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Sökning: WAKA:ref > Inganäs Olle

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21.
  • Andersson, Lars Mattias, et al. (författare)
  • Stoichiometry, mobility, and performance in bulk heterojunction solar cells
  • 2007
  • Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 91:7, s. 071108-
  • Tidskriftsartikel (refereegranskat)abstract
    • Bipolar transport in blends of a copolymer of fluorene, thiophene and electron accepting groups, and the substituted fullerene [6,6]-phenyl-C61-butyric acid methylester have been studied through charge extraction by linearly increasing voltage on solar cells and with field effect transistors. Between 10% and 90% polymer has been used and the results show a clear correlation to solar cell performance. Optimal solar cells comprise 20% polymer and have a power conversion efficiency of 3.5%. The electron mobility is increasing strongly with fullerene content, but is always lower than the hole mobility, thus explaining the low amount of polymer in optimized devices.
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22.
  • Andersson, Mattias, et al. (författare)
  • From short to long - Optical and electrical transients in photovoltaic bulk heterojunctions of polyfluorene/fullerenes
  • 2009
  • Ingår i: Chemical Physics Letters. - : Elsevier BV. - 0009-2614 .- 1873-4448 .- 0301-0104. ; 357:1-3, s. 120-123
  • Tidskriftsartikel (refereegranskat)abstract
    • We combine results from transient optical absorption in a bulk heterojunction polymer donor/fullerene acceptor material, obtained in the optical range as well as in the THz range, with results from electrical transients after a short light pulse, to present a unified interpretation of the transport of charge after the very first act of photoinduced charge transfer. We find that the mobility of charges is initially very high, but dramatically reduced with time, to arrive at values three orders of magnitude lower. We show that this can be understood as a consequence of the transport of hot charges by hopping through the density of states, from higher to lower energies.
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23.
  • Andersson, Mattias, et al. (författare)
  • Intrinsic and extrinsic influences on the temperature dependence of mobility in conjugated polymers
  • 2008
  • Ingår i: Organic electronics. - : Elsevier. - 1566-1199 .- 1878-5530. ; 9:5, s. 569-574
  • Tidskriftsartikel (refereegranskat)abstract
    • The temperature dependence of charge carrier mobility in conjugated polymers and their blends with fullerenes is investigated with different electrical methods, through field effect transistor (FET), space charge limited current (SCLC) and charge extraction (CELIV) measurements. Simple models, such as the Gaussian disorder model (GDM), are shown to accurately predict the temperature behavior, and a good correlation between the different measurement methods is obtained. Inconsistent charge carrier concentrations in the modeling are explained through intrinsic non-equilibrium effects, and are responsible for the limited applicability of existing numerical models. A severe extrinsic influence from water in FETs with a hydrophilic insulator interface is also demonstrated. The presence of water leads to a significant overestimate of the disorder in the materials from measurements close to room temperature and erratic behavior in the 150-350 K range. To circumvent this problem it is shown to be necessary to measure under ultra high vacuum (UHV) conditions. © 2008 Elsevier B.V. All rights reserved.
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24.
  • Andersson, Mattias, et al. (författare)
  • Mixed C60/C70 based fullerene acceptors in polymer bulk-heterojunction solar cells
  • 2012
  • Ingår i: Organic Electronics: physics, materials, applications. - : Elsevier BV. - 1566-1199 .- 1878-5530. ; 13:12, s. 2856-2864
  • Tidskriftsartikel (refereegranskat)abstract
    • Different mixtures of identically substituted C60 and C70 based fullerens have been used as acceptors in three polymer: fullerene systems that strongly express various performance limiting aspects of bulk heterojunction solar cells. Results are correlated with, and discussed in terms of e.g. morphology, charge separation, and charge transport. In these systems, there appears to be no relevant differences in either mobility or energy level positions between the identically substituted C60 and C70 based fullerenes tested. Examples of how fullerene mixtures influence the nano-morphology of the active layer are given. An upper limit to the open circuit voltage that can be obtained with fullerenes is also suggested.
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25.
  • Andersson, Mattias, et al. (författare)
  • Mobility and fill factor correlation in geminate recombination limited solar cells
  • 2011
  • Ingår i: Journal of Applied Physics. - : American Institute of Physics (AIP). - 0021-8979 .- 1089-7550. ; 110:2, s. 024509-
  • Tidskriftsartikel (refereegranskat)abstract
    • Empirical data for the fill factor as a function of charge carrier mobility for two different polymer: fullerene systems is presented and analyzed. The results indicate that charge extraction depth limitations and space charge effects are inconsistent with the observed behavior, and the decrease in the fill factor is, instead, attributed to the field-dependent charge separation and geminate recombination. A solar cell photocurrent limited by the Onsager-Braun charge transfer exciton dissociation is shown to be able to accommodate the experimental observations. Charge dissociation limited solar cells always benefit from increased mobilities, and the negative contribution from the reduced charge separation is shown to be much more important for the fill factor in these material systems than any adverse effects from charge carrier extraction depth limitations or space charge effects due to unbalanced mobilities. The logarithmic dependence of the fill factor on the mobility for such a process is also shown to imply that simply increasing the mobilities is an impractical way to reach very high fill factors under these conditions since unrealistically high mobilities are required. A more controlled morphology is, instead, argued to be necessary for high performance.
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26.
  • Andersson, Mats R., et al. (författare)
  • Electroluminescence from Substituted Poly(thiophenes) : From Blue to Near-Infrared
  • 1995
  • Ingår i: Macromolecules. - : American Chemical Society. - 0024-9297 .- 1520-5835. ; 28:22, s. 7525-7529
  • Tidskriftsartikel (refereegranskat)abstract
    • We report a systematic approach to the control of the conjugation length along the poly(thiophene) backbone. The planarity of the main chain can be permanently modified by altering the pattern of substitution and character of the substituents on the poly(thiophene) chain, and the conjugation length is thus modified. We obtain blue, green, orange, red, and near-infrared electroluminescence from four chemically distinct poly(thiophenes). The external quantum efficiencies are in the range of 0.01-0.6%.
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27.
  • Andersson, Mats R., et al. (författare)
  • Improved photoluminescence efficiency of films from conjugated polymers
  • 1997
  • Ingår i: Synthetic metals. - : Elsevier. - 0379-6779 .- 1879-3290. ; 85:1-3, s. 1383-1384
  • Tidskriftsartikel (refereegranskat)abstract
    • We have demonstrated two general ways to increase the photoluminescence efficiency of films from conjugated polymers. One is to disperse the conjugated polymer on a molecular level by using attractive forces between the conjugated polymer and the matrix. The other method is to substitute the conjugated polymer with side chains which separates the conjugated backbones. Using this idea a new poly(thiophene) with a photoluminescence efficiency of 16% in films has been prepared. LEDs from this polymer exhibit an external efficiency of 0.1% for single layer and 0.7% for double layer diodes.
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28.
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29.
  • Andersson, Mats R., et al. (författare)
  • Regioselective polymerization of 3-(4-octylphenyl)thiophene with FeCl3
  • 1994
  • Ingår i: Macromolecules. - : American Chemical Society. - 0024-9297 .- 1520-5835. ; 27:22, s. 6503-6506
  • Tidskriftsartikel (refereegranskat)abstract
    • We have shown that it is possible to regioselectively polymerize 3-(4-octylphenyl) thiophene with FeCl3. Adding FeCl3 slowly to the monomer leads to a soft and therefore regioselective polymerization. The head-to-tail content was determined by H-1 NMR to be 94 +/- 2%. Thin films of the polymer treated with chloroform vapor have an absorption maximum at 602 nm (2.06 eV) with clear vibronic fine structure. Free standing films have a conductivity of 4 S/cm, which is 100 times higher than for earlier prepared poly(3-(4-octylphenyl)thiophene). A mechanism for the regioregular polymerization is also proposed.
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30.
  • Andersson, Mats R., et al. (författare)
  • Synthesis of poly(alkylthiophenes) for light-emitting diodes
  • 1995
  • Ingår i: Synthetic metals. - : Elsevier. - 0379-6779 .- 1879-3290. ; 71:1-3, s. 2183-2184
  • Tidskriftsartikel (refereegranskat)abstract
    • We have demonstrated a general way to tune the emission of poly(alkylthiophenes) by using steric interaction between the repeating units. Light-emitting diodes prepared of the polymers have blue to near-infrared emission.
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  • Resultat 21-30 av 445
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Zhang, Fengling (78)
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Inganäs, Olle, 1951- (49)
Andersson, Mats R (33)
Wang, Ergang, 1981 (33)
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