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While a detailed knowledge of the hierarchical structure and morphology of the extracellular matrix is considered crucial for understanding the physiological and mechanical properties of bone and cartilage, the orientation of collagen fibres and carbonated hydroxyapatite (HA) crystallites remains a debated topic. Conventional microscopy techniques for orientational imaging require destructive sample sectioning, which both precludes further studies of the intact sample and potentially changes the microstructure. In this work, we use X-ray diffraction tensor tomography to image non-destructively in 3D the HA orientation in a medial femoral condyle of a piglet. By exploiting the anisotropic HA diffraction signal, 3D maps showing systematic local variations of the HA crystallite orientation in the growing subchondral bone and in the adjacent mineralized growth cartilage are obtained. Orientation maps of HA crystallites over a large field of view (~ 3 × 3 × 3 mm 3 ) close to the ossification (bone-growth) front are compared with high-resolution X-ray propagation phase-contrast computed tomography images. The HA crystallites are found to predominantly orient with their crystallite c-axis directed towards the ossification front. Distinct patterns of HA preferred orientation are found in the vicinity of cartilage canals protruding from the subchondral bone. The demonstrated ability of retrieving 3D orientation maps of bone-cartilage structures is expected to give a better understanding of the physiological properties of bones, including their propensity for bone-cartilage diseases.

An emerging theme of modern composites and devices is the coupling of nanostructural properties of materials with their targeted arrangement at the microscale. Of the imaging techniques developed that provide insight into such designer materials and devices, those based on diffraction are particularly useful. However, to date, these have been heavily restrictive, providing information only on materials that exhibit high crystallographic ordering. Here we describe a method that uses a combination of X-ray atomic pair distribution function analysis and computed tomography to overcome this limitation. It allows the structure of nanocrystalline and amorphous materials to be identified, quantified and mapped. We demonstrate the method with a phantom object and subsequently apply it to resolving, in situ, the physicochemical states of a heterogeneous catalyst system. The method may have potential impact across a range of disciplines from materials science, biomaterials, geology, environmental science, palaeontology and cultural heritage to health.

Structure-sensitive catalyzed reactions can be influenced by a number of parameters. So far, it has been established that the formation of Pd-C species is responsible for the behavior of Pd nanoparticles employed as catalysts in a butadiene partial hydrogenation reaction. In this study, we introduce some experimental evidence indicating that subsurface Pd hydride species are governing the reactivity of this reaction. In particular, we detect that the extent of formation/decomposition of PdHx species is very sensitive to the Pd nanoparticle aggregate dimensions, and this finally controls the selectivity in this process. The main and direct methodology applied to determine this reaction mechanism step is time-resolved high-energy X-ray diffraction (HEXRD). [ABSTRACT FROM AUTHOR]

High-pressure high-temperature syntheses that involve volatile-bearing aqueous fluids are typically accomplished by enclosing the samples in gas-tight welded shut noble-metal capsules, from which the bulk volatile content must be extracted to be analyzed with mass spectroscopy, hence making the analysis non-replicable. Here we describe a novel non-destructive method that ensures the identification and the quantitative estimate of the volatiles directly in the sealed capsule, focusing on fluid H2O–CO2 mixtures equilibrated with graphite at conditions of geological interest (1 GPa, 800 °C). We used a high-energy (77 keV) synchrotron X-ray radiation combined with a cryostat to produce X-ray diffraction patterns and X-ray diffraction microtomographic cross-sections of the volatile-bearing samples down to –180 °C, thus encompassing the conditions at which crystalline phases-solid CO2 and clathrate (CO2 hydrate)-form. The uncertainty of the method is < 15 mol%, which reflects the difference between the volatile proportion estimated by both Rietveld refinement of the diffraction data and by image analysis of the microtomograms, and the reference value measured by quadrupole mass spectrometry. Therefore, our method can be reliably applied to the analysis of frozen H2O–CO2 mixtures and, moreover, has the potential to be extended to experimental fluids of geological interest containing other volatiles, such as CH4, SO2 and H2S. [ABSTRACT FROM AUTHOR]

ID15A is a newly refurbished beamline at the ESRF devoted to operando and time‐resolved diffraction and imaging, total scattering and diffraction computed tomography. The beamline is optimized for rapid alternation between the different techniques during a single operando experiment in order to collect complementary data on working systems. The high available energy (up to 120 keV) means that even bulky and highly absorbing systems may be studied. The beamline is equipped with optimized focusing optics and a photon‐counting CdTe pixel detector, allowing for both unprecedented data quality at high energy and for very rapid triggered experiments. A large choice of imaging detectors and ancillary probes and sample environments is also available. [ABSTRACT FROM AUTHOR]

To improve lithium and sodium ion battery technology, it is imperative to understand how the properties of the different components are controlled by their chemical structures. Operando structural studies give us some of the most useful information for understanding how batteries work, but it remains difficult to separate out the contributions of the various components of a battery stack (e.g., electrodes, current collectors, electrolyte, and binders) and examine specific materials. We have used operando X-ray diffraction computed tomography (XRD-CT) to study specific components of an essentially unmodified working cell and extract detailed, space-resolved structural information on both crystalline and amorphous phases that are present during cycling by Rietveld and pair distribution function (PDF) methods. We illustrate this method with the first detailed structural examination of the cycling of sodium in a phosphorus anode, revealing surprisingly different mechanisms for sodiation and desodiation in this promising, high-capacity anode system. [ABSTRACT FROM AUTHOR]

Semiconducting indium sulfide (In2S3) has recently attracted considerable attention as a buffer material in the field of thin film photovoltaics. Compared with this growing interest, however, detailed characterizations of the crystal structure of this material are rather scarce and controversial. In order to close this gap, we have carried out a reinvestigation of the crystal structure of this material with an in situ X-ray diffraction study as a function of temperature using monochromatic synchrotron radiation. For the purpose of this study, high quality polycrystalline In2S3 material with nominally stoichiometric composition was synthesized at high temperatures. We found three modifications of In2S3 in the temperature range between 300 and 1300 K, with structural phase transitions at temperatures of 717 K and above 1049 K. By Rietveld refinement we extracted the crystal structure data and the temperature coefficients of the lattice constants for all three phases, including a high-temperature trigonal γ-In2S3 modification. [ABSTRACT FROM AUTHOR]

An X-ray diffraction computed tomography data-collection strategy that allows, post experiment, a choice between temporal and spatial resolution is reported. This strategy enables time-resolved studies on comparatively short timescales, or alternatively allows for improved spatial resolution if the system under study, or components within it, appear to be unchanging. The application of the method for studying an Mn-Na-W/SiO2 fixed-bed reactor in situ is demonstrated. Additionally, the opportunities to improve the data-collection strategy further, enabling post-collection tuning between statistical, temporal and spatial resolutions, are discussed. In principle, the interlaced scanning approach can also be applied to other pencil-beam tomographic techniques, like X-ray fluorescence computed tomography, X-ray absorption fine structure computed tomography, pair distribution function computed tomography and tomographic scanning transmission X-ray microscopy. [ABSTRACT FROM AUTHOR]

This article reports the creation of tomographic reconstructions giving three-dimensional data on the distribution of various structural features for SAPO-34 zeolite catalyst beds used in the commercially important methanol to olefin conversion process. The data were processed using parametric Rietveld refinement to treat entire slices of the tomograph as single refined data sets, allowing extraction of real structural parameters from all voxels of the reconstruction. This has the advantage over more traditional methods of X-ray diffraction computed tomography using peak intensities, that the structural parameters are independent of the intensity, meaning that information can still be extracted from poor data sets: an example is shown where part of the sample was no longer in the beam during data collection. Reconstructions using several structural parameters are presented and the results compared. Analysis of the variation of the catalyst c axis (linked to the degree of deactivation in earlier work) shows small but significant three-dimensional variations in the degree of deactivation with patterns which depend on the silicon content of the catalyst. Average data for the tomographic slices compare well with the results of earlier operando two-dimensional reactor scanning experiments. [ABSTRACT FROM AUTHOR]

X-ray diffraction (XRD) is typically silent towards information on low loadings of precious metals on solid catalysts because of their finely dispersed nature. When combined with a concentration modulation approach, time-resolved high-energy XRD is able to provide the detailed redox dynamics of palladium nanoparticles with a diameter of 2 nm in 2 wt % Pd/CZ (CZ=ceria-zirconia), which is a difficult sample for extended X-ray absorption fine structure (EXAFS) measurements because of the cerium component. The temporal evolution of the Pd(111) and Ce(111) reflections together with surface information from synchronous diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) measurements reveals that Ce maintains Pd oxidized in the CO pulse, whereas reduction is detected at the beginning of the O2 pulse. Oxygen is likely transferred from Pd to Ce3+ before the onset of Pd re-oxidation. In this context, adsorbed carbonates appear to be the rate-limiting species for re-oxidation. [ABSTRACT FROM AUTHOR]

Abstract: The internal crystalline structure of a human molar tooth has been non-destructively imaged in cross-section using X-ray diffraction computed tomography. Diffraction signals from high-energy X-rays which have large attenuation lengths for hard biomaterials have been collected in a transmission geometry. Coupling this with a computed tomography data acquisition and mathematically reconstructing their spatial origins, diffraction patterns from every voxel within the tooth can be obtained. Using this method we have observed the spatial variations of some key material parameters including nanocrystallite size, organic content, lattice parameters, crystallographic preferred orientation and degree of orientation. We have also made a link between the spatial variations of the unit cell lattice parameters and the chemical make-up of the tooth. In addition, we have determined how the onset of tooth decay occurs through clear amorphization of the hydroxyapatite crystal, and we have been able to map the extent of decay within the tooth. The described method has strong prospects for non-destructive probing of mineralized biomaterials. [Copyright &y& Elsevier]

A new data collection strategy for performing synchrotron energy-dispersive X-ray diffraction computed tomography has been devised. This method is analogous to angle-dispersive X-ray diffraction whose diffraction signal originates from a line formed by intersection of the incident X-ray beam and the sample. Energy resolution is preserved by using a collimator which defines a small sampling voxel. This voxel is translated in a series of parallel straight lines covering the whole sample and the operation is repeated at different rotation angles, thus generating one diffraction pattern per translation and rotation step. The method has been tested by imaging a specially designed phantom object, devised to be a demanding validator for X-ray diffraction imaging. The relative strengths and weaknesses of the method have been analysed with respect to the classic angle-dispersive technique. The reconstruction accuracy of the method is good, although an absorption correction is required for lower energy diffraction because of the large path lengths involved. The spatial resolution is only limited to the width of the scanning beam owing to the novel collection strategy. The current temporal resolution is poor, with a scan taking several hours. The method is best suited to studying large objects ( e.g. for engineering and materials science applications) because it does not suffer from diffraction peak broadening effects irrespective of the sample size, in contrast to the angle-dispersive case. [ABSTRACT FROM AUTHOR]

The evolution of time-resolved experiments, covering a multipurpose surface and bulk characterization of catalytic solids, during their preparation process and under reaction conditions, is presented. Particular emphasis is given to recent studies that attempt to unveil contemporary unresolved questions concerning the control of physicochemical properties of nanosolids, as well as the evolution of such solid materials under reactive atmospheres. To reach this goal, representative in situ and in operando works, using either modern (mostly synchrotron radiation based) approaches or multi-technique methods (mainly, although not exclusively, X-ray-vibrational coupling), and considering experiments in liquid and gas phase, as well as with amorphous, nanocrystalline and surface-deposited materials, are reviewed. [ABSTRACT FROM AUTHOR]

The high flux of high energy X-rays that can be provided through state-of-the-art high energy synchrotron beam lines has enabled a variety of new experiments with the highly absorbing Nb3Sn superconductors. We report different experiments with Nb3Sn strands that have been conducted at the ID15 High Energy Scattering beam line of the European Synchrotron Radiation Facility (ESRF). Synchrotron X-ray diffraction has been used in order to monitor phase transformations during in-situ reaction heat treatments prior to Nb3Sn formation, and to monitor Nb3Sn growth. Fast synchrotron micro-tomography was applied to study void growth during the reaction heat treatment of Internal Tin strands. The elastic strain in the different phases of fully reacted Nb3Sn composite conductors has been measured by high resolution X-ray diffraction during in-situ tensile tests. [ABSTRACT FROM AUTHOR]

The article presents a study which crystallizes CO dissociation and transient carbon storage by Pd nanoparticles through combining diffuse resistance infrared spectroscopy (DRIFTS) and time-resolved hard X-ray diffraction (HRXD). It states that the method allows specification of Al2O3-supported Pd nanoparticles actively participating in de-NOx chemistry. It mentions that method also helped in the discovery of the fundamental events in nanoparticulate catalysis.

[Display omitted] • Computed X-ray diffraction tomography applied to shaped zeolite catalyst extrudates. • Operando monitoring of coking within a single extrudate during methanol conversion. • A strong radial gradient in the coke deposition and incomplete catalyst utilization is observed. • Operando data collection provide the basis for kinetic/diffusion simulation models. We have used operando X-ray diffraction computed tomography (XRD-CT) analysed by rigorous crystallographic methods to reveal the behaviour of a zeolite/alumina based catalyst extrudate in the methanol-to-hydrocarbon reaction under working conditions (T reaction = 440 °C; ambient total pressure; WHSV = 12 g MeOH g extrudate −1 h−1). By doing so, we demonstrate that it is possible to precisely monitor how the cylindrical extrudate is deactivated during the process by gradual filling with coke from the outer surface towards the core. The operando data thus collected are simulated by a model taking both the reaction kinetics and the diffusion within the extrudate into account, and this analysis provides the tools required for future optimization of the degree of utilization of the catalyst. Both the operando experiment and post mortem XRD-CT of fully deactivated extrudates from a test reactor show clearly that the core of the catalyst body, around 1/3 of its volume, remains completely untouched by the reaction, even when the reactor output indicates zero activity. [ABSTRACT FROM AUTHOR]

Residual stresses are considered to be the driving forces for the in-service failure of TBCs. The residual stress distribution through an APS TBC has been experimentally measured by high energy synchrotron X-ray diffraction (XRD) showing two distinct features. Firstly a discontinuity or ‘jump’ in the residual stress trend at a depth of approximately 100 μm from the interface. Secondly we observed a much larger stress gradient than that theoretically predicted. To understand these observations the measured residual stress was compared with analytical and finite element models based on the real 2D and 3D microstructure of the coating visualized by scanning electron microscopy (SEM) and high energy X-ray micro-computed tomography (μ-CT). The effect of the pores in the coating and the rumpled interface between the top coat and the bond coat on the residual stress distribution was studied by image based modelling. It was found that the pores did not have an obvious effect on the overall residual stress distribution. The rumpled interface however was primarily responsible for the jump in the trend. This feature was observed to be located at a depth of approximately 120 μm from the surface with an overall magnitude of approximately 200 MPa. The relaxation of the coating upon in-plane compression was investigated by mechanical testing coupled with DIC. These results are in good agreement with the much larger gradients in the measured residual stress distribution. [ABSTRACT FROM AUTHOR]

Semiconducting indium sulfide (In2S3) has recently attracted considerable attention as a buffer material in the field of thin film photovoltaics. Compared with this growing interest, however, detailed characterizations of the crystal structure of this material are rather scarce and controversial. In order to close this gap, we have carried out a reinvestigation of the crystal structure of this material with an in situ X-ray diffraction study as a function of temperature using monochromatic synchrotron radiation. For the purpose of this study, high quality polycrystalline In2S3 material with nominally stoichiometric composition was synthesized at high temperatures. We found three modifications of In2S3 in the temperature range between 300 and 1300 K, with structural phase transitions at temperatures of 717 K and above 1049 K. By Rietveld refinement we extracted the crystal structure data and the temperature coefficients of the lattice constants for all three phases, including a high-temperature trigonal γ-In2S3 modification. [ABSTRACT FROM AUTHOR]

A combination of time-resolved X-ray absorption spectroscopy (XAS), hard X-ray diffraction (HXRD), diffuse reflectance infrared spectroscopy (DRIFTS), and mass spectrometry (MS) reveals a series of size-dependent phenomena at Pd nanoparticles upon CO/(NO+O2) cycling conditions. The multitechnique approach and analysis show that such size-dependent phenomena are critical for understanding Pd CO elimination behavior and, particularly, that different Pd(I) and Pd(0) centers act as active species for a size estimated by XAS to be, respectively, below and above ca. 3 nm. The relative catalytic performance of these two noble metal species indicates the intrinsic higher activity of the Pd(I) species. [ABSTRACT FROM AUTHOR]

Abstract: The behaviour of Pd/Al2O3 supported catalysts with metal loading in the 0.5–4wt.% interval has been examined during cycling CO/NO conditions in an attempt to interpret the size-dependence of the metal chemical activity within a dynamic redox situation. To this end, a synchronous, multitechnique approach using X-ray absorption (XAS) or hard X-ray diffraction (HXRD) in tandem with diffuse reflectance infrared spectroscopy (DRIFTS) and mass spectrometry (MS) was used to establish the size-dependence of chemically significant steps in formation of N2 and CO2. During cycling, EXAFS and HXRD reveal the existence of a reversible Pd morphology and phase change (PdC x formation and removal) phenomena in response to the gas atmosphere reducing/oxidizing nature. This is observed for Pd particles having dispersion values going from ca. 1–0.4. Using EXAFS Pd–Pd coordination numbers, we dynamically normalized the DRIFTS and MS signals obtained during cycling conditions and find that metal size/phase-effects appear of importance in CO2 formation but can be essentially neglected in N2 formation. Such (size-dependent) metal behaviour appears far from expectations coming from studies using non-cycling gas mixtures. The chemical relevance of NO, CO activation, dissociation and coupling steps are discussed in relation to the product formation and their size-dependence or independence. [Copyright &y& Elsevier]

High capacity sulfur electrodes are expected to be used in the next-generation of high energy density and low cost rechargeable lithium batteries. The positive sulfur electrode undergoes complex electrochemical reactions, which cause morphological changes of the composite electrode while cycling. In the course to deeper understand the failures of this rather complex, but promising technology, the operando technics are in the heart of the advanced characterizations. In this study, a new electrochemical cell was designed which allows, for the first time, the combination operando of multimodal X-ray characterizations: the absorption tomography to study the morphological evolution of electrodes, and the X-ray diffraction computed tomography to probe locally the structural modification of the crystalline active materials S 8 and Li 2 S. The combination of these two techniques simultaneously with the electrochemical cycling, allows the production of correlated 3D-maps of quantitative phase distributions and morphology in the electrode, with time resolution on the scale of battery kinetics. It was thus possible to show the heterogeneous behavior in the bulk of the electrode and to propose kinetics law. • New operando cell designed for coupling XRDCT and X-ray microtomography. • Correlated 3D-maps of phase distributions and morphology in the sulfur electrode. • Evidence of heterogeneous behavior in a 3D-electrode. [ABSTRACT FROM AUTHOR]