Investigation of the electrical properties of polymer–clay nanocomposites is important in the development of nanoelectronic devices. These nanocomposites may be prepared by intercalating suitable monomers within interlayer spaces of expanding layered clay materials, followed by in situ polymerization. We made use of this approach to prepare montmorillonite–polyaniline nanocomposites by ion-exchanging the intergallery cations for anilinium ions and subsequently polymerizing the anilinium ions by peroxydisulphate in the acidic medium to yield emeraldine salt form of polyaniline intercalated in montmorillonite (ES1-MMT). The emeraldine salt form of polyaniline contains one positive charge per three monomer units, and hence, polymerization of anilinium ions reduces the number of cations present within the interlayer. Charge compensation thus requires uptake of required amount of cations from the solution. Further, the emeraldine salt form of polyaniline can be neutralized by treating with excess base such as ammonia. Thus, the neutralization of emeraldine salt results in an uptake of ammonium ions for charge balance. We have, therefore, neutralized ES1-MMT using aqueous ammonium hydroxide, and the cations inserted into the interlayer were again exchanged for anilinium ions. The latter was polymerized in acidic medium to yield more polyaniline in its emeraldine salt form (ES2-MMT). By repeating this procedure we have also prepared ES3-MMT. X-ray diffraction (XRD) spectra recorded at 150 °C reveal the enhancement of d-spacing upon increased amounts of polymer formation, and the Fourier transform infrared (FTIR) analysis also supports this by showing enhanced absorption due to bands typical of emeraldine salt (for example, B–NH+ = Q, where B and Q stand for benzanoid and quinoid, respectively). Careful analyses of FTIR spectra reveal that the polymer is present within the interlayers, as well as adsorbed onto the external surfaces and is bound to clay layers through hydrogen bonding. In this publication, we report the electrical properties of such ES-MMT nanocomposites. Alternating current (AC) impedance analysis shows that the nanocomposites are highly conducting materials, and their bulk conductivity enhances in the order ES1-MMT < ES2-MMT < ES3-MMT. The materials are pure electronic conductors as revealed by the direct current polarization studies. Further, their conductivities decrease with increasing temperature as of pure electronic conductors. By treating kaolinite with anilinium ions in acidic medium followed by peroxydisulphate ions, emeraldine salt–kaolinite (ES-KAL) composites have also been prepared. Because kaolinite is a non-expanding clay, the ion exchange is not possible, and hence, the polymer cannot be incorporated into the interlayer. This is indeed shown in the XRD analysis. The polymer can only reside out of the kaolinite particles. FTIR spectra reveal the hydrogen bonding between the polymer and kaolinite outer surfaces. AC impedance spectra of ES-KAL do not show high bulk conductivity. Thus, the comparison of AC impedance spectra of ES-KAL with ES-MMT systems clearly indicates that the bulk conductivity of the latter systems is predominantly due to intercalated polyaniline. 相似文献
The structural and electronic transport properties of La1−xCexMnO3 (x=0.0–1.0) have been studied. All the samples exhibit orthorhombic crystal symmetry and the unit cell volume decreases with
Ce doping. They also make a metal-insulator transition (MIT) and transition temperature increases with increase in Ce concentration
up to 50% doping. The system La0.5Ce0.5MnO3 also exhibits MIT instead of charge-ordered state as observed in the hole doped systems of the same composition. 相似文献
Brilliance of terbium : Heterodimeric conjugates of trimethoprim covalently linked to sensitized terbium chelates bind to Escherichia coli dihydrofolate reductase fusion proteins with nanomolar affinity (see picture). Terbium luminescence enables sensitive and time‐resolved detection of labeled proteins in vitro and on the surface of living mammalian cells.
Silicon powders of four particle-size ranges were prepared from reagent-grade silicon by the Andreasen pipet method and elutriation. Thin-layer specimens were prepared by a suspension-filtration method using membrane filters. Silicon powder of 1.0–2.5 μm diameter is recommended as internal standard from the study of particle-size effects. Stable suspensions of silicon and hematite were prepared with a 0.05% dextrin solution. Relative standard deviation for determinations by the internal-standard method were < 9% for 100 μg of hematite in a mixed powder sample of 600 μg and < 5% for 400 μg of hematite in mixed samples of 900–1400 μg. Absorption effects in mixed powders are discussed. 相似文献
An asymmetric route to dihydroquinazolinones via the addition of ortho metalated substrates to tert-butanesulfinyl imines is reported. The scope of the nucleophile and electrophile components and the absolute stereochemical outcome are presented. 相似文献
Co/Al2O3/Co magnetic tunnel junctions with an interfacial Cu layer have been investigated with in situ growth characterization and ex situ magnetotransport measurements. Cu interlayers grown on Co give an approximately exponential decay of the tunneling magnetoresistance with xi approximately 0.26 nm while those grown on Al2O3 have a decay length of 0.70 nm. The difference in decay lengths can be explained by different growth morphologies, and in this way clarifies a present disagreement in the literature. For monolayer coverage of Cu, we show that the tunneling spin polarization is suppressed by at least a factor of 2 compared to Co and beyond approximately 5 ML it becomes vanishingly small. 相似文献