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Träfflista för sökning "WAKA:ref ;pers:(Inganäs Olle);srt2:(2005-2009)"

Sökning: WAKA:ref > Inganäs Olle > (2005-2009)

  • Resultat 61-70 av 112
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61.
  • Lindgren, Lars Johan, 1977, et al. (författare)
  • Synthesis, Characterization, and Devices of a Series of Alternating Copolymers for Solar Cells
  • 2009
  • Ingår i: CHEMISTRY OF MATERIALS. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 21:15, s. 3491-3502
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study we report the synthesis, characterization. and photovoltaic properties of a series of six Conjugated polymers based on donor-acceptor-donor (DAD) structure. The polymers are obtained via Suzuki polymerization of different alkoxy-substituted DAD monomers together with a substituted fluorene or phenylene monomer. Application of polymers as light-harvesting and electron-donating materials in solar cells, in conjunction with both [60]PCBM and [70]PCBM as acceptors, show power-conversion efficiencies (PCEs) up to 2.9%, values obtained without extensive optimization work. Furthermore, atomic force microscopy and field-effect transistor (FET) mobility measurements of acceptor-polymer mixtures show that differences in substitution on the polymers affect morphology, mobility, and device performance. Within the series of polymers, all showing similar optical absorption and redox behavior, substituents play an important role in phase separation on a micrometer scale, which in turn has a large impact on device performance. The phase-separation behavior is clearly seen in [70]PCBM devices where the best-performing devices are obtained using the polymers with short alkoxy groups or no substituents together with a high speed of spin coating during device preparation.
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62.
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63.
  • Mammo, W., et al. (författare)
  • New low band gap alternating polyfluorene copolymer-based photovoltaic cells
  • 2007
  • Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248 .- 1879-3398. ; 91:11, s. 1010-1018
  • Tidskriftsartikel (refereegranskat)abstract
    • New low band gap alternating polyfluorene copolymers were synthesized for use in plastic solar cells and their optical, electrochemical, and photovoltaic characteristics were determined. These polymers incorporated fluorene units alternating with groups including electron-withdrawing (A) and electron-donating (D) groups in donor-acceptor-donor (DAD) sequence to achieve the lowering of band gaps. The HOMO-LUMO values were estimated from electrochemical studies. By varying the donor and acceptor strength and position of the solubilizing substituents, similar HOMO values were obtained. These values were also found to correlate well with the open circuit voltage (VOC) values determined from photovoltaic data of the polymers blended with the acceptor PCBM. Despite similar HOMO values, the absorption spectra of the polymers differ significantly. This prompted the preparation of photovoltaic devices consisting of blends of two polymers with complementary absorptions in combination with PCBM to harvest more photons in the polymer solar cells. © 2007 Elsevier B.V. All rights reserved.
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64.
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65.
  • Nemec, Hynek, et al. (författare)
  • Charge carrier dynamics in alternating polyfluorene copolymer : Fullerene blends probed by terahertz spectroscopy
  • 2008
  • Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 112:16, s. 6558-6563
  • Tidskriftsartikel (refereegranskat)abstract
    • Time-resolved terahertz spectroscopy is used for investigation of photoinduced charge carrier dynamics in blends of a polyfluorene copolymer (poly[2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4',7'-di-2-thienyl- 2',1',3-benzo-thiadiazole)]) and an electron acceptor ([6,6]-phenyl-C61-butyric acid methyl ester). The transient far-infrared response appears instantaneously after photoexcitation. We show that the transient conductivity spectrum is dominated by two major contributions: response of separated charge carriers and response of coupled polaron pairs. © 2008 American Chemical Society.
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66.
  • Nemec, Hynek, et al. (författare)
  • Sub-Picosecond Time-Dependent Mobility in Low-Band-Gap Polyphenylene:Fullerene Blend Probed by Terahertz Spectroscopy
  • 2008
  • Ingår i: Conference on Lasers and Electro-Optics, 2008 and 2008 Conference on Quantum Electronics and Laser Science. CLEO/QELS 2008. - : IEEE. - 1092-8081. - 9781557528599 ; , s. 3108-3109
  • Konferensbidrag (refereegranskat)abstract
    • Time-resolved terahertz spectroscopy is used to investigate photoinduced dynamics of charge carriers in a polymer heterojunction. We directly observe instantaneous generation of highly mobile charge carriers followed by a rapid drop in their mobility. (C) 2008 Optical Society of America
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67.
  • Nemec, Hynek, et al. (författare)
  • Ultrafast conductivity in a low-band-gap polyphenylene and fullerene blend studied by terahertz spectroscopy
  • 2009
  • Ingår i: Physical Review B - Condensed Matter and Materials Physics. - 2469-9950 .- 2469-9969 .- 1098-0121. ; 79:24, s. 245326 (art no)-
  • Tidskriftsartikel (refereegranskat)abstract
    • Time-resolved terahertz spectroscopy and Monte Carlo simulations of charge-carrier motion are used to investigate photoinduced transient conductivity in a blend of a low-band-gap polyphenylene copolymer and fullerene derivative. The optical excitation pulse generates free holes delocalized on polymer chains. We show that these holes exhibit a very high initial mobility as their initial excess energy facilitates their transport over defects (potential barriers) on polymer chains. The conductivity then drops down rapidly within 1 ps, and we demonstrate that this decrease occurs essentially by two mechanisms. First, the carriers loose their excess energy and they thus become progressively localized between the on-chain potential barriers-this results in a mobility decay with a rate of (180 fs)(-1). Second, carriers are trapped at defects (potential wells) with a capture rate of (860 fs)(-1). At longer time scales, populations of mobile and trapped holes reach a quasiequilibrium state and further conductivity decrease becomes very slow.
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68.
  • Nilsson, K. Peter R., et al. (författare)
  • Imaging distinct conformational states of amyloid-beta fibrils in Alzheimer's disease using novel luminescent probes
  • 2007
  • Ingår i: ACS Chemical Biology. - : American Chemical Society (ACS). - 1554-8929 .- 1554-8937. ; 2:8, s. 553-560
  • Tidskriftsartikel (refereegranskat)abstract
    • Using luminescent conjugated polyelectrolyte probes (LCPs), we demonstrate the possibility to distinguish amyloid-β 1–42 peptide (Aβ1–42) fibril conformations, by analyzing in vitro generated amyloid fibrils of Aβ1–42 formed under quiescent and agitated conditions. LCPs were then shown to resolve such conformational heterogeneity of amyloid deposits in vivo. A diversity of amyloid deposits depending upon morphology and anatomic location was illustrated with LCPs in frozen ex vivo brain sections from a transgenic mouse model (tg-APP swe) of Alzheimer’s disease. Comparative LCP fluorescence showed that compact-core plaques of amyloid β precursor protein transgenic mice were composed of rigid dense amyloid. A more abundant form of amyloid plaque displayed morphology of a compact center with a protruding diffuse exterior. Surprisingly, the compact center of these plaques showed disordered conformations of the fibrils, and the exterior was composed of rigid amyloid protruding from the disordered center. This type of plaque appears to grow from more loosely assembled regions toward solidified amyloid tentacles. This work demonstrates how application of LCPs can prove helpful to monitor aggregate structure of in vivo formed amyloid deposits such as architecture, maturity, and origin.
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69.
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70.
  • Nilsson, Peter, et al. (författare)
  • Conjugated polyelectrolytes : conformation-sensitive optical probes for detection of amyloid fibril formation
  • 2005
  • Ingår i: Biochemistry. - : American Chemical Society (ACS). - 0006-2960 .- 1520-4995. ; 44:10, s. 3718-3724
  • Tidskriftsartikel (refereegranskat)abstract
    • The in vivo deposition of amyloid fibrils is a hallmark of many devastating diseases known as the amyloidoses. Amyloid formation in vitro may also complicate production of proteins in the biotechnology industry. Simple, sensitive, and versatile tools that detect the fibrillar conformation of amyloidogenic proteins are thus of great importance. We have developed a negatively charged conjugated polyelectrolyte that displays different characteristic optical changes, detected visually or by absorption and emission, depending on whether the protein with which it forms a complex is in its native state or amyloid fibril conformation. This simple, rapid, and novel methodology was applied here to two amyloidogenic proteins, insulin and lysozyme, and its validity for detection of their fibrillar conformation was verified by currently used methods such as circular dichroism, transmission electron microscopy, and Congo red absorption.
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