Oxygen vibrational modes

The best fibers, installed in systems operating at 0.9 )J.m, had losses of 5 dB/km. The lower intrinsic losses in the 1.3 to 1.55-)J.m window were unattainable by this technique. Fundamental cation—oxygen vibrational modes as well as OH contamination were intrinsic to the compositions. 

Massa et al. [76] and Mroginski et al. [77] have reported evidence from reflectivity, transmission, and photo-induced infrared spectra of strong electron coupling to Ni—O vibrational modes. However, a more direct indication that Tt depends sensitively on the oxygen vibrational modes comes from the observation by Medarde et al. [78] of a 10 °C increase in T, on substitution of for 0. 

The strongest mode observed near 800 cm 1 is polarized along c and is a totally symmetrical vibration mode (Ai) corresponding to the niobium-oxygen vibrations vs (NbO) of infinite chains (NbOF4 )n running along the c -axis. The mode observed at 615 cm 1 is polarized perpendicular to c and corresponds to the NbF vibrations of the octahedrons of the same chains. The mode at 626 cm 1 is attributed to NbF vibrations of isolated complex ions - NbF 2 . The lines at 377, 390 and 272 cm 1 correspond to deformation modes 8(FNbF) of the two polyhedrons. 

Assignments for the Raman and IR bands (Table IV) have beeh made by Matsuura and coworkers (12). The molybdenum-oxygen poJjT" hedra, which are assumed to be derived from tetrahedral MoO,, have four vibrational modes, ,(A), vAEI,... 

Raman spectroscopy has been successfully applied to the investigation of oxidic catalysts. According to Wachs, the number of Raman publications rose to about 80-100 per year at the end of the nineties, with typically two thirds of the papers devoted to oxides [41]. Raman spectroscopy provides insight into the structure of oxides, their crystallinity, the coordination of metal oxide sites, and even the spatial distribution of phases through a sample when the technique is used in microprobe mode. As the frequencies of metal-oxygen vibrations found in a lattice are typically between a few hundred and 1000 cm 1 and are thus difficult to investigate in infrared, Raman spectroscopy is clearly the indicated technique for this purpose. 

FIG. 9 Diagram illustrating the three vibrational modes (31V— 6) of water in the gas phase. (A) The first mode is called bending, in which the water molecule moves in a scissors-like manner. (B) The second is the symmetric stretch, where the hydrogen atoms move away from (or toward) the central oxygen atom simultaneously—i.e., in-phase motion. (C) The third is the asymmetric stretch, in which one hydrogen atom approaches the central oxygen atom, while the other moves away—i.e., out-of-phase motion. 

For linear triatomic molecules 3 N - 5 = 4 and we expect form vibrational modes instead of three as shown in the fig. Out of the four there are two vibrations, one in the plane of the paper and the other in which the oxygen atoms move simultaneously into and out of the plane. The two sorts of motion are termed degenerate and so we have only three vibrations. 

On storage in ambient air or immersion in H202 the Si-O-Si vibrational mode becomes detectable for electrochemically formed PS, without a significant change in the number of Si-Hx bonds, as shown in Fig. 6.15 [Th5]. This supports the assumption that oxygen penetrates the Si lattice and breaks the backbonds of the... 

The direct evidence on which our view of cation solvation in polymer electrolytes is based comes mainly from spectroscopic techniques. IR and Raman studies have been carried out on a variety of systems (see Chapter 5, Torell and Schantz, 1989 and Freeh, Manning, Teeters and Black, 1988). Low frequency vibrational modes, around 860-870 cm associated with the cation-ether oxygen interactions in PEG based systems have been observed they are absent in PEO itself... 

When high-temperature products are in an equilibrium state, many of the constituent molecules dissociate thermally. For example, the rotational and vibrational modes of carbon dioxide are excited and their mohons become very intense. As the temperature is increased, the chemical bonds between the carbon and oxygen atoms are broken. This kind of bond breakage is called thermal dissociation. The dissociahon of H2O becomes evident at about 2000 K and produces H2, OH, O2, H, and O at 0.1 MPa. About 50% of H2O is dissociated at 3200 K, rising to 90% at 3700 K. The products H2, O2, and OH dissociate to H and O as the temperature is increased further. The fraction of thermally dissociated molecules is suppressed as the pressure is increased at constant temperature. 

---