Pressure-induced changes in the optical properties of quasi-one-dimensional β\beta-Na0.33_{0.33}V2_2O5_5

The pressure-induced changes in the optical properties of $\beta$-Na$_{0.33}$V$_2$O$_5$ single crystals at room temperature were studied by polarization-dependent Raman and far-infrared reflectivity measurements under high pressure. From the changes in the Raman- and infrared-active phonon modes in the pressure range 9 - 12 GPa a transfer of charge between the different V sites can be inferred. The importance of electron-phonon coupling in the low-pressure regime is discussed.Comment: 7 pages, 5 figure

Boxnep - модульный подводный робот перспективных технологий

The article discusses the relevance of the underwater vehicles are able to solve a wide range of problems. The decision puts in a basis of the research is designing a modular underwater robot. It allows to make a mounting of various equipment and testing it in the water medium. The paper deals with the concept of the robot and its characteristics

Properties of BaTiO3 confined in nanoporous Vycor and artificial opal silica

Using the sol-gel technique, BaTiO3 was embedded into nanoporous Vycor and artificial vitreous opal silica for the first time. About 50 vol% of the pores was filled. In case of the Vycor glass (pore diameter 4–6 nm) only amorphous phase was revealed by XRD, IR reflectivity and Raman spectra. After additional gradual annealing, no crystallization was achieved. Chemical reaction with the SiO2 skeleton started at ~1000 K. The room-temperature IR and Raman spectra clearly show characteristic vibrational modes of the ferroelectrically distorted TiO6 octahedra without any long-range order. In case of the opal matrix (densely packed silica spheres, pore diameter up to ~50 nm), crystallization of the ferroelectric BaTiO3 appeared in coexistence with the amorphous phase, but the penetration depth of the crystalline BaTiO3 was limited. From the apparent temperature independence of the effective wide-frequency dielectric response due to the essentially temperature independent effective soft mode stiffened to ~100 cm-1, we can deduce that no macroscopic percolation of the crystalline BaTiO3 has appeared in our opal matrix. Nevertheless, Raman spectra bring evidence of a diffuse ferroelectric phase transition in the opal-BaTiO3 composite

Optical Contrast and Raman Spectroscopy Techniques Applied to Few-Layer 2D Hexagonal Boron Nitride

The successful integration of few-layer thick hexagonal boron nitride (hBN) into devices based on two-dimensional materials requires fast and non-destructive techniques to quantify their thickness. Optical contrast methods and Raman spectroscopy have been widely used to estimate the thickness of two-dimensional semiconductors and semi-metals. However, they have so far not been applied to two-dimensional insulators. In this work, we demonstrate the ability of optical contrast techniques to estimate the thickness of few-layer hBN on SiO2/Si substrates, which was also measured by atomic force microscopy. Optical contrast of hBN on SiO2/Si substrates exhibits a linear trend with the number of hBN monolayers in the few-layer thickness range. We also used bandpass filters (500–650 nm) to improve the effectiveness of the optical contrast methods for thickness estimations. We also investigated the thickness dependence of the high frequency in-plane E2g phonon mode of atomically thin hBN on SiO2/Si substrates by micro-Raman spectroscopy, which exhibits a weak thickness-dependence attributable to the in-plane vibration character of this mode. Ab initio calculations of the Raman active phonon modes of atomically thin free-standing crystals support these results, even if the substrate can reduce the frequency shift of the E2g phonon mode by reducing the hBN thickness. Therefore, the optical contrast method arises as the most suitable and fast technique to estimate the thickness of hBN nanosheets

Structure Determination and Compositional Modification of Body-Centered Tetragonal PX-Phase Lead Titanate

The fibrous PX-phase of lead titanate (PT), which can be synthesized by a hydrothermal method, has been studied to clarify its structural aspects on the atomic level. By combining synchrotron X-ray diffraction and electron microscope analysis with a first-principles calculation, a unique open-channel structure with a 5.529 angstrom diameter bore through the whole wire is determined. First-principle modeling reveals that the PX-phase structure has an indirect wide band gap and a higher formation enthalpy than the tetragonal perovskite phase. Both the frequency and symmetry of Raman-active lattice vibrational modes have been identified with polarized Raman spectra on individual monocrystalline PX-phase PT wires, showing a good match with the first-principles calculation. Furthermore, the doping of Zr in the PX-phase PT and the influence on the structure were investigated, showing a limit of 17% incorporation of Zr in the PX-phase PT

Photoanodes with Fully Controllable Texture: The Enhanced Water Splitting Efficiency of Thin Hematite Films Exhibiting Solely (110) Crystal Orientation

Hematite, α-Fe₂O₃, is considered as one of the most promising materials for sustainable hydrogen production <i>via</i> photoelectrochemical water splitting with a theoretical solar-to-hydrogen efficiency of 17%. However, the poor electrical conductivity of hematite is a substantial limitation reducing its efficiency in real experimental conditions. Despite of computing models suggesting that the electrical conductivity is extremely anisotropic, revealing up to 4 orders of magnitude higher electron transport with conduction along the (110) hematite crystal plane, synthetic approaches allowing the sole growth in that direction have not been reported yet. Here, we present a strategy for controlling the crystal orientation of very thin hematite films by adjusting energy of ion flux during advanced pulsed reactive magnetron sputtering technique. The texture and effect of the deposition mode on the film properties were monitored by XRD, conversion electron Mössbauer spectroscopy, XPS, SEM, AFM, PEC water splitting, IPCE, transient photocurrent measurements, and Mott–Schottky analysis. The precise control of the synthetic conditions allowed to fabricate hematite photoanodes exhibiting fully textured structures along (110) and (104) crystal planes with huge differences in photocurrents of 0.65 and 0.02 mA cm^–2 (both at 1.55 V <i>versus</i> RHE), respectively. The photocurrent registered for fully textured (110) film is among record values reported for thin planar films. Moreover, the developed fine-tuning of crystal orientation having a huge impact on the photoefficiency would induce further improvement of thin hematite films mainly if cation doping will be combined with the controllable texture