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Abstract: Nanoscale interconnects are an important component of molecular electronics. Here we use X-ray spectromicroscopy techniques as well as scanning probe methods to explore the self-assembled growth of insulated iron nanowires as a potential means of supplying an earth abundant solution. The intrinsic anisotropy of a TiO2(110) substrate directs the growth of micron length iron wires at elevated temperatures, with a strong metal–support interaction giving rise to ilmenite (FeTiO3) encapsulation. Iron nanoparticles that decorate the nanowires display magnetic properties that suggest other possible applications.

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Abstract: Graphene oxide (GO) forms a well-aligned lyotropic liquid crystal (LC) phase in aqueous dispersions at relatively low concentrations. Under a remarkably wide range of shear rates, we report hitherto unobserved shear-induced polarized light image patterns, a Maltese cross combined with shear banding, recorded in real time and in situ during rheological measurements. This is shown to be a result of elastic flow instabilities that manifest as a helical flow in alternating bands of left- and right-handed helices, arising from a combination of shear flow and Taylor-type vortex flow. The instability is observed for LCs formed from large aspect ratio GO particles owing to their unique viscoelastic properties, but not for smaller aspect ratio particles. This phenomenon coincides with rheopecty and anomalous small-angle X-ray scattering patterns under shear flow, which confirm the instabilities. The results presented here could lead to advanced control over macroscopic periodic alignment in technologically relevant dispersions of two-dimensional material particles.

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Abstract: Fabrics—materials consisting of layers of woven fibres—are some of the most important materials in everyday life. Previous nanoscale weaves include isotropic crystalline covalent organic frameworks that feature rigid helical strands interlaced in all three dimensions, rather than the two-dimensional layers of flexible woven strands that give conventional textiles their characteristic flexibility, thinness, anisotropic strength and porosity. A supramolecular two-dimensional kagome weave and a single-layer, surface-supported, interwoven two-dimensional polymer have also been reported. The direct, bottom-up assembly of molecular building blocks into linear organic polymer chains woven in two dimensions has been proposed on a number of occasions, but has not previously been achieved. Here we demonstrate that by using an anion and metal ion template, woven molecular ‘tiles’ can be tessellated into a material consisting of alternating aliphatic and aromatic segmented polymer strands, interwoven within discrete layers. Connections between slowly precipitating pre-woven grids, followed by the removal of the ion template, result in a wholly organic molecular material that forms as stacks and clusters of thin sheets—each sheet up to hundreds of micrometres long and wide but only about four nanometres thick—in which warp and weft single-chain polymer strands remain associated through periodic mechanical entanglements within each sheet. Atomic force microscopy and scanning electron microscopy show clusters and, occasionally, isolated individual sheets that, following demetallation, have slid apart from others with which they were stacked during the tessellation and polymerization process. The layered two-dimensional molecularly woven material has long-range order, is birefringent, is twice as stiff as the constituent linear polymer, and delaminates and tears along well-defined lines in the manner of a macroscopic textile. When incorporated into a polymer-supported membrane, it acts as a net, slowing the passage of large ions while letting smaller ions through.

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Abstract: Thick corrosion scales form within carbon steel oilfield pipelines in sweet (CO2 saturated) environments. The morphology and the extent of the resultant pseudo-protective nature of these scales has been seen to be dependent on multiple factors including solution pH, temperature, flow rate, and partial pressure of CO2 present. Different techniques (SEM, XRD, FIB, etc.) have been used in the past to characterise these corrosion scales. However, limitations in these techniques occur due to the fact that only small regions of the scale can be characterised in a feasible time. Further limitations may result in difficulty to relate local scale features with corrosion morphology on the evolving metal surface (i.e. localised corrosion) as the morphology of the substrate surface can only be characterised once the scale is removed. The aim of this work is to address this issue through the use of high resolution x-ray absorption tomography to characterise the internal morphology of the corrosion scales from ex situ specimens exposed to CO2 environments as a function of pH and temperature. X-65 pipeline steel, high purity 99.99 Fe and low purity 99.0 Fe pins were used in these experiments. Specimens were exposed to CO2saturated solutions using two different methods, notably open circuit potential (OCP) immersion for 7-12 days and electrochemical polarisation for two hours at 200 mV(vs OCP). After the scaling experiments, samples were characterised using XRD and SEM. X-ray tomography was subsequently performed at the University of Manchester X-ray Imaging Facilities to characterise the corrosion morphology. Transmission X-ray microscopy (TXM) was used in absorption mode and phase contrast mode to obtain three dimensional reconstructions of the specimens, where the different features of the scale and the internal corroded substrate were imaged and characterised simultaneously. Results indicate differences in the morphology of the corrosion scale depending on the method that was used to corrode the samples. As a consequence of the supersaturation in Fe2+, polarised samples present a thicker scale than the scales obtained by immersion at OCP conditions. The polarisation process also produces a less uniform corroded substrate than when the sample is immersed for 7 days at open circuit in the corroding environments used. In this work high resolution X-ray tomography has been proven to be a very powerful technique to study the scale morphology as well as the features of localised corrosion occurring under scale in the substrate.

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Abstract: The redox behaviour modification following the addition of zirconia to ceria nanostructures supported on Rh(111) has been investigated using a combination of Low Energy Electron Diffraction (LEED) and X-ray Photoemission Electron Microscopy (XPEEM). Soft X-ray irradiation was employed to reduce ZrO2-x(111) supported on Rh(111) and, by introducing oxygen, the reoxidation process of the thin film was monitored. CeO2(111) was then deposited on zirconia/Rh(111) and, using XPEEM, we determined that the mixed metal oxide formed a phase-separated structure with CeO2(111) nanoparticles on top of the zirconia. Upon exposure of CeO2-x/ZrO2-x/Rh(111) to X-ray illumination, the zirconia no longer undergoes any observable reduction while at the same time the ceria is reduced. Our results indicate a synergy between the zirconia and ceria in the phase-separated system expected in the working catalyst, with oxygen transfer between the metal oxides. This sheds light on the mechanism of the enhancement of catalytic properties seen with the addition of zirconia to ceria and highlights the oxygen storage and release ability of ceria.