Vortex Dynamics in Bi2Sr2CaCu2O8 Single Crystal with Low Density Columnar Defects Studied by Magnetic Force Microscope

We have studied vortex dynamics in Bi₂Sr₂CaCu₂O₈ single crystal with low density columnar defects by using a magnetic force microscope. Single crystal Bi₂Sr₂CaCu₂O₈ sample was irradiated by 1.3 GeV uranium ion to form artificial pinning centers along the crystalline c-axis. The irradiation dose corresponded to a matching field of 20 gauss. The radius of an individual vortex is approximately 140 nm, which is close to the penetration depth of this material. Magnetic force microscope (MFM) images show that intrinsic crystalline defects such as stacking fault dislocations are very effective pinning centers for vortices in addition to the pinning centers due to ion bombardment. By counting the number of vortex, we found that the flux trapped at each pinning center is a single flux quantum. At higher magnetic field, the vortex structure showed an Abrikosov lattice disturbed only by immobile vortices located at pinning centers. When increasing or decreasing the external magnetic field, the spatial distribution of vortices showed a Bean model like behavior.     

Melt filtration of recycled PVC

The separation of PVC from contaminants is one of the most important steps in recycling PVC. Earlier works have shown that one can separate PVC from other polymers by using the X-ray fluorescence technique. However, in many cases, even after careful separation, there is a remaining impurity level of about 0.1% due to the limitations of the separation processes. In many applications, impurities, particularly nonmeltables, cause defects in the PVC matrix and must be removed for best performance and appearance. Melt filtration appears to be the best technique to remove the nonmeltable impurities.     

Proximity electron tunneling spectroscopy. IV. Electron-phonon coupling and superconductivity of tantalum

An extensive superconducting electron tunneling study of Ta, using both a proximity method and an optimized conventional spectroscopy, is reported. The results for Ta confirm the electron-phonon origin of superconductivity in this element, and provide slightly improved superconducting parameters: =0.73 and _ph ^* = 0.11. The results from the PET and optimized conventional methods are in substantial agreement, although the proximity method appears to provide somewhat better resolution of structure in the Eliashberg function ² F(E).Operated for the U.S. Department of Energy by Iowa State University under contract No. W-7405-Eng-82. This research was supported by the Director for Energy Research, Office of Basic Energy Sciences, WPAS-KC-02-02-02.     

Mechanical Activation-Assisted Synthesis of Pb(Fe2/3W1/3)O3

Perovskite Pb(Fe_2/3W_1/3)O₃ (PFW) was prepared via a mechanical activation-assisted synthesis route from mixed oxides of PbO, Fe₂O₃, and WO₃. The mechanically activated oxide mixture, which exhibited a specific area of >10 m²/g, underwent phase conversion from nanocrystalline lead tungstate (PbWO₄) and pyrochlore (Pb₂FeWO_6.5) phases on sintering to yield perovskite PFW, although the formation of perovskite phase was not triggered by mechanical activation. When heated to 700°C, >98% perovskite phase was formed in the mechanically activated oxide mixture. The perovskite phase was sintered to a density of ∼99% of theoretical density at 870°C for 2 h. The sintered PFW exhibited a dielectric constant of 9800 at 10 kHz, which was ∼30% higher than that of the PFW derived from the oxide mixture that was not subjected to mechanical activation.     

Magnetic properties of Co- and Mn-implanted BaTiO3, SrTiO3 and KTaO3

Implantation of Co or Mn into single-crystal BaTiO₃(K), SrTiO₃ or KTaO₃(Ca), followed by annealing at 700 °C, produced ferromagnetic behavior over a broad range of transition metal concentrations. For BaTiO₃, both Co and Mn implantation produced magnetic ordering temperatures near 300 K with coercivities 70 Oe. The M–T plots showed either a near-linear decrease of magnetization with increasing temperature for Co and a non-Brillouin shaped curve for Mn. No secondary phases were detected by high-resolution X-ray diffraction. The same basic trends were observed for both SrTiO₃ and KTaO₃, with the exception that at high Mn concentrations (5 at.%) the SrTiO₃ was no longer ferromagnetic. Our results are consistent with recent reports of room temperature ferromagnetism in other perovskite systems (e.g. LaBaMnO₃) and theoretical predictions for transition metal doping of BaTiO₃ [Nakayama et al., Jap. J. Appl. Phys. 40 (2001) L1355].     

Determination of lumped rate coefficients of proteins: Effect of adsorption

The equilibria and kinetics of adsorption of lysozyme and bovine serum albumin on the Fractogel-EMD tentacle-type cation exchanger and the Fractogel-TSK conventional cation exchanger have been studied experimentally by batch stirred-tank method. Adsorption equilibrium data corresponded well to the Langmuir isotherm. For both proteins, the tentacle-type exchanger exhibited a higher binding capacity than the conventional exchanger. This is attributed to the flexibility of the functional groups in the tentacle-type exchanger which enhance optimal electrostatic interactions. The dynamic data were analyzed by a simplified data model which lumped mass transfer resistances and intrinsic adsorption kinetics into a single rate constant. For both proteins, it was found that the tentacle-type exchanger showed a smaller lumped rate coefficient than the conventional exchanger. The difference in the values of the lumped rate coefficients was shown to be due to the influence of nonlinear equilibrium constants rather than due to any difference in rate of adsorption.     

Analysis of additional leakage resulting from the feeding motion of a vacuum-compatible air bearing stage

A rise in pressure is generated when a vacuum-compatible air bearing stage moves in a vacuum condition. This study analyzed this pressure rise phenomenon theoretically and verified it experimentally. Results indicate that the pressure rise was caused by additional leakage resulting from stage velocity, along with adsorption and outgassing of gas molecules from the guide rail surface. Tilting of the stage had a negligible effect because the tilting time was very short. Additional leakage caused by stage velocity was inevitable if the stage incorporated mechanical movements, but rises in pressure caused by adsorption and outgassing could be suppressed by coating the guide rail surface with titanium nitride, to which gas molecules are less likely to adhere. The results also indicate that the pressure rise ratio increased when the air bearing stage operated under high-vacuum conditions.     

Uniaxial Alignment of Conjugated Polymer Films for High‐Performance Organic Field‐Effect Transistors

Polymer semiconductors have been experiencing a remarkable improvement in electronic and optoelectronic properties, which are largely related to the recent development of a vast library of high‐performance, donor–acceptor copolymers showing alternation of chemical moieties with different electronic affinities along their backbones. Such steady improvement is making conjugated polymers even more appealing for large‐area and flexible electronic applications, from distributed and portable electronics to healthcare devices, where cost‐effective manufacturing, light weight, and ease of integration represent key benefits. Recently, a strong boost to charge carrier mobility in polymer‐based field‐effect transistors, consistently achieving the range from 1.0 to 10 cm² V^?1 s^?1 for both holes and electrons, has been given by uniaxial backbone alignment of polymers in thin films, inducing strong transport anisotropy and favoring enhanced transport properties along the alignment direction. Herein, an overview on this topic is provided with a focus on the processing–structure–property relationships that enable the controlled and uniform alignment of polymer films over large areas with scalable processes. The key aspects are specific molecular structures, such as planarized backbones with a reduced degree of conformational disorder, solution formulation with controlled aggregation, and deposition techniques inducing suitable directional flow.     

Systematic Study of Widely Applicable N‐Doping Strategy for High‐Performance Solution‐Processed Field‐Effect Transistors

A specific design for solution‐processed doping of active semiconducting materials would be a powerful strategy in order to improve device performance in flexible and/or printed electronics. Tetrabutylammonium fluoride and tetrabutylammonium hydroxide contain Lewis base anions, F^? and OH^?, respectively, which are considered as organic dopants for efficient and cost‐effective n‐doping processes both in n‐type organic and nanocarbon‐based semiconductors, such as poly[[N,N′‐bis(2‐octyldodecyl)‐naphthalene‐1,4,5,8‐bis(dicarboximide)‐2,6‐diyl]‐alt‐5,5′‐(2,2′‐bithiophene)] (P(NDI2OD‐T2)) and selectively dispersed semiconducting single‐walled carbon nanotubes by π‐conjugated polymers. The dramatic enhancement of electron transport properties in field‐effect transistors is confirmed by the effective electron transfer from the dopants to the semiconductors as well as controllable onset and threshold voltages, convertible charge‐transport polarity, and simultaneously showing excellent device stabilities under ambient air and bias stress conditions. This simple solution‐processed chemical doping approach could facilitate the understanding of both intrinsic and extrinsic charge transport characteristics in organic semiconductors and nanocarbon‐based materials, and is thus widely applicable for developing high‐performance organic and printed electronics and optoelectronics devices.