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  • 1
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The fully vibrationally resolved participator Auger spectra originating from the decay of the C 1s(2σ)−12π1 resonance in CO are presented. The C 1s(2σ)−12π1 v'=0 resonance has been excited with a 75 meV monochromator bandpass, i.e., in Auger resonant Raman conditions, and the participator Auger spectrum observed. The C 1s(2σ)−12π1 v'=1 resonance is also excited and the corresponding participator Auger spectrum observed with a monochromator bandpass slightly larger than the inherent width. The results are compared to theoretical simulations using coherent lifetime-vibrational interference theory which accounts for the details of the spectrum. We have observed an interference shift on the transitions to different vibrational sublevels in the final state. A high resolution C 1s photoelectron spectrum of CO is also presented. The lifetime width of the C 1s core–hole state is determined to be 97(10) meV, whereas the C 1s(2σ)−12π1 resonance is measured to have a width of 86(10) meV. © 1995 American Institute of Physics.
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 10719-10724 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The decay of core-excited electronic states in free 1,3 trans butadiene molecules has been studied using high-resolution synchrotron radiation and electron spectrometry. The core-level energy shift between the terminal and central carbon atoms is 0.64 eV making selective excitation of core electrons from these atoms possible. Resonant excitation to the au(π*) valence state leads to autoionizing decay channels which proceed according to the atomic site in the molecule. The radiationless decay is localized, and certain molecular orbitals are excluded from the decay depending upon the site of the core hole. This phenomenon is confirmed by semiempirical INDO calculations based upon the equivalent core approximation. The vibrational structure of the resonances below the carbon K edge has been measured and fit to extract vibrational energies and intensities, chemical shifts, and the lifetimes of the centrally and terminally excited states. The C 1s spectrum is also measured with vibrational resolution and the energies of the normal vibrational modes are extracted. The bond lengths are derived by application of a linear coupling analysis. © 1996 American Institute of Physics.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 106 (1997), S. 1661-1668 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Recent progress in the development of high-resolution electron spectrometers in combination with highly monochromatized undulator radiation has allowed observation of the vibrationally resolved gas-phase C 1s photoelectron spectra of methane and ethane. For both molecules, the C–H stretching modes are well resolved and for ethane the active C–C stretching mode has been observed for the first time. The spectra have been measured at low kinetic energies and detailed fittings using post-collision interaction line profiles have been made both, using a free parameter fit and a fit adhering to a linear coupling model. The free parameter fit allows for any anharmonicity in the vibrational energies. The linear coupling model, on the other hand, assumes that the initial and final state potential curves are harmonic and differ only in the normal coordinates. This simple model is used to reduce the number of free parameters in the fit, which greatly simplifies the analysis. An intensity model based on the linear coupling predicts that the intensities of the C–H stretching modes are directly related to the number of C–H bonds around the core ionized atom. The result is verified for ethane and shows a potential for further reduction of free parameters for large molecules and polymers. Ab initio calculations of molecular geometry and vibrational frequencies have also been carried out using the equivalent core (Z+1) approximation. The values predicted for the decrease in bond length have then been compared to those determined empirically by the linear coupling approach. The calculation of ethane indicates that symmetric C–H and C–C stretching modes are important upon core ionization. The corresponding vibrational frequencies have been calculated and agree well with observed values. © 1997 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 4475-4480 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High-resolution Auger electron spectra from the decay of the Cl 2p→σ* excitation in HCl and DCl have been measured. The spectra are analyzed, separating molecular and atomic features, which are assigned to transitions to the HCl (5σ2π)4σ* and Cl (3s3p)6 states, respectively. Auger line shapes, as affected by the molecular dissociation, are studied by comparing the experiment with the results of Monte-Carlo computer simulations based on a semiclassical model. © 1996 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 66 (1995), S. 2729-2733 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A modular system of techniques and software has been developed for the calibration and correction of intensity linearity, uniformity of response, spatial distortion, and image plate decay. With calibration the Molecular DynamicsTM Imaging Plate scanner system has been shown to give comparable results to the MarResearchTM scanner. The ESRF x-ray image intensifier/charge-coupled device detectors inherently cause large spatial and uniformity of response distortions, and successful data analysis depends on calibration and correction. Results of synchrotron radiation experiments are presented. © 1995 American Institute of Physics.
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  • 6
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A new end station equipped with a very high-resolution SES-200 electron energy analyzer has been constructed for the study of gases and soft molecular materials. The analyzer is rotatable around the direction of the photon beam, allowing angular-dependent studies. The system has been built in a way allowing the investigation of free molecules and atoms, metal vapors, liquid interfaces as well as solid films. The first electron spectroscopy results for gases, liquids, and polymer films are presented. © 1996 American Institute of Physics.
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  • 7
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A modular system of techniques and software has been developed for the calibration and correction of intensity linearity, uniformity of response, spatial distortion, and image plate decay. With calibration the Molecular DynamicsTM Imaging Plate scanner system has been shown to give comparable results to the MarResearchTM scanner. The ESRF x-ray image intensifier/charge-coupled device detectors inherently cause large spatial and uniformity of response distortions, and successful data analysis depends on calibration and correction. Results of synchrotron radiation experiments are presented. © 1995 American Institute of Physics.
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  • 8
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: The photon energy resolution of the modified SX-700 plane grating monochromator at the Finnish beamline (BL51) at MAX-laboratory in Lund, Sweden, has improved considerably after proper alignment of the monochromator. Resolving powers of about 10 000 at hν≈90 eV and 5000 at hν≈400 eV have been achieved at the first diffraction order, as inferred from total ion yield measurements at the Kr 3d5/2→5p and N2 N1s→π* resonances. The total linewidth of ≤121 meV recorded for the Ar 2p3/2→4s excitation suggests that the lifetime broadening could be smaller than 116 meV obtained from electron energy-loss spectroscopy. © 1995 American Institute of Physics.
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  • 9
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 67 (1995), S. 1800-1802 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Gratings of different period spacings are fabricated on quantum well infrared photodetectors having two-stack multiple quantum wells (MQW) to determine the grating coupling efficiency in multicolor detection. The peak wavelength of each MQW is 4.8 and 9.4 μm, respectively, covering the two atmospheric windows. 2D gratings of box-shaped cavities with grating period either in 3 or 4.6 μm spacing are used to coupled normal incident light into the detector. Comparing detectors with and without gratings at either normal or 45° facet incidence, the detectors with an optimized grating show efficient light coupling for both wavelengths due to the fact that the longer wavelength in the present case is an integral multiple of the shorter wavelength. The optimized long wavelength grating couples the shorter wavelength through additional higher orders of diffraction. © 1995 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 30 (1997), S. 957-962 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: A high-resolution structural study of magnesium formate dihydrate was performed using high-energy synchrotron radiation (0.22 Å) and an X-ray image intensifier/CCD (charge-coupled device) detector. The complete data collection was performed in less than 2 h. The data were treated by two different integration programs and the results are compared. The data quality was sufficiently high to produce good-quality electron difference density maps.
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