Measurement of higher order chromatic dispersion in a photonic bandgap fiber: comparative study of spectral interferometric methods.

Chromatic dispersion of a 37 cm long, solid-core photonic bandgap (PBG) fiber was studied in the wavelength range of 740-840 nm with spectral interferometry employing a Mach-Zehnder interferometer and a high resolution spectrometer. The interferometer was illuminated by a Ti:sapphire laser providing 20 fs pulses. A comparative study has been carried out to find the most accurate spectral phase retrieval method that is suitable for measuring higher order chromatic dispersion. The stationary phase point, the minima-maxima, the cosine function fit, the Fourier transform, and the windowed Fourier transform methods were tested. It was shown that out of these five techniques, the Fourier-transform method provided the dispersion coefficients with the highest accuracy, and it could also detect rapid phase changes in the vicinity of leaking mode frequencies within the transmission band of the PBG fiber.

The structure of hyperalkaline aqueous solutions containing high concentrations of gallium--a solution X-ray diffraction and computational study.

Highly concentrated alkaline NaOH-Ga(OH)3 solutions with 1.18 M ≤ [Ga(III)]T ≤ 2.32 M and 2.4 M ≤ [NaOH]T ≤ 4.9 M (where the subscript T denotes total or analytical concentrations) have been prepared and investigated by solution X-ray diffraction and also by ab initio quantum chemical calculations. The data obtained are consistent with the presence of only one predominant Ga(III)-bearing species in these solutions, which is the tetrahedral hydroxo complex Ga(OH)4(-). This finding is in stark contrast to that found for Al(III)-containing solutions of similar concentrations, in which, besides the monomeric complex, an oxo-bridged dimer was also found to form. From the solution X-ray diffraction measurements, the formation of the dimeric (OH)3Ga-O-Ga(OH)3(2-) could not unambiguously be shown, however, from the comparison of experimental IR, Raman and (71)Ga NMR spectra with calculated ones, its formation can be safely excluded. Moreover, higher mononuclear stepwise hydroxo complexes, like Ga(OH)6(3-), which have been claimed to exist by others in the literature, were not possible to experimentally detect in these solutions with any of the spectroscopic techniques used.

Structural studies of water in hydrophilic and hydrophobic mesoporous silicas: an x-ray and neutron diffraction study at 297 K.

Water confined in a sol-gel network has been characterized by x-ray and neutron diffraction for two samples of mesoporous silica: one with a hydrophilic character (a nonmodified one) and another with a hydrophobic character (a modified one with a methylated internal pore surface). The pore size has been previously characterized [J. Jelassi et al., Phys. Chem. Chem. Phys. 134, 1039 (2010)] to have a mean pore diameter of approximately 55 Å. The diffraction measurements presented in this paper have been made at room temperature [293 K] for a filling factor of 0.45, giving a mean thickness of 8-9 Å for the water layer. The results show that the local order of the confined water molecules in the intermediate region of 3-6 Å is significantly different from that of the bulk water and also for the two different environments. For the hydrophilic sample, the siloxyl groups at the surface modify the water structure through the effects of interfacial hydrogen-bonding, which influences the orientational configuration of local water molecules and creates a modified spatial arrangement in the pore. In the case of the hydrophobic sample, there is no specific interaction with the pore wall, which is primarily van der Waals type, and the water molecules at the interface are differently oriented to create a hydrogen-bonded network linked more directly to the rest of the water volume. In the present circumstances, the thickness of the water layer has a relatively small dimension so that the interpretation of the measured diffraction pattern is not as straightforward as for the bulk liquids, and it is necessary to consider the effects of diffraction-broadening from a distributed sample volume and also the contribution from cross-terms that remain after conducting a "wet-minus-dry" analysis procedure. These analytic difficulties are discussed in the context of the present measurements and compared with the work of other groups engaged in the study of water confined in different environments. The present results, again, emphasize the complexity influencing the properties of water in a confined geometry and the strong influence of surface interactions on its behavior.