Explore the vast range of titles available.

In this work, the multiferroic bismuth ferrite materials Bi 0.9 RE 0.1 FeO 3 doped by rare-earth (RE = La, Eu, and Er) elements were obtained by the solution combustion synthesis. Structure, electrical, and magnetic properties of prepared samples were investigated by X-ray photoelectron spectroscopy, Mössbauer spectroscopy, electrical hysteresis measurement, broadband dielectric spectroscopy, and SQUID magnetometry. All obtained nanomaterials are characterized by spontaneous electrical polarization, which confirmed their ferroelectric properties. Investigation of magnetic properties at 300.0 K and 2.0 K showed that all investigated Bi 0.9 RE 0.1 FeO 3 ferrites possess significantly higher magnetization in comparison to bismuth ferrites obtained by different methods. The highest saturation magnetisation of 5.161 emu/g at 300.0 K was observed for the BLaFO sample, while at 2.0 K it was 12.07 emu/g for the BErFO sample. Several possible reasons for these phenomena were proposed and discussed.

At this time, the development of advanced elastic dielectric materials for use in organic devices, particularly in organic field-effect transistors, is of considerable interest to the scientific community. In the present work, flexible poly(dimethylsiloxane) (PDMS) specimens cross-linked by means of ZnCl2-bipyridine coordination with an addition of 0.001 wt. %, 0.0025 wt. %, 0.005 wt. %, 0.04 wt. %, 0.2 wt. %, and 0.4 wt. % of gold nanoparticles (AuNPs) were prepared in order to understand the effect of AuNPs on the electrical properties of the composite materials formed. The broadband dielectric spectroscopy measurements revealed one order of magnitude decrease in loss tangent, compared to the coordinated system, upon an introduction of 0.001 wt. % of AuNPs into the polymeric matrix. An introduction of AuNPs causes damping of conductivity within the low-temperature range investigated. These effects can be explained as a result of trapping the Cl− counter ions by the nanoparticles. The study has shown that even a very low concentration of AuNPs (0.001 wt. %) still brings about effective trapping of Cl− counter anions, therefore improving the dielectric properties of the investigated systems. The modification proposed reveals new perspectives for using AuNPs in polymers cross-linked by metal-ligand coordination systems.

Core−shell nanocomposites comprising barium titanate, BaTiO3 (BTO), and poly(methyl methacrylate) (PMMA) chains grafted from its surface with varied grafting densities were prepared. BTO nanocrystals are high-k inorganic materials, and the obtained nanocomposites exhibit enhanced dielectric permittivity, as compared to neat PMMA, and a relatively low level of loss tangent in a wide range of frequencies. The impact of the molecular dynamics, structure, and interactions of the BTO surface on the polymer chains was investigated. The nanocomposites were characterized by broadband dielectric and vibrational spectroscopies (IR and Raman), transmission electron microscopy, differential scanning calorimetry, and nuclear magnetic resonance. The presence of ceramic nanoparticles in core–shell composites slowed down the segmental dynamic of PMMA chains, increased glass transition temperature, and concurrently increased the thermal stability of the organic part. It was also evidenced that, in addition to segmental dynamics, local β relaxation was affected. The grafting density influenced the self-organization and interactions within the PMMA phase, affecting the organization on a smaller size scale of polymeric chains. This was explained by the interaction of the exposed surface of nanoparticles with polymer chains.

The article describes three different ways of polymer light-emitting diode (PLED) degradation, caused by damage of the protective layer. The electroluminescence and charge-transport properties of a completely encapsulated diode, the diodes with a leaky protective layer and diodes without encapsulation were compared under long-time exploitation. The studied devices incorporated Super Yellow light-emitting poly-(1,4-phenylenevinylene) PPV copolymer as an electroluminescence component, and (poly-(3,4-ethylenedioxythiophene)–poly-(styrene sulfonate) (PEDOT:PSS) as a charge-transport layer between the indium tin oxide (ITO) anode and aluminum–calcium cathode. To analyze the PLED degradation mechanism regarding charge transport, impedance spectroscopy was used. The values of resistance and capacitance of the internal layers revealed an effect of applied voltage on charge carrier injection and recombination. The factors responsible for the device degradation were analyzed on a macromolecular level by comparing the plots of voltage dependence of resistance and capacitance at different operation times elapsed.

In this study, nanocrystalline (18–28 nm) perovskite-like bismuth ferrite rare earth-doped powders (Bi0.9RE0.1FeO3, where RE = La (BLaFO), Eu (BEuFO), and Er (BErFO)) were obtained by microwave-assisted modification of solution combustion synthesis (SCS). The influence of high load La3+, Eu3+, and Er3+ doping on structural, optical, and electrical properties of BiFeO3 was investigated. It was found that rare earth doping along with fast phase formation and quenching significantly distorts the crystal cells of the obtained materials, which results in the formation of mixed rhombohedral- (R3c-) orthorhombic (Pbnm) crystal structures with decreased lengths of Bi-O and Fe-O bonds along with a decreasing radius size of doping ions. This promotes reduction of the optical band gap energy and suppression of ionic polarization at high frequencies and results in enhanced dielectric permittivity of the materials at 1 MHz.

There is an urgent need for the development of elastic dielectric materials for flexible organic field effect transistors (OFETs). In this work, detailed analysis of the AC and DC electrical conductivity of a series of flexible poly(dimethylsiloxane) (PDMS) polymers crosslinked by metal-ligand coordination in comparison to neat PDMS was performed for the first time by means of broadband dielectric spectroscopy. The ligand was 2,2-bipyridine-4,4-dicarboxylic amide, and Ni2+, Mn2+, and Zn2+ were introduced for Cl−, Br−, and I− salts. Introduction of metal salt and creation of coordination bonds resulted in higher permittivity values increasing in an order: neat PDMS < Ni2+ < Mn2+ < Zn2+; accompanied by conductivity values of the materials increasing in an order: neat PDMS < Cl− < I− < Br−. Conductivity relaxation time plot as a function of temperature, showed Vogel-Fulcher–Tammann dependance for the Br− salts and Arrhenius type for the Cl− and I− salts. Performed study revealed that double-edged challenge can be obtained, i.e., dielectric materials with elevated value of dielectric permittivity without deterioration too much the non-conductive nature of the polymer. This opens up new perspectives for the production of flexible dielectrics suitable for gate insulators in OFETs. Among the synthesized organometallic materials, those with chlorides salts are the most promising for such applications.

Poly(dimethylosiloxane) (PDMS) cross-linked by metal-ligand coordination has a potential functionality for electronic devices applications. In this work, the molecular dynamics of bipyridine (bpy)–PDMS-MeCl2 (Me: Mn2+, Fe2+, Ni2+, and Zn2+) are investigated by means of broadband dielectric spectroscopy and supported by differential scanning calorimetry and density functional theory calculations. The study of molecular motions covered a broad range of temperatures and frequencies and was performed for the first time for metal-ligand cross-linked PDMS. It was found that the incorporation of bpy moieties into PDMS chain prevents its crystallization. The dielectric permittivity of studied organometallic systems was elevated and almost two times higher (ε′ ~4 at 1 MHz) than in neat PDMS. BpyPDMS-MeCl2 complexes exhibit slightly higher glass transition temperature and fragility as compared to a neat PDMS. Two segmental type relaxations (α and αac) were observed in dielectric studies, and their origin was discussed in relation to the molecular structure of investigated complexes. The αac relaxation was observed for the first time in amorphous metal-ligand complexes. It originates from the lower mobility of PDMS polymer chains, which are immobilized by metal-ligand coordination centers via bipyridine moieties.

In this study, nanocrystalline (18–28 nm) perovskite-like bismuth ferrite rare earth-doped powders (Bi 0.9 RE 0.1 FeO 3 , where RE = La (BLaFO), Eu (BEuFO), and Er (BErFO)) were obtained by microwave-assisted modification of solution combustion synthesis (SCS). The influence of high load La 3+ , Eu 3+ , and Er 3+ doping on structural, optical, and electrical properties of BiFeO 3 was investigated. It was found that rare earth doping along with fast phase formation and quenching significantly distorts the crystal cells of the obtained materials, which results in the formation of mixed rhombohedral- (R3c-) orthorhombic (Pbnm) crystal structures with decreased lengths of Bi-O and Fe-O bonds along with a decreasing radius size of doping ions. This promotes reduction of the optical band gap energy and suppression of ionic polarization at high frequencies and results in enhanced dielectric permittivity of the materials at 1 MHz.

We report a strategy for preparing barium titanate precursor, being the composite of titanate nanosheets (TN) with barium ions (Ba-TN), which subjected to step sintering allows obtaining TiO2 rich barium titanate ceramics of stoichiometry BaTi4O9 or Ba2Ti9O20. These compounds are important in modern electronics due to their required dielectric properties and grains’ size that can be preserved in nanometric range. The morphology studies, structural characterization, and dielectric investigations were performed simultaneously in each step of Ba-TN calcinations in order to properly characterize type of obtained ceramic, its grains’ morphology, and dielectric properties. The Ba-TN precursor can be sintered at given temperatures, so that its dielectric permittivity can be tuned between 25 and 42 with controlled temperature coefficients that change from negative 32 ppm/°C for Ba-TN sintered at 900°C up to positive 37 ppm/°C after calcination at 1300°C. XRD analysis and Raman investigations performed for the Ba-TN in the temperature range of 900÷1250°C showed that below 1100°C we obtained as a main phase BaTi4O9, whereas the higher calcinations temperature transformed Ba-TN into Ba2Ti9O20. Taking into account trend of device miniaturization and nanoscopic size requirements, temperatures of 900°C and 1100°C seem to be an optimal condition for Ba-TN precursor calcinations that guarantee the satisfactory value of dielectric permittivity (ε=26 and 32) and ceramic grains with a mean size of ~180 nm and ~550 nm, respectively.