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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 5568-5577 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Self-broadened nitrogen isotropic Q(J) Raman linewidths have been inverted to obtain effective rotation–translation (R–T) state-to-state rate constants using the energy corrected sudden (ECS) formalism. These rate constants are discussed as a function of the rotational levels J and temperature T. Collisional Q(J) line shifts have been investigated by high-resolution inverse Raman spectroscopy (IRS) over a wide temperature range. Semiclassical calculations lead to a clear understanding of their J and T dependence. This exhaustive study of both diagonal and off-diagonal relaxation matrix elements has allowed us to calculate the collisionally narrowed Q branch at high pressure. New measurements of N2 Q branch at high pressure have been performed by IRS. The good agreement of ECS profiles with IRS data, for various pressures and temperatures, underlines the consistency of the present R–T ECS scaling analysis.
    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 91 (1989), S. 5916-5925 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In order to understand the influence of H2O on the stimulated Raman Q-branch spectra of nitrogen in combusting media, an exhaustive theoretical and experimental study has been carried out. Starting from a semiclassical model, particularly convenient at high temperature, the Q-line broadening and shifting coefficients have been calculated over a wide temperature range and for a large number of lines. Stimulated Raman Spectra (SRS) measurements have allowed us to test these calculated line broadening coefficients and thus establish the high accuracy of semiclassical values. The theoretical broadening coefficients have been inverted to deduce state-to-state rotational relaxation rates by using two types of fitting laws. A partial test of the resulting Q-branch profiles has been realized at moderate pressures leading to a discrimination between these two laws. Furthermore, the effect of rotational energy transfers on collisionally narrowed profiles at higher densities has been simulated and compared with the pure N2 case.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 1774-1784 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Accurate values of linewidth and line shift in the isotropic vibrational Raman spectrum of compressed liquid N2 have been obtained by using inverse Raman spectroscopy. Experiments have been performed for eight isotherms, from the normal boiling point to the critical point temperatures of N2, the number density varying between the value on the coexistence line, and the maximum value of 2.1×1022 cm−3. Minima of the linewidth have been observed above 86 K, showing the increasing influence of vibration–rotation coupling (motional narrowing) competing with the broadening due to pure vibrational dephasing. Moreover, for the first time, maxima of the red line shifts have been found, exhibiting increasing values as temperature increases. As far as the linewidth is concerned, the comparison with two existing models shows that negative interference of the attractive and repulsive forces must be taken into account for obtaining reasonable agreement between the experimental and theoretical parameters. The experimental density dependence of the linewidth can be described well enough with the Schweizer–Chandler model by taking only into account a soft-core, hard-sphere approximation for the calculation of the radial distribution functions. In the case of the frequency shifts, there is only qualitative agreement between the experimental and theoretical density dependences for the effective repulsive contributions calculated within the framework of the Schweizer–Chandler model.
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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. 6584-6589 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The influence of CO2 and H2O on the rotational relaxation processes of N2 in ternary mixtures N2–CO2–H2O is investigated. The efficiency of these perturbers is responsible for significant modifications of the state-to-state relaxation rates and broadening coefficients. Flame data are well reproduced by taking into account these modifications. The role of these minor species in the determination of temperatures in premixed flames is analyzed. The present relaxation model allows us to understand why the discrepancy between observed and calculated coherent anti-Stokes Raman spectroscopy (CARS) spectra in flames is sometimes resolved by empirically adding a dephasing component to pure nitrogen linewidths. Moreover, this model improves the accuracy of CARS temperature measurements.
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  • 5
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The 2ν2 component of the Fermi dyad ν1/2ν2 of CO2 has been studied with high-resolution stimulated Raman spectroscopy (SRS). The behavior of the band shape has been explored in a large density range: 0.2 to 50 amagat at a temperature of 295 K and 0.5 to 20 amagat at 500 K. Energy corrected sudden (ECS) and modified energy gap (MEG) laws are used to model the relaxation matrix in order to account for the collisional narrowing induced by rotational energy transfers. ECS model allows us to accurately determine the vibrational shift and width as a function of density by fitting the experimental spectra, leading to the determination of the vibrational relaxation coefficients for the 2ν2 mode. Connection is established between the present calculations of the collisionally narrowed SRS spectra based on the diagonalization of the relaxation matrix, which applies for any line overlap, and the usual spectral line shape for weak line coupling. Particular emphasis is put on the situation of strong collapse and on the concomitant predominance of the vibrational dephasing.
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  • 6
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An experimental (SRS) and theoretical analysis for the ν1 component of the ν1/2ν2 Fermi dyad of CO2 has been performed for densities lying from 0.01 to 50 amagat at 295 K, and from 0.01 to 20 amagat at 500 K. At subatmospheric pressure, both line mixing and Dicke narrowing take place for this component due to the very weak Q line spacings. A simple method to account for both diffusional narrowing (due to velocity changing collisions) and collisional narrowing (due to energy transfers) on isotropic Raman Q-branch profile is proposed. This method is based on the transformation of the collapsed Q-branch profile as a sum of individual Lorentzian plus dispersive components whose parameters are density-dependent. Such an exact transformation permits to easily introduce the averaging effect of velocity changing collisions on each component, and then on the collapsed Q-branch itself. In the present study, the Galatry soft collision model is used to define a generalized complete profile for each Lorentzian plus dispersive component. Such a procedure allows us to take into account the velocity changing collision's effects not only on isolated lines (the well-known Dicke narrowing) but also on the line couplings resulting from collisionally induced rotational energy transfers. The present analysis permits an accurate description of the observed modifications on the SRS profile of the ν1 band of CO2 (1388 cm−1) as a function of density. The straightforward extension to other spectroscopies (linear and nonlinear) is suggested.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 4951-4956 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A speed-dependent line profile combining soft and hard fully correlated Dicke-narrowing collisions was recently successfully tested on Ar-broadened H2 spectra in a wide density and temperature range. A further test for mixtures of H2 in nitrogen molecules (instead of Ar atoms) is presented. This test is also based on high resolution Raman investigation of the isotropic Q(1) line of H2 from low to high density at various temperatures. The same consistency of the speed-dependent line profile as for H2–Ar is obtained for H2–N2 through a remarkable agreement with all the data by using a unique set of four parameters (the collisional width and shift, the kinetic frequency, and a characteristic velocity memory parameter). The present study is a preliminary step for the hydrogen CARS thermometry in H2–air flames at high pressure. © 2000 American Institute of Physics.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 158-166 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The paper presents high resolution Raman investigations of the Q(1) line of H2 in Ar mixture from low density (Doppler regime) to high density (collisional regime) analyzed with a unique line shape profile. Measurements are performed by stimulated Raman gain spectroscopy between 300 and 1000 K in a wide density range (from 0.2 to 11 amagat). All the observed spectral features are accurately described by a unified model recently proposed by two of the authors. This model accounts for a velocity-memory process, not restricted to the usual hard and soft limits. It also includes correlation between velocity- and phase-changing collisions. An exhaustive analysis of various possible mechanisms on the line shape is achieved. These mechanisms are the Dicke narrowing, the radiator speed dependence of the collisional broadening and shifting parameters, the collisionally induced speed-class exchange and the nonimpact effect. The present test shows the high consistency of the unified model, since it allows one to get a remarkable agreement with all the data by using a unique set of parameters. This model should be useful for optical diagnostics at moderate density, as required for combusting media or atmospheric work. © 2000 American Institute of Physics.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 951-961 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High resolution stimulated gain Raman spectroscopy is used to investigate the collisional parameters of pure rotational S0(j=0–4) lines of H2 in pure H2 and H2–He mixture. Measurements are performed between 300 and 1000 K in a density regime where the lines are essentially collisionally broadened (typically 10 amagat). For the first time, these highly accurate measurements of the frequencies of pure rotational lines allow one to correct previously measured values that did not take into account the collisional frequency shift. For both collisional systems, the shifting coefficients exhibit a linear behavior with the square root of temperature, similar to the behavior already observed in the Q branch. The broadening coefficients of the S0 branch increase nonlinearly with temperature contrary to the Q branch. For the H2–He system, both these new S0(j) data and previously measured Q(j) data are analyzed using a modeling of the broadening coefficients in terms of elastic and inelastic contributions. These different contributions are analyzed as a function of temperature and of the rotational quantum number j. Preliminary quantum calculations are used to assess the validity of the model. Further calculations will be presented in paper II. © 1998 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 73 (1998), S. 1859-1861 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Photoemission spectromicroscopy data on Si–GaSe with 0.2 μm lateral resolution revealed laterally inhomogeneous interface Se–Si chemical reactions. The local Si 2p fits agrees with interface Si selenide parameters; the Se 3d peaks indicate a Si–selenide component; the Ga 3d peaks exhibit a metallic component whose intensity increases with Si coverage. This local interface reaction is related to lateral changes in the band lineup. © 1998 American Institute of Physics.
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