29 research outputs found

    High efficiency arrays of polymer solar cells fabricated by spray-coating in air

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    We present bulk heterojunction organic solar cells fabricated by spray-casting both the PEDOT:PSS hole-transport layer (HTL) and active PBDTTT-EFT:PC71BM layers in air. Devices were fabricated in a (6 × 6) array across a large-area substrate (25 cm2) with each pixel having an active area of 6.45 mm2. We show that the film uniformity and operational homogeneity of the devices are excellent. The champion device with spray cast active layer on spin cast PEDOT:PSS had an power conversion efficiency (PCE) of 8.75%, and the best device with spray cast active layer and PEDOT:PSS had a PCE of 8.06%. The impacts of air and light exposure of the active layer on device performance are investigated and found to be detrimental

    Polymer-based solar cells having an active area of 1.6 cm2 fabricated via spray coating

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    We demonstrate the fabrication of polymersolar cells in which both a PEDOT:PSS hole transport and a PCDTBT:PC71BM photoactive layer are deposited by spray-casting. Two device geometries are explored, with devices having a pixel area of 165 mm2 attaining a power conversion efficiency of 3.7%. Surface metrology indicates that the PEDOT:PSS and PCDTBT:PC71BM layers have a roughness of 2.57 nm and 1.18 nm over an area of 100 μm2. Light beam induced current mapping reveals fluctuations in current generation efficiency over length-scales of ∼2 mm, with the average photocurrent being 75% of its maximum value

    Organic photovoltaic devices with enhanced efficiency processed from non-halogenated binary solvent blends

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    The development of processing routes to fabricate organic photovoltaic devices (OPVs) using non-halogenated solvents is a necessary step towards their eventual commercialisation. To address this issue, we have used Hansen solubility parameter analysis to identify a non-halogenated solvent blend based on a mixture of carbon disulphide and acetone. This solvent blend was then used to deposit a donor–acceptor polymer–fullerene thin-film that was then used as the active layer of bulk-heterojunction OPV. For the benchmark polymer:fullerene system PCDTBT:PC70BM, a power conversion efficiency of 6.75% was achieved; a 20% relative improvement over reference cells processed using the chlorinated-solvent chlorobenzene. Improvements in device efficiency are attributed to an increase in electron and hole conductivity resulting from enhanced fullerene crystallisation; a property that leads to enhanced device efficiency through improved charge extraction

    The emission of X-rays by fission fragments

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    Approximately 5% of the γ-ray transitions in fission fragments are internally converted, giving rise to X-rays. X-ray energies are characteristic of Z, but yields depend strongly and not smoothly on Z and A of the fragments and on time. If these biases can be accepted, X-rays can be used to identify the atomic number of fission fragments. More generally, internal conversion and X-ray emission must be interpreted in the context of detailed knowledge of γ-ray transitions.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/43110/1/10967_2005_Article_BF02039468.pd

    Parental origin of sequence variants associated with complex diseases

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    To access publisher full text version of this article. Please click on the hyperlink in Additional Links fieldEffects of susceptibility variants may depend on from which parent they are inherited. Although many associations between sequence variants and human traits have been discovered through genome-wide associations, the impact of parental origin has largely been ignored. Here we show that for 38,167 Icelanders genotyped using single nucleotide polymorphism (SNP) chips, the parental origin of most alleles can be determined. For this we used a combination of genealogy and long-range phasing. We then focused on SNPs that associate with diseases and are within 500 kilobases of known imprinted genes. Seven independent SNP associations were examined. Five-one with breast cancer, one with basal-cell carcinoma and three with type 2 diabetes-have parental-origin-specific associations. These variants are located in two genomic regions, 11p15 and 7q32, each harbouring a cluster of imprinted genes. Furthermore, we observed a novel association between the SNP rs2334499 at 11p15 and type 2 diabetes. Here the allele that confers risk when paternally inherited is protective when maternally transmitted. We identified a differentially methylated CTCF-binding site at 11p15 and demonstrated correlation of rs2334499 with decreased methylation of that site.info:eu-repo/grantAgreement/EC/FP7/21807

    Meta-analysis of type 2 Diabetes in African Americans Consortium

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    Type 2 diabetes (T2D) is more prevalent in African Americans than in Europeans. However, little is known about the genetic risk in African Americans despite the recent identification of more than 70 T2D loci primarily by genome-wide association studies (GWAS) in individuals of European ancestry. In order to investigate the genetic architecture of T2D in African Americans, the MEta-analysis of type 2 DIabetes in African Americans (MEDIA) Consortium examined 17 GWAS on T2D comprising 8,284 cases and 15,543 controls in African Americans in stage 1 analysis. Single nucleotide polymorphisms (SNPs) association analysis was conducted in each study under the additive model after adjustment for age, sex, study site, and principal components. Meta-analysis of approximately 2.6 million genotyped and imputed SNPs in all studies was conducted using an inverse variance-weighted fixed effect model. Replications were performed to follow up 21 loci in up to 6,061 cases and 5,483 controls in African Americans, and 8,130 cases and 38,987 controls of European ancestry. We identified three known loci (TCF7L2, HMGA2 and KCNQ1) and two novel loci (HLA-B and INS-IGF2) at genome-wide significance (4.15 × 10(-94)<P<5 × 10(-8), odds ratio (OR)  = 1.09 to 1.36). Fine-mapping revealed that 88 of 158 previously identified T2D or glucose homeostasis loci demonstrated nominal to highly significant association (2.2 × 10(-23) < locus-wide P<0.05). These novel and previously identified loci yielded a sibling relative risk of 1.19, explaining 17.5% of the phenotypic variance of T2D on the liability scale in African Americans. Overall, this study identified two novel susceptibility loci for T2D in African Americans. A substantial number of previously reported loci are transferable to African Americans after accounting for linkage disequilibrium, enabling fine mapping of causal variants in trans-ethnic meta-analysis studies.Peer reviewe

    Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits : A Multi-Ethnic Meta-Analysis of 45,891 Individuals

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    J. Kaprio, S. Ripatti ja M.-L. Lokki työryhmien jäseniä.Peer reviewe
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