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Träfflista för sökning "WFRF:(Berggren Magnus 1968 ) srt2:(2015-2019)"

Sökning: WFRF:(Berggren Magnus 1968 ) > (2015-2019)

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1.
  • Brooke, Robert, 1989-, et al. (författare)
  • Greyscale and paper electrochromic polymer displays by UV patterning
  • 2019
  • Ingår i: Polymers. - : MDPI AG. - 2073-4360. ; 11:2
  • Tidskriftsartikel (refereegranskat)abstract
    • Electrochromic devices have important implications as smart windows for energy efficient buildings, internet of things devices, and in low-cost advertising applications. While inorganics have so far dominated the market, organic conductive polymers possess certain advantages such as high throughput and low temperature processing, faster switching, and superior optical memory. Here, we present organic electrochromic devices that can switch between two high-resolution images, based on UV-patterning and vapor phase polymerization of poly(3,4- ethylenedioxythiophene) films. We demonstrate that this technique can provide switchable greyscale images through the spatial control of a UV-light dose. The color space was able to be further altered via optimization of the oxidant concentration. Finally, we utilized a UV-patterning technique to produce functional paper with electrochromic patterns deposited on porous paper, allowing for environmentally friendly electrochromic displays.
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2.
  • Che, Canyan, 1988-, et al. (författare)
  • Twinning Lignosulfonate with a Conducting Polymer via Counter-Ion Exchange for Large-Scale Electrical Storage
  • 2019
  • Ingår i: Advanced Sustainable Systems. - : Wiley-VCH Verlag. - 2366-7486. ; 3:9
  • Tidskriftsartikel (refereegranskat)abstract
    • Lignosulfonate (LS) is a large-scale surplus product of the forest and paper industries, and has primarily been utilized as a low-cost plasticizer in making concrete for the construction industry. LS is an anionic redox-active polyelectrolyte and is a promising candidate to boost the charge capacity of the positive electrode (positrode) in redox-supercapacitors. Here, the physical-chemical investigation of how this biopolymer incorporates into the conducting polymer PEDOT matrix, of the positrode, by means of counter-ion exchange is reported. Upon successful incorporation, an optimal access to redox moieties is achieved, which provides a 63% increase of the resulting stored electrical charge by reversible redox interconversion. The effects of pH, ionic strength, and concentrations, of included components, on the polymer–polymer interactions are optimized to exploit the biopolymer-associated redox currents. Further, the explored LS-conducting polymer incorporation strategy, via aqueous synthesis, is evaluated in an up-scaling effort toward large-scale electrical energy storage technology. By using an up-scaled production protocol, integration of the biopolymer within the conducting polymer matrix by counter-ion exchange is confirmed and the PEDOT-LS synthesized through optimized strategy reaches an improved charge capacity of 44.6 mAh g−1. 
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3.
  • Kim, Nara, 1985-, et al. (författare)
  • Electric transport properties in PEDOT thin films
  • 2019. - 4
  • Ingår i: Conjugated polymers. - Boca Raton : CRC Press. - 9780429190520 ; , s. 45-128
  • Bokkapitel (refereegranskat)abstract
    • In this chapter, the authors summarize their understanding of Poly(3,4-ethylenedioxythiophene) (PEDOT), with respect to its chemical and physical fundamentals. They focus upon the structure of several PEDOT systems, from the angstrom level and up, and the impact on both electronic and ionic transport. The authors discuss the structural properties of PEDOT:X and PEDOT:poly(styrenesulfonate) based on experimental data probed at the scale ranging from angstrom to submicrometer. The morphology of PEDOT is influenced by the nature of counter-ions, especially at high oxidation levels. The doping anions intercalate between PEDOT chains to form a “sandwich” structure to screen the positive charges in PEDOT chains. The authors provide the main transport coefficients such as electrical conductivity s, Seebeck coefficient S, and Peltier coefficient σ, starting from a general thermodynamic consideration. The optical conductivity of PEDOT has also been examined based on the effective medium approximation, which is normally used to describe microscopic permittivity properties of composites made from several different constituents.
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4.
  • Mitraka, Evangelia, 1986- (författare)
  • Conducting Polymer Electrodes for Oxygen Reduction Reaction
  • 2018
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Both the pollution level of the environment and the increasing energy demands have stimulated intense research on the development of low-cost environmentally-friendly energy conversion and storage systems with high efficiency, such as metal-air batteries and fuel cells.One of the most essential parts of both fuel cells and metal–air batteries is the air-electrode which is responsible for the reduction of O2. The air-electrode can use O2 from air facilitating the layout of the device; however, the process taking place on it is significantly complex. Currently, platinum (Pt) is the benchmark for air-electrodes in such technologies, although it is expensive and exhibits other important disadvantages which diminish the fuel cell performance. Therefore, extensive research has been devoted to reduce the amount of Pt used in air-electrodes and to develop a noble metal-free version of these electrodes.The area of printed electronics could facilitate the development of low-cost electrodes produced in high volume for such applications. Conducting polymers are attractive materials for this technology because they may combine several desired properties, like electronic conduction, ionic conduction and catalysis of electrochemical reactions.Among other conducting polymers, poly(3,4-ethylenedioxythiophene) (PEDOT) emerged as an alternative cathode catalyst material to Pt, due to its ability to effectively catalyze the oxygen reduction reaction (ORR), while it also exhibits high electrical and ionic conductivity.The focus of this thesis is to study the electrocatalytic activity and mechanism of the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) when employed as an airelectrode in energy storage devices, such as fuel cells and metal-air batteries. Although PEDOT is extensively studied during the last decade as an air-electrode for fuel cell and metal-air batteries, vital pieces of the catalytic mechanism that PEDOT follows remain unknown, namely: (i) the sites of PEDOT on which O2 interacts and (ii) the intermediate species which are formed during the ORR. The content of this thesis tackles these topics, both from experimental and theoretical point of view. Moreover, it investigates the use of PEDOT as an active electrocatalyst in a polymer exchange membrane (PEM) fuel cell, by embedding the polymer in a cellulose matrix, aiming to fabricate a gas diffusion electrode for the ORR side of the device. Finally, the goal of the thesis surpasses the limit of the p-doped PEDOT and undertakes the evaluation of a n-type conjugated polymer of high electron affinity as a cathode in reduction processes.  
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5.
  • Shiran Chaharsoughi, Mina, 1986-, et al. (författare)
  • Hybrid Plasmonic and Pyroelectric Harvesting of Light Fluctuations
  • 2018
  • Ingår i: Advanced Optical Materials. - : Wiley-Blackwell. - 2162-7568 .- 2195-1071.
  • Tidskriftsartikel (refereegranskat)abstract
    • State-of-the-art solar energy harvesting systems based on photovoltaic technology require constant illumination for optimal operation. However, weather conditions and solar illumination tend to fluctuate. Here, a device is presented that extracts electrical energy from such light fluctuations. The concept combines light-induced heating of gold nanodisks (acting as plasmonic optical nanoantennas), and an organic pyroelectric copolymer film (poly(vinylidenefluoride-co-trifluoroethylene)), that converts temperature changes into electrical signals. This hybrid device can repeatedly generate current pulses, not only upon the onset of illumination, but also when illumination is blocked. Detailed characterization highlights the key role of the polarization state of the copolymer, while the copolymer thickness has minor influence on performance. The results are fully consistent with plasmon-assisted pyroelectric effects, as corroborated by combined optical and thermal simulations that match the experimental results. Owing to the tunability of plasmonic resonances, the presented concept is compatible with harvesting near infrared light while concurrently maintaining visible transparency.
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6.
  • Andersson Ersman, Peter, et al. (författare)
  • Screen printed digital circuits based on vertical organicelectrochemical transistors
  • 2017
  • Ingår i: Flexible and Printed Electronics. - : IOP Publishing. - 2058-8585. ; 2
  • Tidskriftsartikel (refereegranskat)abstract
    • Vertical organic electrochemical transistors (OECTs) have been manufactured solely using screenprinting. The OECTs are based on PEDOT:PSS (poly(3,4-ethylenedioxythiophene) doped with poly(styrene sulfonic acid)), which defines the active material for both the transistor channel and the gateelectrode. The resulting vertical OECT devices and circuits exhibit low-voltage operation, relativelyfast switching, small footprint and high manufacturing yield; the last three parameters are explainedby the reliance of the transistor configuration on a robust structure in which the electrolyte verticallybridges the bottom channel and the top gate electrode. Two different architectures of the verticalOECT have been manufactured, characterized and evaluated in parallel throughout this report. Inaddition to the experimental work, SPICE models enabling simulations of standalone OECTs andOECT-based circuits have been developed. Our findings may pave the way for fully integrated, lowvoltageoperating and printed signal processing systems integrated with e.g. printed batteries, solarcells, sensors and communication interfaces. Such technology can then serve a low-cost basetechnology for the internet of things, smart packaging and home diagnostics applications.
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7.
  • Berggren, Magnus, 1968-, et al. (författare)
  • How conducting polymer electrodes operate
  • 2019
  • Ingår i: Science. - Washington, DC, United States : American Association for the Advancement of Science (A A A S). - 0036-8075 .- 1095-9203. ; 364:6437, s. 233-234
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • n/a
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8.
  • Berggren, Magnus, 1968-, et al. (författare)
  • Organic bioelectronics based on Mixed Ion–Electron conductors
  • 2019. - 4
  • Ingår i: Conjugated polymers. - Boca Raton : CRC Press. - 9780429190520 ; , s. 679-696
  • Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
    • This chapter focuses on two specific areas of organic mixed ion–electron conductors: surfaces and scaffolds for controlling cell cultures, and “iontronic”-controlled delivery of ions and biomolecules. It draws on iontronic technology based on ion exchange materials, which is compatible with physiological salt concentrations. Iontronics is attractive for bioelectronic applications, as it provides a means for the manipulation of flows of ions and charged biomolecules – species that can possess chemical and biological functionality. The organic electronic ion pump (OEIP) is a delivery device where charged (bio)molecules are transported within a polyelectrolyte membrane. The electronic control of the delivery flux, together with micrometer-sized channel outlets, enables OEIPs to achieve high spatiotemporal resolution; biomolecule delivery can be tightly controlled to a specific site and dose amount. High spatiotemporal control of ion and biomolecule concentrations is attractive for a wide range of in vitro studies of biological systems.??
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9.
  • Brooke, Robert, 1989-, et al. (författare)
  • Supercapacitors on demand : All-printed energy storage devices with adaptable design
  • 2019
  • Ingår i: Flexible and Printed Electronics. - : Institute of Physics Publishing. - 2058-8585. ; 4:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Demands on the storage of energy have increased for many reasons, in part driven by household photovoltaics, electric grid balancing, along with portable and wearable electronics. These are fast-growing and differentiated applications that need large volume and/or highly distributed electrical energy storage, which then requires environmentally friendly, scalable and flexible materials and manufacturing techniques. However, the limitations on current inorganic technologies have driven research efforts to explore organic and carbon-based alternatives. Here, we report a conducting polymer:cellulose composite that serves as the active material in supercapacitors which has been incorporated into all-printed energy storage devices. These devices exhibit a specific capacitance of ≈90 F g -1 and an excellent cyclability (>10 000 cycles). Further, a design concept coined 'supercapacitors on demand' is presented, which is based on a printing-cutting-folding procedure, that provides us with a flexible production protocol to manufacture supercapacitors with adaptable configuration and electrical characteristics.
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10.
  • Fahlman, Mats, 1967-, et al. (författare)
  • Interfaces in organic electronics
  • 2019
  • Ingår i: Nature Reviews Materials. - : Nature Publishing Group. - 2058-8437. ; 4:10, s. 627-650
  • Forskningsöversikt (refereegranskat)abstract
    • Undoped, conjugated, organic molecules and polymers possess properties of semiconductors, including the electronic structure and charge transport, which can be readily tuned by chemical design. Moreover, organic semiconductors (OSs) can be n-doped or p-doped to become organic conductors and can exhibit mixed electronic and ionic conductivity. Compared with inorganic semiconductors and metals, organic (semi)conductors possess a unique feature: no insulating oxide forms on their surface when exposed to air. Thus, OSs form clean interfaces with many materials, including metals and other OSs. OS–metal and OS–OS interfaces have been intensely investigated over the past 30 years, from which a consistent theoretical description has emerged. Since the 2000s, increased attention has been paid to interfaces in organic electronics that involve dielectrics, electrolytes, ferroelectrics and even biological organisms. In this Review, we consider the central role of these interfaces in the function of organic electronic devices and discuss how the physico-chemical properties of the interfaces govern the interfacial transport of light, excitons, electrons and ions, as well as the transduction of electrons into the molecular language of cells.
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