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Magnons have proven to be a promising candidate for low-power wave-based computing. The ability to encode information not only in amplitude but also in phase allows for increased data transmission rates. However, efficiently exciting nanoscale spin waves for a functional device requires sophisticated lithography techniques and therefore, remains a challenge. Here, we report on a method to measure the full spin wave isofrequency contour for a given frequency and field. A single antidot within a continuous thin film excites wave vectors along all directions within a single excitation geometry. Varying structural parameters or introducing Dzyaloshinskii–Moriya interaction allows the manipulation and control of the isofrequency contour, which is desirable for the fabrication of future magnonic devices. Additionally, the same antidot structure is utilized as a multipurpose spin wave device. Depending on its position with respect to the microstrip antenna, it can either be an emitter for short spin waves or a directional converter for incoming plane waves. Using simulations we show that such a converter structure is capable of generating a coherent spin wave beam. By introducing a short wavelength spin wave beam into existing magnonic gate logic, it is conceivable to reduce the size of devices to the micrometer scale. This method gives access to short wavelength spin waves to a broad range of magnonic devices without the need for refined sample preparation techniques. The presented toolbox for spin wave manipulation, emission, and conversion is a crucial step for spin wave optics and gate logic.

Vegetation and crops in agricultural areas are a significant source of both biogenic secondary organic aerosols and of directly emitted primary biological atmospheric particles (PBAPs) composed of ...

The interaction mechanisms of heavy metals with organo-Fe hydroxides co-precipitates (OFC) remain unclear due to the structural complexity of the OFC. In this study, batch experiments were conducted to investigate the immobilization mechanisms of Cr(III) by the OFC, which was prepared by co-precipitating Fe3+ with rice/rape straw-derived dissolved organic carbon, through sorption and co-precipitation using synchrotron-based X-ray absorption near-edge structure (XANES) spectroscopy and scanning transmission X-ray microscopy (STXM). At an Fe/C molar ratio ≥ 0.3, both the sorption and co-precipitation immobilized the majority of Cr(III), but the co-precipitation desorbed less Cr(III) than the sorption regardless of DOC loadings and sources. In contrast, Cr(III) immobilization was significantly reduced at an Fe/C molar ratio of 0.1 for both reactions. Linear combination fitting of Cr K-edge XANES spectra revealed the predominance of ferrihydrite-bound Cr(III), but enhanced organic Cr(III) occurred with increased organic carbon (OC) loading for both the sorption and co-precipitation. STXM coupled with multi-edge XANES analysis confirmed the primary association of Cr(III) with ferrihydrite and directly probed carboxyl as the binding site for Cr(III) retention on the OC constituents of the OFC. These results provided new molecular-level insights into the Cr(III) retention mechanisms on the OFC, particularly for the interactions of Cr(III) and OC constituents of the OFC, which could benefit the management of Cr-contaminated soils with straw returning.

Phosphorene, single- or few-layered black phosphorus, has been rediscovered as a promising two-dimensional material owing to its unique optical, thermal, and electrical properties with potential applications in optoelectronics, nanoelectronics, and energy storage. However, rapid degradation under ambient condition highly limits the practical applications of phosphorene. Solving the degradation problem demands an understanding of the oxidization process. We, for the first time, apply synchrotron-based X-ray photoelectron spectroscopy (XPS), X-ray absorption near-edge structure (XANES), and scanning transmission X-ray microscopy (STXM) for the nanoscale chemical imaging of phosphorene degradation. Through these methods, we have identified chemical details of the morphological effect and clarified thickness and proximity effects, which control the oxidization process. Furthermore, the entire oxidization process of phosphorene has also been studied by in situ XPS and XANES, showing the step-by-step oxidization process under the ambient condition. Theoretical calculations at the density functional theory level support experimental findings. This detailed study provides a better understanding of phosphorene degradation and is valuable for the development of phosphorene-based materials.

Selenium (Se) is an element of growing environmental concern, because low aqueous concentrations can lead to biomagnification through the aquatic food web. Biofilms, naturally occurring microbial consortia, play numerous important roles in the environment, especially in biogeochemical cycling of toxic elements in aquatic systems. The complexity of naturally forming multispecies biofilms presents challenges for characterization because conventional microscopic techniques require chemical and physical modifications of the sample. Here, multispecies biofilms biotransforming selenium oxyanions were characterized using X-ray fluorescence imaging (XFI) and scanning transmission X-ray microscopy (STXM). These complementary synchrotron techniques required minimal sample preparation and were applied correlatively to the same biofilm areas. Sub-micrometer XFI showed distributions of Se and endogenous metals, while Se K-edge X-ray absorption spectroscopy indicated the presence of elemental Se (Se0). Nanoscale carbon K-edge STXM revealed the distributions of microbial cells, extracellular polymeric substances (EPS), and lipids using the protein, saccharide, and lipid signatures, respectively, together with highly localized Se0 using the Se LIII edge. Transmission electron microscopy showed the electron-dense particle diameter to be 50-700 nm, suggesting Se0 nanoparticles. The intimate association of Se0 particles with protein and polysaccharide biofilm components has implications for the bioavailability of selenium in the environment.

Polarization dependent X-ray absorption spectroscopy (XAS) is a powerful probe of the anisotropic electronic structure of bulk single crystals, but its application to nanostructured samples is challenging. Here we describe a method for obtaining linearly polarized XAS spectra along three orthogonal axes of an individual nano-object using scanning transmission X-ray microscopy (STXM). The technique is applied to a single sodium titanate nanoribbon [(Na,H)Ti NR]. Significant linear dichroism is observed at both the Ti 2p and O 1s edges. The experimental results are compared with first-principles calculations; good agreement is achieved. The spectral changes among the three axes are attributed to the anisotropic Ti–O bonding of the various Ti and O sites in the monoclinic crystal structure of the nanoribbon. The methodology for 3D dichroic STXM measurements developed in this study is a powerful way to investigate the anisotropic geometric and electronic structure of nanomaterials.

The electronic structure of graphdiyne exposed to air is investigated utilizing X-ray absorption spectroscopy and scanning transmission X-ray microscopy. It is found that carbon–carbon triple bonds at defect sites in graphdiyne have been changed to double bonds after 3 months in air. The experimental results reveal the existence of oxygen and nitrogen functional groups and indicate that the oxidation takes place throughout the aged graphdiyne while the nitrogen contamination is mainly on its surface. Buckling of the aged graphdiyne is observed, resulting from bond length change due to the opening of triple bonds. It is also shown that annealing at a high temperature such as 800 °C may remove most of the functional groups in the aged graphdiyne.

The electronic structure of individual carbon nanotubes (CNTs) with different diameters has been investigated by scanning transmission X-ray microscopy (STXM). Various factors that may alter the STXM spectral features in CNT bundles have been discussed. Tube diameter has been found to be proportional to the spectral intensity, whereas it has negligible effect on the spectral shape. Disordered structure in CNTs introduced in the synthesis process was observed, which significantly affected the X-ray absorption spectrum by a reduction of the π* excitation. Moreover, tube–tube interaction in CNT bundles was detected, which can enhance the π* excitation. Insights into the nature of CNT bundles with various electronic structures may provide a new vision to understand the performance of CNT-based devices.

The C 1s inner shell excitation spectra of individual metallic and semiconducting single-walled carbon nanotubes (SWCNTs) were measured using high-resolution electron energy loss spectroscopy in an aberration-corrected transmission electron microscope (TEM-EELS). On the basis of its diameter, the metallic SWCNT is most likely a (10,10) sample, whereas (11,12) and a number of other chiral vectors are consistent with the diameter of the semiconducting SWCNTs. The C 1s X-ray absorption spectra of the same electronically pure SWCNT materials were measured as individual bundles or agglomerations of bundles by scanning transmission X-ray microscopy. Spectral differences in the C 1s → π* transitions of metallic and semiconducting species, related to differences in the van Hove singularities in their unoccupied states, are observed by both methods. The fine structure of the C 1s → π* transitions is similar to that recently reported from nonspatially resolved X-ray absorption spectroscopy of ensemble samples of high-purity metallic and semiconducting SWCNTs. The quality of the TEM-EELS spectra of individual SWCNTs is such that the line shape can be used to identify if they are metallic or semiconducting, thereby opening up the possibility to interrogate the electronic state of single-SWCNT devices. A strong X-ray linear dichroism in the C 1s → π* band of both types of SWCNTs was observed.

An important feature of microbial communities is the spatial heterogeneity of extracellular chemistry. Scanning transmission X-ray microscopy (STXM) was used to map the spatial distribution of iron speciesthroughout Pseudomonas aeruginosa biofilms to assess the influence of chemical heterogeneity on biomineralization. P. aeruginosa biofilms were treated with Fe(III)-amended media. Speciation and quantitative mapping using STXM image sequences in the Fe 2p(3/2) (L3) absorption edge region revealed both Fe(II) and Fe(III) in localized microenvironments. Fe(III) was mainly associated with cell surfaces, while small amounts of Fe(II) was found in the extracellular space. Biofilms were also characterized using C 1s edge STXM image sequences. Anaerobic growth assays and confocal microscopy revealed the inability of P. aeruginosa to directly reduce Fe(III), implicating indirect iron reduction mechanisms in the formation of fine-grained, multivalent minerals. These studies suggest that geochemical microenvironments found throughout microbial communities are even more complex than previously believed.

Scanning transmission X-ray microscopy (STXM) has been used to probe the electronic structure of individual multiwall carbon nanotubes by chemical mapping at the nanoscale. Carbon 1s near-edge X-ray absorption fine structure (NEXAFS) spectra of individual structures are shown to be able to differentiate carbon nanotubes from onionlike carbon nanoparticles and to differentiate nanotubes synthesized by different growth methods. Imaging of the very same region by both STXM and transmission electron microscopy is shown to be a very useful and complementary approach.

Carbonaceous particles originating from biomass burning can account for a large fraction of organic aerosols in a local environment. Presently, their composition, physical and chemical properties, as well as their environmental effects are largely unknown. Tar balls, a distinct type of highly spherical carbonaceous biomass burn particles, have been observed in a number of field campaigns. The Yosemite Aerosol Characterization Study that took place in summer 2002 occurred during an active fire season in the western United States; tar balls collected during this field campaign are described in this article. Scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure spectroscopy are used to determine the shape, structure, and size-dependent chemical composition of approximately 150 individual spherical particles ranging in size from 0.15 to 1.2 mum. The elemental composition of tar balls is approximately 55% atomic carbon and approximately 45% atomic oxygen. Oxygen is present primarily as carboxylic carbonyls and oxygen-substituted alkyl (O-alkyl-C) functional groups, followed by moderate amounts of ketonic carbonyls. The observed chemical composition, density, and carbon functional groups are distinctly different from soot or black carbon and more closely resemble high molecular weight polymeric humic-like substances, which could account for their reported optical properties. A detailed examination of the carboxylic carbonyl and O-alkyl-C functional groups as a function of particle size reveals a thin oxygenated interface layer. The high oxygen content, as well as the presence of water-soluble carboxylic carbonyl groups, could account for the reported hygroscopic properties of tar balls. The presence of the oxygenated layer is attributed to atmospheric processing of biomass burn particles.

In situ characterization of colloidal particles under hydrous conditions is one of the key requirements for understanding their state of aggregation and impact on the transport of pollutants in aqueous environments. Scanning transmission X-ray microscopy (STXM) is one of the few techniques that can satisfy this need by providing element- and chemical-state-specific 2-D maps at a spatial resolution better than 50 nm using soft X-rays from synchrotron radiation wiggler or undulator sources tuned to the absorption edges of different elements. X-ray absorption near-edge structure (XANES) spectra can also be collected simultaneously at a similar spatial resolution and can provide phase identification in many cases. In this study, we report STXM images and XANES spectroscopy measurements at or above the Al K-edge (E = 1559.6 eV) of various Al-containing minerals and synthetic oxides [alpha-Al2O3 (corundum), gamma-Al2O3, gamma-AlOOH (boehmite), alpha-Al(OH)3 (bayerite), KAl2(AlSi3O10)(OH)2 (muscovite), (Al,Mg)8(Si4O10)4(OH)8.nH2O (montmorillonite), and Mg6Al2(OH)16CO3.4H2O (hydrotalcite)] and demonstrate the capability of this spectromicroscopic tool to identify different Al-containing mineral colloids in multiphase mixtures in aqueous solution. We also demonstrate that STXM imaging at or above the C K-edge (E = 284.2 eV) and Al K-edge can provide unique information on the interactions between bacteria and Al-containing nanoparticles in aqueous suspensions. STXM images of a mixture of Caulobacter crescentus and montmorillonite and corundum particles just above the C and Al K-edges show that the mineral particles and bacteria are closely associated in aggregates, which is likely due to the binding of bacteria to clay and corundum particles by extracellular polysaccharides.

Scanning transmission X-ray microscopy (STXM) was used to spatially map aromatic and aliphatic carbon distributions in ultramicrotomed coal thin sections at the submicron level. In addition, microfocus X-ray absorption spectra recorded at the carbon K absorption edge allowed analysis of the variations in fundamental chemistry at maceral interfaces and within maceral boundaries. The ability of STXM to map the chemical composition of coal to this resolution has provided rich detail into the chemical and physical heterogeneity of macerals and of submaceral domains, as well as to the identification of microfine mineral particles that are present