Surface characterisation of oxygen plasma treated electrospun polyurethane fibres and their interaction with red blood cells

In this work, the effects of oxygen plasma surface modification have been studied on electrospun polyether-based polyurethane in order to investigate the imposed limitations and possibilities to improve surface characteristics on fibrous assemblies. The evolution of induced changes in surface morphology, chemistry and wettability by the plasma treatment has been characterised for increasing plasma exposure time using scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS) and water contact angle measurements. Significant reduction in fibre diameter concomitant with progressing rough surface textures are found on the fibres in surface layers during early treatment phases while extended exposure eventually causes the fibre structure to deteriorate. Surface oxygen content and functionalities such as carbonyl and carboxyl increase slightly with longer treatments until loss of material integrity occurs. The results have also shown that oxygen plasma rapidly alters the initially strong hydrophobic character of the non-woven fibres to hydrophilic behaviour, allowing water penetration into the network, but without significant changes for increased exposure time. In addition, the response of red blood cell shape to pristine and oxygen plasma treated fibres were found to be similar. In both cases, a population of cells having fibre contact displayed protrusions while measurements showed that the cell function remain intact and indicated that the adhesion was non-specific. The reported findings yield useful process knowledge that can support the formation of well-defined fibre architectures and are valuable in the designs of electrospun polyurethane material systems utilising oxygen plasma surface modification.     

Sn-containing liquid crystalline side group homopolymers with two glass transitions

Three homologous tin-containing homopolymers with a terminal CN-dipole in the side group have been synthesized and characterized by dynamical calorimetry, polarization microscopy, X-ray and dielectric methods. AFM was used to evaluate the texture at room temperature. Four different phase transitions were detected by DSC. The high temperature phases were identified by polarization microscopy as SmA and SmC. AFM-measurements show focal-conic domains at room temperature and confirm so the smectic nature of all phases. X-ray measurements on nonoriented samples give hints to a phase segregation on nanometer scale. Dielectric investigation and temperature-modulated DSC (TMDSC) confirm clearly phase separation by appearance of two glass transitions related to the liquid order of the main chains and the liquid crystalline of the side groups.     

Expansion of random field gradients using hierarchical matrices

We present two expansions for the gradient of a random field. In the first approach, we differentiate its truncated Karhunen-Loève expansion. In the second approach, the Karhunen-Loève expansion of the random field gradient is computed directly. Both strategies require the solution of dense, symmetric matrix eigenvalue problems which can be handled efficiently by combining hierachical matrix techniques with a thick-restart Lanczos method. (© 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Photoelectron spectroscopy in the energy region 30 to 800 eV using synchrotron radiation

With the advent of synchrotron radiation, the photoemission techniques were extended to a continuous range of excitation energies in the far ultraviolet and soft x-ray regions, adding tremendously to the usefulness of photoemission as a probe of the electronic structure of materials. In this paper, we discuss the application of photoelectron spectroscopy using synchrotron radiation to the studies of oxygen chemisorption/oxidation of Si surfaces, metal overlayers on III-V semiconductor surfaces, chemisorption on transition metal surfaces, and the surface electronic structure of CuNi alloys.     

Bonding of column 3 and 5 atoms on GaAs (110)

Experimental data, in strong disagreement with current theoretical work, shows that the bonding of column 3 elements to GaAs (110) is mainly nondirectional (metallic), with no significant change in GaAs surface lattice reconstruction. Adsorbed Sb, however, is characterized by highly directional bonding. Based on these conclusions, a model of the mechanism of molecular beam epitaxy is presented.     

An exploratory study of the reactive Ni-GaAs (1 1 0) interface

Soft X-ray photoemission spectroscopy measurements have been carried out on cleaved n-type GaAs (1 1 0) surfaces covered with Ni overlayers ranging in thickness from 0.05 to 53 Å. The results of these room temperature measurements show that we have band bending effects occurring in conjunction with strong interfacial chemical reactions. Deconvolution of the Ga 3d core line into substrate and metallic components shows dissolution of the substrate at the interface with Ga diffusing into the surface of the metal overlayer for the intermediate coverages (1–15 Å). Observation of the As 3d core level shows out-diffusion of As to the surface over the entire Ni coverage range. Using this deconvolution scheme we are able to follow the band bending of the Schottky barrier formed here up to the 8 Å coverage. The Schottky barrier height is 1.0 ± 0.1 eV for this overlayer thickness.     

Do the Au 5d-bands narrow at the surface: Comparison with Au alloys

Synchrotron radiation studies indicate no systematic narrowing of the Au surface 5d-bands. Comparison with Au alloys reveals an insensitivity to the number of nearest Au neighbours. The applicability of simple tight-binding theory to noble metal surfaces is questioned.     

O KVV Auger emission versus resonant photoemission at the O K edge of high-Tc superconductors

Photoelectron spectroscopy results on single crystals of the superconductors Bi₂Sr₂CaCu₂O₈,Bi₂Sr₂CuO₆, Ba_0.6K_0.4BiO₃ and the semiconductor Ba_0.9K_0.1BiO₃ are reported for the photon energy region around the O K absorption threshold. The development of the O-KVV Auger structure has been carefully monitored as a function of photon energy. A non-monotonic behavior displaying a feature at a constant binding energy of about 14 eV was found for Bi₂Sr₂CaCu₂O₈ and Bi₂Sr₂CuO₆ in a narrow photon energy region of 1 eV at the main edge of the O K absorption spectrum around 530 eV. The corresponding enhancement, connected with the autoionization of O 2p states, is absent in Ba_1−xK_xBiO ₃ in contrast to Bi₂Sr₂CaCu₂O₈ and Bi₂Sr₂CuO₆. The resonant enhancement is more pronounced for Bi₂Sr₂CuO₆ as compared to Bi₂Sr₂CaCu₂O₈, which can be explained by a lower charge carrier concentration in the former case, leading to a more localized nature of intermediate O 2p states. The model parameters Cu d–d and O p–p Coulomb interactions and the charge transfer energy Δ are estimated from the experiments.