SwePub
Tyck till om SwePub Sök här!
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Jonsson Magnus P.) "

Sökning: WFRF:(Jonsson Magnus P.)

  • Resultat 1-10 av 31
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Adloff, C, et al. (författare)
  • Energy flow and rapidity gaps between jets in photoproduction at HERA
  • 2002
  • Ingår i: European Physical Journal C. Particles and Fields. - : Springer Science and Business Media LLC. - 1434-6044. ; 24:4, s. 517-527
  • Tidskriftsartikel (refereegranskat)abstract
    • Dijet events in photon-proton collisions in which there is a large pseudorapidity separation, Deltaeta > 2.5 between the two highest E-T jets are studied with the H1 detector at HERA. The inclusive dijet cross sections are measured as functions of the longitudinal momentum fractions of the proton and photon which participate in the production of the jets, x(p)(jets) and x(gamma)(jets) respectively, Deltaeta, the pseudorapidity P separation between the two highest E-T jets, and E-T(gap), the total summed transverse energy between the jets. Rapidity gap events are defined as events in which E-T(gap) is less than E-T(cut), for E-T(cut) varied between jets 0.5 and 2.0 GeV. The fraction of dijet events with a rapidity gap is measured differentially in Deltaeta, x(p)(jets) and x(gamma)(jets). An excess of events with rapidity gaps at low values of E-T(cut) is observed above the expectation from standard photoproduction processes. This excess can be explained by the exchange of a strongly interacting colour singlet object between the jets.
  •  
2.
  • Aidas, Kestutis, et al. (författare)
  • The Dalton quantum chemistry program system
  • 2014
  • Ingår i: Wiley Interdisciplinary Reviews. Computational Molecular Science. - : Wiley. - 1759-0876. ; 4:3, s. 269-284
  • Tidskriftsartikel (refereegranskat)abstract
    • Dalton is a powerful general-purpose program system for the study of molecular electronic structure at the Hartree-Fock, Kohn-Sham, multiconfigurational self-consistent-field, MOller-Plesset, configuration-interaction, and coupled-cluster levels of theory. Apart from the total energy, a wide variety of molecular properties may be calculated using these electronic-structure models. Molecular gradients and Hessians are available for geometry optimizations, molecular dynamics, and vibrational studies, whereas magnetic resonance and optical activity can be studied in a gauge-origin-invariant manner. Frequency-dependent molecular properties can be calculated using linear, quadratic, and cubic response theory. A large number of singlet and triplet perturbation operators are available for the study of one-, two-, and three-photon processes. Environmental effects may be included using various dielectric-medium and quantum-mechanics/molecular-mechanics models. Large molecules may be studied using linear-scaling and massively parallel algorithms. Dalton is distributed at no cost from for a number of UNIX platforms.
  •  
3.
  • Brooke, Robert, et al. (författare)
  • Infrared electrochromic conducting polymer devices
  • 2017
  • Ingår i: Journal of Materials Chemistry C. - : The Royal Society of Chemistry. - 2050-7526 .- 2050-7534. ; 5:23, s. 5824-5830
  • Tidskriftsartikel (refereegranskat)abstract
    • The conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) is well known for its electrochromic properties in the visible region. Less focus has been devoted to the infrared (IR) wavelength range, although tunable IR properties could enable a wide range of novel applications. As an example, modern day vehicles have thermal cameras to identify pedestrians and animals in total darkness, but road and speed signs cannot be easily visualized by these imaging systems. IR electrochromism could enable a new generation of dynamic road signs that are compatible with thermal imaging, while simultaneously providing contrast also in the visible region. Here, we present the first metal-free flexible IR electrochromic devices, based on PEDOT:Tosylate as both the electrochromic material and electrodes. Lateral electrochromic devices enabled a detailed investigation of the IR electrochromism of thin PEDOT:Tosylate films, revealing large changes in their thermal signature, with effective temperature changes up to 10 [degree]C between the oxidized (1.5 V) and reduced (-1.5 V) states of the polymer. Larger scale (7 [times] 7 cm) vertical electrochromic devices demonstrate practical suitability and showed effective temperature changes of approximately 7 [degree]C, with good optical memory and fast switching (1.9 s from the oxidized state to the reduced state and 3.3 s for the reversed switching). The results are highly encouraging for using PEDOT:Tosylate for IR electrochromic applications.
  •  
4.
  • Brooke, Robert, 1989-, et al. (författare)
  • Infrared electrochromic conducting polymer devices
  • 2017
  • Ingår i: Journal of Materials Chemistry C. - : Royal Society of Chemistry (RSC). - 2050-7526 .- 2050-7534. ; 5:23, s. 5824-5830
  • Tidskriftsartikel (refereegranskat)abstract
    • The conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) is well known for its electrochromic properties in the visible region. Less focus has been devoted to the infrared (IR) wavelength range, although tunable IR properties could enable a wide range of novel applications. As an example, modern day vehicles have thermal cameras to identify pedestrians and animals in total darkness, but road and speed signs cannot be easily visualized by these imaging systems. IR electrochromism could enable a new generation of dynamic road signs that are compatible with thermal imaging, while simultaneously providing contrast also in the visible region. Here, we present the first metal-free flexible IR electrochromic devices, based on PEDOT:Tosylate as both the electrochromic material and electrodes. Lateral electrochromic devices enabled a detailed investigation of the IR electrochromism of thin PEDOT:Tosylate films, revealing large changes in their thermal signature, with effective temperature changes up to 10 °C between the oxidized (1.5 V) and reduced (-1.5 V) states of the polymer. Larger scale (7 × 7 cm) vertical electrochromic devices demonstrate practical suitability and showed effective temperature changes of approximately 7 °C, with good optical memory and fast switching (1.9 s from the oxidized state to the reduced state and 3.3 s for the reversed switching). The results are highly encouraging for using PEDOT:Tosylate for IR electrochromic applications.
  •  
5.
  • 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. 
  •  
6.
  • Gisladottir, Rosa S, et al. (författare)
  • Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.
  • 2020
  • Ingår i: Current biology : CB. - : Elsevier BV. - 1879-0445 .- 0960-9822. ; 30:23, s. 4643-4653.e3
  • Tidskriftsartikel (refereegranskat)abstract
    • Olfactory receptor (OR) genes in humans form a special class characterized by unusually high DNA sequence diversity, which should give rise to differences in perception and behavior. In the largest genome-wide association study to date based on olfactory testing, we investigated odor perception and naming with smell tasks performed by 9,122 Icelanders, with replication in a separate sample of 2,204 individuals. We discovered an association between a low-frequency missense variant in TAAR5 and reduced intensity rating of fish odor containing trimethylamine (p.Ser95Pro, pcombined = 5.6 × 10-15). We demonstrate that TAAR5 genotype affects aversion to fish odor, reflected by linguistic descriptions of the odor and pleasantness ratings. We also discovered common sequence variants in two canonical olfactory receptor loci that associate with increased intensity and naming of licorice odor (trans-anethole: lead variant p.Lys233Asn in OR6C70, pcombined = 8.8 × 10-16 and pcombined = 1.4 × 10-9) and enhanced naming of cinnamon (trans-cinnamaldehyde; intergenic variant rs317787-T, pcombined = 5.0 × 10-17). Together, our results show that TAAR5 genotype variation influences human odor responses and highlight that sequence diversity in canonical OR genes can lead to enhanced olfactory ability, in contrast to the view that greater tolerance for mutations in the human OR repertoire leads to diminished function.
  •  
7.
  • Håkansson, H., et al. (författare)
  • In vivo and in vitro toxicity of fractionated fish lipids, with particular regard to their content of chlorinated organic compounds
  • 1991
  • Ingår i: Pharmacology and Toxicology. - : Wiley. - 0901-9928 .- 1600-0773. ; 69:6, s. 459-471
  • Tidskriftsartikel (refereegranskat)abstract
    • Six different lipid matrices (the intact lipid (IL), four lipid fractions with different polarity, and the free fatty acids (FFAs) obtained by hydrolysis of the triacylglycerol (TAG) containing fraction) were obtained from salmon (Salmo salar) and eel (Anguilla anguilla), each collected at a contaminated and a comparatively uncontaminated catch site along the coast of Scandinavia. The lipid matrices were studied in toxicological test systems representing various biological functions of different organ systems from several species and trophic levels. The results were evaluated with particular respect to the concentrations of extractable organically bound chlorine (EOCl) in the matrices tested. In some test systems, the specimens with a higher EOCl concentration appeared to be more toxic. For example, the TAG containing fraction (F2) from Idefjord eel, having a higher EOCl content than F2 from Oslofjord eel, reduced the number and hatchability of eggs laid by zebrafish. Both IL and F2 of Idefjord eel increased mortality and reduced the oxygen/nitrogen-ratio in blue mussels. Non-polar compounds (F1) from Bothnian Sea salmon induced 7-ethoxyresurofin O-deethylase (EROD) activity in rainbow trout hepatocytes, whereas F1 from Senja salmon did not. F1 from Bothnian Sea salmon also reduced the number of T-cells in foetal mouse thymus anlagen in vitro compared with the cell number in anlagen exposed to F1 from Senja salmon. A positive correlation between EOCl concentration and test response was found for EROD activity in rainbow trout hepatocytes and for ATP-leakage in Erlich ascites tumour cells when testing the phospolipid containing fraction (F4). However, in most test systems the fish oils, irrespective of EOCl content, were of low toxicity, and the observed effects need to be verified in future studies.
  •  
8.
  • Jonsson, Magnus P., et al. (författare)
  • Simultaneous Nanoplasmonic and Quartz Crystal Microbalance Sensing: Analysis of Biomolecular Conformational Changes and Quantification of the Bound Molecular Mass
  • 2008
  • Ingår i: Analytical Chemistry. - : American Chemical Society. - 0003-2700 .- 1520-6882. ; 80:21, s. 7988-7995
  • Tidskriftsartikel (refereegranskat)abstract
    • This paper presents a study of supported lipid bilayer (SIB) formation and subsequent protein binding using a sensor that combines localized surface plasmon resonance (LSPR) and quartz crystal microbalance with dissipation (QCM-D) monitoring. The LSPR activity arises from silicon oxide (SiOx) coated nanometric apertures in a thin gold film, which also serves as the active electrode of a QCM-D crystal. Both transducer principles provide signatures for the formation of a SLB upon adsorption and subsequent rupture of adsorbed lipid vesicles. However, the two techniques are sensitive over different regions of the sample: LSPR primarily inside and on the rim of the holes and QCM-D primarily on the planar areas between the holes. Although the dimension of the lipid vesicles is on the same order as the dimension of the nanoholes, it is concluded from the response of the combined system that vesicle rupture in the nanoholes and on the planar region between the holes is synchronized. Furthermore, by determining the thickness of the SLB from the QCM-D response, the characteristic decay length of the LSPR field intensity could be determined. This made it possible not only to determine the mass and refractive index of the homogeneous SLB but also to postulate a generic means to quantify the LSPR response in terms of mass-uptake also for nonhomogeneous films. This is exemplified by measuring the adsorbed lipid mass during vesicle adsorption, yielding the critical lipid vesicle coverage at which spontaneous rupture into a planar bilayer occurs. The generic applicability and versatility of the method is demonstrated from specific protein binding to a functionalized SLB. From the absolute refractive index of the protein, provided from the LSPR data alone, it was possible to determine both the effective thickness of the protein film and the molecular mass (or number) of bound protein.
  •  
9.
  • Sandberg, Mats, et al. (författare)
  • Photoconductive zinc oxide-composite paper by pilot paper machine manufacturing
  • 2016
  • Ingår i: Flexible and Printed Electronics. - : IOP Publishing. - 2058-8585. ; 1
  • Tidskriftsartikel (refereegranskat)abstract
    • Smartmaterials can be used for awide variety of applications, including sensing and energy harvesting.Implementation of smartmaterials in large area devices requires scalablemanufacturing. The use ofpaper-making techniques would offer an enormous production capacity, allowing for low-cost andlarge-scalemanufacturing. In thisworkwe present a successful pilot scale papermachinemanufacturingof functional composite papers(100mmin−1 with aweb width of 30 cm) based on cellulose fibres andcommercial tetrapodal zinc oxidemicrowhiskers(ZnO-Ts).Carbon electrodes could successfully beprinted on the paper to form complete electronic devices where the paper itself is the active material.Thisenabled development of aZnO-composite paper photosensor,where we characterized its stability,sensitivity and speed. The devices show excellent photosensing properties over awide range of lightirradiances(0.01–1Sun), including short response times (∼10 s) and long-term stability. Under simulatedsunlight and a bias voltage of 1 V, small(0.5 cm2) two-probe interdigitated photosensor devices provided12μAphotocurrent.Under the same conditions, four-probe measurements of the composite papershowed a sheet resistance of 6.9·107Ω/sq. Four-probe measurements also demonstrated that the paperconductivity varies linearlywith light irradiance. To the best of ourknowledge, this is thefirst example ofpilot paper machine production of an optoelectronic paper, demonstrating the potential for large-scalepapermanufacturing of active smart paper from low-cost industrial bulk materials.
  •  
10.
  • Stavrinidou, Eleni, et al. (författare)
  • In vivo polymerization and manufacturing of wires and supercapacitors in plants
  • 2017
  • Ingår i: Proceedings of the National Academy of Sciences of the United States of America. - : National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 114:11, s. 2807-2812
  • Tidskriftsartikel (refereegranskat)abstract
    • Electronic plants, e-Plants, are an organic bioelectronic platform that allows electronic interfacing with plants. Recently we have demonstrated plants with augmented electronic functionality. Using the vascular system and organs of a plant, we manufactured organic electronic devices and circuits in vivo, leveraging the internal structure and physiology of the plant as the template, and an integral part of the devices. However, this electronic functionality was only achieved in localized regions, whereas new electronic materials that could be distributed to every part of the plant would provide versatility in device and circuit fabrication and create possibilities for new device concepts. Here we report the synthesis of such a conjugated oligomer that can be distributed and form longer oligomers and polymer in every part of the xylem vascular tissue of a Rosa floribunda cutting, forming long-range conducting wires. The plant’s structure acts as a physical template, whereas the plant’s biochemical response mechanism acts as the catalyst for polymerization. In addition, the oligomer can cross through the veins and enter the apoplastic space in the leaves. Finally, using the plant’s natural architecture we manufacture supercapacitors along the stem. Our results are preludes to autonomous energy systems integrated within plants and distribute interconnected sensor-actuator systems for plant control and optimization
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 31
Typ av publikation
tidskriftsartikel (28)
konferensbidrag (2)
rapport (1)
Typ av innehåll
refereegranskat (30)
övrigt vetenskapligt/konstnärligt (1)
Författare/redaktör
Bruncko, D. (1)
Caron, S. (1)
Dingfelder, J. (1)
Heinemann, B. (1)
Hoffmann, D. (1)
Issever, C. (1)
visa fler...
Klein, M. (1)
Kroseberg, J. (1)
Laycock, P. (1)
Lobodzinska, E. (1)
Loginov, A. (1)
Mehta, A. (1)
Meier, K. (1)
Meyer, J. (1)
Naumann, T. (1)
Rizvi, E. (1)
Schmitt, S. (1)
Schoeffel, L. (1)
Schwanenberger, C. (1)
South, D. (1)
Stamen, R. (1)
Tasevsky, M. (1)
Tsipolitis, G. (1)
Valkar, S. (1)
Werner, M. (1)
Wessels, M. (1)
Zhang, Z. (1)
Diaconu, C. (1)
zur Nedden, M. (1)
Eisenhandler, E. (1)
Ferencei, J. (1)
Greenshaw, T. (1)
Ibbotson, M. (1)
Kluge, T. (1)
Lendermann, V. (1)
Garvey, J. (1)
Haller, J. (1)
Weber, M. (1)
Zhokin, A. (1)
Alonso, Alejandro (1)
Astvatsatourov, A. (1)
Collard, C. (1)
Koblitz, B. (1)
Kostka, P. (1)
Lebedev, A. (1)
Kennedy, J. (1)
Levonian, S. (1)
Marshall, R. (1)
Andrieu, B. (1)
Heinrich, J. (1)
visa färre...
Lärosäte
Linköpings universitet (15)
RISE (5)
Kungliga Tekniska Högskolan (4)
Lunds universitet (4)
Chalmers tekniska högskola (4)
Göteborgs universitet (3)
visa fler...
Umeå universitet (2)
Uppsala universitet (2)
Karolinska Institutet (2)
Luleå tekniska universitet (1)
Högskolan i Halmstad (1)
Örebro universitet (1)
Högskolan i Borås (1)
visa färre...
Språk
Engelska (31)
Forskningsämne (UKÄ/SCB)
Naturvetenskap (17)
Teknik (8)
Medicin och hälsovetenskap (5)
Lantbruksvetenskap (1)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy