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Complexes containing rare-earth ions attract great attention for their technological applications ranging from spintronic devices to quantum information science. While charged rare-earth coordination complexes are ubiquitous in solution, they are challenging to form on materials surfaces that would allow investigations for potential solid-state applications. Here we report formation and atomically precise manipulation of rare-earth complexes on a gold surface. Although they are composed of multiple units held together by electrostatic interactions, the entire complex rotates as a single unit when electrical energy is supplied from a scanning tunneling microscope tip. Despite the hexagonal symmetry of the gold surface, a counterion at the side of the complex guides precise three-fold rotations and 100% control of their rotational directions is achieved using a negative electric field from the scanning probe tip. This work demonstrates that counterions can be used to control dynamics of rare-earth complexes on materials surfaces for quantum and nanomechanical applications.

An ultra-high-vacuum compatible X-ray chopper system has been designed, constructed and integrated into the XTIP beamline at the Advanced Photon Source at Argonne National Laboratory. The XTIP beamline can operate at soft X-ray energies from 400 eV to 1900 eV while providing a focused beam down to about 10 µm × 10 µm into the synchrotron X-ray scanning tunneling microscopy (SX-STM) endstation instrument. The X-ray chopper is a critical component for separating topographic information from chemical information in SX-STM through phase-sensitive current detection. Depending on the experimental needs, the modulation frequency can be controlled from 100 Hz to 10 kHz. In addition, the chopper system is fully bakeable and can achieve a base pressure of 10−10 mbar. Facilities for active water cooling have been designed, but passive cooling through copper braids has been shown to be sufficient at standard chopping frequencies. Using an Fe/Al2O3/CoAl(111) sample, the separation of the SX-STM current into a chemical component and a stable feedback signal is demonstrated.

Side reactions involving surface reduction play a critical role in the failure of LiNi0.8Co0.15Al0.05O2 to reach its theoretical capacity as a cathode material for Li-ion batteries. While macroscop...

Impurity contamination in thin-film solar cells remains an uncertain risk due to the little-known impact of impurities on recombination. Building upon previous work, in which we intentionally contaminated lead halide perovskite (LHP) solar cells with iron, we further examine the distribution and charge state of iron-induced defects in LHP films using synchrotron-based X-ray techniques. X-ray absorption measurements suggest that iron-rich regions, which form among iron feedstock concentrations that exceed 100 ppm, most closely resemble the chemistry of Fe2O3. Iron distributed within the bulk may form a mix of Fe2+and Fe3+, the latter of which is not expected to be recombination active, potentially allowing LHPs to incorporate more iron than traditional semiconductors. X-ray beam induced current measurements show little correlation between the presence of iron-rich regions and charge collection, which further suggests low recombination activity at these sites. These results further elucidate the recombination behavior caused by iron incorporation in LHP films, revealing insight into how inhomogeneous incorporation of impurities may mitigate photovoltaic performance degradation., National Science Foundation (U.S.). Materials Research Science and Engineering Centers (Program) (award number DMR-1419807), United States. Department of Energy. Office of Science User Facility (Contract No. DE-AC02-06CH11357), National Science Foundation (U.S.) (NSF EECS Award No. 1541959), Martin Family Society of Fellows for Sustainability, National Science Foundation (U.S.). Graduate Research Fellowship (Grant No. 1122374), National Science Foundation (U.S.). (CA No. EEC-1041895)

There is no doubt about the potential offered by the low-cost fabrication and high efficiency of hybrid organic–inorganic perovskite solar cells. However, the service lifetimes of these devices must be increased from months to years to capitalize on their potential. The archetypal hybrid perovskite for solar cells, methylammonium lead iodide (CH3NH3PbI3, abbreviated MAPI), readily degrades in ambient atmosphere under standard operating conditions. Understanding the origin and effects of this degradation can pave the way to better engineer photovoltaic devices and the perovskite material itself. Herein we present the effects of varying pressure on the electrical performance of MAPI solar cells. Solar cell parameters, especially open circuit voltage, are significantly affected by the total ambient pressure and present an unexpected reversible behavior upon pressure cycling. We complement photoluminescence studies as a function of ambient atmosphere and temperature with first-principles density functional t...

In situ and operando measurement techniques combined with nanoscale resolution have proven invaluable in multiple fields of study. We argue that evaluating device performance as well as material behavior by correlative X-ray microscopy with

Statistical and correlative analysis are increasingly important in the design and study of new materials, from semiconductors to metals. Non-destructive measurement techniques, with high spatial resolution, capable of correlating composition and/or structure with device properties, are few and far between. For the case of polycrystalline and inhomogeneous materials, the added challenge is that nanoscale resolution is in general not compatible with the large sampling areas necessary to have a statistical representation of the specimen under study. For the study of grain cores and grain boundaries in polycrystalline solar absorbers this is of particular importance since their dissimilar behavior and variability throughout the samples makes it difficult to draw conclusions and ultimately optimize the material. In this study, we present a nanoscale in-operando approach based on the multimodal utilization of synchrotron nano x-ray fluorescence and x-ray beam induced current collected for grain core and grain boundary areas and correlated pixel-by-pixel in fully operational Cu ( In ( 1 − x ) Ga x ) Se 2 solar cells. We observe that low gallium cells have grain boundaries that over perform compared to the grain cores and high gallium cells have boundaries that under perform. These results demonstrate how nanoscale correlative X-ray microscopy can guide research pathways towards grain engineering low cost, high efficiency solar cells.

The reasons for the start and end of the induction period of cement hydration remain topic of controversy. One long-standing hypothesis is that a thin metastable hydrate forming on the surface of cement grains significantly reduces the particle dissolution rate; the eventual disappearance of this layer re-establishes higher dissolution rates at the beginning of the acceleration period. However, the importance, or even the existence, of this metastable layer has been questioned because it cannot be directly detected in most experiments. In this work, a combined analysis using nano-tomography and nano-X-ray fluorescence makes the direct imaging of early hydration products possible. These novel X-ray imaging techniques provide quantitative measurements of 3D structure, chemical composition, and mass density of the hydration products during the induction period. This work does not observe a low density product on the surface of the particle, but does provide insights into the formation of etch pits and the subsequent hydration products that fill them.

Spatial heterogeneities in the chemical makeup of thin film photovoltaic devices are pivotal in determining device efficiency. We report the in-plane spatial distribution and degree of chlorine incorporation in organic–inorganic lead halide perovskite absorbers by means of nondestructive synchrotron-based nanoprobe X-ray fluorescence. The presence of chlorine is positively identified in CH3NH3PbI3 films synthesized with Cl-containing precursors and as an impurity in some films synthesized with nominally Cl-free precursors. The impurity may be introduced from precursors or as contaminants during film synthesis. The films formed from Cl-containing precursors contain roughly an order of magnitude higher amount of chlorine, with Cl:I values greater than 0.02 found whether Cl is present in either the organic or the inorganic precursor for both one- and two-step fabrication processes. A spatial variation in the Cl incorporation is observed within single particles and as well as between particles within a given ...

Lead halide perovskites have emerged as promising absorber materials over the last decade to increase the efficiency of photovoltaics beyond its current limits. However, to further optimize the performance of perovskites more detailed studies need to be performed, which allow for the correlation of film morphology and local electronic properties at the nanoscale. Here, we present a scanning tunneling microscopy (STM) approach to probe the effect of an applied electric field of a methylammonium formamidinium lead triiodide perovskite thin film on the film response by current–voltage spectroscopy, current imaging tunneling spectroscopy, differential conductance mapping, and x-ray absorption spectroscopy by means of synchrotron x-ray STM. We find a strong correlation between the measurement conditions and the obtained current–voltage characteristics when imaging under opposite bias polarities. In particular, we find similarities to already observed poling effects for lead halide perovskites, which result in either a positively or negatively charged interface due to ion and vacancy migration. Our results provide insight into the influence of measurement conditions such as bias polarity on the performance assessment of perovskite thin films by STM.

Disagreements about the mechanisms of cement hydration remain despite the fact that portland cement has been studied extensively for over 100 years. One reason for this is that direct observation of the change in microstructure and chemistry are challenging for many experimental techniques. This paper presents results from synchrotron nano X-ray tomography and fluorescence imaging. The data show unprecedented direct observations of small collections of C3S particles before and after different periods of hydration in 15 mmol/L lime solution. X-ray absorption contrast is used to make three dimensional maps of the changes of these materials with time. The chemical compositions of hydration products are then identified with X-ray fluorescence mapping and scanning electron microscopy. These experiments are used to provide insight into the rate and morphology of the microstructure formation.

X-ray beam-induced damage in nanoscale metal islands was investigated. Monolayer-high Ni islands were prepared on a Cu(111) substrate. High brilliance X-rays with photon energies between 8.45 and 8.85 keV illuminated the sample for about 11 hours. In order to track changes in the morphology of the islands, the synchrotron X-ray scanning tunneling microscopy (SX-STM) technique was utilized. The result shows that X-ray illumination onto Ni islands does not induce noticeable damage. The study demonstrates that local beam-induced changes can be studied using SX-STM.

The efficiency of solar cells with a polycrystalline absorber is typically limited by grain boundaries. Many questions need to be answered such as: which roles do elemental and structural inhomogeneities play with respect to electrical performance? By which mechanisms does degradation occur and how can it be mitigated? The answers to these questions lie at the nanoscale. Ideally, we would measure performance, composition, and structure in-situ and operando all at once. Correlative, synchrotron-based X-ray microscopy offers a step in this direction. Here, we present a novel technique, X-ray beam induced voltage (XBIV) measurements, which complements the set of X-ray microscopy techniques. Combining the penetration depth of visible-light microscopy with the spatial resolution of electron-beam methods, XBIV measurements shine light on recombination and absorber-layer bandgap variations at nanoscale resolution. We give experimental details and discuss the use of lock-in amplification based on first applications of XBIV measurements to $\text{CuIn}_{x} \text{Ga}_{1}-x\text{Se}_{2}$ solar cells.

The root cause of light- and elevated temperature-induced degradation (LeTID) in multicrystalline silicon p-type passivated emitter and rear cell (PERC) devices is still unknown. Some researchers hypothesize that high temperature firing processes dissolve metal-rich precipitates which can then participate in LeTID. To address this hypothesis, synchrotron-based X-ray techniques, including fluorescence and absorption near-edge spectroscopy, are employed. In as-grown industrial material, we observe collocated copper- and nickel-rich precipitates, which persist after firing and are below the detection limit after phosphorous diffusion. We conclude that precipitates decrease in size due to the firing process and that this may result in an increase in bulk interstitial metal concentration. We further employ microphotoluminescence at a grain versus grain boundary to highlight similarities and possible differences in degradation and regeneration behavior.

While there is great interest in characterizing and modifying materials at the nanoscale, progress has been slow because few techniques allow for critical observations at this length scale. This work presents a data fusion technique that combines synchrotron-based X-ray nano computed tomography and nano X-ray fluorescence to non-destructively investigate complex nanoscale materials and provide combined three-dimensional (3-D) renderings of microstructure and chemistry. The technique has been named nano tomography-assisted chemical correlation (nTACCo) and is demonstrated on fly ash particles with nanoscale chemical inhomogeneities. Our findings show that nTACCo is capable of providing the concentration and location of seven different nano-inclusions within a particle. This work also provides direct observations of reactivity and chemical distribution of fly ash. This ability to combine 3-D structure and chemistry at the nanoscale will provide unprecedented tools for nanoscience in material science, biology, chemistry and medical science.

Synchrotron nanoprobe X-ray fluorescence maps show for the first time discrete iron-rich, titanium-rich and manganese/silicon-rich particles present in blast furnace slag grains, and these particles remain intact when the slag is used as a precursor for alkali-activated slag (AAS) binders. These particles appear to be entrained during slag production, and remain stable under the reducing conditions prevailing during alkali-activation. There is no evidence of chemical interaction between these particles and the AAS binder, which mainly comprises calcium silicate hydrates. These results are important for the understanding of iron chemistry in AAS, and the potential reactivity of metallic and other redox-sensitive species within AAS binders.

This review discusses recent progress in the development of hard X-ray microscopy techniques for materials characterization at the nanoscale. Although the utility of traditionally ensemble-based X-ray techniques in materials research has been widely recognized, the utility of X-ray techniques as a tool for local characterization of nanoscale materials properties has undergone rapid development in recent years. Owing to a confluence of improvements in synchrotron source brightness, focusing optics fabrication, detection, and data analysis, nanoscale X-ray imaging techniques have moved beyond proof-of-principle experiments to play a central role in synchrotron user programs worldwide with high-impact applications made to materials science questions. Here, we review the current state of synchrotron-based, hard X-ray nanoscale microscopy techniques—including 3D tomographic visualization, spectroscopic elemental and chemical mapping, microdiffraction-based structural analysis, and coherent methods for nanomaterials imaging—with particular emphasis on applications to materials research.

The combination of the high spatial resolution of scanning tunneling microscopy with the chemical and magnetic contrast provided by synchrotron X-rays has the potential to allow a unique characterization of advanced functional materials. While the scanning probe provides the high spatial resolution, synchrotron X-rays that produce photo-excitations of core electrons add chemical and magnetic contrast. However, in order to realize the method's full potential it is essential to maintain tunneling conditions, even while high brilliance X-rays irradiate the sample surface. Different from conventional scanning tunneling microscopy, X-rays can cause a transition of the tip out of the tunneling regime. Monitoring the reaction of the z-piezo (the element that controls the tip to sample separation) alone is not sufficient, because a continuous tip current is obtained. As a solution, an unambiguous and direct way of fingerprinting such near to far field transitions of the tip that relies on the simultaneous analysis of the X-ray-induced tip and sample current is presented. This result is of considerable importance because it opens the path to the ultimate resolution in X-ray enhanced scanning tunneling microscopy.

The effect of the activator concentration on the structure of alkali silicate-activated slag/metakaolin pastes is assessed through synchrotron radiation-based X-ray techniques. As main reaction products, both calcium aluminosilicate hydrate (C–A–S–H) and sodium/calcium aluminosilicate hydrate [(C,N)–A–S–H] type gels are formed in activated binders solely based on slag, along with the zeolitic products gismondine and garronite. In activated blended pastes, the inclusion of metakaolin in the binder hinders the formation of zeolite products, instead favoring the formation of a (C,N)–A–S–H type gel consistent with the activation of metakaolin in the presence of high concentrations of Ca. The formation of the two distinct binding products is confirmed by high-resolution X-ray fluorescence microscopy, where the “inner” products and the “outer” products have compositions consistent with (C,N)–A–S–H and C–A–S–H type gels, respectively. These results provide important new insights into the gel chemistry and micro/nanostructure of blended alkali-activated binder systems.

This paper presents the outcomes of a series of beamline-based studies, the results of which are combined to provide a more detailed multiscale understanding of the structure and chemistry of geopolymer binders. The range of beamline-based characterization techniques which have been applied to the study of geopolymer binders is increasing rapidly; although no single technique can provide a holistic view of binder structure across all the length scales which are of importance in determining strength development and durability, the synergy achievable through the combination of multiple beamline techniques is leading to rapid advances in knowledge in this area. Studies based around beamline infrared and X-ray fluorescence microscopy, in situ and ex situ neutron pair distribution function analysis, and nano- and micro-tomography, are combined to provide an understanding of geopolymer gel chemistry, nano- and microstructure in two and three dimensions, and the influences of seeded nucleation and precursor chemistry in these key areas. The application of advanced characterization methods in recent years has brought the understanding of geopolymer chemistry from a point, not more than a decade ago, when the analysis of the detailed chemistry of the aluminosilicate binder gel was considered intractable due to its disordered (“X-ray amorphous”) nature, to the present day where the influence of key compositional parameters on nanostructure is well understood, and both gel structure and reaction kinetics can be manipulated through methods including seeding, temperature variation, and careful mix design. This paper therefore provides a review outlining the value of nanotechnology – and particularly nanostructural characterization – in the development and optimization of a new class of environmentally beneficial cements and concretes. Key engineering parameters, in particularly strength development and permeability, are determined at a nanostructural level, and so it is essential that gel structures can be analyzed and manipulated at this level; beamline-based characterization techniques are critical in providing the ability to achieve this goal.

Here for the first time we describe the use of high resolution nanoprobe X-ray fluorescence (XRF) mapping for the analysis of artists’ paints, hierarchically complex materials typically composed of binder, pigments, fillers, and other additives. The work undertaken at the nanoprobe sought to obtain highly spatially resolved, highly sensitive mapping of metal impurities (Pb, Cd, Fe, and other metals) in submicron particles of zinc oxide pigments used in early 20th century artists’ tube paints and enamel paints, with particular emphasis on Ripolin, a popular brand of French house paint used extensively by Pablo Picasso and some of his contemporaries. Analysis revealed that the Zn oxide particles only contain a little Fe, proving that the highest quality Zn oxide pigment, free of Pb and Cd, was used for Ripolin house paints as well as artists’ paints. Nanoprobe XRF mapping also demonstrated that artists’ tube paints generally have more abundant fillers and additional whites (based on Pb, Ti, Ca) than Ripolin paints, which contain mostly pure zinc oxide. The chemical characterization of paints at the nanoscale opens the path to a better understanding of their fabrication and chemical reactivity.

The real-space observation of magnetic structure using scanning probe microscopy (SPM) methods or synchrotron-based microscopy continues to have a tremendous impact on our understanding of functional magnetic materials. However, although SPM methods provide high spatial resolution, they lack direct chemical contrast and the ability to quantify magnetic moments. X-ray microscopy, on the other hand, can provide chemical as well as magnetic sensitivity, but the spatial resolution is limited.

It is well known that the addition of alkali elements such as Na and K during and after growth of Cu(In, Ga)Se 2 (CIGS) has beneficial effects on the electronic properties of bulk material, improving device performance significantly. While the device level effects have been measured and reported, a direct observations of the localization of Na including its chemical nature are missing, and the impact of Na on elemental and phase segregation during CIGS growth is not fully understood. We investigate these aspects to shine light on the role of Na in CIGS solar cells with the ultimate goal of increasing their conversion efficiency. Utilizing a suite of synchrotron based x-ray characterization techniques, we discuss the challenges and advantages of these techniques for investigating segregation of main constituents of CIGS, Na distribution, chemical bonding of Na, and collection efficiency in CIGS as well as their correlations.

Spatial heterogeneities in the chemical makeup of thin film photovoltaic devices are pivotal in determining device efficiency. In this study, the presence of chlorine is identified in perovskite films synthesized with Cl-containing precursors by means of nanoprobe X-ray fluorescence (Nano-XRF). Additionally, a spatial variation in the Cl incorporation is observed within a given film, and the standard deviation of Cl: I ratio across the film is large. Using Nano-XRF, the Cl incorporation in methylammonium lead iodide perovskite films can be manipulated by precursor stoichiometry ratio.

Unveiling the correlation between elemental composition, fermi-level splitting, and charge collection in perovskite solar cells (PSCs) exposed to different environments is crucial to understanding the origin of defects. This will enable defect engineering to achieve high performing and long lasting perovskite solar cells. In this contribution we measured for the first time the spatial distribution and charge collection efficiency at the nano-scale by synchrotron-based x-ray fluorescence (XRF) and x-ray beam induced current (XBIC) with sub-grain resolution, and we observe a correlation between Pb/I ratio and charge collection efficiency. In contrast to other thin-film solar cells, perovskite solar cells are highly sensitive to ambient conditions (atmosphere and illumination). As the XRF and XBIC measurements were conducted in vacuum under an x-ray source illumination, the impact of measurement conditions on the measurements need to be taken into account. Furthermore, necessary conditions for quantification of XRF/XBIC measurements are not fulfilled for perovskite solar cells. Therefore, we will discuss fundamentals of XRF/XBIC measurements of perovskite solar cells that will enable reliable quantitative, high-resolution measurements of elemental distribution and charge collection.

A tunneling smart tip of a synchrotron X-ray scanning tunneling microscope provides simultaneously localized topographic, elemental and magnetic information., Localized spectroscopy with simultaneous topographic, elemental and magnetic information is presented. A synchrotron X-ray scanning tunneling microscope has been employed for the local study of the X-ray magnetic circular dichroism at the Fe L 2,3-edges of a thin iron film grown on Cu(111). Polarization-dependent X-ray absorption spectra have been obtained through a tunneling smart tip that serves as a photoelectron detector. In contrast to conventional spin-polarized scanning tunneling microscopy, X-ray excitations provide magnetic contrast even with a non-magnetic tip. Intensity variations in the photoexcited tip current point to chemical variations within a single magnetic Fe domain.

Durability of alkali-activated binders is of vital importance in their commercial application, and depends strongly on microstructure and pore network characteristics. X-ray microtomography (μCT) offers, for the first time, direct insight into microstructural and pore structure characteristics in three dimensions. Here, μCT is performed on a set of sodium metasilicate-activated fly ash/slag blends, using a synchrotron beamline instrument. Segmentation of the samples into pore and solid regions is then conducted, and pore tortuosity is calculated by a random walker method. Segmented porosity and diffusion tortuosity are correlated, and vary as a function of slag content (slag addition reduces porosity and increases tortuosity), and sample age (extended curing gives lower porosity and higher tortuosity). This is particularly notable for samples with ≥ 50% slag content, where a space-filling calcium (alumino)silicate hydrate gel provides porosity reductions which are not observed for the sodium aluminosilicate (‘geopolymer’) gels which do not chemically bind water of hydration.

Nanotomographic reconstruction of a sample of low-CO2 “geopolymer” cement provides the first three-dimensional view of the pore structure of the aluminosilicate geopolymer gel, as well as evidence for direct binding of geopolymer gel onto unreacted fly ash precursor particles. This is central to understanding and optimizing the durability of concretes made using this new class of binder, and demonstrates the value of nanotomography in providing a three-dimensional view of nanoporous inorganic materials.

Structural evolution in pastes produced from alkali silicate-activated granulated blast furnace slag (GBFS)/metakaolin (MK) blends is assessed. In the initial period of the reaction, the addition of MK leads to an increase in the total setting time, reduces the heat release, and affects the reaction mechanism by introduction of a large quantity of additional Al. This effect is more significant when an activating solution with a higher silicate modulus is used, and leads to a slight reduction in the final mechanical strength of mortars but a significant increase in setting time, which is valuable in the development of alkali-activated slag binders as these are known to sometimes harden more rapidly than is desirable. High-energy synchrotron X-ray diffractometry reveals that the main reaction products in alkali-activated GBFS/MK blends are segregated and partially crystalline calcium silicate hydrate and aluminosilicate phases, including a small component with a zeolitic (gismondine) structure. No hydrotalcite-type phases are observed in these samples, which are synthesized from a low-Mg slag. A secondary reaction product (Na-substituted C–S–H) is also identified in pastes activated with a modulus of solution of 2.0. Infrared spectroscopy carried out over a period of 180 days shows the development of the gel structure, with aluminum incorporation leading to an increase in the extent of crosslinking, and higher alkalinity giving a more depolymerized gel structure.

Magnetism at buried interfaces plays a crucial role in many emerging phenomena, but detection of interfacial magnetism in close proximity to a surface with elemental and chemical sensitivity is a challenging task. Here, we use low temperature synchrotron x-ray scanning tunneling microscopy to investigate x-ray magnetic circular dichroism and the near edge x-ray absorption fine structure of La0.67Sr0.33MnO3-LaNiO3 superlattices. In stark contrast to the weak magnetic signal of Mn when the La0.67Sr0.33MnO3 layers are located on top, a robust x-ray magnetic circular dichroism signal is detected when they are buried underneath the LaNiO3 layers. The near edge x-ray absorption fine structure reveals the valence states of manganese, while the oxygen K-edge x-ray absorption spectra show an increase in hole formation, indicating a cogent charge transfer at the LaNiO3/La0.67Sr0.33MnO3 interface. This work demonstrates that scanning tunneling microscopy can be extended to the synchrotron X-ray study of buried interfaces by controlling the tip-sample separation in the nanometer regime.

Accelerated carbonation is induced in pastes and mortars produced from alkali silicate-activated granulated blast furnace slag (GBFS)–metakaolin (MK) blends, by exposure to CO2-rich gas atmospheres. Uncarbonated specimens show compressive strengths of up to 63 MPa after 28 days of curing when GBFS is used as the sole binder, and this decreases by 40–50% upon complete carbonation. The final strength of carbonated samples is largely independent of the extent of metakaolin incorporation up to 20%. Increasing the metakaolin content of the binder leads to a reduction in mechanical strength, more rapid carbonation, and an increase in capillary sorptivity. A higher susceptibility to carbonation is identified when activation is carried out with a lower solution modulus (SiO2/Na2O ratio) in metakaolin-free samples, but this trend is reversed when metakaolin is added due to the formation of secondary aluminosilicate phases. High-energy synchrotron X-ray diffractometry of uncarbonated paste samples shows that the main reaction products in alkali-activated GBFS/MK blends are C–S–H gels, and aluminosilicates with a zeolitic (gismondine) structure. The main crystalline carbonation products are calcite in all samples and trona only in samples containing no metakaolin, with carbonation taking place in the C–S–H gels of all samples, and involving the free Na+ present in the pore solution of the metakaolin-free samples. Samples containing metakaolin do not appear to have the same availability of Na+ for carbonation, indicating that this is more effectively bound in the presence of a secondary aluminosilicate gel phase. It is clear that claims of exceptional carbonation resistance in alkali-activated binders are not universally true, but by developing a fuller mechanistic understanding of this process, it will certainly be possible to improve performance in this area.

High-speed beam choppers are a crucial part of time-resolved x-ray studies as well as a necessary component to enable elemental contrast in synchrotron x-ray scanning tunneling microscopy (SX-STM). However, many chopper systems are not capable of operation in vacuum, which restricts their application to x-ray studies with high photon energies, where air absorption does not present a significant problem. To overcome this limitation, we present a fully ultra-high vacuum (UHV) compatible chopper system capable of operating at variable chopping frequencies up to 4 kHz. The lightweight aluminum chopper disk is coated with Ti and Au films to provide the required beam attenuation for soft and hard x-rays with photon energies up to about 12 keV. The chopper is used for lock-in detection of x-ray enhanced signals in SX-STM.

In conventional magnetic materials, oxidation is a disagreeable effect that often lowers or destroys the magnetic capabilities of those materials. By contrast, we report on the decisive paramagnetic-ferromagnetic phase transition in CoAl(100) at room temperature, utilizing oxidation of stoichiometric CoAl. We also discuss the control and drastic increase of the coercive field by subsequent annealing of the oxidized sample. The alumina film grown by selective oxidation protects the alloy from oxidation of Co, despite the accumulation of Al vacancies and the resulting enrichment in Co of the metallic phase underneath the oxide film. As a result, a ferromagnetic thin Co-rich phase is formed at the interface between the insulating aluminum oxide and the paramagnetic Co50Al50 bulk. The creation via simple oxidation of a ferromagnetic thin film underneath a surface insulator demonstrates a novel path to building the majority of a magnetic tunnel junction. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

We have investigated the growth of Co nanoparticles on {theta}-Al{sub 2}O{sub 3}/CoAl(1 0 0) by means of Auger electron spectroscopy (AES), high-resolution electron energy loss spectroscopy (EELS), low energy electron diffraction (LEED) and scanning tunneling microscopy (STM). Due to Volmer--Weber growth, Co forms particles with a mean diameter of approximately 2.5 nm and height of 0.8 nm. Even on the entirely covered oxide, there is no Ostwald ripening and Co particles stay structurally isolated. The nanoparticles exhibit a small size distribution and tend to form chains, as predetermined by the streak structure of the oxide template. For sufficient high coverages Co-core-CoO-shell nanoparticles may be evidenced, which is explained as a result of surfactant oxygen. The nanostructured particles may open the door to numerous applications, such as in catalysis and magnetoelectronic applications, where large areas of ordered nanodots are desired.

The study of a multilayered and multicomponent system by spatially resolved X-ray fluorescence microscopy poses unique challenges in achieving accurate quantification of elemental distributions. This is particularly true for the quantification of materials with high X-ray attenuation coefficients, depth-dependent composition variations and thickness variations. A widely applicable procedure for use after spectrum fitting and quantification is described. This procedure corrects the elemental distribution from the measured fluorescence signal, taking into account attenuation of the incident beam and generated fluorescence from multiple layers, and accounts for sample thickness variations. Deriving from Beer–Lambert's law, formulae are presented in a general integral form and numerically applicable framework. The procedure is applied using experimental data from a solar cell with a Cu(In,Ga)Se2 absorber layer, measured at two separate synchrotron beamlines with varied measurement geometries. This example shows the importance of these corrections in real material systems, which can change the interpretation of the measured distributions dramatically.

We present the latest developments in the characterization of thin-film solar cells based on the combination of elemental mapping from fluorescence measurements using synchrotron x-rays, with beam induced current from electron and x-ray beams. This is a powerful method to directly correlate compositional variations with charge collection efficiency. We compare different approaches for mapping solar cells both in cross-section and in plan view on CIGS and CdTe solar cells. Based on examples from our latest research, we discuss the experimental approaches and highlight the advantages and limitations of each technique. Finally, we present an outlook to experiments that will allow x-ray based characterization to enter new fields of research that were not accessible before.

We have employed Auger electron spectroscopy (AES), high resolution electron energy loss spectroscopy (EELS), low energy electron diffraction (LEED) and scanning tunneling microscopy (STM) to investigate the growth of an Al2O3 film on CoAl(1 0 0). While exposure to oxygen at room temperature leads to the formation of amorphous alumina, subsequent annealing at higher temperatures results in the growth of well-ordered θ-Al2O3. Well-ordered Al2O3 films are also formed by oxidation at temperatures of 800 K and above. The oxide is characterized by Fuchs–Kliewer modes at around 430, 630, 780 and 920 cm−1. Oxide islands grow in two sets of domains perpendicular to each other. Under ultra-high vacuum conditions, self-limiting thickness of the oxide layer (9–10 A) has been found. The band gap of the θ-Al2O3 film on CoAl(1 0 0) is 4.3–4.5 eV.

The seventh edition of the international conference on Synchrotron Radiation and Neutrons in Art and Archaeology (SR2A 2016) was held September 6–8, 2016, at the Stock Exchange Room of The Art Institute of Chicago, USA. The conference was jointly organized by seven research laboratories and museums; more precisely, the Center for Scientific Studies in the Arts (NU-ACCESS) of Northwestern University, the Art Institute of Chicago, the Field Museum Chicago, the Advanced Photon Source (APS), the Oriental Institute Chicago, the Detroit Institute of Arts, and the Indianapolis Museum of Art, in close interaction with the SR2A International Committee. Nine years after the organization of the first SR2A conference in Grenoble, the Art Institute hosted the second biennial interdisciplinary meeting in the US.

The oxidation of a CoAl(1 0 0) surface at 300 K was studied by means of Auger electron spectroscopy, high resolution electron energy loss spectroscopy (EELS), low energy electron diffraction and scanning tunneling microscopy (STM). For an exposure ⩽0.3 L, the oxygen atoms are chemisorbed on the CoAl(1 0 0) surface, while for a larger O2 exposure the oxidation of the surface sets in. For an exposure ⩾300 L the surface is entirely covered with amorphous Al2O3 (a-Al2O3) whereas the Co atoms seem to be unaffected. The EEL spectra of a-Al2O3 exhibit Fuchs–Kliewer modes at around 640 and 890 cm−1. The thickness of the a-Al2O3 film is estimated to be 7.1 ± 0.7 A. The STM images show that the oxide grows as large islands which cover the whole surface. The band gap of the ultra-thin a-Al2O3 film on CoAl(1 0 0) is found to be 3.2 eV and thus it is strongly diminished with respect to the bulk value.

We use a nanofabricated scanning tunneling microscope tip as a detector to investigate local X-ray induced tunneling and electron emission from a single cobalt nanocluster on a Au(111) surface. The tip-detector is positioned a few angstroms above the nanocluster, and ramping the incident X-ray energy across the Co photoabsorption K-edge enables the detection of element specific electrons. Atomic-scale spatial dependent changes in the X-ray absorption cross section are directly measured by taking the X-ray induced current as a function of X-ray energy. From the measured sample and tip currents, element specific X-ray induced current components can be separated and thereby the corresponding yields for the X-ray induced processes of the single cobalt nanocluster can be determined. The detection of element specific synchrotron X-ray induced electrons of a single nanocluster opens an avenue for materials characterization on a one particle at-a-time basis.

By using synchrotron X-rays as a probe and a nanofabricated smart tip of a tunneling microscope as a detector, we have achieved chemical fingerprinting of individual nickel clusters on a Cu(111) surface at 2 nm lateral resolution, and at the ultimate single-atomic height sensitivity. Moreover, by varying the photon energy, we have succeeded to locally measure photoionization cross sections of just a single Ni nanocluster, which opens new exciting opportunities for chemical imaging of nanoscale materials.

The distributions of chemical elements within cells are of prime importance in a wide range of basic and applied biochemical research. An example is the role of the subcellular Zn distribution in Zn homeostasis in insulin producing pancreatic beta cells and the development of type 2 diabetes mellitus. We combined transmission electron microscopy with micro- and nano-synchrotron X-ray fluorescence to image unequivocally for the first time, to the best of our knowledge, the natural elemental distributions, including those of trace elements, in single organelles and other subcellular features. Detected elements include Cl, K, Ca, Co, Ni, Cu, Zn and Cd (which some cells were supplemented with). Cell samples were prepared by a technique that minimally affects the natural elemental concentrations and distributions and without using fluorescent indicators. It could likely be applied to all cell types and provide new biochemical insights at the single organelle level not available from organelle population level studies.

In order to achieve elemental and chemical sensitivity in scanning tunneling microscopy (STM), synchrotron x-rays have been applied to excite core-level electrons during tunneling. The x-ray photo-excitations result in tip currents that are superimposed onto conventional tunneling currents. While carrying important physical information, the varying x-ray induced currents can destabilize the feedback loop causing it to be unable to maintain a constant tunneling current, sometimes even causing the tip to retract fully or crash. In this paper, we report on an easy-to-implement filter circuit that can separate the x-ray induced currents from conventional tunneling currents, thereby allowing simultaneous measurements of topography and chemical contrasts. The filter and the schematic presented here can also be applied to other variants of light-assisted STM such as laser STM.