Activation level in boron-doped thin germanium-on-insulator (GeOI): Extraction method and impact of mobility

We hereby present a non-destructive method for extracting the activation level on boron-doped germanium-on-insulator (GeOI) wafers, with a discussion on the impact of the hole mobility model. This method combines Monte Carlo boron profile simulations with optical Ge layer thickness T_Ge and electrical sheet resistance R_sh measurements. As B atoms are known not to diffuse in Ge for the usual activation temperatures (<800 °C), we can assume that the as-implanted dopant profile remains unchanged after annealing (no modelling of boron diffusion required). We highlight that the knowledge of the hole mobility dependence on activated impurities concentration in Ge is of paramount importance. Several experimental and theoretical models are available in the literature. After relative validity assessments, all of them have been implemented for extraction and unfortunately yield different values scattered over nearly one decade. Still, the lower-bound concentration 2.7×10¹⁹ cm⁻³ is in the range of the state-of-the-art values for B-implanted crystalline Ge and has proven suitable for functional GeOI pMOSFET demonstration.     

RAFT controlled synthesis of six-armed biodegradable star polymeric architectures via a ‘core-first’ methodology

Six-armed biodegradable star polymers made from polystyrene (polySt), poly(polyethylene glycol) acrylate (polyPEG-A) and the block copolymer, polySt-b-polyPEG-A were synthesized using a ‘core-first’ methodology via RAFT polymerization. Disulfide linkages between the core and the arms conferred biodegradability on the stars. The star architectures were found to degrade rapidly on treatment with DL-dithiothreitol (DTT) and degrade more slowly in the presence of glutathione (GSH), the most abundant intracellular thiol tethered peptide. These star polymers were well characterized using gel permeation chromatography (GPC), nuclear magnetic resonance (NMR), electrospray ionization mass spectroscopy (ESI-MS) and dynamic light scattering (DLS).     

Release of Volatile Aldehydes by the Brown Algal Kelp Laminaria digitata in Response to Both Biotic and Abiotic Stress

With a little kelp from my friends : In response to biotic and abiotic stress, the brown algal kelp Laminaria digitata releases volatile fatty acid aldehydes under laboratory conditions and in its natural environment (red). In response to 4‐HHE treatment, L. digitata releases (13S)‐HOTrE (green). These results support the hypothesis that these compounds may mediate kelp responses to stress.

     

Acid and enzymic hydrolysis of Kappa carrageenan

Summary This paper describes the acid and enzymic hydrolysis of Kappa carrageenan and the gel permeation chromatography of the charged oligosaccharides.     

Liveness Checking as Safety Checking

Temporal logic is widely used for specifying hardware and software systems. Typically two types of properties are distinguished, safety and liveness properties. While safety can easily be checked by reachability analysis, and many efficient checkers for safety properties exist, more sophisticated algorithms have always been considered to be necessary for checking liveness. In this paper we describe an efficient translation of liveness checking problems into safety checking problems. A counter example is detected by saving a previously visited state in an additional state recording component and checking a loop closing condition. The approach handles fairness and thus extends to full LTL.     

Structure and Formation Kinetics of Millimeter-Size Single Domain Supercrystals

Organizing nanoparticles (NPs) into periodic structures is a central goal in materials science. Despite progress in the last decades, it is still challenging to produce macroscopic assemblies reliably. In this work, the analysis of the pervaporation-induced organization of gold octahedra into supercrystals within microfluidic channels using a combination of X-ray scattering techniques and FIB-SEM tomography is reported. The results reveal the formation of a single-domain supercrystal with a monoclinic C2/m symmetry and long-range order extending over the dimensions of the microfluidic channel, covering at least 1.7 × 0.3 mm². Time-resolved small angle X-ray scattering analysis shows that the formation of the superlattice involves an accumulation of the NPs within the channel before the nucleation and growth of the supercrystal. The orientation of the crystal remains unchanged during its formation, suggesting a growth mechanism directed by the channel interface. Together, these results show the potential application of the pervaporation strategy to providing spatially determined control over NP crystallization, which can be used for the rational fabrication of nanomaterial architectures.     

Aflatoxin Exposure during Early Life Is Associated with Differential DNA Methylation in Two-Year-Old Gambian Children

Background: DNA methylation is an epigenetic control mechanism that may be altered by environmental exposures. We have previously reported that in utero exposure to the mycotoxin and liver carcinogen aflatoxin B1 from the maternal diet, as measured using biomarkers in the mothers’ blood, was associated with differential DNA methylation in white blood cells of 6-month-old infants from The Gambia. Methods: Here we examined aflatoxin B1-associated differential DNA methylation in white blood cells of 24-month-old children from the same population (n = 244), in relation to the child’s dietary exposure assessed using aflatoxin albumin biomarkers in blood samples collected at 6, 12 and 18 months of age. HM450 BeadChip arrays were used to assess DNA methylation, with data compared to aflatoxin albumin adduct levels using two approaches; a continuous model comparing aflatoxin adducts measured in samples collected at 18 months to DNA methylation at 24 months, and a categorical time-dose model that took into account aflatoxin adduct levels at 6, 12 and 18 months, for comparison to DNA methylation at 24 months. Results: Geometric mean (95% confidence intervals) for aflatoxin albumin levels were 3.78 (3.29, 4.34) at 6 months, 25.1 (21.67, 29.13) at 12 months and 49.48 (43.34, 56.49) at 18 months of age. A number of differentially methylated CpG positions and regions were associated with aflatoxin exposure, some of which affected gene expression. Pathway analysis highlighted effects on genes involved with with inflammatory, signalling and growth pathways. Conclusions: This study provides further evidence that exposure to aflatoxin in early childhood may impact on DNA methylation.     

Donor‐Stabilized Phosphenium Adducts as New Efficient and Immobilizing Ligands in Palladium‐Catalyzed Alkynylation and Platinum‐Catalyzed Hydrogenation in Ionic Liquids

The straightforward synthesis of a new donor‐stabilized phosphenium ligand 3d by addition of bromodifurylphosphine to 1,3‐dimethylimidazolium‐2‐carboxylate 1 is described. The obtained ligand exhibits a very strong π‐acceptor character, comparable to that of triphenyl phosphite [P(OPh)₃] or of tris‐halogenophosphines, with a ν_CO(A₁) at 2087 cm⁻¹ for its nickel tricarbonyl complex. This ligand, as well as the related 3a which was obtained from chlorodiphenylphosphine, were tested in palladium‐catalyzed aryl alkynylation and in the platinum‐catalyzed selective hydrogenation of chloronitrobenzenes, both in an ionic liquid phase. In C C bond cross‐coupling we observed that the increase of the π‐acceptor character in ligand 3d , due to the introduction of an additional electron‐withdrawing group, provides a very efficient catalyst in the alkynylation reaction of aryl bromides with phenylacetylene, including the deactivated 4‐bromoanisole or the sterically hindered 2‐bromonaphthalene. The catalytic activity decreases with recycling due to the sensitiveness of ligands to protonation in the ionic phase. Conversely, a multiple recycling of the metal/ligand system in non‐acidic media was achieved from platinum‐catalyzed hydrogenation of m‐chloronitrobenzene. The catalytic results obtained by employing the complex of platinum(II) chloride with 3a [trans‐PtCl₂( 3a )₂] in comparison with the non‐ionic related trans‐tris(triphenylphosphine)platinum dichloride [trans‐PtCl₂(PPh₃)₂] complex clearly indicate that the simultaneous existence of a strong π‐acceptor character and a positive charge within the ligand 3a significantly increases the life‐time of the platinum catalyst. The selectivity of the reaction is also improved by decreasing the undesirable formation of dehalogenation products. This cationic platinum complex trans‐PtCl₂( 3a )₂ is the first example of a highly selective catalyst for hydrogenation of chloronitroarenes immobilized in an ionic liquid phase. The system was recycled six times without noticeable metal leaching in the organic phase, and no loss of activity.     

How Bromate and Ozone Concentrations Can be Modeled at Full-Scale Based on Lab-Scale Experiments – A Case Study

This article presents a full-scale modeling study of an industrial ozonation unit for practical application. The modeling framework combines an integrated hydraulic model (systematic network) with a quasi-mechanistic chemical model. Dealing with natural water, the chemical model has to be parameterized, and the parameters calibrated. This was done based on lab-scale experiments. The calibration results showed that the chemical model is able to account for changes in contact time with ozone, pH, temperature, ozone dose, NOM concentration, bromide concentration. Comparison of residence time distributions showed that the hydraulic model accurately reproduces flow conditions. Six sampling points were installed along an industrial ozonation unit of 487 m³ consisting of two baffled tanks in series. Bromate and ozone concentrations were monitored under varying operational process conditions. After the selection of a value for the k_La, simulations were run. Using the lab-scale calibrated models, simulated and experimental data were found in close agreement: 84% of the simulated concentrations for ozone matched measurements (±experimental error), 60 % for bromate. A readjustment of the kinetics of a single reaction (out of 65) showed that seasonal changes in NOM activity may easily be taken into account based on regular concentration measurements (90% of the bromate concentrations were then modeled accurately).