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Multiple lobes in the far-field distribution of terahertz quantum-cascade lasers due to self-interference

2016, Röben, B., Wienold, M., Schrottke, L., Grahn, H.T.

The far-field distribution of the emission intensity of terahertz (THz) quantumcascade lasers (QCLs) frequently exhibits multiple lobes instead of a single-lobed Gaussian distribution. We show that such multiple lobes can result from selfinterference related to the typically large beam divergence of THz QCLs and the presence of an inevitable cryogenic operation environment including optical windows. We develop a quantitative model to reproduce the multiple lobes. We also demonstrate how a single-lobed far-field distribution can be achieved.

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Discovery of chitin in skeletons of non-verongiid Red Sea demosponges

2018, Ehrlich, Hermann, Shaala, Lamiaa A., Youssef, Diaa T. A., Żółtowska- Aksamitowska, Sonia, Tsurkan, Mikhail, Galli, Roberta, Meissner, Heike, Wysokowski, Marcin, Petrenko, Iaroslav, Tabachnick, Konstantin R., Ivanenko, Viatcheslav N., Bechmann, Nicole, Joseph, Yvonne, Jesionowski, Teofil

Marine demosponges (Porifera: Demospongiae) are recognized as first metazoans which have developed over millions of years of evolution effective survival strategies based on unique metabolic pathways to produce both biologically active secondary metabolites and biopolymer-based stiff skeletons with 3D architecture. Up to date, among marine demosponges, only representatives of the Verongiida order have been known to synthetize biologically active substances as well as skeletons made of structural polysaccharide chitin. This work, to our knowledge, demonstrates for the first time that chitin is an important structural component within skeletons of non-verongiid demosponges Acarnus wolffgangi and Echinoclathria gibbosa collected in the Red Sea. Calcofluor white staining, FTIR and Raman analysis, ESI-MS, SEM, and fluorescence microscopy as well as a chitinase digestion assay were applied in order to confirm, with strong evidence, the finding of α-chitin in the skeleton of both species. We suggest that, the finding of chitin within these representatives of Poecilosclerida order is a promising step in the evaluation of these sponges as novel renewable sources for both biologically active metabolites and chitin, which are of prospective application for pharmacology and biomedicine.

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Comparison of nano-structured transition metal modified tri-metal MgMAl–LDHs (M = Fe, Zn, Cu, Ni, Co) prepared using co-precipitation

2019, Gevers, Bianca R., Naseem, Sajid, Leuteritz, Andreas, Labuschagné, Frederick J. W. J.

Comparison of layered double hydroxides (LDHs) synthesised using different methods, conditions and post-treatment is difficult to achieve because these greatly modify their material properties. This paper aims to provide a comparison of material properties for modified quintinite, where all LDHs were synthesised at the same conditions-thus allowing for direct comparison of the material properties obtained. Nano-structured materials were formed in all cases. The nano-structured transition metal (TM) MgMAl-LDHs were synthesised using constant pH co-precipitation. Five TMs (M = Fe, Co, Ni, Cu, Zn) were included in the LDH layers with molar substitutions of 0.5%, 1%, 5%, 10%, and 25% based on Mg-replacement for divalent TM cations and Al-replacement for trivalent TM cations. The materials were characterised using powder X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), scanning electron microscopy (SEM), attenuated total reflectance Fourier transform infrared analysis (ATR-FTIR), thermogravimetric analysis (TGA) and particle size analysis (PSA). The modified LDHs were synthesised free of major by-products and with similar morphologies. It could be shown that the crystallite dimensions varied between the different TM substitutions, that morphological changes were visible for some of the TMs used, that the processability depended on the TMs substituted, and that the substitution of TMs influenced the thermal stability of the LDHs. This journal is © 2019 The Royal Society of Chemistry.