| 1. |
- Mauri, Massimiliano, 1987, et al.
(författare)
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Click chemistry-type crosslinking of a low-conductivity polyethylene copolymer ternary blend for power cable insulation
- 2020
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Ingår i: Polymer International. - : Wiley. - 1097-0126 .- 0959-8103. ; 69:4, s. 404-412
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Tidskriftsartikel (refereegranskat)abstract
- High-voltage direct-current power cables are vital for the efficient transport of electricity derived from renewable sources of energy. The most widely used material for high-voltage power cable insulation - low-density polyethylene (LDPE) - is usually crosslinked with peroxides, a process that releases unwanted by-products. Hence, by-product-free crosslinking concepts that mitigate the associated increase in electrical conductivity are in high demand. Click chemistry-type crosslinking of polyethylene copolymer mixtures that contain glycidyl methacrylate and acrylic acid co-monomers is a promising alternative, provided that the curing reaction can be controlled. Here, we demonstrate that the rate of the curing reaction can be adjusted by tuning the number of epoxy and carboxyl groups. Both dilution of copolymer mixtures with neat LDPE and the selection of copolymers with a lower co-monomer content have an equivalent effect on the curing speed. Ternary blends that contain 50 wt% of neat LDPE feature an extended extrusion window of up to 170 degrees C. Instead, at 200 degrees C rapid curing is possible, leading to thermosets with a low direct-current electrical conductivity of about 10(-16) S cm(-1) at an electric field of 20 kV mm(-1) and 70 degrees C. The conductivity of the blends explored here is comparable to or even lower than values measured for both ultraclean LDPE and a peroxide-cured commercial crosslinked polyethylene grade. Hence, click chemistry curing represents a promising alternative to radical crosslinking with peroxides. (c) 2019 Society of Chemical Industry
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| 2. |
- Untilova, Viktoriia, et al.
(författare)
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High Thermoelectric Power Factor of Poly(3-hexylthiophene) through In-Plane Alignment and Doping with a Molybdenum Dithiolene Complex
- 2020
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Ingår i: Macromolecules. - : American Chemical Society (ACS). - 1520-5835 .- 0024-9297. ; 53:15, s. 6314-6321
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Tidskriftsartikel (refereegranskat)abstract
- We report a record thermoelectric power factor of up to 160 μW m-1 K-2 for the conjugated polymer poly(3-hexylthiophene) (P3HT). This result is achieved through the combination of high-temperature rubbing of thin films together with the use of a large molybdenum dithiolene p-dopant with a high electron affinity. Comparison of the UV-vis-NIR spectra of the chemically doped samples to electrochemically oxidized material reveals an oxidation level of 10%, i.e., one polaron for every 10 repeat units. The high power factor arises due to an increase in the charge-carrier mobility and hence electrical conductivity along the rubbing direction. We conclude that P3HT, with its facile synthesis and outstanding processability, should not be ruled out as a potential thermoelectric material. ©
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| 3. |
- Campbell, PJ, et al.
(författare)
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Pan-cancer analysis of whole genomes
- 2020
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Ingår i: Nature. - : Springer Science and Business Media LLC. - 1476-4687 .- 0028-0836. ; 578:7793, s. 82-
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Tidskriftsartikel (refereegranskat)abstract
- Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale1–3. Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4–5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter4; identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation5,6; analyses timings and patterns of tumour evolution7; describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity8,9; and evaluates a range of more-specialized features of cancer genomes8,10–18.
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| 4. |
- Hofmann, Anna, 1987, et al.
(författare)
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All-Polymer Conducting Fibers and 3D Prints via Melt Processing and Templated Polymerization
- 2020
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Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8252 .- 1944-8244. ; 12:7, s. 8713-8721
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Tidskriftsartikel (refereegranskat)abstract
- Because of their attractive mechanical properties, conducting polymers are widely perceived as materials of choice for wearable electronics and electronic textiles. However, most state-of-the-art conducting polymers contain harmful dopants and are only processable from solution but not in bulk, restricting the design possibilities for applications that require conducting micro-to-millimeter scale structures, such as textile fibers or thermoelectric modules. In this work, we present a strategy based on melt processing that enables the fabrication of nonhazardous, all-polymer conducting bulk structures composed of poly(3,4-ethylenedioxythiophene) (PEDOT) polymerized within a Nafion template. Importantly, we employ classical polymer processing techniques including melt extrusion followed by fiber spinning or fused filament 3D printing, which cannot be implemented with the majority of doped polymers. To demonstrate the versatility of our approach, we fabricated melt-spun PEDOT:Nafion fibers, which are highly flexible, retain their conductivity of about 3 S cm(-1) upon stretching to 100% elongation, and can be used to construct organic electrochemical transistors (OECTs). Furthermore, we demonstrate the precise 3D printing of complex conducting structures from OECTs to centimeter-sized PEDOT:Nafion figurines and millimeter-thick 100-leg thermoelectric modules on textile substrates. Thus, our strategy opens up new possibilities for the design of conducting, all-polymer bulk structures and the development of wearable electronics and electronic textiles.
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| 5. |
- Hofmann, Anna, 1987, et al.
(författare)
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Chemical Doping of Conjugated Polymers with the Strong Oxidant Magic Blue
- 2020
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Ingår i: Advanced Electronic Materials. - : Wiley. - 2199-160X .- 2199-160X. ; 6:8
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Tidskriftsartikel (refereegranskat)abstract
- Molecular doping of organic semiconductors is a powerful tool for the optimization of organic electronic devices and organic thermoelectric materials. However, there are few redox dopants that have a sufficiently high electron affinity to allow the doping of conjugated polymers with an ionization energy of more than 5.3 eV. Here, p-doping of a broad palette of conjugated polymers with high ionization energies is achieved by using the strong oxidant tris(4-bromophenyl)ammoniumyl hexachloroantimonate (Magic Blue). In particular diketopyrrolopyrrole (DPP)-based copolymers reach a conductivity of up to 100 S cm−1 and a thermoelectric power factor of 10 µW m−1 K−2. Further, both electron paramagnetic resonance (EPR) as well as a combination of spectroelectrochemistry and chronoamperometry is used to estimate the charge-carrier density of the polymer PDPP-3T doped with Magic Blue. A molar attenuation coefficient of 6.0 ± 0.2 × 103 m2 mol−1 is obtained for the first polaronic sub-bandgap absorption of electrochemically oxidized PDPP-3T. Comparison with chemically doped PDPP-3T suggests a charge-carrier density on the order of 1026 m−3, which yields a charge-carrier mobility of up to 0.5 cm2 V−1 s−1 for the most heavily doped material.
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| 6. |
- Kim, Youngseok, et al.
(författare)
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Robust PEDOT:PSS Wet‐Spun Fibers for Thermoelectric Textiles
- 2020
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Ingår i: Macromolecular Materials and Engineering. - : Wiley. - 1439-2054 .- 1438-7492. ; 305:3, s. 1900749-
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Tidskriftsartikel (refereegranskat)abstract
- To realize thermoelectric textiles that can convert body heat to electricity, fibers with excellent mechanical and thermoelectric properties are needed. Although poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is among the most promising organic thermoelectric materials, reports that explore its use for thermoelectric fibers are all but absent. Herein, the mechanical and thermoelectric properties of wet‐spun PEDOT:PSS fibers are reported, and their use in energy‐harvesting textiles is discussed. Wet‐spinning into sulfuric acid results in water‐stable semicrystalline fibers with a Young's modulus of up to 1.9 GPa, an electrical conductivity of 830 S cm−1, and a thermoelectric power factor of 30 μV m−1 K−2. Stretching beyond the yield point as well as repeated tensile deformation and bending leave the electrical properties of these fibers almost unaffected. The mechanical robustness/durability and excellent underwater stability of semicrystalline PEDOT:PSS fibers, combined with a promising thermoelectric performance, opens up their use in practical energy‐harvesting textiles, as illustrated by an embroidered thermoelectric fabric module.
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