1,083 research outputs found

    Understanding the Role Thin Film Interfaces Play in Solar Cell Performance and Stability

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    As more efficient and cost-effective photovoltaic (PV) architectures are developed, solar becomes an ever more competitive and viable replacement for fossil fuels. Full grid electrification necessitates the development of efficient, reliable, cost-effective technologies - and there is room for many different kinds of PV in this expanding market. The practical challenges and constraints of terawatt PV production have brought scalability and durability into sharp scientific focus. From a materials perspective, there are commonalities in the materials questions and challenges across different PV technologies. Whereas most PV technology is referred to by the absorber layer - e.g. silicon, or perovskite solar cells, other layers in the device are equally important to performance and durability. These layers are often composed of metal oxides, and are common across device technologies - for example, interfacial layers (such as charge transport layers, CTLs), and transparent conducting oxides (TCOs) used as electrodes.This work addresses materials oxide characterization and its relationship to materials and device performance and degradation across PV technologies. Among the most promising PVs to date are two technologies with different levels of thin film incorporation: silicon heterojunction (SHJ) and perovskite PV. SHJ cells are part of the industrial Si PV portfolio, and perovskite cells are starting to be commercially produced after a decade of intensive research. However, there are well-known stability and cost limitations associated with each technology. Understanding the thin film materials science in these devices, and using that understanding to enhance device performance and stability is key to more reliable and cost effective electricity production. Under practical aging conditions, careful materials-level characterization is required to understand the degradation mechanisms of these materials and the complex effects of aging on the multilayer system. This work details the effects of practical degradation challenges such as damp heat (DH) exposure and encapsulation degradation on the stability of inorganic metal oxides in both the SHJ and perovskite thin film photovoltaic architectures. For perovskite devices, MAPbI3 films were deposited by spin coating onto a range of substrates and CTLs; substrates of glass and indium tin oxide (ITO) were paired with metal oxides (MOs) including MoOX, NiOX, and ZnO. SE and SEM were used to characterize the surface and bulk properties of the perovskite films. Results demonstrate that the underlying layers affect the rate of absorber degradation when exposed to heat and moisture. Unencapsulated SHJ cells (a subset of which were exposed to low concentrations of acetic acid under an applied voltage) were aged under DH 85°C/85% relative humidity conditions. The contact-ITO interface was examined via optical profilometry (OP), spectroscopic ellipsometry (SE), and scanning electron microscopy (SEM). SHJ cells have interfaces unique to their architecture, namely the c-Si/a-Si:H and a-Si:H/ITO interfaces at the top of the device. Examining the degradation of unencapsulated SHJ cells and comparing those results to historical degradation profiles of encapsulated SHJ cells in addition to the simulated effects of acetic acid exposure will help to decouple the effects of encapsulation on ITO stability in this architecture. It is well known that ethylene vinyl acetate (EVA) encapsulation degrades and produces acetic acid upon exposure to heat and humidity. When under an applied voltage, even small concentrations of acetic acid can quickly corrode the contact-ITO interface, leading to decreases in efficiency and increases in series resistance of the cell. Here, XPS was used to monitor the changes in the front contact of the SHJ cells during DH and acetic acid exposure. Changes to the materials will be correlated to changes in device performance under the same aging conditions

    Cardiopulmonary assessment in primary ciliary dyskinesia.

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    Background Primary ciliary dyskinesia (PCD) is a rare, usually autosomal recessive disorder of ciliary dysfunction associated with lung involvement, which has a great impact on health. There is limited information concerning the aerobic fitness of children and adolescents with PCD. The aim of this study was to assess cardiopulmonary functional capacity and its relationship with pulmonary function and physical activity (PA) levels in patients with PCD. Design Ten patients with PCD (age 13·2±2·8years) underwent spirometry and cardiopulmonary exercise testing. PA was investigated through a questionnaire. Eight age- and body mass index-matched healthy children were enrolled as controls. Main variables were forced expiratory volume at 1s, peak oxygen uptake (VO 2peak) and time spent in PA. Results Forty per cent of patients with PCD had impaired lung function as expressed by FEV 1<85% predicted. Only patients with impaired lung function exhibited reduced VO 2peak (18·1±7·9mL/kg/min). Time spent in total daily PA was slightly lower in patients than controls, with no difference between patients with normal or reduced lung function. In multiple regression models, male gender (??=0·518, P=0·018), age (??=0·752, P=0·035) and time spent in vigorous PA (??=0·353, P=0·049) were independent predictors of aerobic fitness. Conclusions Assessment of resting pulmonary function and cardiopulmonary functional capacity could contribute to the evaluation of pulmonary impairment in PCD. Given the benefit of physical exercise on airway clearance and on general health and quality of life, patients with PCD should be encouraged to adopt an active lifestyle

    The Non-Canonical Wnt/PKC Pathway Regulates Mitochondrial Dynamics through Degradation of the Arm-Like Domain-Containing Protein Alex3

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    The regulation of mitochondrial dynamics is vital in complex cell types, such as neurons, that transport and localize mitochondria in high energy-demanding cell domains. The Armcx3 gene encodes a mitochondrial-targeted protein (Alex3) that contains several arm-like domains. In a previous study we showed that Alex3 protein regulates mitochondrial aggregation and trafficking. Here we studied the contribution of Wnt proteins to the mitochondrial aggregation and dynamics regulated by Alex3. Overexpression of Alex3 in HEK293 cells caused a marked aggregation of mitochondria, which was attenuated by treatment with several Wnts. We also found that this decrease was caused by Alex3 degradation induced by Wnts. While the Wnt canonical pathway did not alter the pattern of mitochondrial aggregation induced by Alex3, we observed that the Wnt/PKC non-canonical pathway regulated both mitochondrial aggregation and Alex3 protein levels, thereby rendering a mitochondrial phenotype and distribution similar to control patterns. Our data suggest that the Wnt pathway regulates mitochondrial distribution and dynamics through Alex3 protein degradation

    A factor analytic study of the Italian National Institute of Health Quality of Life – Core Evaluation Form (ISSQoL-CEF)

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    Objectives: The Italian National Institute of Health Quality of Life - Core Evaluation Form (ISSQoL-CEF) is a specific questionnaire measuring health-related quality of life for human immunodeficiency virus-infected people in the era of highly active antiretroviral therapy. The main goal of this study was to examine the construct validity of this questionnaire by confirmation of its hypothesized dimensional structure. Methods: Baseline quality of life data from four clinical studies were collected and a confirmatory factor analysis of the ISSQoL-CEF items was carried out. Both first-order and secondorder factor models were tested: Model 1 with nine correlated first-order factors; Model 2 with three correlated second-order factors (Physical, Mental, and Social Health); Model 3 with two correlated second-order factors (Physical and Mental/Social Health); Model 4 with only one second-order factor (General Health). Results: A total of 261 patients were surveyed. Model 1 had a good fit to the data. Model 2 had an acceptable fit to the data and it was the best of all hierarchical models. However, Model 2 fitted the data worse than Model 1. Conclusions: The findings of in this study, consistent with the results of previous study, pointed out the construct validity of the ISSQoL-CEF. © 2010 Lauriola et al, publisher and licensee Dove Medical Press Ltd

    Beam test, simulation, and performance evaluation of PbF2_2 and PWO-UF crystals with SiPM readout for a semi-homogeneous calorimeter prototype with longitudinal segmentation

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    Crilin (Crystal Calorimeter with Longitudinal Information) is a semi-homogeneous, longitudinally segmented electromagnetic calorimeter based on high-ZZ, ultra-fast crystals with UV-extended SiPM readout. The Crilin design has been proposed as a candidate solution for both a future Muon Collider barrel ECAL and for the Small Angle Calorimeter of the HIKE experiment. As a part of the Crilin development program, we have carried out beam tests of small (10×10×4010\times10\times40~mm3^3) lead fluoride (PbF2_2) and ultra-fast lead tungstate (PbWO4_4, PWO) crystals with 120~GeV electrons at the CERN SPS to study the light yield, timing response, and systematics of light collection with a proposed readout scheme. For a single crystal of PbF2_2, corresponding to a single Crilin cell, a time resolution of better than 25~ps is obtained for >>3 GeV of deposited energy. For a single cell of \pwo, a time resolution of better than 45~ps is obtained for the same range of deposited energy. This timing performance fully satisfies the design requirements for the Muon Collider and HIKE experiments. Further optimizations of the readout scheme and crystal surface preparation are expected to bring further improvements

    The Pervasive Effects of ER Stress on a Typical Endocrine Cell: Dedifferentiation, Mesenchymal Shift and Antioxidant Response in the Thyrocyte

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    none13noThe endoplasmic reticulum stress and the unfolded protein response are triggered following an imbalance between protein load and protein folding. Until recently, two possible outcomes of the unfolded protein response have been considered: life or death. We sought to substantiate a third alternative, dedifferentiation, mesenchymal shift, and activation of the antioxidant response by using typical endocrine cells, i.e. thyroid cells. The thyroid is a unique system both of endoplasmic reticulum stress (a single protein, thyroglobulin represents the majority of proteins synthesized in the endoplasmic reticulum by the thyrocyte) and of polarized epithelium (the single layer of thyrocytes delimiting the follicle). Following endoplasmic reticulum stress, in thyroid cells the folding of thyroglobulin was disrupted. The mRNAs of unfolded protein response were induced or spliced (X-box binding protein-1). Differentiation was inhibited: mRNA levels of thyroid specific genes, and of thyroid transcription factors were dramatically downregulated, at least in part, transcriptionally. The dedifferentiating response was accompanied by an upregulation of mRNAs of antioxidant genes. Moreover, cadherin-1, and the thyroid (and kidney)-specific cadherin-16 mRNAs were downregulated, vimentin, and SNAI1 mRNAs were upregulated. In addition, loss of cortical actin and stress fibers formation were observed. Together, these data indicate that ER stress in thyroid cells induces dedifferentiation, loss of epithelial organization, shift towards a mesenchymal phenotype, and activation of the antioxidant response, highlighting, at the same time, a new and wide strategy to achieve survival following ER stress, and, as a sort of the other side of the coin, a possible new molecular mechanism of decline/loss of function leading to a deficit of thyroid hormones formation.openUlianich L.; Mirra P.; Garbi C.; Cali G.; Conza D.; Treglia A.S.; Miraglia A.; Punzi D.; Miele C.; Raciti G.A.; Beguinot F.; Consiglio E.; Di Jeso B.Ulianich, L.; Mirra, P.; Garbi, C.; Cali, G.; Conza, D.; Treglia, A. S.; Miraglia, A.; Punzi, D.; Miele, C.; Raciti, G. A.; Beguinot, F.; Consiglio, E.; Di Jeso, B
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