ABSTRACT
The possibility of doping ZnO in its metastable rock salt structure with Li, Na, and K intended to act as acceptor dopants was investigated. For the first time, MgxZn1-xO alloys and pure ZnO with a rock salt structure doped with Li, Na, and K metals was obtained by high-pressure synthesis from pure oxides with the addition of carbonates or acetates of the corresponding metals as dopant sources. Successful stabilization of the metastable rock salt structure and phase purity were confirmed by X-ray diffraction. Transmission electron microscopy was used to study the particle size of nanocrystalline precursors, while the presence of Li, Na, and K metals in rock salt ZnO was detected by electron energy-loss spectroscopy and X-ray photoelectron spectroscopy in MgxZn1-xO alloys. Electron paramagnetic resonance measurements revealed the acceptor behavior of Li, Na, and K dopants based on the influence of the latter on native defects and natural impurities in ZnO-MgO alloys. In addition, diffuse reflectance spectroscopy was used to derive band gaps of quenched rock salt ZnO and its alloys with MgO.
ABSTRACT
Titanium dioxide is a widely used photocatalytic material possessing such advantages as safety, low cost, and high reactivity under the ultraviolet light illumination. However, its applicability in sunlight is limited due to the wide band gap and, as a consequence, the low quantum yield. Doping of titanium dioxide with metal or non-metal atoms and creating heterojunctions based on it are some of the most efficient ways to overcome this drawback. Herein we propose a new facile way of synthesis of nitrogen-doped TiO2/MoO3 and TiO2/WO3 microsphere-shaped nanocomposite photocatalysts, combining the advantages of these two methods. It is revealed that such structures are not only photo-active when exposed to visible light, but can also accumulate a photoinduced charge, thus allowing the catalytic reaction to be prolonged for a long time after the illumination is switched off (up to 48 h). With the help of EPR spectroscopy, paramagnetic defects in the samples were determined. The obtained results show good application prospects of the visible-light-driven TiO2-based nanoheterostructured microspheres in the environmental purification.
ABSTRACT
The Re3As7- x In x solid solution was prepared for x ≤ 0.5 by heating the elements in stoichiometric ratios in evacuated silica tubes at 1073 K. It crystallizes with the Ir3Ge7 crystal structure, space group Im-3m, with a unit-cell parameter a ranging from 8.716 to 8.747 Å. The crystal structure and properties were investigated for a composition with x = 0.4. It is shown that indium substitutes arsenic exclusively at one crystallographic site, such that the As-As dumbbells with d As-As = 2.54 Å remain intact. Re3As6.6In0.4 behaves as a bad metal or heavily doped semiconductor, with electrons being the dominant charge carriers. It possesses high values of Seebeck coefficient and low thermal conductivity, but relatively low electrical conductivity, which leads to rather low values of the thermoelectric figure of merit.
ABSTRACT
The after-pulse time-resolved microwave conductivity (TRMC) decays observed in P3HT:PCBM blends display a dependence on time close to t(-beta), independent of excitation intensity, in the 10 ns-1 micros range. This is explained in terms of the relaxation of carriers in a Gaussian density of states (DOS). The model is based on a demarcation level that moves with time by thermal release and retrapping of initially trapped carriers. The model shows that when the disorder is large the after-pulse decay of the type t(-beta) is obtained, while at low disorder and large temperature the carrier distribution becomes independent of time. In the measurements different beta values were observed depending on the solvent used for spin-coating: 0.4-0.6 for chlorobenzene and 0.3-0.4 for toluene. The model was applied to extract the shape of the DOS from the TRMC decays, giving a dispersion parameter of about 120 meV for blends with high P3HT content.