| 1. |
- Aasmundtveit, K.E., et al.
(författare)
-
Structural anisotropy of poly(alkylthiophene) films
- 2000
-
Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 33:8, s. 3120-3127
-
Tidskriftsartikel (refereegranskat)abstract
- The structural anisotropy of various poly(alkylthiophene) films have been studied by X-ray diffraction, using both conventional methods and synchrotron radiation at grazing incidence. Solution-cast films orient with the side chains preferably normal to the film surface, whereas spin-cast films of nonstereoregular material orient with both the main and the side chains in the film plane. For thick (10-50 µm) solution-cast films, the degree of orientation depends strongly on the solvent used for casting, and on the stereoregularity of the polymer, films of stereoregular materials being more oriented than those of nonregular materials. The most oriented nonregular films are those cast from mixtures of chloroform and tetrahydrofuran. Thin (50-500 nm) solution-cast films are more oriented than the thicker ones, and the effects of different stereoregularity or different casting solvents are small. For spin-cast films, the degree of orientation is independent of substrate and solvent. Spin-cast films of stereoregular material have two different phases: One with the side chains normal to the substrate, and another where they are parallel to the substrate. The diffraction peaks of spin-cast poly(octylthiophene) narrow considerably upon heating.
|
|
| 2. |
- Aasmundtveit, K.E., et al.
(författare)
-
Structural aspects of electrochemical doping and dedoping of poly(3,4-ethylenedioxythiophene)
- 2000
-
Ingår i: Synthetic metals. - 0379-6779 .- 1879-3290. ; 113:1, s. 93-97
-
Tidskriftsartikel (refereegranskat)abstract
- Electrochemical dedoping and redoping of p-toluene sulfonate doped poly(3,4-ethylenedioxythiophene) (PEDOT) has been studied with in situ grazing incidence diffraction with water used as an electrolyte. The diffraction peak positions and integrated intensities do not change significantly during doping and dedoping, while the peak widths increase upon dedoping and decrease upon doping. This implies that the lattice parameters and the relative positions of the polymer chains and the p-toluene sulfonate ions remain unchanged, the redox processes being carried out by the motion of smaller ions between the polymer and the electrolyte, and that the structural order decreases upon dedoping and increases upon doping in a reversible manner.
|
|
| 3. |
- Aasmundtveit, K.E., et al.
(författare)
-
Structural ordering in phenyl-substituted polythiophenes
- 2000
-
Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 33:15, s. 5481-5489
-
Tidskriftsartikel (refereegranskat)abstract
- Various substituted poly(phenylthiophene)s have been studied by X-ray diffraction. They are semicrystalline, with very different degrees of crystallinity. Those with para-substituted phenyl groups have a low degree of crystallinity, whereas those with ortho-substituted phenyl groups are more crystalline. The most crystalline materials in this study have two equally long substituents on the phenyl ring, one at the ortho position and the other at the ortho or meta position on the opposite side of the phenyl ring. Poly(3-(2,5-dioctylphenyl)thiophene) (PDOPT) was most thoroughly studied, and a structural model is proposed. The structure of PDOPT is quite different from previously studied substituted polythiophenes in that the octyl side chains are directed normal to the thiophene planes. In this way, the conjugated polymer chains are kept separated from each other. Solution-cast and spin-cast PDOPT films are anisotropic, with the octyl side chains oriented normal to the film surface in both cases. This is contrary to the situation for poly(3-alkylthiophene)s, where solution-cast and spin-cast films orient in different ways.
|
|
| 4. |
- Abramavicius, Vytautas, et al.
(författare)
-
Carrier motion in as-spun and annealed P3HT:PCBM blends revealed by ultrafast optical electric field probing and Monte Carlo simulations
- 2014
-
Ingår i: Physical Chemistry Chemical Physics. - : Royal Society of Chemistry (RSC). - 1463-9084 .- 1463-9076. ; 16:6, s. 2686-2692
-
Tidskriftsartikel (refereegranskat)abstract
- Charge transport dynamics in solar cell devices based on as-spun and annealed P3HT:PCBM films are compared using ultrafast time-resolved optical probing of the electric field by means of field-induced second harmonic generation. The results show that charge carriers drift about twice as far during the first 3 ns after photogeneration in a device where the active layer has been thermally annealed. The carrier dynamics were modelled using Monte-Carlo simulations and good agreement between experimental and simulated drift dynamics was obtained using identical model parameters for both cells, but with different average PCBM and polymer domain sizes. The calculations suggest that small domain sizes in as-spun samples limit the carrier separation distance disabling their escape from geminate recombination.
|
|
| 5. |
|
|
| 6. |
- Admassie, Shimelis, et al.
(författare)
-
A polymer photodiode using vapour-phase polymerized PEDOT as an anode
- 2006
-
Ingår i: Solar Energy Materials & Solar Cells. ; 90:2, s. 133-141
-
Tidskriftsartikel (refereegranskat)abstract
- We report the photovoltaic properties of devices made using a highly conducting polymer electrode, from vapor-phase polymd. poly (3,4-ethylenedioxy) thiophene (VPP PEDOT) on glass substrate as an anode and a polyfluorene copolymer poly[2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4',7'-di-2thienyl-2',1'3'-benzothiadiazole)] (APFO-3) mixed with [6,6]-phenyl-C61-butyric acid methylester (PCBM) in the ratio of 1:4 as the active layer. The device performance was compared with that of devices made with PEDOT-PSS on glass substrates. The surfaces of VPP PEDOT were imaged using at. force microscopy (AFM). [on SciFinder (R)]
|
|
| 7. |
- Admassie, Shimelis, et al.
(författare)
-
A renewable biopolymer cathode with multivalent metal ions for enhanced charge storage
- 2014
-
Ingår i: JOURNAL OF MATERIALS CHEMISTRY A. - : Royal Society of Chemistry. - 2050-7488. ; 2:6, s. 1974-1979
-
Tidskriftsartikel (refereegranskat)abstract
- A ternary composite supercapacitor electrode consisting of phosphomolybdic acid (HMA), a renewable biopolymer, lignin, and polypyrrole was synthesized by a simple one-step simultaneous electrochemical deposition and characterized by electrochemical methods. It was found that the addition of HMA increased the specific capacitance of the polypyrrole-lignin composite from 477 to 682 F g(-1) ( at a discharge current of 1 A g(-1)) and also significantly improved the charge storage capacity from 6(to 128 mA h g(-1).
|
|
| 8. |
|
|
| 9. |
- Admassie, Shimelis, et al.
(författare)
-
Electrochemical and optical studies of the band gaps of alternating polyfluorene copolymers
- 2006
-
Ingår i: Synthetic Metals. ; 156:7-8, s. 614-623
-
Tidskriftsartikel (refereegranskat)abstract
- The electrochem. and optical properties of alternating polyfluorene copolymers with low band gaps were detd. 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 polymers were solvent-casted on Pt disk electrode and the band gaps were estd. from cyclic voltammetry (CV). These values were compared with values obtained from optical absorption measurements. Although the electrochem. detd. band gaps are slightly higher than the optical band gap in most cases, values are well correlated. The values of the band gaps detd. range from 2.1 to 1.3 eV. [on SciFinder (R)]
|
|
| 10. |
|
|
