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Through Monte Carlo simulations, we investigate how various experimental parameters can influence the quality of time-resolved scanning transmission X-ray microscopy images. In particular, the effect of the X-ray photon flux, of the thickness of the investigated samples, and of the frequency of the dynamical process under investigation on the resulting time-resolved image are investigated. The ideal sample and imaging conditions that allow for an optimal image quality are then identifed.

Nature Communications 10(1), 2600 (2019). doi:10.1038/s41467-019-10670-7, Reaching the full potential of X-ray nanotomography, in particular for biological samples, is limited by many factors, of which one of the most serious is radiation damage. Although sample deformation caused by radiation damage can be partly mitigated by cryogenic protection, it is still present in these conditions and, as we exemplify here using a specimen extracted from scales of the Cyphochilus beetle, it will pose a limit to the achievable imaging resolution. We demonstrate a generalized tomographic model, which optimally follows the sample morphological changes and attempts to recover the original sample structure close to the ideal, damage-free reconstruction. Whereas our demonstration was performed using ptychographic X-ray tomography, the method can be adopted for any tomographic imaging modality. Our application demonstrates improved reconstruction quality of radiation-sensitive samples, which will be of increasing relevance with the higher brightness of 4th generation synchrotron sources., Published by Nature Publishing Group UK, [London]

Recent studies in three dimensional spintronics propose that the \OE rsted field plays a significant role in cylindrical nanowires. However, there is no direct report of its impact on magnetic textures. Here, we use time-resolved scanning transmission X-ray microscopy to image the dynamic response of magnetization in cylindrical Co$_{30}$Ni$_{70}$ nanowires subjected to nanosecond \OE rsted field pulses. We observe the tilting of longitudinally magnetized domains towards the azimuthal \OE rsted field direction and create a robust model to reproduce the differential magnetic contrasts and extract the angle of tilt. Further, we report the compression and expansion, or breathing, of a Bloch-point domain wall that occurs when weak pulses with opposite sign are applied. We expect that this work lays the foundation for and provides an incentive to further studying complex and fascinating magnetization dynamics in nanowires, especially the predicted ultra-fast domain wall motion and associated spin wave emissions., Comment: 6 pages, 3 figures in main text and supplementary materials

Diffraction gratings are key components in experiments with UV, VUV and soft x-ray radiation at synchrotron radiation and free-electron laser (FEL) facilities. They areused in monochromators to produce beams with narrow energy distribution, and in analyzers to provide high-resolution spectral analysis of scattered radiation. Today, such diffraction gratings consist of a large number of periodic grooves (typically tens to thousands per millimeter) arranged on the reflecting surface on a plane or concave substrate. The performance of the grating is also ultimately limited by the surface quality of the substrate. For best spectral resolution, the substrates need to be ultra-precise and superpolished, with typical lengths of 100 – 300 mm and shape errors of 1-2 nanometers, slope errors in the order of 100 nrad, and a roughness in the Angstrom scale. Today, the line patterns of x-ray gratings are mostly produced either by holographic exposures of interfering laser beams into a photo resist, or by ruling machines that imprint the grating groves in a line-by-line manner into a soft metal layer. As an alternative to these established methods, we present a strategy of grating fabrication by electron-beam lithography (EBL). This technique can expose arbitrary patterns with high resolution and placement accuracy at a speed sufficient for x-ray grating fabrication. We have performed optical metrology of a low-cost grating substrate, which served as the basis for an aligned exposure of a corrected grating pattern to yield a laminar grating with a constant deflection angle along the substrate surface. We have confirmed that the effects of slope errors were strongly compensated over an extended wavelength range by using synchrotron radiation in the soft x-ray range. This work shows a path for circumventing the limited availability of high quality reflective substrates to obtain gratings with performance beyond what is possible today.

We employ xenon (Xe) plasma focused ion beam (PFIB) milling to obtain soft X-ray transparent windows out of bulk samples. The use of a Xe PFIB allows for the milling of thin windows (several 100 nm thick) with areas of the order of 100 µm × 100 µm into bulk substrates. In addition, we present an approach to empirically determine the transmission level of such windows during fabrication by correlating their electron and soft X-ray transparencies. We perform scanning transmission X-ray microscopy (STXM) imaging on a sample obtained by Xe PFIB milling to demonstrate the conceptual feasibility of the technique. Our thinning approach provides a fast and simplified method for facilitating soft X-ray transmission measurements of epitaxial samples and it can be applied to a variety of different sample systems and substrates that are otherwise not accessible, Crystals, 11 (5), ISSN:2073-4352

A setup for time-resolved scanning transmission X-ray microscopy imaging is presented, which allows for an increase in the temporal resolution without the requirement of operating the synchrotron light source with low-α optics through the measurement of the time-of-arrival of the X-ray photons. Measurements of two filling patterns in hybrid mode of the Swiss Light Source are presented as a first proof-of-principle and benchmark for the performances of this new setup. From these measurements, a temporal resolution on the order of 20–30 ps could be determined., Journal of Synchrotron Radiation, 27 (Part 5), ISSN:0909-0495, ISSN:1600-5775

A new endstation to perform operando chemical analysis at solid–liquid interfaces by means of ambient pressure x-ray photoelectron spectroscopy (APXPS) is presented. The endstation is located at the Swiss Light Source and can be attached to the soft x-ray in situ spectroscopy beamline (X07DB) for solid–gas type experiments and to a tender x-ray beamline (PHOENIX I) for solid–liquid interface experiments. The setup consists of three interconnected ultrahigh vacuum chambers: one for sample preparation using surface science techniques, the analysis chamber for APXPS experiments, and an entry-lock chamber for sample transfer across the two pressure regimes. The APXPS chamber is designed to study solid–liquid interfaces stabilized by the dip and pull method. Using a three-electrode setup, the potential difference across the solid-electrolyte interface can be controlled, as is demonstrated here using an Ir(001) electrode dipped and pulled from a 0.1M KOH electrolyte. The new endstation is successfully commissioned and will offer unique opportunities for fundamental studies of phenomena that take place at solid–liquid interfaces and that are relevant for fields such as electrochemistry, photochemistry, or biochemistry, to name a few., Review of Scientific Instruments, 91 (2), ISSN:0034-6748, ISSN:1089-7623

X-ray tomography has become an indispensable tool for studying complex 3D interior structures with high spatial resolution. Three-dimensional imaging using soft X-rays offers powerful contrast mechanisms but has seen limited success with tomography due to the restrictions imposed by the much lower energy of the probe beam. The generalized geometry of laminography, characterized by a tilted axis of rotation, provides nm-scale 3D resolution for the investigation of extended (mm range) but thin (μm to nm) samples that are well suited to soft X-ray studies. This work reports on the implementation of soft X-ray laminography (SoXL) at the scanning transmission X-ray spectromicroscope of the PolLux beamline at the Swiss Light Source, Paul Scherrer Institut, which enables 3D imaging of extended specimens from 270 to 1500 eV. Soft X-ray imaging provides contrast mechanisms for both chemical sensitivity to molecular bonds and oxidation states and magnetic dichroism due to the much stronger attenuation of X-rays in this energy range. The presented examples of applications range from functionalized nanomaterials to biological photonic crystals and sophisticated nanoscaled magnetic domain patterns, thus illustrating the wide fields of research that can benefit from SoXL.

Using time-lapsed ambient-pressure X-ray photoelectron spectroscopy, we investigate the thermal oxidation of single-crystalline Ir(100) films toward rutile IrO2(110) in situ. We initially observe the formation of a carbon-free surface covered with a complete monolayer of oxygen, based on the binding energies of the Ir 4f and O 1s core level peaks. During a rather long induction period with nearly constant oxygen coverage, the work function of the surface changes continuously as sensed by the gas phase O 1s signal. The sudden and rapid formation of the IrO2 rutile phase with a thickness above 3 nm, manifested by distinct binding energy changes and substantiated by quantitative XPS analysis, provides direct evidence that the oxide film is formed via an autocatalytic growth mechanism that was previously proposed for PbO and RuO2.

We report on the investigation of current-induced domain wall motion of Neel domain walls in perpendicularly magnetized microwires with curved geometries in the flow regime. The investigation was performed by time-resolved scanning transmission x-ray microscopy. In particular, we studied the dynamical tilting of the Neel domain walls, observing that an asymmetric behavior in the domain wall tilt appears upon an inversion of the polarity of the current pulse driving the motion, an effect not predicted by state-of-the-art theories and micromagnetic modeling.

Nanometer-thin rare-earth iron garnet films with perpendicular magnetic anisotropy are among the most promising materials for fast and low-energy spintronics applications. Here, the authors demonstrate ultrafast control of intrinsically stabilized submicrometer bubble domains in these materials. By employing powerful x-ray imaging techniques both in transmission and with surface sensitivity, and by combining this with nanosecond electrical pulses and femtosecond laser excitation, they deterministically create, and image, these bubble states $i\phantom{\rule{0}{0ex}}n$ $s\phantom{\rule{0}{0ex}}i\phantom{\rule{0}{0ex}}t\phantom{\rule{0}{0ex}}u$. The topology, the chirality, and the switching phase diagram of these twisted spin structures are all resolved by direct imaging.

Optica 7(11), 1602 - 1608 (2020). doi:10.1364/OPTICA.399885, The availability of intense soft x-ray beams with tunable energy and polarization has pushed the development of highlysensitive, element-specific, and noninvasive microscopy techniques to investigate condensed matter with high spatialand temporal resolution. The short wavelengths of soft x-rays promise to reach spatial resolutions in the deep single-digitnanometer regime, providing unprecedented access to magnetic phenomena at fundamental length scales. Despiteconsiderable efforts in soft x-ray microscopy techniques, a two-dimensional resolution of 10 nm has not yet been surpassedin direct imaging. Here, we report on a significant step beyond this long-standing limit by combining newlydeveloped soft x-ray Fresnel zone plate lenses with advanced precision in scanning control and careful optical design.With this approach, we achieve an image resolution of 7 nm. By combining this highly precise microscopy techniquewith the x-ray magnetic circular dichroism effect,we reveal dimensionality effects in an ensemble of interacting magneticnanoparticles. Such effects are topical in current nanomagnetism research and highlight the opportunities of highresolutionsoft x-ray microscopy in magnetism research and beyond., Published by OSA, Washington, DC

X-ray free-electron lasers (XFELs) are paving the way towards new experiments in many scientific fields, such as ultrafast science, nonlinear spectroscopy, and coherent imaging. However, the strong intensity fluctuations inherent to the lasing process in these sources often lead to problems in signal normalization. In order to address this challenge, we designed, fabricated, and characterized diffractive x-ray optics that combine the focusing properties of a Fresnel zone plate with the beam-splitting capability of a grating in a single diffractive optical element. The possibility to split the incident beam into identical copies allows for direct shot-to-shot normalization of the sample signal, thereby greatly enhancing the signal-to-noise ratio in experiments with XFEL radiation. Here we propose two schemes for the design of such diffractive x-ray optical elements for splitting and focusing an incoming beam into up to three foci by merging a grating with a focusing zone plate. By varying the duty cycle of the grating or the relative shift of the Fresnel zone plate structure, we are able to tune the relative intensities of the different diffraction orders to achieve the desired splitting ratios. Experimental confirmation of the design is provided with soft x-ray light (540 eV) and shows a good agreement with calculations, confirming the suitability of this approach for XFEL experiments.

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Magnetic skyrmions promise breakthroughs in future memory and computing devices due to their inherent stability and small size. Their creation and current driven motion have been recently observed at room temperature, but the key mechanisms of their formation are not yet well-understood. Here it is shown that in heavy metal/ferromagnet heterostructures, pulsed currents can drive morphological transitions between labyrinth-like, stripe-like, and skyrmionic states. Using high-resolution X-ray microscopy, the spin texture evolution with temperature and magnetic field is imaged and it is demonstrated that with transient Joule heating, topological charges can be injected into the system, driving it across the stripe-skyrmion boundary. The observations are explained through atomistic spin dynamic and micromagnetic simulations that reveal a crossover to a global skyrmionic ground state above a threshold magnetic field, which is found to decrease with increasing temperature. It is demonstrated how by tuning the phase stability, one can reliably generate skyrmions by short current pulses and stabilize them at zero field, providing new means to create and manipulate spin textures in engineered chiral ferromagnets.

We present a detailed study on the static magnetic properties of individual permalloy nanotubes (NTs) with hexagonal cross-sections. Anisotropic magnetoresistance (AMR) measurements and scanning transmission X-ray microscopy (STXM) are used to investigate their magnetic ground states and its stability. We find that the magnetization in zero applied magnetic field is in a very stable vortex state. Its origin is attributed to a strong growth-induced anisotropy with easy axis perpendicular to the long axis of the tubes. AMR measurements of individual NTs in combination with micromagnetic simulations allow the determination of the magnitude of the growth-induced anisotropy for different types of NT coatings. We show that the strength of the anisotropy can be controlled by introducing a buffer layer underneath the magnetic layer. The magnetic ground states depend on the external magnetic field history and are directly imaged using STXM. Stable vortex domains can be introduced by external magnetic fields and can be erased by radio-frequency magnetic fields applied at the center of the tubes via a strip line antenna.

Recent progress in the performance of polymer electronics devices has depended heavily on detailed knowledge of the properties of the active polymer materials. While many advanced conjugated polymer materials are being synthesized, the limited quantities produced severely restrict opportunities to measure their physical properties. In particular, the absolute mass density is a basic material property that impacts on many other important properties, yet it is very difficult to measure when in limited quantity. Here, we report a method to spatially resolve the absolute mass density of polymer materials at the nanoscale and measure values for polystyrene (1028 (43) kg/m3), PMMA (1140 (26) kg/m3), PFB (727 (51) kg/m3), and F8BT (749 (26) kg/m3). We estimate that the measurement method could be applied to sample quantities less than 1 picogram.

Ultrafast dynamics are generally investigated using stroboscopic pump-probe measurements, which characterize the sample properties for a single, specific time delay. These measurements are then repeated for a series of discrete time delays to reconstruct the overall time trace of the process. As a consequence, this approach is limited to the investigation of fully reversible phenomena. We recently introduced an off-axis zone plate based X-ray streaking technique, which overcomes this limitation by sampling the relaxation dynamics with a single femtosecond X-ray pulse streaked over a picosecond long time window. In this article we show that the X-ray absorption cross section can be employed as the contrast mechanism in this novel technique. We show that changes of the absorption cross section on the percent level can be resolved with this method. To this end we measure the ultrafast magnetization dynamics in CoDy alloy films. Investigating different chemical compositions and infrared pump fluences, we demonstrate the routine applicability of this technique. Probing in transmission the average magnetization dynamics of the entire film, our experimental findings indicate that the demagnetization time is independent of the specific infrared laser pump fluence. These results pave the way for the investigation of irreversible phenomena in a wide variety of scientific areas., Comment: 9 pages, 5 figures

Performance combined with simplicity: we demonstrate that thick Permalloy films exhibiting a weak growth-induced perpendicular magnetic anisotropy can be employed as an ideal test system for the study of magnetodynamical processes in perpendicularly magnetized systems exhibiting magnetic textures ranging from isolated magnetic bubbles to more complex n"pi" states.

We investigated the influence of an isotropic strain on the magnetization dynamics of microstructured magnetostrictive Co40Fe40B20 (CoFeB) elements with time-resolved scanning transmission x-ray microscopy. We observed that the application of isotropic strain leads to changes in the behavior of the microstructured magnetostrictive elements that cannot be fully explained by the volume magnetostriction term. Therefore, our results prompt for an alternative explanation to the current models used for the interpretation of the influence of mechanical strain on the dynamical processes of magnetostrictive materials.

Moving towards significantly smaller nanostructures, direct structuring techniques such as electron beam lithography approach fundamental limitations in feature size and aspect ratios. Application of nanostructures like diffractive X-ray lenses requires feature sizes of below 10 nm to enter a new regime in high resolution X-ray microscopy. As such dimensions are difficult to obtain using conventional electron beam lithography, we pursue a line-doubling approach. We demonstrate that this method yields structure sizes as small as 6.4 nm. X-ray lenses fabricated in this way are tested for their efficiency and microscopic resolution. In addition, the line-doubling technique is successfully extended to a six-fold scheme, where each line in a template structure written by electron beam lithography evolves into six metal lines.

The influence of a strain-induced uniaxial magnetoelastic anisotropy on the magnetic vortex core dynamics in microstructured magnetostrictive ${\mathrm{Co}}_{40}{\mathrm{Fe}}_{40}{\mathrm{B}}_{20}$ elements was investigated with time-resolved scanning transmission x-ray microscopy. The measurements revealed a monotonically decreasing eigenfrequency of the vortex core gyration with the increasing magnetoelastic anisotropy, which follows closely the predictions from micromagnetic modeling.

Scientific reports 7(1), 7253(2017). doi:10.1038/s41598-017-07069-z, The advent of x-ray free electron lasers has extended the unique capabilities of resonant x-ray spectroscopy techniques to ultrafast time scales. Here, we report on a novel experimental method that allows retrieving with a single x-ray pulse the time evolution of an ultrafast process, not only at a few discrete time delays, but continuously over an extended time window. We used a single x-ray pulse to resolve the laser-induced ultrafast demagnetisation dynamics in a thin cobalt film over a time window of about 1.6 ps with an excellent signal to noise ratio. From one representative single shot measurement we extract a spin relaxation time of (130 ± 30) fs with an average value, based on 193 single shot events of (113 ± 20) fs. These results are limited by the achieved experimental time resolution of 120 fs, and both values are in excellent agreement with previous results and theoretical modelling. More generally, this new experimental approach to ultrafast x-ray spectroscopy paves the way to the study of non-repetitive processes that cannot be investigated using traditional repetitive pump-probe schemes., Published by Macmillan, London

High-throughput three-dimensional cryogenic imaging of thick biological specimens is valuable for identifying biologically- or pathologically-relevant features of interest, especially for subsequent correlative studies. Unfortunately, high-resolution imaging techniques at cryogenic conditions often require sample reduction through sequential physical milling or sectioning for sufficient penetration to generate each image of the 3-D stack. This study represents the first demonstration of using ptychographic hard X-ray tomography at cryogenic temperatures for imaging thick biological tissue in a chemically-fixed, frozen-hydrated state without heavy metal staining and organic solvents. Applied to mammalian brain, this label-free cryogenic imaging method allows visualization of myelinated axons and sub-cellular features such as age-related pigmented cellular inclusions at a spatial resolution of ~100 nanometers and thicknesses approaching 100 microns. Because our approach does not require dehydration, staining or reduction of the sample, we introduce the possibility for subsequent analysis of the same tissue using orthogonal approaches that are expected to yield direct complementary insight to the biological features of interest.

Integrated optically inspired wave-based processing is envisioned to outperform digital architectures in specific tasks, such as image processing and speech recognition. In this view, spin waves represent a promising route due to their nanoscale wavelength in the gigahertz frequency range and rich phenomenology. Here, a versatile, optically inspired platform using spin waves is realized, demonstrating the wavefront engineering, focusing, and robust interference of spin waves with nanoscale wavelength. In particular, magnonic nanoantennas based on tailored spin textures are used for launching spatially shaped coherent wavefronts, diffraction-limited spin-wave beams, and generating robust multi-beam interference patterns, which spatially extend for several times the spin-wave wavelength. Furthermore, it is shown that intriguing features, such as resilience to back reflection, naturally arise from the spin-wave nonreciprocity in synthetic antiferromagnets, preserving the high quality of the interference patterns from spurious counterpropagating modes. This work represents a fundamental step toward the realization of nanoscale optically inspired devices based on spin waves.

The thickness- and temperature-induced in-plane spin reorientation transitions (SRT) in epitaxial Fe films on a W(110) single crystal were investigated using X-ray photoemission electron microscopy. We present the real time evolution of the magnetisation switching, and we demonstrate differences between the two transition mechanisms. Whereas both the transitions involve the magnetic domain wall motion, the temperature SRT is additionally accompanied by nucleation of domains. Before and after the thickness-induced SRTs, the sample is in the almost single domain state, which is not the case for the final magnetic configuration after the temperature-induced transition.

The X-ray excited optical luminescence response of sapphire (α-Al 2 O 3 ), aluminium lanthanate (LaAlO 3 ), and magnesium oxide (MgO) were measured at room temperature as a function of incident photon energy in the range from 500 to 1000 eV. The luminescence yield varies weakly with energy above 600 eV and is dominated by the presence of the O K absorption edge in all cases and the La M 2,3 edge for LaAlO 3 . The emission spectra in the visible range measured at a fixed incidence X-ray photon energy of 1000 eV shows for LaAlO 3 a simple spectrum composed of two broad lines, a dominant sharp line for sapphire arising from Cr 3+ impurities, and a complex spectrum for MgO, containing both broad and sharp spectral lines originating predominantly from impurities. SrTiO 3 and Nb-doped SrTiO 3 crystals were also measured and are found to have much smaller luminescence yields than the other materials investigated. Our results show that residual impurities that are inevitably present in high quality bulk crystals can be employed as colour centres for the detection of X-ray light in X-ray transmission spectroscopy.

We present a setup that allows for the in situ generation of tensile strains by bending x-ray transparent Si3N4 membranes with the application of a pressure difference between the two sides of the membrane, enabling the possibility to employ high resolution space- and time-resolved scanning transmission x-ray microscopy for the investigation of the magneto-elastic coupling.

Advanced materials 30(19), 1702057 (2017). doi:10.1002/adma.201702057, Most studies of structural color in nature concern periodic arrays, which through the interference of light create color. The “color” white however relies on the multiple scattering of light within a randomly structured medium, which randomizes the direction and phase of incident light. Opaque white materials therefore must be much thicker than periodic structures. It is known that flying insects create “white” in extremely thin layers. This raises the question, whether evolution has optimized the wing scale morphology for white reflection at a minimum material use. This hypothesis is difficult to prove, since this requires the detailed knowledge of the scattering morphology combined with a suitable theoretical model. Here, a cryoptychographic X‐ray tomography method is employed to obtain a full 3D structural dataset of the network morphology within a white beetle wing scale. By digitally manipulating this 3D representation, this study demonstrates that this morphology indeed provides the highest white retroreflection at the minimum use of material, and hence weight for the organism. Changing any of the network parameters (within the parameter space accessible by biological materials) either increases the weight, increases the thickness, or reduces reflectivity, providing clear evidence for the evolutionary optimization of this morphology., Published by Wiley-VCH, Weinheim

Recent studies have shown that material structures, which lack structural inversion symmetry and have high spin-orbit coupling can exhibit chiral magnetic textures and skyrmions which could be a key component for next generation storage devices. The Dzyaloshinskii-Moriya Interaction (DMI) that stabilizes skyrmions is an anti-symmetric exchange interaction favoring non-collinear orientation of neighboring spins. It has been shown that material systems with high DMI can lead to very efficient domain wall and skyrmion motion by spin-orbit torques. To engineer such devices, it is important to quantify the DMI for a given material system. Here we extract the DMI at the Heavy Metal (HM) /Ferromagnet (FM) interface using two complementary measurement schemes namely asymmetric domain wall motion and the magnetic stripe annihilation. By using the two different measurement schemes, we find for W(5 nm)/Co20Fe60B20(0.6 nm)/MgO(2 nm) the DMI to be 0.68 +/- 0.05 mJ/m2 and 0.73 +/- 0.5 mJ/m2, respectively. Furthermore, we show that this DMI stabilizes skyrmions at room temperature and that there is a strong dependence of the DMI on the relative composition of the CoFeB alloy. Finally we optimize the layers and the interfaces using different growth conditions and demonstrate that a higher deposition rate leads to a more uniform film with reduced pinning and skyrmions that can be manipulated by Spin-Orbit Torques.

International audience; Sub-100-nm skyrmions are stabilized in magnetic metallic multilayers and observed using transmission electron microscopy, magnetic force microscopy, scanning transmission X-ray microscopy and X-ray resonant magnetic scattering. All these advanced imaging techniques demonstrate the presence of "pure" Néel skyrmion textures with a determined chirality. Combining these observations with electrical measurements allows us to demonstrate reproducible skyrmion nucleation using current pulses, and measure their contribution to the transverse resistivity to detect them electrically. Once nucleated, skyrmions can be moved using charge currents. We find predominantly a creep-like regime, characterized by disordered skyrmion motion, as observed by atomic force microscopy and scanning transmission X-ray microscopy. These observations are explained qualitatively and to some extent quantitatively by the presence of crystalline grains of about 20 nm lateral size with a distribution of magnetic properties.

Techniques exist for imaging the magnetization patterns of magnetic thin films and at the surfaces of magnets, but here hard-X-ray tomography is used to image the three-dimensional magnetic structure within a micrometre-sized magnet in the vicinity of Bloch points. Techniques have long existed for imaging the two-dimensional magnetization patterns of thin-film magnets, but the three-dimensional complexities of magnetization structure within the body of a magnet is not so amenable to direct investigation. Claire Donnelly et al. have made substantial progress in lifting this veil by harnessing hard-X-ray tomography to determine the inner magnetic structure of micrometre-sized magnets. The properties of current X-ray sources limit the spatial resolution to about 100 nanometres, but it is anticipated that future instrumental developments could greatly improve on this. In soft ferromagnetic materials, the smoothly varying magnetization leads to the formation of fundamental patterns such as domains, vortices and domain walls1. These have been studied extensively in thin films of thicknesses up to around 200 nanometres, in which the magnetization is accessible with current transmission imaging methods that make use of electrons or soft X-rays. In thicker samples, however, in which the magnetization structure varies throughout the thickness and is intrinsically three dimensional, determining the complex magnetic structure directly still represents a challenge1,3. We have developed hard-X-ray vector nanotomography with which to determine the three-dimensional magnetic configuration at the nanoscale within micrometre-sized samples. We imaged the structure of the magnetization within a soft magnetic pillar of diameter 5 micrometres with a spatial resolution of 100 nanometres and, within the bulk, observed a complex magnetic configuration that consists of vortices and antivortices that form cross-tie walls and vortex walls along intersecting planes. At the intersections of these structures, magnetic singularities—Bloch points—occur. These were predicted more than fifty years ago4 but have so far not been directly observed. Here we image the three-dimensional magnetic structure in the vicinity of the Bloch points, which until now has been accessible only through micromagnetic simulations, and identify two possible magnetization configurations: a circulating magnetization structure5 and a twisted state that appears to correspond to an ‘anti-Bloch point’. Our imaging method enables the nanoscale study of topological magnetic structures6 in systems with sizes of the order of tens of micrometres. Knowledge of internal nanomagnetic textures is critical for understanding macroscopic magnetic properties and for designing bulk magnets for technological applications7.

We report on in-plane magnetic anisotropy in epitaxial bcc Co/Fe(110) bilayers on W(110). The magnetic surface anisotropy in the Co/Fe(110) bilayers exhibited a strong nonmonotonic dependence on Co coverage. Magneto-optical studies revealed a sharp maximum of the magnetic surface anisotropy, $2.44\phantom{\rule{0.16em}{0ex}}\mathrm{mJ}/{\mathrm{m}}^{2}$, at ${d}_{\mathrm{Co}}=5\phantom{\rule{0.16em}{0ex}}\AA{}$. This giant interfacial magnetic anisotropy allowed a small fraction of a Co monolayer to reorient the magnetization of the bulk-like Fe film. We conclude that the mono- and double-layer bcc Co(110) exhibited in-plane magnetic anisotropy with a $[1\overline{1}0]$ easy axis.

Polarization dependent X-ray absorption spectroscopy and microscopy enables the element selective investigation of magnetic systems at the nanoscale. At the Swiss Light Source a photoemission electron microscope is used for the study of a broad variety of systems. Here, a review of recent activities is presented with a focus on instrumental and analytical developments. A new procedure for the 3 dimensional determination of the magnetization vector has been developed, and is demonstrated for GdFeCo microstructures displaying in-plane and out-of-plane domains, and sub-20 nm Fe nanoparticles. The recent progress for measurements in applied magnetic fields is presented and a new set-up for time-resolved measurements employing femtosecond laser pulses is described.

Thin films of organic semiconducting materials are of increasing technological importance in optoelectronic devices such as light emitting diodes (LEDs), lasers, field effect transistors (FETs) and solar cells. However, the morphology of such films is complex, often displaying three dimensional composition structure or molecular alignment effects. The structure of the polymer film incorporated into a device can strongly affect its performance characteristics, e.g. via the connectedness of polymer domains and to the device electrodes, or due to anisotropic material properties due to molecular alignment. Scanning transmission X-ray spectro-microscopy (STXM) has been demonstrated to be an excellent tool for the study of organic materials due to its high spatial resolution (down to about 20 nm) and strong contrast based on a variety of spectroscopic mechanisms. In particular, tuning the probing X-ray beam to resonances in the near edge X-ray absorption fine structure (NEXAFS) spectra provides a mechanism for molecular-structure based contrast which is a very powerful tool for studying blends of organic components. A further advantage of STXM is that strategic use of spectroscopic information allows quantitative compositional analysis of imaged areas. Recent work at the PolLux STXM has demonstrated two new developments in the imaging of thin organic films: simultaneous surface and bulk imaging via an additional channeltron electron detector, and molecular orientation mapping via anisotropic near edge resonances.

The geometry of magnetic flux penetration in a high temperature superconductor at a buried interface was imaged using element-specific x-ray excited luminescence. We performed low temperature observation of the flux penetration in YBa2Cu3O7–δ (YBCO) at a buried interface by imaging of the perpendicular magnetization component in square Permalloy (Py) mesostructures patterned superjacent to a YBCO film. Element specific imaging below the critical temperature of YBCO reveals a cross-like geometry of the perpendicular magnetization component which is decorated by regions of alternating out-of-plane magnetization at the edges of the patterned Py structures. The cross structure can be attributed to the geometry of flux penetration originating from the superconductor and is reproduced using micromagnetic simulations. Our experimental method opens up possibilities for the investigation of flux penetration in superconductors at the nanoscale.

We report on the design and first tests of a novel instrument aimed at combining the benefits of scanning force microscopy with those of X-ray spectroscopy. For this we built an instrument combining a scanning transmission X-ray microscope with a beam-deflection atomic force microscope in a coaxial geometry. This allows to combine X-ray absorption spectroscopy and high resolution topography in-situ. When replacing the conventional scanning probe tip by a coaxially shielded tip the instrument will allow detection of the photoelectrons produced by resonant X-ray absorption. This could yield spectroscopic information with a spatial resolution approaching the values achievable with atomic force microscopy.

Imaging the magnetic structure of a material is essential to understanding the influence of the physical and chemical microstructure on its magnetic properties. Magnetic imaging techniques, however, have been unable to probe three-dimensional micrometer-size systems with nanoscale resolution. Here we present the imaging of the magnetic domain configuration of a micrometer-thick FeGd multilayer with hard x-ray dichroic ptychography at energies spanning both the Gd ${L}_{3}$ edge and the Fe $K$ edge, providing a high spatial resolution spectroscopic analysis of the complex x-ray magnetic circular dichroism. With a spatial resolution reaching $45\phantom{\rule{0.28em}{0ex}}\mathrm{nm}$, this advance in hard x-ray magnetic imaging is a first step towards the investigation of buried magnetic structures and extended three-dimensional magnetic systems at the nanoscale.

International audience; The manipulation of magnetic domain walls in thin films and nanostructures opens new opportunities for fundamental and applied research. But controlling reliably the position of a moving domain wall still remains challenging. So far, most of the studies aimed at understanding the physics of pinning and depinning processes in the magnetic layer in which the wall moves (active layer). In these studies, the role of other magnetic layers in the stack has been often ignored. Here, we report an indirect localization process of 180° domain walls that occurs in magnetic tunnel junctions, commonly used in spintronics. Combining Scanning Transmission X-Ray Microscopy and micromagnetic simulations, magnetic configurations in both layers are resolved. When nucleating a 180° domain wall in the active layer, a quasi wall is created in the reference layer, atop the wall. The wall and its quasi wall must then be moved or positioned together, as a unique object. As a mutual effect, a localized change of the magnetic properties in the reference layer induces a localized quasi wall in the active layer. The two types of quasi walls are shown to be responsible for an indirect localization process of the 180° domain wall in the active layer.

International audience; Calcium silicate hydrates (C−S−H) are the most abundant hydration products in ordinary Portland cement paste. Yet, despite the critical role they play in determining mechanical and transport properties, there is still a debate about their density and exact composition. Here, the site-specific mass density and composition of C−S−H in hydrated cement paste are determined with nanoscale resolution in a nondestructive approach. We used ptychographic X-ray computed tomography in order to determine spatially resolved mass density and water content of the C−S−H within the microstructure of the cement paste. Our findings indicate that the C−S−H at the border of hydrated alite particles possibly have a higher density than the apparent inner-product C−S−H, which is contrary to the common expectations from previous works on hydrated cement paste.

The penetration of spherical and rod-like gold nanoparticles into human skin is reported. Several skin preparation techniques are applied, including cryo techniques, such as plunge freezing and freeze drying, and the use of wet cells. Their advantages and drawbacks for observing nanoparticle uptake are discussed. Independent of the particle shape no uptake into intact skin is observed by a combination of imaging approaches, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), and scanning X-ray microscopy (STXM). These results are discussed along with suitable skin preparation approaches. Experiments on barrier-disrupted skin, i.e. mechanical lesions made by pricking, indicate, however, that gold particles can be identified deep in the dermis, as follows from STXM studies on wet skin samples.

HighlightsX-ray lithography was performed in direct write (maskless) geometry using a STXM.Sub-25nm free form features were created in PMMA.The ultimate feature size limitations of this technique are discussed. Sub-25nm continuous, reproducible features of arbitrary geometry were created by X-ray lithography in direct write (maskless) geometry, analogous to conventional electron beam lithography. This was achieved through the use of a laser interferometer-controlled scanning transmission X-ray microscope (STXM) equipped with a zone doubled Fresnel zone plate lens, and a cold development procedure. These features are among the smallest created with photons in direct write geometry.

Recent advances in fabrication techniques to create mesoscopic 3D structures have led to significant developments in a variety of fields including biology, photonics, and magnetism. Further progress in these areas benefits from their full quantitative and structural characterization. We present resonant ptychographic tomography, combining quantitative hard x-ray phase imaging and resonant elastic scattering to achieve ab initio element-specific 3D characterization of a cobalt-coated artificial buckyball polymer scaffold at the nanoscale. By performing ptychographic x-ray tomography at and far from the Co K edge, we are able to locate and quantify the Co layer in our sample to a 3D spatial resolution of 25 nm. With a quantitative determination of the electron density we can determine that the Co layer is oxidized, which is confirmed with microfluorescence experiments.