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We report a new approach for reflection mode Fourier ptychographic microscopy using the Scheimpflug geometry. Successful recovery of a USA resolution target is shown with 2NAb synthetic aperture.

Computational microscopy algorithms can be used to improve resolution by synthesizing a bigger numerical aperture. Fourier Ptychographic (FP) microscopy utilizes multiple exposures, each illuminated with a unique incidence angle coherent source. The recorded images are often corrupted with background noises and preprocessing improves the quality of the FP recovered image. The preprocessing involves data denoising, thresholding and intensity balancing. We propose a wavelet-based thresholding scheme for noise removal. Any image can be decomposed into its coarse approximation, horizontal details, vertical details, and diagonal details using suitable wavelets. The details are extracted to find a suitable threshold, which is used to perform thresholding. In the proposed algorithm, two wavelet families, Daubechies and Biorthogonal with compact support of db4, db30, bior2.2 and bior6.8, have been used in conjunction with ptychographic phase retrieval. The obtained results show that the wavelet-based thresholding significantly improves the quality of the reconstructed FP microscopy image.

High-throughput microscopy in the sense of large areas imaged at high-resolution demands costly hardware such as objective lenses with high numerical aperture and high sensitivity cameras, typically combined with lateral mechanical scanning of the sample. The field of view and the resolution of an imaging system depend strongly on the applied objective lens, with higher resolution coming at the cost of a smaller field of view. To address this limitation of conventional microscopes, both aperture synthesis and phase retrieval techniques are combined in the recent computational imaging approach of Fourier Ptychographic Microscopy (FPM). Gigapixel space-bandwidth product of FPM is obtained by combining low-resolution images obtained with illumination diversity through phase retrieval, which is facilitated by ensuring that the input images overlap in the Fourier domain. In practice, the illumination is achieved using one lamp at a time from an LED array. A drawback of FPM is that it requires long acquisition times and has significant computational cost. Here, we present a refined FPM procedure by using Fresnel propagation and reducing the number of exposures by multiplexing and symmetry considerations, thus slashing the amount of data and the processing time. The multiplexing strategy works by illuminating groups of three LEDs that are chosen from one-half plane of the LED array – an approach valid for pure amplitude samples. We have experimentally demonstrated that the FPM recovered image has approximately the same resolution as recovery based on one exposure from each of the LEDs.

Multislice Fourier ptychography (MFP) uses angularly diverse illumination to compute a three-dimensional image of the sample. We present an improved MFP algorithm, demonstrating better convergence properties and reduced noise in reconstructions. © 2019 The Author(s)

This study explores the vaguely defined concept of sustainableexperiences. Specifically, it questions how perceived experiencevalue at tourism destinations can be enhanced through sustainableexperience dimensions. Although experiences and sustainabletourism are intrinsically interlinked, knowledge of sustainableexperiences and how they can be included in experience design toenhance perceived value is limited. Within a lake context, localstakeholders, researchers and students were invited to activelyidentify and co-design sustainable experience dimensions using,among others, interviews with residents and tourists. Ourfindingssuggest four sustainable experience dimensions: interaction withthe natural environment; interaction with the cultural environment;insights and views; and lake-based activities. The study advocatesfor future research and management to better incorporatesustainable experience dimensions to holistically enhance tourists’perceived experience value and destination sustainability.

Fourier ptychography setup is developed using 61 LEDs installed on a spherical dome which illuminate the sample sequentially. The resolution is improved by 4.9 times by Fourier Ptychographic recovery.

Au–Sn SLID bonding is a technique originally developed for harsh environment applications. The technology has recently shown promising results for ultrasound transducer fabrication. Characterizing the spatial and size distributions of voids is crucial for developing a fabrication process that satisfies acoustic requirements. This measurement is traditionally done by optical or electron cross-section microscopy that gives the void distribution in a randomly selected physically cut plane. X-ray micro computed tomography is a powerful tool for non-destructive three-dimensional imaging of void distributions, but is challenging to use in high-density materials like the ones used in ultrasound transducers. We demonstrate that monochromatic, high-energy synchrotron X-ray tomography can give 3D images of such a challenging sample, resolving $\mu \mathrm{m}$-sized voids in the bondline. The void distribution is highly non-uniform, implying that traditional cross-section microscopy would give different results depending on the plane of sectioning. Computed tomography allows the voids to be parametrized and treated statistically, revealing a wide distribution of void sizes, a tendency to form oblate voids with size-dependent orientation, as well as porous networks.

Glass fibres with silicon cores have emerged as a versatile platform for all-optical processing, sensing and microscale optoelectronic devices. Using SiGe in the core extends the accessible wavelength range and potential optical functionality because the bandgap and optical properties can be tuned by changing the composition. However, silicon and germanium segregate unevenly during non-equilibrium solidification, presenting new fabrication challenges, and requiring detailed studies of the alloy crystallization dynamics in the fibre geometry. We report the fabrication of SiGe-core optical fibres, and the use of CO2 laser irradiation to heat the glass cladding and recrystallize the core, improving optical transmission. We observe the ramifications of the classic models of solidification at the microscale, and demonstrate suppression of constitutional undercooling at high solidification velocities. Tailoring the recrystallization conditions allows formation of long single crystals with uniform composition, as well as fabrication of compositional microstructures, such as gratings, within the fibre core., Using SiGe in the core of optical fibres extends the wavelength range and potential optical functionality, but fabrication challenges exist. Here, Coucheron et al. report the fabrication and tailoring of SiGe-core optical fibres using CO2 laser irradiation to heat the glass cladding and recrystallize the core.

In this paper, we present a study of wafer-level process for deposition of amorphous thin film MoS2 by radio-frequency (RF) magnetron sputtering technique. Thin film deposition was performed in argon atmosphere with pressure around 10-2 to 10-4 Torr, RF power between 100-250 W and temperature from room temperature up to 250°C. X-ray diffraction indicates that the thin films are amorphous. Deposition rate and sulphur concentration showed a clear dependence on variation in RF power. Surface roughness increase as temperature was increased from room temperature up to 250°C. Photocurrent increases about 20% under white light illumination. The thin films are continuous with low roughness which might make it a potential candidate for wafer-scale production for advanced electronics or sensor applications.

Experimental nondestructive methods for probing the spatially varying arrangement and orientation of ultrastructures in hierarchical materials are in high demand. While conventional computed tomography (CT) is the method of choice for nondestructively imaging the interior of objects in three dimensions, it retrieves only scalar density fields. In addition to the traditional absorption contrast, other contrast mechanisms for image formation based on scattering and refraction are increasingly used in combination with CT methods, improving both the spatial resolution and the ability to distinguish materials of similar density. Being able to obtain vectorial information, like local growth directions and crystallite orientations, in addition to scalar density fields, is a longstanding scientific desire. In this work, it is demonstrated that, under certain conditions, the spatially varying preferred orientation of anisotropic particles embedded in a homogeneous matrix can be retrieved using CT with small-angle X-ray scattering as the contrast mechanism. Specifically, orientation maps of filler talc particles in injection-moulded isotactic polypropylene are obtained nondestructively under the key assumptions that the preferred orientation varies slowly in space and that the orientation of the flake-shaped talc particles is confined to a plane. It is expected that the method will find application inin situstudies of the mechanical deformation of composites and other materials with hierarchical structures over a range of length scales.

International audience; Characterization of the wavefront of an X-ray beam is of primary importance for all applications where coherence plays a major role. Imaging techniques based on numerically retrieving the phase from interference patterns are often relying on an a-priori assumption of the wavefront shape. In Coherent X-ray Diffraction Imaging (CXDI) a planar incoming wave field is often assumed for the inversion of the measured diffraction pattern, which allows retrieving the real space image via simple Fourier transformation. It is therefore important to know how reliable the plane wave approximation is to describe the real wavefront. Here, we demonstrate that the quantitative wavefront shape and flux distribution of an X-ray beam used for CXDI can be measured by using a micrometer size metal-coated polymer sphere serving in a similar way as the hole array in a Hartmann wavefront sensor. The method relies on monitoring the shape and center of the scattered intensity distribution in the far field using a 2D area detector while raster-scanning the microsphere with respect to the incoming beam. The reconstructed X-ray wavefront was found to have a well-defined central region of approximately 16 mu m diameter and a weaker, asymmetric, intensity distribution extending 30 mu m from the beam center. The phase front distortion was primarily spherical with an effective radius of 0.55 m which matches the distance to the last upstream beam-defining slit, and could be accurately represented by Zernike polynomials. (C) 2016 Optical Society of America

Coherent x-ray diffraction imaging (CXDI) is becoming an important 3D quantitative microscopy technique, allowing structural investigation of a wide range of delicate mesoscale samples that cannot be imaged by other techniques like electron microscopy. Here we report high-resolution 3D CXDI performed on spherical microcomposites consisting of a polymer core coated with a triple layer of nickel–gold–silica. These composites are of high interest to the microelectronics industry, where they are applied in conducting adhesives as fine-pitch electrical contacts—which requires an exceptional degree of uniformity and reproducibility. Experimental techniques that can assess the state of the composites non-destructively, preferably also while embedded in electronic chips, are thus in high demand. We demonstrate that using CXDI, all four different material components of the composite could be identified, with radii matching well to the nominal specifications of the manufacturer. Moreover, CXDI provided detailed maps of layer thicknesses, roughnesses, and defects such as holes, thus also facilitating cross-layer correlations. The side length of the voxels in the reconstruction, given by the experimental geometry, was 16 nm. The effective resolution enabled resolving even the thinnest coating layer of ∼20 nm nominal width. We discuss critically the influence of the weak phase approximation and the projection approximation on the reconstructed electron density estimates, demonstrating that the latter has to be employed. We conclude that CXDI has excellent potential as a metrology tool for microscale composites.

Producing surfaces textured with a homogeneous pattern of nanoscale structures is increasingly important for fabrication of semiconductor devices. Although techniques exist for imaging surface nanostructures on a local scale, these techniques are often impractical for use over large areas for finding average structural information. The nanostructured surface in this study consists of densely packed cones produced by sputtering a mono-crystalline GaSb substrate with a low-energy unfocused ion beam, yielding self-organized cones that are slightly tilted away from the sample normal. Here, we devise an all-optical non-destructive characterization scheme using Grazing-Incidence Small-Angle X-ray Scattering (GISAXS) and Spectroscopic Mueller Matrix Ellipsometry (MME) for obtaining all main dimensions including average height, lateral spacing and packing motifs, and the cone top and bottom diameters. It is further shown that both MME and GISAXS are sensitive to small tilts of the nanocone axis from the surface normal.

The internal microstructure of injection-molded dogbone specimens of talc-filled isotactic polypropylene has been investigated using a home laboratory scanning wide-angle X-ray scattering setup, yielding two-dimensional maps of molecular orientation and ordering for cross-sections parallel and perpendicular to the flow direction with unprecedented details. In addition to demonstrating a high degree of alignment of both the iPP b-axis and the talc c-axis parallel to the sample wall normals, thus corroborating earlier reports, the synthesized maps also yield new insights into the molecular organization. We find an asymmetry in the orientation maps, which we ascribe to a lateral temperature gradient across the mold during solidification. This interpretation is supported by numerical simulations of heat transport during the solidification following material flow, leading to orientation maps in full qualitative agreement with the experimental data. Recent developments in X-ray scattering equipment, in particular fast-readout low-noise area detectors, have facilitated the present experiments, which demonstrate the usability of raster scanning for advanced polymer characterization.

Au-Sn solid–liquid interdiffusion (SLID) bonding is an established reliable high temperature (HT) die attach and interconnect technology. This article presents the life cycle of an optimized HT Au-Sn SLID bond, from fabrication, via thermal treatment, to mechanical rupture. The layered structure of a strong and uniform virgin bond was identified by X-ray diffraction to be Au/ζ (Au0.85Sn0.15)/Au. During HT exposure, it was transformed to Au/β (Au1.8Sn0.2)/Au. After HT exposure, the die shear strength was reduced by 50 pct, from 14 Pa to 70 MPa, which is still remarkably high. Fractographic studies revealed a change in fracture mode; it was changed from a combination of adhesive Au/Ni and cohesive SiC fracture to a cohesive β-phase fracture. Design rules for high quality Au-Sn SLID bonds are given.

As data sets continue to grow in size, visualization has become a vitally important tool for extracting meaningful knowledge. Scattered point data, which are unordered sets of point coordinates with associated measured values, arise in many contexts, such as scientific experiments, sensor networks, and numerical simulations. In this paper, we present a method for visualizing such scattered point data sets. Our method is based on volume ray casting, and distinguishes itself by operating directly on the unstructured samples, rather than resampling them to form voxels. We estimate the intensity of the volume at points along the rays by interpolation using nearby samples, taking advantage of an octree to facilitate efficient range search. The method has been implemented on multi-core CPUs, GPUs as well as multi-GPU systems. 1 To test our method, actual X-ray diffraction data sets have been used, consisting of up to 240 million data points. We are able to generate images of good quality and achieve interactive frame rates in favorable cases. The GPU implementation (Nvidia Tesla K20) achieves speedups of 8-14 compared with our parallelized CPU version (4-core, hyperthreaded Intel i7 3770K). Open Access

We show that charge-transporting polymer chains in the brush conformation can be synthesized from a variety of substrates of interest, displaying a high degree of stretching and showing up to a 3 orders of magnitude increase in current density normal to the substrate as compared with a spin-coated film. These nanostructured polymeric films may prove to be suitable for electronic devices based on molecular semiconductors as current fabrication techniques often provide little control over film structure.

Optimizing the morphology of bulk heterojunctions is known to significantly improve the photovoltaic performance of organic solar cells, but available quantitative imaging techniques are few and have severe limitations. We demonstrate X-ray ptychographic coherent diffractive imaging applied to all-organic blends. Specifically, the phase-separated morphology in bulk heterojunction photoactive layers for organic solar cells, prepared from a 50:50 blend of poly(3-hexylthiophene) (P3HT) and phenyl-C61-butyric acid methyl ester (PCBM) and thermally treated for different annealing times is imaged to high resolution. Moreover, using a fast-scanning calorimetry chip setup, the nano-morphological changes caused by repeated thermal annealing applied to the same sample could be monitored. X-ray ptychography resolves to better than 100 nm the phase-segregated domains of electron donor and electron acceptor materials over a large field of view within the active layers. The quantitative phase contrast images further allow us to estimate the local volume fraction of PCBM across the photovoltaically active layers. The volume fraction gradient for different regions provides insight on the PCBM diffusion across the depletion zone surrounding PCBM aggregates. Phase contrast X-ray microscopy is under rapid development, and the results presented here are promising for future studies of organic-organic blends, also under in situ conditions, e.g., for monitoring the structural stability during UV-Vis irradiation. © 2016 Patil et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Ordered graphene films have been fabricated on Fe-treated SiC and diamond surfaces using the catalytic conversion of sp(3) to sp(2) carbon. In comparison with the bare SiC(0 0 0 1) surface, the graphitization temperature is reduced from over 1000 degrees C to 600 degrees C and for diamond (111), this new approach enables epitaxial graphene to be grown on this surface for the first time. For both substrates, a key development is the in situ monitoring of the entire fabrication process using real-time electron spectroscopy that provides the necessary precision for the production of films of controlled thickness. The quality of the graphene/graphite layers has been verified using angle-resolved photoelectron spectroscopy, scanning tunneling microscopy and low energy electron diffraction. Graphene is only formed on treated regions of the surface and so this offers a method for fabricating and patterning graphene structures on SiC and diamond in the solid-state at industrially realistic temperatures. (c) 2012 Elsevier Ltd. All rights reserved. (Less)

A convenient method to induce face-on orientation of an alkoxy phtalocyanine discotic mesogen is described. The alignment is imposed by the confinement of the discotic thin films with a top sacrificial polymer layer that is easily removed by washing with a selective solvent, after thermal annealing. Thin films have been characterized by optical and atomic force microscopy, UV-Vis absorption spectroscopy, and grazing incidence wide angle X-ray scattering. The data converge in showing the central role of the sacrificial layer in promoting alignment with the planar molecules orienting parallel to the substrate in an essentially homeotropic arrangement over large lateral length scales and the persistence of this desirable alignment after removal of the layer.

We investigate the growth and field-effect transistor performance of aligned pentacene thin films deposited by zone-casting from a solution of unsubstituted pentacene molecules in a chlorinated solvent. Polarized optical microscopy shows that solution processed pentacene films grow as large crystalline domains with pronounced anisotropy in the substrate plane, in contrast to vacuum sublimed pentacene films, which consist of small crystalline grains with random in-plane orientation. The high structural alignment is confirmed by in-plane and out-of-plane X-ray diffraction analysis, with out-of-plane 00n reflections up to at least the seventh order, and a pronounced in-plane anisotropy with the a-axis of the triclinic unit cell predominantly aligned parallel to the zone-casting direction and the ab-plane parallel to the substrate. The average charge carrier mobility of the zone-cast pentacene devices depends strongly on the underlying dielectric. Divinylsiloxane-bis-benzocyclobutene (BCB) resin is found to b...

Computationally efficient simulations of grazing-incidence X-ray diffraction (GIXD) are discussed, with particular attention given to textured thin polycrystalline films on supporting substrates. A computer program has been developed for simulating scattering from thin films exhibiting varying degrees of preferred orientation. One emphasized common case is that of a `fibre' symmetry axis perpendicular to the sample plane, resulting from crystallites having one well defined crystal facet towards the substrate, but no preferred in-plane orientation. Peak splitting caused by additional scattering from the totally substrate-reflected beam (two-beam approximation) and refraction effects are also included in the program, together with the geometrical intensity corrections associated with GIXD measurements. To achieve `user friendliness' for scientists less familiar with diffraction, the mathematically simplest possible descriptions are sought whenever feasible. The practical use of the program is demonstrated for a selected thin-film example, perylene, which is of relevance for organic electronics.

Semiconducting diblock copolymers of polyethylene (PE) and regioregular poly(3-hexylthiophene) (P3HT) are demonstrated to exhibit a rich phase behaviour, judicious use of which permitted us to fabricate field-effect transistors that show saturated charge carrier mobilities, ?FET, as high as 2 × 10-2 cm2V-1 s-1 and ON-OFF ratios, Ion/Ioff ?105 at contents of the insulating PE moiety as high as 90 wt %. In addition, the diblock copolymers display outstanding flexibility and toughness with elongations at break exceeding 600 % and true tensile strengths around 70 MPa, opening the path towards robust and truly flexible electronic components. © 2007 WILEY-VCH Verlag GmbH & Co. KGaA

Organic electronics technology, in which at least the semiconducting component of the integrated circuit is an organic material, offers the potential for fabrication of electronic products by low-cost printing technologies, such as ink jet, gravure offset lithography and flexography. The products will typically be of lower performance than those using the present state of the art single crystal or polysilicon transistors, but comparable to amorphous silicon. A range of prototypes are under development, including rollable electrophoretic displays, active matrix liquid crystal (LC) displays, flexible organic light emitting diode displays, low frequency radio frequency identification tag and other low performance electronics. Organic semiconductors that offer both electrical performance and stability with respect to storage and operation under ambient conditions are required. This work describes the development of reactive mesogen semiconductors, which form large crosslinked LC domains on polymerization within mesophases. These crosslinked domains offer mechanical stability and are inert to solvent exposure in further processing steps. Reactive mesogens containing conjugated aromatic cores, designed to facilitate charge transport and provide good oxidative stability, were prepared and their liquid crystalline properties evaluated. The organization and alignment of the mesogens, both before and after crosslinking, were probed by grazing incidence wide-angle X-ray scattering of thin films. Both time-of-flight and field effect transistor devices were prepared and their electrical characterization reported.

Discotic mesophases are known for their ability to self-assemble into columnar structures and can serve as semiconducting molecular wires. Charge carrier mobility along these wires strongly depends on molecular packing, which is controlled by intermolecular interactions. By combining wide-angle X-ray scattering experiments with molecular dynamics simulations, we elucidate packing motifs of a perylene tetracarboxdiimide derivative, a task which is hard to achieve by using a single experimental or theoretical technique. We then relate the charge mobility to the molecular arrangement, both by pulse-radiolysis time-resolved microwave conductivity experiments and simulations based on the non-adiabatic Marcus charge transfer theory. Our results indicate that the helical molecular arrangement with the 45 degrees twist angle between the neighboring molecules favors hole transport in a compound normally considered as an n-type semiconductor. Statistical analysis shows that the transport is strongly suppressed by structural defects. By linking molecular packing and mobility, we eventually provide a pathway to the rational design of perylenediimide derivatives with high charge mobilities.

Blends and other multicomponent systems are used in various polymer applications to meet multiple requirements that cannot be fulfilled by a single material. In polymer optoelectronic devices it is often desirable to combine the semiconducting properties of the conjugated species with the excellent mechanical properties of certain commodity polymers. Here we investigate bicomponent blends comprising semicrystalline regioregular poly(3-hexylthiophene) and selected semicrystalline commodity polymers, and show that, owing to a highly favourable, crystallization-induced phase segregation of the two components, during which the semiconductor is predominantly expelled to the surfaces of cast films, we can obtain vertically stratified structures in a one-step process. Incorporating these as active layers in polymer field-effect transistors, we find that the concentration of the semiconductor can be reduced to values as low as 3 wt% without any degradation in device performance. This is in stark contrast to blends containing an amorphous insulating polymer, for which significant reduction in electrical performance was reported. Crystalline-crystalline/semiconducting-insulating multicomponent systems offer expanded flexibility for realizing high-performance semiconducting architectures at drastically reduced materials cost with improved mechanical properties and environmental stability, without the need to design all performance requirements into the active semiconducting polymer itself.

X-ray waveguides are successfully produced employing standard silicon technology of UV photolithography and wafer bonding. Contrary to theoretical expectations for similar systems even 100 mu m broad guides of less than 80 nm height do not collapse and can be used as one dimensional waveguides to excite single guided modes at typical x-ray energies.

Charge transport properties in organic semiconductors depend strongly on molecular order. Here we demonstrate field-effect transistors where drain current flows through a precisely defined array of nanostripes made of crystalline and highly ordered molecules. The molecular stripes are fabricated across the channel of the transistor by a stamp-assisted deposition of the molecular semiconductors from a solution. As the solvent evaporates, the capillary forces drive the solution to form menisci under the stamp protrusions. The solute precipitates only in the regions where the solution is confined by the menisci once the critical concentration is reached and self-organizes into molecularly ordered stripes 100-200 nm wide and a few monolayers high. The charge mobility measured along the stripes is 2 orders of magnitude larger than the values measured for spin-coated thin films.

This work describes the development of solution processable liquid crystalline semiconductors and their applications in field-effect transistors. The relationship between liquid crystal molecular structure, its corresponding phase behaviour and electrical performance is examined. Molecular design methodology is employed to control the liquid crystalline morphology. The thermal, optical and electrical behaviour of these materials is characterised and X-ray diffraction scattering technique is used to reveal details of morphology and molecular orientation.

Imaging nanoparticles under relevant reaction conditions of high temperature and gas pressure is difficult because conventional imaging techniques, like transmission electron microscopy, cannot be used. Here we demonstrate that the coherent diffractive imaging technique of X-ray ptychography can be used for in situ phase contrast imaging in structure studies at atmospheric pressure and elevated temperatures. Lithium zirconate, a candidate CO2 capture material, was studied at a pressure of one atmosphere in air and in CO2, at temperatures exceeding 600 °C. Images with a spatial resolution better than 200 nm were retrieved, and possibilities for improving the experiment are described.