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Loss peak

Figure Bl.25.12. Excitation mechanisms in electron energy loss spectroscopy for a simple adsorbate system Dipole scattering excites only the vibration perpendicular to the surface (v ) in which a dipole moment nonnal to the surface changes the electron wave is reflected by the surface into the specular direction. Impact scattering excites also the bending mode v- in which the atom moves parallel to the surface electrons are scattered over a wide range of angles. The EELS spectra show the higlily intense elastic peak and the relatively weak loss peaks. Off-specular loss peaks are in general one to two orders of magnitude weaker than specular loss peaks. Figure Bl.25.12. Excitation mechanisms in electron energy loss spectroscopy for a simple adsorbate system Dipole scattering excites only the vibration perpendicular to the surface (v ) in which a dipole moment nonnal to the surface changes the electron wave is reflected by the surface into the specular direction. Impact scattering excites also the bending mode v- in which the atom moves parallel to the surface electrons are scattered over a wide range of angles. The EELS spectra show the higlily intense elastic peak and the relatively weak loss peaks. Off-specular loss peaks are in general one to two orders of magnitude weaker than specular loss peaks.
L of CO was adsorbed at a pressure of 1 x 10 mbar and T= 200 K. At zero energy loss one observes the highly intense elastic peak. The other peaks in the spectrum are loss peaks. At high energy, loss peaks due to dipole scattering are visible. In this case they are caused by CO vibration perpendicular to the surface. The... [Pg.1866]

Figure 3.16a shows the storage and loss components of the compliance of crystalline polytetrafluoroethylene at 22.6°C. While not identical to the theoretical curve based on a single Voigt element, the general features are readily recognizable. Note that the range of frequencies over which the feature in Fig. 3.16a develops is much narrower than suggested by the scale in Fig. 3.13. This is because the sample under investigation is crystalline. For amorphous polymers, the observed loss peaks are actually broader than predicted by a... Figure 3.16a shows the storage and loss components of the compliance of crystalline polytetrafluoroethylene at 22.6°C. While not identical to the theoretical curve based on a single Voigt element, the general features are readily recognizable. Note that the range of frequencies over which the feature in Fig. 3.16a develops is much narrower than suggested by the scale in Fig. 3.13. This is because the sample under investigation is crystalline. For amorphous polymers, the observed loss peaks are actually broader than predicted by a...
Dynamic mechanical measurements were made on PTEE samples saturated with various halocarbons (88). The peaks in loss modulus associated with the amorphous relaxation near —90°C and the crystalline relaxation near room temperature were not affected by these additives. An additional loss peak appeared near —30° C, and the modulus was reduced at all higher temperatures. The amorphous relaxation that appears as a peak in the loss compliance at 134°C is shifted to 45—70°C in the swollen samples. [Pg.352]

Figure 4 Experimental low-loss profiles for Mg (10.0)< Ti (17.2), Zr(16.6), and their hydrides MgH2 (14.2), TiH 97 (20.0), and ZrHj g (18.1). The values in parentheses represent the experimental plasmon-loss peak energies in eV. Figure 4 Experimental low-loss profiles for Mg (10.0)< Ti (17.2), Zr(16.6), and their hydrides MgH2 (14.2), TiH 97 (20.0), and ZrHj g (18.1). The values in parentheses represent the experimental plasmon-loss peak energies in eV.
The width and shape of the energy loss peaks in HREELS are usually completely determined by the relatively poor instrumental resolution. This means that no information can be obtained from HREELS about such interesting chemical physics questions as vibrational energy transfer, since the influence of the time scale and mechanism of vibrational excitations at surfaces on the lifetimes, and therefore the line widths and shapes, is swamped. (Adsorbates on surfaces have intrinsic vibra-... [Pg.446]

Figure 2.36 A shows a typical low-loss spectrum taken from boron nitride (BN). The structure of BN is similar to that of graphite, i. e. sp -hybridized carbon. For this reason the low-loss features are quite similar and comprise a distinct plasmon peak at approximately 27 eV attributed to collective excitations of both n and a electrons, whereas the small peak at 7 eV comes from n electrons only. Besides the original spectrum the zero-loss peak and the low-loss part derived by deconvolution are also drawn. By calculating the ratio of the signal intensities hot and Iq a relative specimen thickness t/2 pi of approximately unity was found. Owing to this specimen thickness there is slight indication of a second plasmon. Figure 2.36 A shows a typical low-loss spectrum taken from boron nitride (BN). The structure of BN is similar to that of graphite, i. e. sp -hybridized carbon. For this reason the low-loss features are quite similar and comprise a distinct plasmon peak at approximately 27 eV attributed to collective excitations of both n and a electrons, whereas the small peak at 7 eV comes from n electrons only. Besides the original spectrum the zero-loss peak and the low-loss part derived by deconvolution are also drawn. By calculating the ratio of the signal intensities hot and Iq a relative specimen thickness t/2 pi of approximately unity was found. Owing to this specimen thickness there is slight indication of a second plasmon.
AF correction, in EDXS 205 Zero-loss peak, in EELS 57... [Pg.336]

Thermal treatment and the nature of the casting solvent can also affect the deformation modes achieved in strained films of ionomers. For example, in films cast from polar dimethylformamide (DMF), the solvent interacts with ion-rich clusters and essentially destroys them, as is evident form absence of a second, higher temperature loss peak in such samples. As a result, even in a cast DMF sample of Na-SPS ionomer of high ion content (8.5 mol%), the only deformation mode observed in tensile straining is crazing. However, when these films are given an additional heat treatment (41 h at 210°C), shear... [Pg.148]

Die Tg can be determined readily only by observing the temperature at which a significant change takes place in a specific electric, mechanical, or physical property. Moreover, the observed temperature can vary significantly, depending on the specific property chosen for observation and on details of the experimental technique (for example, the rate of heating, or frequency). Therefore, the observed Tg should be considered to be only an estimate. The most reliable estimates are normally obtained from the loss peak observed in dynamic mechanical tests or from dilatometric data (ASTM D-20). [Pg.396]

Dynamic mechanical analysis of siloxane-urea copolymers show a sharp loss peak around —110 °C corresponding to the Tg of the siloxane segment. The transition in... [Pg.65]

In addition, use of the scanning principle allows mlcroanalysls of very small specimen regions to be performed by detection of either the characteristic X-rays emitted cr the characteristic energy loss peaks in the energy spectrum of transmitted electrons. [Pg.330]

Figure 6.9 HREEL evidence for carbonate formation when C02 is chemisorbed at Cu(110)-Cs at 110K and warmed to 298 K with a strong loss peak at 1500 cm-1 characteristic of a bidentate structure. (Reproduced from Ref. 6). Figure 6.9 HREEL evidence for carbonate formation when C02 is chemisorbed at Cu(110)-Cs at 110K and warmed to 298 K with a strong loss peak at 1500 cm-1 characteristic of a bidentate structure. (Reproduced from Ref. 6).

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