90 research outputs found

    Minireview on Disordered Optical Metasurfaces

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    The use of coherent wave phenomena to enhance device performance is a cornerstone of modern optics. In juxtaposition to (locally) periodic metasurfaces, their disordered counterparts exhibit an interplay of destructive and constructive interferences occurring at the same spatial and spectral frequencies. This attribute provides disordered metasurfaces with a remarkable degree of flexibility, setting them apart from the constraints of periodic arrangements. Hereafter, we provide a concise overview of the cutting-edge developments and offer insights into the forthcoming research in this dynamic field

    Relationships between spectral features, iron oxides and colours of surface soils in northern Jordan

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    Ground data on spectral characteristics of Jordan's soils remain sparse, which makes the interpretation of remote sensing datasets challenging. These are, however, very useful for predicting soil properties and agricultural suitability. Previous studies have shown that soil colours correlate well with degrees of weathering intensity, as indicated by magnetic parameters and dithionite‐extractable iron (Fed) contents along a climosequence in northern Jordan. This study enlarges the database by the results of 160 bulk samples that were collected systematically from the soil surface at 40 locations. In addition to soil colour and contents of Fed, we explore mean soil reflectance spectra (MSRS) measured by analytical spectral devices (ASD) and analyse the morphological conditions of the spectra referring to the effects of iron oxides on spectral behaviours. Results show a high correlation of spectral behaviours and colour variations with Fe oxides, and no correlation with soil organic carbon Corg. The influence of the Fe oxide contents is clearly apparent in the visible range (VIS). The presence of CaCO3 increases the reflectance in all spectral ranges. Six soil groups (Gr. I ‐ Gr. VI) were discerned qualitatively and quantitatively in the study area, which largely mirror the intensity of red colour expressed by redness indices

    Multi-method study of the Middle Pleistocene loess–palaeosol sequence of Köndringen, SW Germany

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    Loess–palaeosol sequences (LPSs) remain poorly investigated in the southern part of the Upper Rhine Graben but represent an important element to understand the environmental context controlling sediment dynamics in the area. A multi-method approach applied to the LPS at Köndringen reveals that its formation occurred during several glacial–interglacial cycles. Field observations, as well as colour, grain size, magnetic susceptibility, organic carbon, and carbonate content measured in three profiles at 5 cm resolution, provide detailed stratigraphical information. Only minor parts of the LPS are made up of loess sediment, whereas the major parts are polygenetic palaeosols and pedosediments of varying development that are partly intersected, testifying to a complex local geomorphic evolution. The geochronological framework is based on 10 cm resolution infrared-stimulated luminescence (IRSL) screening combined with 18 multi-elevated-temperature post-IR IRSL ages. The luminescence ages indicate that two polygenetic, truncated Luvisols formed during marine isotope stages (MISs) 9(–7?) and MIS 5e, whereas unaltered loess units correspond to the last glacial (MISs 5d–2) and MIS 8. The channel-like structure containing the two truncated Luvisols cuts into &gt; 2 m thick pedosediments apparently deposited during MIS 12. At the bottom of the LPS, a horizon with massive carbonate concretions (loess dolls) occurs, which may correspond to at least one older interglacial.</p

    Sulfur-Functionalized Mesoporous Carbons as Sulfur Hosts in Li–S Batteries: Increasing the Affinity of Polysulfide Intermediates to Enhance Performance

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    The Li–S system offers a tantalizing battery for electric vehicles and renewable energy storage due to its high theoretical capacity of 1675 mAh g^(–1) and its employment of abundant and available materials. One major challenge in this system stems from the formation of soluble polysulfides during the reduction of S_8, the active cathode material, during discharge. The ability to deploy this system hinges on the ability to control the behavior of these polysulfides by containing them in the cathode and allowing for further redox. Here, we exploit the high surface areas and good electrical conductivity of mesoporous carbons (MC) to achieve high sulfur utilization while functionalizing the MC with sulfur (S–MC) in order to modify the surface chemistry and attract polysulfides to the carbon material. S–MC materials show enhanced capacity and cyclability trending as a function of sulfur functionality, specifically a 50% enhancement in discharge capacity is observed at high cycles (60–100 cycles). Impedance spectroscopy suggests that the S-MC materials exhibit a lower charge-transfer resistance compared with MC materials which allows for more efficient electrochemistry with species in solution at the cathode. Isothermal titration calorimetry shows that the change in surface chemistry from unfunctionalized to S-functionalized carbons results in an increased affinity of the polysulfide intermediates for the S–MC materials, which is the likely cause for enhanced cyclability

    Casting new light on the chronology of the loess/paleosol sequences in Lower Austria

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    Der vorliegende Artikel gibt einen Überblick ĂŒber neu datierte Abschnitte in bekannten Löss/PalĂ€oboden-Sequenzen Niederösterreichs. Die Ergebnisse der Datierungen im Profil Joching deuten darauf hin, dass es im letzten Hochglazial zur Lösssedimentation kam. Die meisten erfassten Alter sind jedoch Ă€lter als das letzte Hochglazial, was auf Erosionsprozesse hindeutet, die zur Abtragung der jĂŒngeren Lösse gefĂŒhrt hat. In dem Abschnitt zwischen ~28 ka and ~35 ka wurden ĂŒberwiegend Tundragleye gebildet. Eine intensivere interstadiale Bodenbildung ist nicht nachzuweisen. Dieses Ergebnis kann auch fĂŒr die stratigraphische Einstufung von ‚Stillfried B‘ (sensu Fink) von Bedeutung sein. Der folgende chronologische Abschnitt liegt zwischen ~35 ka and ~57 ka in Lösssedimenten mit eingeschalteten Tundragleyen. Auch dieser Abschnitt ist durch Umlagerungsprozesse charakterisiert. Im Zeitraum von ~57 ka bis ~106 ka befindet sich eine markante ZeitlĂŒcke, die vermutlich auf langandauernde und intensive Erosionsprozesse im Untersuchungsgebiet zurĂŒckzufĂŒhren ist. Die Ă€lteste Datierung in den Sedimenten des letzten Glazials mit 106 ± 12 ka befindet sich in Paudorf direkt ĂŒber dem ‚Stillfried A‘- Komplex (Paudorfer Bodenbildung). Direkt unter diesem Pedokomplex, bzw. vergleichbaren Pedokomplexen treten in Lössablagerungen Alter von 124 ± 2 5 ka (Göttweig-Aigen), 159 ± 20 ka (Paudorf 1), and 170 ± 16 ka (Joching) auf. DarĂŒber hinausgehende Alter konnten in Stratzing, Paudorf 2, Göttweig-Furth und Langenlois nachgewiesen werden

    Supramolecular nesting of cyclic polymers

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    Advances in template-directed synthesis make it possible to create artificial molecules with protein-like dimensions, directly from simple components. These synthetic macromolecules have a proclivity for self-organization that is reminiscent of biopolymers. Here, we report the synthesis of monodisperse cyclic porphyrin polymers, with diameters of up to 21 nm (750 C–C bonds). The ratio of the intrinsic viscosities for cyclic and linear topologies is 0.72, indicating that these polymers behave as almost ideal flexible chains in solution. When deposited on ​gold surfaces, the cyclic polymers display a new mode of two-dimensional supramolecular organization, combining encapsulation and nesting; one nanoring adopts a near-circular conformation, thus allowing a second nanoring to be captured within its perimeter, in a tightly folded conformation. Scanning tunnelling microscopy reveals that nesting occurs in combination with stacking when nanorings are deposited under vacuum, whereas when they are deposited directly from solution under ambient conditions there is stacking or nesting, but not a combination of both

    Spin Exchange Monitoring of the Strong Positive Homotropic Allosteric Binding of a Tetraradical by a Synthetic Receptor in Water

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