Internal Dynamics of Ionic Liquids over a Broad Temperature Range—The Role of the Cation Structure

1H and 19F spin-lattice relaxation experiments have been performed for a series of ionic liquids sharing the same anion: bis(trifluoromethanesulfonyl)imide but including cations of different alkyl chain lengths: butyltriethylammonium, triethyloctylammonium, dodecyltriethylammo-nium and hexadecyltriethylammonium. The studies have been carried out in the temperature range from 383 to 108 K at the resonance frequency of 200 MHz (for 1H). A quantitative analysis of the relaxation data has revealed two dynamical processes for both kinds of ions. The dynamics have been successfully modeled in terms of the Arrhenius law. The timescales of the dynamical processes and their temperature evolution have been discussed in detail, depending on the structure of the cation.

SURFACE LUMINESCENCE OF A2B6 SEMICONDUCTOR QUANTUM DOTS (REVIEW)

Semiconductor zero-dimensional nanocrystals – quantum dots (QDs) – have been increasingly used in various fields of opto- and nanoelectronics in recent decades. This is because of the exciton nature of their luminescence, which can be controlled via the well known quantum-dimensional effect. At the same time, at small nanocrystall sizes, the influence of the surface on the optical and structural properties of nanocrystals increases significantly. The presence of broken bonds of surface atoms and point defects – vacancies and interstial atoms – can both weaken the exciton luminescence and create new effective channels of radiant luminescence. In some cases, these surface luminescence becomes dominant, leading to optical spectra broadening up to the quasi-white light. The nature of such localized states often remains unestablished due to the large number of the possible sorts of defects in both of QD and its surrounding. In contrast to exciton luminescence, which can be properly described within effective-mass approximations, the optical properties of defects relay on chemical nature of both defect itsself and its surrounding, what cannot be provided by “hydrogen-type coulomb defect” approximation. Moreover, charge state and related to this lattice relaxation must be taken into account, what requires an application of atomistic approach, such as Density functioal theory (DFT). Therefore, this review is devoted to the study of surface (defect) states and related luminescence, as well as the analysis of possible defects in nanocrystals of semiconductor compounds A2B6 (CdS, CdZnS, ZnS), responsible for luminescence processes, within ab initio approach. The review presents the results of the authors' and literature sources devoted to the study of the luminescent characteristics of ultra-small (<2 nm) QDs.

Plan-view TEM observation of a single-domain κ-Ga2O3 thin film grown on ε-GaFeO3 substrate using GaCl3 precursor by mist chemical vapor deposition

We demonstrated the growth of a single-domain κ-Ga2O3 thin film on ε-GaFeO3 by using an organic-free compound as a precursor for mist chemical vapor deposition. X-ray diffraction analysis revealed that an 87-nm-thick κ-Ga2O3 thin film was grown almost coherently with slight lattice relaxation. The surface morphology of the κ-Ga2O3 thin film exhibited a step-terrace structure without island growth. Furthermore, plan-view TEM observations revealed that the κ-Ga2O3 thin film grown on ε-GaFeO3 had a single domain, whereas the previously reported κ-Ga2O3 thin film grown on AlN template had a domain structure.

Mixing, Domains, and Fast Li-ion Dynamics in Ternary Li-Sb-Bi Battery Anode Alloys

Antimony and bismuth can both alloy with up to three molar equivalents of lithium and are therefore attractive candidates for replacing graphite in Li-ion battery anodes. Li3Sb and Li3Bi have the same cubic structure (Fm3 ̅m), but the ternary Li-Sb-Bi system has not been studied. We synthesized Li3(SbxBi1-x) with different Sb mole fractions at room temperature by ball-milling. These ternary alloys all have cubic crystal structures, as determined by XRD, but show a tendency towards phase segregation for x = 0.25 and 0.50. For x = 0.25, the lattice parameter presents a clear positive deviation from Vegard’s law in XRD, while for x = 0.50, XRD reveals two phases after milling, with the Bi-rich minority phase diminishing after thermal annealing. Solid-state nuclear magnetic resonance spectroscopy provides evidence for a Sb-enriched environment around the Li atoms for Li3Sb0.25Bi0.75, and nuclear spin-lattice relaxation measurements of the binary and ternary alloy phases point to low activation energies and rapid Li ion diffusion in Li3Bi.

Water Behavior of Aerogels Obtained from Chemically Modified Potato Starches during Hydration

Aerogels are highly porous materials that are prepared by removing water held within a hydrogel in a manner that maintains the three-dimensional structure of the gel. Recently, there has been much interest in the preparation of aerogels from biopolymers, including starch. The applicability of native starches in the food industry is partially limited; therefore, the functional properties of starch are often improved by means of physical and/or chemical modification. The aim of the work was the analysis of molecular dynamics and the transport of water in aerogels obtained from native and chemically modified potato starches of the normal and waxy variety. Chemical modification with OSA (E 1450) as well as cross-linking with adipic anhydrite and acetylation (E 1422) had no significant impact on the hydration of potato starch aerogels as well as equilibrium water activity. The introduction of chemical moieties into starch macromolecules led to the improved binding of water by the biopolymer matrix; this was especially evident in the case of waxy starch derivatives. A increase in the amylopectin-to-amylose ratio of starch used for production of aerogels resulted in a decrease of equilibrium water activity along with spin-lattice relaxation time.

EPR study of Mn site substituted Pr based Doped Rare Earth Manganites

In this paper, we present the investigations of Electron Paramagnetic Resonance (EPR) on Mn site substituted Pr based Doped rare Earth Manganites i.e. Pr0.60Ca0.40MnO3 and Pr0.60Ca0.40Mn0.85Zn0.15O3. Changes in physical properties as lattice parameters, average valence of Mn site was observable of those manganites. X-ray diffraction pattern shows that both Pr0.60Ca0.40MnO3 and Pr0.60Ca0.40Mn0.85Zn0.15O3 have single phase and without the other secondary or impurity phase and indexed supported the Pbnm space group. The value of x in Pr0.60Ca0.40Mn1-xZnxO3 increases, the average valence V was increased except for a fixed composition, i.e. x remains unchanged, the average valence V was decreased as we go from less valency to high valency (i.e., from divalent to trivalent and from trivalent to tetravalent. The EDXS analysis of those materials shows good homogeneity, but there are experimental errors in composition. It is seen from the SEM images that is formed in different shape grains. The average grain sizes of the samples are different for Pr0.60Ca0.40MnO3 and Pr0.06Ca0.40Mn0.85Zn0.15O3 The paramagnetic resonance spectra parameters (effective g-factor, peak-to-peak line width) of Pr0.60Ca0.40MnO3 and Pr0.60Ca0.40Mn0.85Zn0.15O3.have been used to study the paramagnetic spin correlations and spin dynamics. As for Pr0.60Ca0.40MnO3 the line width becomes wider because of the contribution of small polaron jumping within the PM mechanism. However, as for Pr0.60Ca0.40Mn0.85Zn0.15O3 the broadening of EPR line-width is understood with the spin-lattice relaxation mechanism, g value decreased from 1.99 to 1.79. Therefore, the Zn dopant not solely changes the parent spin correlation in the PM regime however additionally suppresses the development of orbital ordering.

Soliton Generation in Negative Thermal Expansion Materials

Strain solitons have been observed statically in several 2D materials and dynamically in substrate materials using ultrafast laser pulses. The latter case relies on lattice relaxation in response to ultrafast heating in a light-absorbing transducer material, a process which is sensitive to the thermal expansion coefficient. Here we consider an unusual case where the sign of the thermal expansion coefficient is negative, a scenario which is experimentally feasible in light of rapid and recent advances in the discovery of negative thermal expansion materials. We present numerical solutions to a nonlinear differential equation which has been repeatedly demonstrated to quantitatively model experimental data and discuss the salient results using realistic parameters for material linear and nonlinear elasticity. The solitons that emerge from the initial value problem with negative and positive thermal expansion are qualitatively different in several ways. The new case of negative thermal expansion gives rise to a nearly-periodic soliton train with chirped profile and free of an isolated shock front. We suggest this unanticipated result may be realized experimentally and assess the potential for certain applications of this generic effect.