We present the results of a temperature-dependent photoluminescence (PL) spectroscopy study on CuInS2 quantum dots (QDs). In order to elucidate the influence of QD size on PL temperature dependence, size-selective precipitation was used to obtain several nanoparticle fractions. Additionally, the nanoparticles’ morphology and chemical composition were studied using transmission electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The obtained QDs showed luminescence in the visible–near infrared range. The PL energy, linewidth, and intensity were studied within an 11–300 K interval. For all fractions, a temperature decrease led to a shift in the emission maximum to higher energies and pronounced growth of the PL intensity down to 75–100 K. It was found that for large particle fractions, the PL intensity started to decrease, with temperature decreasing below 75 K, while the PL intensity of small nanoparticles remained stable.
A synthesis protocol of polyvinylpyrrolidone-capped AgInS2 quantum dots in aqueous solution is reported. Nanoparticle morphology and chemical composition were studied by means of TEM, XRD, XPS, and FTIR. The obtained quantum dots were luminescent in the visible range. The photoluminescence intensity dependence on the polyvinylpyrrolidone amount was demonstrated. The wavelength of the emission maximum varied with changing the [Ag]:[In] molar ratio. The temperature dependence of the photoluminescence intensity of the polyvinylpyrrolidone-capped AgInS2 quantum dots was investigated within the temperature range of 11–294 K.
The current–voltage characteristics (IVCs) of anodic TiO2 films in a thin-film structure (Carbon paste/TiO2/Ti/Al) were investigated in the temperature range of T = 80–300 K with bias voltages from −0.5 V to +0.5 V. Anodic oxide film, with a thickness of 14 nm, was obtained by electrochemical oxidation of Ti at a voltage of 10 V. The obtained data for various temperatures showed that the IVCs in the forward (negative on the Ti electrode) and reverse (positive on the Ti electrode) bias of the thin film structure are not symmetrical. Based on the analysis, three temperature ranges (sections) were identified in which the IVCs differ in their behavior. Examination of the IVCs revealed that the conductivity mechanism in Section I (temperature range from 298 to 263 K) is determined by the Space Charge Limited Current (SCLC). Section II, in the temperature range from 243 to 203 K, is characterized by the onset of conductivity involving donor centers, in the case where the concentration of electrons on traps is significantly higher than the concentration of electrons in the conduction band. In Section III, within the temperature range from 183 to 90 K, the conduction mechanism is the Poole–Frenkel process involving donor centers. These donor centers are located below the level of traps in the forbidden band. The results obtained indicate that anodic TiO2 is an n-type semiconductor, in the bandgap of which there are both electron traps and donor centers formed by anionic (oxygen) vacancies. The different behavior of the characteristic energy with different sample biasing in the case of the Poole–Frenkel mechanism indicates a two-layer structure of anodic TiO2.
Today, air pollution is a global environmental problem. A huge amount of explosive and combustible gas emissions that negatively affect nature and human health. Gas sensors are one of the ways to prevent this impact. Several types of sensors have been developed, but the main problem with them is the high operating temperature. This leads to a decrease in reproducibility and stability over time. The aim of the work is to synthesize zinc stannate nanoparticles, study their phase composition, and modify the structure with silver nanoparticles to improve gas-sensing characteristics. This paper presents the synthesis of zinc stannate nanoparticles by the coprecipitation method and annealing at varying temperatures. A method of decorating zinc stannate with silver nanoparticles was proposed. Using XRD, it was found that a change in the annealing temperature leads to a change in the initial phase composition of the sample. Decoration with silver nanoparticles allows for increasing the sensor response of zinc stannate layers to isopropyl alcohol by 20 times. The corresponding increase in response to ethanol is 16 times.
The conductivity of direct and alternating current for graphite-like amorphous carbon films after annealing in vacuum at a temperature of 700 °C was studied. The I–V characteristics of such films are symmetrical. The I–V curve in logarithmic coordinates demonstrated the presence of two linear sections. A study of the frequency dependences of structures with a thin graphite-like amorphous carbon film showed a sharp increase in capacitance at low frequencies and a decrease in the high-frequency region. The increase in capacitance in the low-frequency region is explained by the Maxwell–Wagner polarization, which is observed in inhomogeneous dielectrics with conducting inclusions. The results of temperature measurements of resistance showed that at room temperatures, there is a mechanism of conduction of electrons with a variable jump length along localized states lying in a narrow energy band near the Fermi level. At the same time, with an increase in the injection current, an additional mechanism of hopping electrical transport with a variable jump length along localized states in the tail of the valence band arises, which leads to an increase in the conductivity of the films.
Porous nickel oxide nanoparticles with a hierarchical structure and high specific surface area were obtained by green synthesis followed by thermal annealing. The influence of the choice of precursor plant extract (Fumaria officinalis L. and Origanum vulgare L.) and the extractants in aqueous solutions on the parameters of the synthesized particles was studied. Characterization of the NiO morphology and composition, as well as the specific surface area, was performed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and the BET method of nitrogen thermal desorption. Resulting particles have a spherical shape and a size from 30 to 50 nm. According to the data obtained, it can be seen that when the precursor is changed from Fumaria officinalis L. to Origanum vulgare L., the size of the synthesized particles increases, while the structure becomes more friable. It has been revealed that certain parameters and the nature of the assembly of porous particles lead to an increase in the surface area: the highest value of the SSA of 130.0 m2/g is observed in NiO nanoparticles obtained using Fumaria officinalis L. extract based on isopropyl alcohol. Also, a relatively high SSA value of 73.5 m2/g is observed in nanoparticles obtained using the same extractant for Origanum vulgare L. extract, while the use of an ethyl alcohol-based extractant for Fumaria officinalis L. resulted in the lowest value of 40.2 m2/g. The developed semiconductor particles are promising for use in catalysis, sensors, and as part of supercapacitor electrodes and functional layers in device structures for solar cells.