the intensities for the CO+(A˜,B˜)⋅CO PIPECO bands are found to be negligibly small compared to that for the CO+(X˜)⋅CO PIPECO band. This observation supports the conclusion that the excited CO+(A˜,B˜)⋅CO ions are dissociative, with dissociation lifetimes〈42 μs. This conclusion is contrary to that of the preliminary study which is based on the PIPECO spectrum for (CO)+2 measured at P0=350 Torr and T=120 K. Assuming that the radiative lifetimes of CO+(A˜ or B˜) and CO+(A˜ or B˜)⋅CO are identical, we estimate that the dissociation lifetimes for CO+(A˜)⋅CO and CO+(B˜)⋅CO are (approximately-less-than)4 μs and (approximately-less-than)50 ns, respectively.
    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 88 (1988), S. 4098-4099 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The photoion–photoelectron coincidence (PIPECO) spectrum for (CO)+2 has been measured in the wavelength region of ∼600–1 000 A(ring). The lower limits for the bond dissociation energies of CO+ (X˜)⋅CO, CO+ (A˜)⋅CO, and CO+ (B˜)⋅CO are determined to be 29.8, 17, and 16 kcal/mol, respectively. Evidence supporting the existence of long-lived (CO)+2 states with dissociation lifetimes 〉40 μs at energies above the CO+ (X˜,v=0)+CO asymptote is found. The dissociative lifetimes of CO+ (A˜)⋅CO and CO+(B˜)⋅CO are estimated to be longer than 4 μs and 50 ns, respectively.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2015-11-20
    Description: Negative thermal expansion (NTE) was investigated for Ga 1− x Mn x N 0.8 Mn 3 (0.1 ≤  x  ≤ 0.3). As x increases, the temperature range where lattice contracts upon heating becomes broad and shifts to lower temperatures. The coefficient of linear thermal expansion beyond −40 ppm/K with a temperature interval of ∼50 K was obtained around room temperature in x  = 0.2 and 0.25. Local lattice distortion which was thought to be intimately related to NTE is invisible in the X-ray pair distribution function of x  = 0.3. Furthermore, a zero-field-cooling exchange bias was observed as a result of competing ferromagnetic (FM) and antiferromagnetic (AFM) orders. The concomitant FM order serves as an impediment to the growth of the AFM order, and thus broadens the temperature range of NTE. Our result suggests that NTE can be achieved in antiperovskite manganese nitrides by manipulating the magnetic orders without distorting the local structure.
    Print ISSN: 0003-6951
    Electronic ISSN: 1077-3118
    Topics: Physics
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