Band structure and electronic transport across Ta2O5/Nb:SrTiO3 interfaces

Resistive switching devices promise significant progress in memory and logic technologies. One of the hurdles toward their practical realization is the high forming voltages required for their initial activation, which may be incompatible with standard microelectronic architectures. This work studies the conduction mechanisms of Ta2O5 layers, one of the most studied materials for memristive devices, in their initial, as-fabricated state (“pre-forming”). By separating this aspect and resolving the current mechanisms, we provide the input that may guide future design of resistive switching devices. For this purpose, Ta2O5 layers were sputtered on conductive Nb:SrTiO3 substrates. Ta2O5/Nb:SrTiO3 structures exhibit diode behavior with an ideality factor of n ≈ 1.3 over four current decades. X-ray photoelectron spectroscopy analysis of the interfacial band offsets reveals a barrier of 1.3 ± 0.3 eV for electrons injected from the semiconductor into Ta2O5. Temperature-dependent current–voltage analysis exhibits rectifying behavior. While several conduction mechanisms produce good fits to the data, comparing the physical parameters of these models to the expected physical parameters led us to conclude that trap-assisted tunneling (TAT) is the most likely conduction mechanism. Fitting the data using a recent TAT model and with the barrier that was measured by spectroscopy fully captures the temperature dependence, further validating this conduction mechanism.Fil: Miron, Dror. Technion - Israel Institute of Technology; IsraelFil: Cohen Azarzar, Dana. Technion - Israel Institute of Technology; IsraelFil: Segev, Noa. Technion - Israel Institute of Technology; IsraelFil: Baskin, Maria. Technion - Israel Institute of Technology; IsraelFil: Palumbo, Félix Roberto Mario. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Tecnológica Nacional. Facultad Regional Buenos Aires. Unidad de Investigación y Desarrollo de las Ingenierías; ArgentinaFil: Yalon, Eilam. Technion - Israel Institute of Technology; IsraelFil: Kornblum, Lior. Technion - Israel Institute of Technology; Israe

Dynamic assessment of the tear film muco-aqueous and lipid layers using a novel tear film imager (TFI)

Purpose The objective of the study was to assess a new technology, the tear film imager (TFI), which can dynamically image the muco-aqueous and lipid layers. Methods Prospective pilot case series of individuals with and without dry eye (DE). Two sequential images were obtained with the TFI. Measurements were assessed for reproducibility and compared with clinically derived DE metrics. Individuals were grouped into DE categories based on signs of DE. Results 49 patients participated in the study with a mean age of 58.8 years (SD 15.9) and a female majority (69%). Reproducibility of the muco-aqueous layer thickness (MALT) was excellent (r=0.88). MALT measurements significantly correlated with the Schirmer score (r=0.31). Lipid break up time (LBUT) as measured by the TFI significantly correlated with the clinical measure of tear break up time (TBUT) (r=0.73). MALT and LBUT were significantly thinner and shorter, respectively, in the DE groups (mild–moderate and severe) compared with the control group. When comparing TFI parameters to clinically assessed signs, sensitivity of the device was 87% and specificity was 88%. Conclusion The TFI is the first machine capable of reproducibly measuring muco-aqueous thickness in human subjects which correlates with Schirmer score. In parallel, it assesses other important aspects of tear film function which correlate with clinician assessed DE metrics

Muscle-Bound Primordial Stem Cells Give Rise to Myofiber-Associated Myogenic and Non-Myogenic Progenitors

Myofiber cultures give rise to myogenic as well as to non-myogenic cells. Whether these myofiber-associated non-myogenic cells develop from resident stem cells that possess mesenchymal plasticity or from other stem cells such as mesenchymal stem cells (MSCs) remain unsolved. To address this question, we applied a method for reconstructing cell lineage trees from somatic mutations to MSCs and myogenic and non-myogenic cells from individual myofibers that were cultured at clonal density

Resolution Revolution—Seeing the Molecules of Life With Electron Cryomicroscopy

Peer reviewed: TrueAcknowledgements: We thank Alex Bernstein for providing the figures and Susan Debad for copyediting the manuscript.This article is based on an interview between the two authors.Structural biology is a field that seeks to find the structures of all the components that make up living things—from molecules that exist in humans and other animals, through molecules present in tiny microorganisms, to the molecules that make up plants. To determine these structures, structural biologists use sophisticated imaging techniques that are becoming more and more accurate at “seeing”, or determining the structure of smaller and more diverse molecules. Electron cryomicroscopy is one very advanced and powerful imaging technique. In this technique, electrons are sent through frozen specimens to determine the structures of single molecules, at magnifications that are enough to see atoms. These images are taking us one step further toward understanding the structure and function of the basic building blocks of life. In this article, we will tell you about the developments that led to what is called “the resolution revolution” in electron cryomicroscopy, which Dr. Henderson was part of and that eventually allowed him to share the Nobel Prize in Chemistry in 2017.</jats:p

An efficient analytical reduction of detailed nonlinear neuron models

Detailed conductance-based nonlinear neuron models consisting of thousands of synapses are key for understanding of the computational properties of single neurons and large neuronal networks, and for interpreting experimental results. Simulations of these models are computationally expensive, considerably curtailing their utility. Neuron_Reduce is a new analytical approach to reduce the morphological complexity and computational time of nonlinear neuron models. Synapses and active membrane channels are mapped to the reduced model preserving their transfer impedance to the soma; synapses with identical transfer impedance are merged into one NEURON process still retaining their individual activation times. Neuron_Reduce accelerates the simulations by 40–250 folds for a variety of cell types and realistic number (10,000–100,000) of synapses while closely replicating voltage dynamics and specific dendritic computations. The reduced neuron-models will enable realistic simulations of neural networks at unprecedented scale, including networks emerging from micro-connectomics efforts and biologically-inspired “deep networks”. Neuron_Reduce is publicly available and is straightforward to implement

Colon Stem Cell and Crypt Dynamics Exposed by Cell Lineage Reconstruction

Stem cell dynamics in vivo are often being studied by lineage tracing methods. Our laboratory has previously developed a retrospective method for reconstructing cell lineage trees from somatic mutations accumulated in microsatellites. This method was applied here to explore different aspects of stem cell dynamics in the mouse colon without the use of stem cell markers. We first demonstrated the reliability of our method for the study of stem cells by confirming previously established facts, and then we addressed open questions. Our findings confirmed that colon crypts are monoclonal and that, throughout adulthood, the process of monoclonal conversion plays a major role in the maintenance of crypts. The absence of immortal strand mechanism in crypts stem cells was validated by the age-dependent accumulation of microsatellite mutations. In addition, we confirmed the positive correlation between physical and lineage proximity of crypts, by showing that the colon is separated into small domains that share a common ancestor. We gained new data demonstrating that colon epithelium is clustered separately from hematopoietic and other cell types, indicating that the colon is constituted of few progenitors and ruling out significant renewal of colonic epithelium from hematopoietic cells during adulthood. Overall, our study demonstrates the reliability of cell lineage reconstruction for the study of stem cell dynamics, and it further addresses open questions in colon stem cells. In addition, this method can be applied to study stem cell dynamics i