Analysis of Vibrational Spectra of Tetrafluoroethane Glasses Deposited by Physical Vapor Deposition.

This paper presents the results obtained in the study of structural phase transitions in thin films of R134A. The samples were condensed on a substrate by physical deposition of R134A molecules from the gas phase. Structural phase transformations in samples were investigated by observing the changes in characteristic frequencies of Freon molecules in the mid-infrared range with the help of Fourier-transform infrared spectroscopy. The experiments were carried out in the temperature range from 12 to 90 K. A number of structural phase states, including glassy forms, were detected. The changes in thermogram curves at fixed frequencies of half-widths of absorption bands of R134A molecules were revealed. These changes indicate a large bathochromic shift of these bands at frequencies of ν = 842 cm-1, ν = 965 cm-1, and ν = 958 cm-1 and a hypsochromic shift of the bands at frequencies of ν = 1055 cm-1, ν = 1170 cm-1, and ν = 1280 cm-1 at temperatures from T = 80 K to T = 84 K. These shifts are related to the structural phase transformations in the samples.

IR Spectroscopic Degradation Study of Thin Organometal Halide Perovskite Films.

The advantages of IR spectroscopy include relatively fast analysis and sensitivity, which facilitate its wide application in the pharmaceutical, chemical and polymer sectors. Thus, IR spectroscopy provides an excellent opportunity to monitor the degradation and concomitant evolution of the molecular structure within a perovskite layer. As is well-known, one of the main limitations preventing the industrialization of perovskite solar cells is the relatively low resistance to various degradation factors. The aim of this work was to study the degradation of the surface of a perovskite thin film CH3NH3PbI3-xClx caused by atmosphere and light. To study the surface of CH3NH3PbI3-xClx, a scanning electron microscope, infrared (IR) spectroscopy and optical absorption were used. It is shown that the degradation of the functional layer of perovskite proceeds differently depending on the acting factor present in the surrounding atmosphere, whilst the chemical bonds are maintained within the perovskite crystal structure under nitrogen. However, when exposed to an ambient atmosphere, an expansion of the NH3+ band is observed, which is accompanied by a shift in the N-H stretching mode toward higher frequencies; this can be explained by the degradation of the perovskite surface due to hydration. This paper shows that the dissociation of H2O molecules under the influence of sunlight can adversely affect the efficiency and stability of the absorbing layer. This work presents an approach to the study of perovskite structural stability with the aim of developing alternative concepts to the fabrication of stable and sustainable perovskite solar cells.

Optical Studies of Thin Films of Cryocondensed Mixtures of Water and Admixture of Nitrogen and Argon.

The interaction of host molecules with water molecules is of primary importance in astrophysical and atmospheric studies. Water-binding interactions continue to attract a broad interest in various fields, especially those related to the formation of assembly structures. Using the physical vapor deposition (PVD) method and a two-beam interferometer with a wavelength of 406 nm, the refractive indices of thin films of a water and nitrogen (argon) mixture were calculated in the range from 15 to 35 K. The results of temperature transformations of the obtained films from a two-beam interferometer, and thermal desorption characteristics from the temperature of condensation to the temperature of evaporation of water (15-180 K), are presented. The relationship between the signal of the interferometer, the refractive index, and the film thickness during glass transition is demonstrated.