Changes in the structure of amorphous solid water films, grown by vapour deposition on a copper substrate at 75 K and then held at 120 K for 10 min to effect pore collapse, have been observed in the ranges 122-139 K and 150-162 K using positronium annihilation spectroscopy. It is proposed that the former is associated with the glass transition, with an effective activation energy of 0.266(3) eV. The data for the latter, which exhibit minima suggesting the temporary introduction of molecular disorder, can be processed to yield an effective activation energy of 0.47(2) eV, and are consistent with either a structural reorganization of the crystalline lattice or a relaxation of the amorphous structure mediated by defect migration.
Stimulated Rayleigh-Mie scattering (SRMS) in two-photon absorption liquids is realized by a Fourier-transform-limited pulsed Nd-glass laser. For the first time, to the best of our knowledge, we have measured anti-Stokes spectral shifts of SRMS in toluene and hexane colloids of Ag nanoparticles, as well as in pure toluene. These values appreciably exceed the Rayleigh line width in those liquids. The four-wave mixing method is applied both experimentally and theoretically to display the process as Rayleigh-induced parametric generation. We show that the amplification effect is provided predominantly by thermally induced coherent polarization oscillations, while an interference-assisted thermal grating provides formation of a self-induced optical cavity inside the interaction region.
A number of features of stimulated thermal Rayleigh scattering (STRS) in pure liquids and nanoparticle solutions are investigated in this work. It is shown that scattering efficiency is not reduced in the case of wide spectral bandwidth pump radiation. It is shown experimentally that the frequency shift of the scattered signal relative to the pump frequency greatly exceeds the theoretical value. It is also shown theoretically that the frequency shift value does not depend on the linewidth of the pump.
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