70 research outputs found
Impact of internal Faraday shields on RF driven hydrogen discharges
At RF plasma reactors operated at high power, internal Faraday shields are required to shield dielectric vessel or windows from erosion due to isotropic heat and particle fluxes. By utilizing a flexible and diagnostically well-equipped laboratory setup, crucial effects that accompany the application of internal Faraday shields at low-pressure hydrogen (and deuterium) RF discharges are identified and quantified in this contribution. Both an inductively coupled plasma (ICP) utilizing a helical coil and a low-field helicon discharge applying a Nagoya-type III antenna at magnetic fields of up to 12 mT are investigated. Discharges are driven at 4 MHz and in the pressure range between 0.3 and 10 Pa while the impact of the Faraday shields on both the RF power transfer efficiency and spectroscopically determined bulk plasma parameters (electron density and temperature, atomic density) is investigated. Three main effects are identified and discussed: (i) due to the Faraday shield, the measured RF power transfer efficiency is globally reduced. This is mainly caused by increased power losses due to induced eddy currents within the electrostatic shield, as accompanying numerical simulations by a self-consistent fluid model demonstrate. (ii) The Faraday shield reduces the atomic hydrogen density in the plasma by one order of magnitude, as the recombination rate of atoms on the metallic (copper) surfaces of the shield is considerably higher compared to the dielectric quartz walls. (iii) The Faraday shield suppresses the transition of the low-field helicon setup to a wave heated regime at the present conditions. This is attributed to a change of boundary conditions for wave propagation, as the plasma is in direct contact with the conductive surfaces of the Faraday shield rather than being operated in a laterally fully dielectric vessel
Evidence for electronically-driven ferroelectricity in the family of strongly correlated dimerized BEDT-TTF molecular conductors
By applying measurements of the dielectric constants and relative length
changes to the dimerized molecular conductor
-(BEDT-TTF)Hg(SCN)Cl, we provide evidence for order-disorder
type electronic ferroelectricity which is driven by charge order within the
(BEDT-TTF) dimers and stabilized by a coupling to the anions. According to
our density functional theory calculations, this material is characterized by a
moderate strength of dimerization. This system thus bridges the gap between
strongly dimerized materials, often approximated as dimer-Mott systems at 1/2
filling, and non- or weakly dimerized systems at 1/4 filling exhibiting charge
order. Our results indicate that intra-dimer charge degrees of freedom are of
particular importance in correlated -(BEDT-TTF)X salts and can
create novel states, such as electronically-driven multiferroicity or
charge-order-induced quasi-1D spin liquids.Comment: 6 pages, 4 figures + Supplementary Information (8 pages, 8 figures
DINI-Zertifikat 2013 - Request for Comments
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Characterisation of Human Embryonic Stem Cells Conditioning Media by 1H-Nuclear Magnetic Resonance Spectroscopy
BACKGROUND: Cell culture media conditioned by human foreskin fibroblasts (HFFs) provide a complex supplement of protein and metabolic factors that support in vitro proliferation of human embryonic stem cells (hESCs). However, the conditioning process is variable with different media batches often exhibiting differing capacities to maintain hESCs in culture. While recent studies have examined the protein complement of conditioned culture media, detailed information regarding the metabolic component of this media is lacking. METHODOLOGY/PRINCIPAL FINDINGS: Using a (1)H-Nuclear Magnetic Resonance ((1)H-NMR) metabonomics approach, 32 metabolites and small compounds were identified and quantified in media conditioned by passage 11 HFFs (CMp11). A number of metabolites were secreted by HFFs with significantly higher concentration of lactate, alanine, and formate detected in CMp11 compared to non-conditioned media. In contrast, levels of tryptophan, folate and niacinamide were depleted in CMp11 indicating the utilisation of these metabolites by HFFs. Multivariate statistical analysis of the (1)H-NMR data revealed marked age-related differences in the metabolic profile of CMp11 collected from HFFs every 24 h over 72 h. Additionally, the metabolic profile of CMp11 was altered following freezing at -20°C for 2 weeks. CM derived from passage 18 HFFs (CMp18) was found to be ineffective at supporting hESCs in an undifferentiated state beyond 5 days culture. Multivariate statistical comparison of CMp11 and CMp18 metabolic profiles enabled rapid and clear discrimination between the two media with CMp18 containing lower concentrations of lactate and alanine as well as higher concentrations of glucose and glutamine. CONCLUSIONS/SIGNIFICANCE: (1)H-NMR-based metabonomics offers a rapid and accurate method of characterising hESC conditioning media and is a valuable tool for monitoring, controlling and optimising hESC culture media preparation
Novel genetic loci associated with hippocampal volume
The hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness. Structural abnormalities in hippocampal volume and shape are found in several common neuropsychiatric disorders. To identify the genetic underpinnings of hippocampal structure here we perform a genome-wide association study (GWAS) of 33,536 individuals and discover six independent loci significantly associated with hippocampal volume, four of them novel. Of the novel loci, three lie within genes (ASTN2, DPP4 and MAST4) and one is found 200 kb upstream of SHH. A hippocampal subfield analysis shows that a locus within the MSRB3 gene shows evidence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure. Further, we show that genetic variants associated with decreased hippocampal volume are also associated with increased risk for Alzheimer's disease (rg =-0.155). Our findings suggest novel biological pathways through which human genetic variation influences hippocampal volume and risk for neuropsychiatric illness
Novel genetic loci underlying human intracranial volume identified through genome-wide association
Intracranial volume reflects the maximally attained brain size during development, and remains stable with loss of tissue in late life. It is highly heritable, but the underlying genes remain largely undetermined. In a genome-wide association study of 32,438 adults, we discovered five novel loci for intracranial volume and confirmed two known signals. Four of the loci are also associated with adult human stature, but these remained associated with intracranial volume after adjusting for height. We found a high genetic correlation with child head circumference (ρgenetic=0.748), which indicated a similar genetic background and allowed for the identification of four additional loci through meta-analysis (Ncombined = 37,345). Variants for intracranial volume were also related to childhood and adult cognitive function, Parkinson’s disease, and enriched near genes involved in growth pathways including PI3K–AKT signaling. These findings identify biological underpinnings of intracranial volume and provide genetic support for theories on brain reserve and brain overgrowth
Vaccination with intestinal tract antigens does not induce protective immunity in a permissive model of filariasis
Graphene-Based Nanocomposites for Energy Storage
Since the first report of using micromechanical cleavage method to produce graphene sheets in 2004, graphene/graphene-based nanocomposites have attracted wide attention both for fundamental aspects as well as applications in advanced energy storage and conversion systems. In comparison to other materials, graphene-based nanostructured materials have unique 2D structure, high electronic mobility, exceptional electronic and thermal conductivities, excellent optical transmittance, good mechanical strength, and ultrahigh surface area. Therefore, they are considered as attractive materials for hydrogen (H2) storage and high-performance electrochemical energy storage devices, such as supercapacitors, rechargeable lithium (Li)-ion batteries, Li–sulfur batteries, Li–air batteries, sodium (Na)-ion batteries, Na–air batteries, zinc (Zn)–air batteries, and vanadium redox flow batteries (VRFB), etc., as they can improve the efficiency, capacity, gravimetric energy/power densities, and cycle life of these energy storage devices. In this article, recent progress reported on the synthesis and fabrication of graphene nanocomposite materials for applications in these aforementioned various energy storage systems is reviewed. Importantly, the prospects and future challenges in both scalable manufacturing and more energy storage-related applications are discussed
The transcriptional landscape of age in human peripheral blood
Disease incidences increase with age, but the molecular characteristics of ageing that lead to increased disease susceptibility remain inadequately understood. Here we perform a whole-blood gene expression meta-analysis in 14,983 individuals of European ancestry (including replication) and identify 1,497 genes that are differentially expressed with chronological age. The age-associated genes do not harbor more age-associated CpG-methylation sites than other genes, but are instead enriched for the presence of potentially functional CpG-methylation sites in enhancer and insulator regions that associate with both chronological age and gene expression levels. We further used the gene expression profiles to calculate the 'transcriptomic age' of an individual, and show that differences between transcriptomic age and chronological age are associated with biological features linked to ageing, such as blood pressure, cholesterol levels, fasting glucose, and body mass index. The transcriptomic prediction model adds biological relevance and complements existing epigenetic prediction models, and can be used by others to calculate transcriptomic age in external cohorts.Peer reviewe
Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa
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