A convenient route at ambient conditions was employed to prepare narrow-dispersed ZnO nanorods in terms of size and morphology. Transmission electron microscopy and X-ray diffraction were used to characterize the structurally uniform and well-proportioned products. The as-prepared specimen exhibits strong ultraviolet exciton emission at 385 nm and disappearance of visible defect emission.
The magnetostructural coupling between the structural and the magnetic transition has a crucial role in magnetoresponsive effects in a martensitic-transition system. A combination of various magnetoresponsive effects based on this coupling may facilitate the multifunctional applications of a host material. Here we demonstrate the feasibility of obtaining a stable magnetostructural coupling over a broad temperature window from 350 to 70 K, in combination with tunable magnetoresponsive effects, in mnniGe:Fe alloys. The alloy exhibits a magneticfield-induced martensitic transition from paramagnetic austenite to ferromagnetic martensite. The results indicate that stable magnetostructural coupling is accessible in hexagonal phasetransition systems to attain the magnetoresponsive effects with broad tunability.
The ionic liquid (IL) 1‐butyl‐3‐methylimidazolium tetrafluoroborate (bmimBF4) forms nonaqueous microemulsions with p‐xylene, with the aid of the nonionic surfactant TX‐100. The phase behavior of the ternary system is investigated, and three microregions of the microemulsions—ionic liquid‐in‐oil (IL/O), bicontinuous, and oil‐in‐ionic liquid (O/IL)—are identified by conductivity measurements, according to percolation theory. On the basis of a phase diagram, a series of IL/O microemulsions are chosen and characterized by dynamic light scattering (DLS). The size of aggregates increases on increasing the amount of added polar component (bmimBF4), which is a similar phenomenon to that observed for typical water‐in‐oil (W/O) microemulsions, suggesting the formation of IL/O microemulsions. The microstructural characteristics of the microemulsions are investigated by FTIR and 1H NMR spectroscopy. The results indicate that the interaction between the electronegative oxygen atoms of the oxyethylene (OE) units in TX‐100 and the electropositive imidazolium ring may be the driving force for the solubilization of bmimBF4 into the core of the TX‐100 aggregates. In addition, the micropolarity of the microemulsions is investigated by using methyl orange (MO) as a UV/Vis spectroscopic probe. A relatively constant polarity of the microemulsion droplets is obtained in the IL microemulsion. Finally, a plausible structure for the IL/O microemulsion is presented.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.