| 1. |
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| 2. |
- Gadisa, Abay, et al.
(författare)
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A new donor-acceptor-donor polyfluorene copolymer with balanced electron and hole mobility
- 2007
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Ingår i: Adv. Funct. Mater. FIELD Full Journal Title:Advanced Functional Materials. ; 17:18, s. 3836-3842
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Tidskriftsartikel (refereegranskat)abstract
- A new alternating polyfluorene copolymer poly[2,7-(9,9-dioctylfluoren)-alt-5,5-(5',8'-di-2-thienyl-(2',3'-bis-(3''-octyloxyphenyl)-quinoxaline))] (APFO-15), which has electron donor-acceptor-donor units in between the fluorene units, is synthesized and characterized. This polymer has a strong absorption and emission in the visible range of the solar spectrum. Its electroluminescence and photolumin escence emissions extend from about 560 to 900 nm. Moreover, solar cells with efficiencies in excess of 3.5 % have been realized from blends of APFO-15 and an electron acceptor mol., a mathanofullerene [6,6]-phenyl-C61-butyric acid Me ester (PCBM). It has also been obsd. that electron and hole transport is balanced both in the pure polymer phase and in polymer/PCBM bulk heterojunction films, which makes this material quite attractive for applications in opto-electronic devices. [on SciFinder (R)]
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| 3. |
- Gadisa, Abay, et al.
(författare)
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Bipolar Charge Transport in Fullerene Molecules in a Bilayer and Blend of Polyfluorene Copolymer and Fullerene
- 2010
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Ingår i: ADVANCED MATERIALS. - : Wiley. - 0935-9648. ; 22:9, s. 1008-
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Tidskriftsartikel (refereegranskat)abstract
- Efficient polymer solar cells typically contain the fullerene derivative [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), which promotes dissociation of excited states and enhances charge transport. The ability of PCBM to transport holes in solar cell bulk heterojunction films is monitored via the electroluminescence emission of a bulk heterojunction blend of PCBM and a polyfluorene copolymer. In polymer/fullerene bilayer diodes, fullerene emission is also observed.
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| 4. |
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| 5. |
- Gadisa, Abay, et al.
(författare)
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Correlation between oxidation potential and open-circuit voltage of composite solar cells based on blends of polythiophenes/fullerene derivative
- 2004
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 84:9, s. 1609-1611
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Tidskriftsartikel (refereegranskat)abstract
- The photovoltaic parameters of donor/acceptor blend organic solar cells are highly influenced by several parameters, such as the strength of the acceptor species, the morphology of the film due to the solvent, and the mobility of the free charge carriers. In this work, the open-circuit voltage (Voc) of solar cells based on series of conjugated polythiophene polymers were measured and compared. In every cell, the donor polymer was blended with an electron acceptor fullerene molecule. The devices were constructed in a sandwich structure with indium tin oxide (ITO)/metallic polymer (PEDOT:PSS) acting as an anode and Al or LiF/Al acting as a cathode. Comparing the Voc of all the cells shows that this important photovoltaic parameter is systematically varying with the polymer. The variation of photovoltage is attributed to the variation of the oxidation potential of the donor conjugated polymers after due consideration of the different injection conditions in the varying polymers.
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| 6. |
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| 7. |
- Gadisa, Abay, et al.
(författare)
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Improvements of fill factor in solar cells based on blends of polyfluorene copolymers as electron donors
- 2007
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Ingår i: Thin Solid Films. - : Elsevier BV. - 0040-6090 .- 1879-2731. ; 515:5, s. 3126-3131
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Tidskriftsartikel (refereegranskat)abstract
- The photovoltaic characteristics of solar cells based on alternating polyfluorene copolymers, poly(2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)) (APFO-3), and poly(2,7-(9,9-didodecyl-fluorene)-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)) (APFO-4), blended with an electron acceptor fullerene molecule [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), have been investigated and compared. The two copolymers have the same aromatic backbone structure but differ by the length of their alkyl side chain. The overall photovoltaic performance of the solar cells is comparable irrespective of the copolymer used in the active layer. However, the fill factor (FF) values of the devices are strongly affected by the copolymer type. Higher FF values were realized in solar cells with APFO-4 (with longer alkyl side chain)/PCBM bulk heterojunction active layer. On the other hand, devices with blends of APFO-3/APFO-4/PCBM were found to render fill factor values that are intermediate between the values obtained in solar cells with APFO-3/PCBM and APFO-4/PCBM active film. Upon using APFO-3/APFO-4 blends as electron donors, the cell efficiency can be enhanced by about 16% as compared to cells with either APFO-3 or APFO-4. The transport of holes in each polymer obeys the model of hopping transport in disordered media. However, the degree of energetic barrier against hopping was found to be larger in APFO-3. The tuning of the photovoltaic parameters will be discussed based on studies of hole transport in the pure polymer films, and morphology of blend layers. The effect of bipolar transport in PCBM will also be discussed.
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| 8. |
- Gadisa, Abay, et al.
(författare)
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Red and near infrared polarized light emission from polyfluorene copolymer based light emitting diodes
- 2007
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 90:11, s. 113510-
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Tidskriftsartikel (refereegranskat)abstract
- The authors report polarized red, electroluminescence peak at 705 nm and near infrared, electroluminescence peak at 950 nm, light emission from light emitting diodes based on two polyfluorene copolymers. The copolymers are synthesized from a fluorene monomer combined with donor-acceptor-donor comonomers and designed to have a low band gap and form birefringent liquid crystalline phases. Emission occurs from aligned thin films of polymer layers. The emissive layers are aligned by spin coating on a layer of rubbed conducting polymer poly(3,4-ethylene dioxythiophene)-poly(styrene sulphonate) and thermally converted into glassy nematic liquid crystalline state.
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| 9. |
- Gadisa, Abay, et al.
(författare)
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Red and near infrared polarized light emissions from polyfluorene copolymer based light emitting diodes
- 2007
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Ingår i: Appl. Phys. Lett. FIELD Full Journal Title:Applied Physics Letters. ; 90:11, s. 113510/1-113510/3
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Tidskriftsartikel (refereegranskat)abstract
- The authors report polarized red, electroluminescence peak at 705 nm and near IR, electroluminescence peak at 950 nm, light emission from light emitting diodes based on two polyfluorene copolymers. The copolymers are synthesized from a fluorene monomer combined with donor-acceptor-donor comonomers and designed to have a low band gap and form birefringent liq. cryst. phases. Emission occurs from aligned thin films of polymer layers. The emissive layers are aligned by spin coating on a layer of rubbed conducting polymer poly(3,4-ethylene dioxythiophene)-poly(styrene sulfonate) and thermally converted into glassy nematic liq. cryst. state. [on SciFinder (R)]
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| 10. |
- Gadisa, Abay, et al.
(författare)
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Stoichiometry dependence of charge transport in polymer/methanofullerene and polymer/C70 derivative based solar cells
- 2006
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Ingår i: Organic electronics. - : Elsevier BV. - 1566-1199. ; 7:4, s. 195-204
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Tidskriftsartikel (refereegranskat)abstract
- Charge transport in a near infrared absorbing polyfluorene copolymer (APFO-Green1) and its blends with methanofullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM), and 3′-(3,5-bis-trifluoromethylphenyl)-1′-(4-nitrophenyl)pyrazolino[70]fullerene (BTPF70) is reported. PCBM and BTPF70 are electron acceptor and transporting molecules in polymer based solar cells. The BTPF70 has emerged as a new electron acceptor molecule that provides adequate exciton dissociation when blended with the low band gap polyfluorene copolymer APFO-Green1. Electron transport in both net PCBM and BTPF70 films are subjected to positional and energetic disorder, with the degree of disorder being more pronounced in BTPF70. On the other hand, mixing PCBM with conjugated polymers usually leads to increased hole mobility. We have investigated and compared the acceptor concentration dependence of charge transport in APFO-Green1/PCBM and APFO-Green1/BTPF70 blend films. For better understanding of the charge transport in the heterojunction films, the field and temperature dependence of hole transport in pure APFO-Green1 films has also been studied. It is observed that the behavior of hole mobility in the blend layer is sensitive to the acceptor type. For APFO-Green1/PCBM hole only devices, the hole mobility attains a local maximum at 67 wt.% of PCBM, while on the contrary mixing any amount of BTPF70 with APFO-Green1 results into degradation of hole transport. Electron transport in both blends, however, increases monotonically as a function of acceptor loading.
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| 11. |
- Gadisa, Abay, et al.
(författare)
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Stoichiometry dependence of charge transport in polymer/methanofullerene and polymer/C70 derivative based solar cells
- 2006
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Ingår i: Organic Electronics. ; 7:4, s. 195-204
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Tidskriftsartikel (refereegranskat)abstract
- Charge transport in a near IR absorbing polyfluorene copolymer (APFO-Green1) and its blends with methanofullerene [6,6]-Ph C61-butyric acid Me ester (PCBM), and 3'-(3,5-bis-trifluoromethylphenyl)-1'-(4-nitrophenyl)pyrazolino[70]fullerene (BTPF70) is reported. PCBM and BTPF70 are electron acceptor and transporting mols. in polymer based solar cells. The BTPF70 has emerged as a new electron acceptor mol. that provides adequate exciton dissocn. when blended with the low band gap polyfluorene copolymer APFO-Green1. Electron transport in both net PCBM and BTPF70 films are subjected to positional and energetic disorder, with the degree of disorder being more pronounced in BTPF70. On the other hand, mixing PCBM with conjugated polymers usually leads to increased hole mobility. We have investigated and compared the acceptor concn. dependence of charge transport in APFO-Green1/PCBM and APFO-Green1/BTPF70 blend films. For better understanding of the charge transport in the heterojunction films, the field and temp. dependence of hole transport in pure APFO-Green1 films has also been studied. It is obsd. that the behavior of hole mobility in the blend layer is sensitive to the acceptor type. For APFO-Green1/PCBM hole only devices, the hole mobility attains a local max. at 67 wt.% of PCBM, while on the contrary mixing any amt. of BTPF70 with APFO-Green1 results into degrdn. of hole transport. Electron transport in both blends, however, increases monotonically as a function of acceptor loading. [on SciFinder (R)]
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| 12. |
- Gadisa, Abay, 1972-
(författare)
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Studies of Charge Transport and Energy Level in Solar Cells Based on Polymer/Fullerene Bulk Heterojunction
- 2006
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- π-Conjugated polymers have attracted considerable attention since they are potential candidates for various opto-electronic devices such as solar cells, light emitting iodes, photodiodes, and transistors. Electronic de vices based on conjugated polymers can be easily processed at low temperature using inexpensive technologies. This leads to cost reduction, a key-deriving factor for choosing conjugated polymers for various types of applications. In particular, polymer based solar cells are of special interest due to the fact that they can play a major role in generating clean and cheap energy in the future.The investigations described in thesis are aimed mainly at understanding charge transport and the role of energy le vels in solar cells based on polymer/acceptor bulk heterojunction (BHJ) active films. Best polymer based solar cells, with efficiency 4 to 5%, rely on polymer/fullerene BHJ active films. These solar cells are in an immature state to be used for energy conversion purposes. In order to enhance their performance, it is quite important to understand the efficiency-limiting factors. Solid films of conjugated polymers compose conjugation segments that are randomly distributed in space and energy. Such distributio n gives rise to the localization of charge carriers and hence broadening of electron density of states. Consequently, electronic wave functions have quite poor overlap resulting into absence of continuous band transport. Charge transport in polymers and organic materials, in general, takes place by hopping among the localized states. This makes a bottleneck to the performance of polymer-based solar cells. In this context, the knowledge of charge transport in the solar cell materials is quite important to develop materials and device architectures that boost the efficiency of such solar cells.Most of the transport studies are based on polyfluorene copolymers and fullerene electron acceptor molecules. Fullerenes are blended with polymers to enhance the dissociation of excited state into free carriers and transport free electrons to the respective electrode. The interaction within the polymer-fullerene complex, therefore, plays a major role in the generation and transport of both electrons and holes. In this thesis, we present and discuss the effect of various polymer/fullerene compositions on hole percolation paths. We mainly focus on hole transport since its mobility is quite small as compared to electron mobility in the fullerenes, leading to creation of spa ce charges within the bulk of the solar cell composite. Changing a polymer band gap may necessitate an appropriate acceptor type in order to fulfill the need for sufficient driving force for dissociation of photogenerated electron-hole pairs. We have observed that different acceptor types give rise to completely different hole mobility in BHJ films. The change of hole transport as a function of acceptor type and concentration is mainly attributed to morphological changes. The effect of the acceptors in connection to hole transport is also discussed. The later is supported by studies of bipolar transport in pure electron acceptor layers. Moreover, the link between charge carrier mobility and photovoltaic parameters has also been studied and presented in this thesis.The efficiency of polymer/fullerene-based solar cells is also significantly limited by its open-circuit voltage (Voc), a parameter that does not obey the metal-insulator-metal principle due to its complicated characteristics. In this thesis, we address the effect of varying polymer oxidation potential on Voc of the polymer/fullerene BHJ based solar cells. Systematic investigations have been performed on solar cells that comprise several polythiophene polymers blended with a fullerene derivative electron acceptor molecule. The Voc of such solar cells was found to have a strong correlation with the oxidation potential of the polymers. The upper limit to Voc of the aforementioned solar cells is thermodynamically limited by the net internal electric filed generated by the difference in energy levels of the two materials in the blend.The cost of polymer-based solar cells can be reduced to a great extent through realization of all-plastic and flexible solar cells. This demands the replacement of the metallic components (electrodes) by highly conducting polymer films. While hole conductor polymers are available, low work function polymer electron conductors are rare. In this thesis, prototype solar cells that utilizes a highly conducting polymer, which has a work function of ~ 4.3 eV, as a cathode are demonstrated. Development of this material may eventually lead to fabrication of large area, flexible and cheap solar cells. The transparent nature of the polymer cathode may also facilitate fabrication of multi-layer and tandem solar cells.In the last chapter of this thesis, we demonstrate generation of red and near infrared polarized light by employing thermally converted thin films of polyfluorene copolymers in light emitting diodes. This study, in particular, aims at fabricating polarized infrared light emitting devices.
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| 13. |
- Gadisa, Abay, et al.
(författare)
-
Transparent polymer cathode for organic photovoltaic devices
- 2006
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Ingår i: Synthetic metals. - : Elsevier BV. - 0379-6779 .- 1879-3290. ; 156:16-17, s. 1102-1107
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Tidskriftsartikel (refereegranskat)abstract
- We demonstrate a prototype solar cell with a transparent polymer cathode, and indium-tin-oxide (ITO)/poly (3, 4-ethylene dioxythiophene)-poly (styrene sulphonate) (PEDOT:PSS) anode. As an active layer, thin film of a bulk heterojunction of polyfluorene copolymer poly[2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4′,7′-di-2thienyl-2′,1′3′-benzothiadiazole)] (APFO-3) and an electron acceptor molecule [6] and [6]-phenyl-C61-butyric acid methyl ester (PCBM) (1:4 wt.) was sandwiched between the two transparent polymer electrodes. The cathode is another form of PEDOT formed by vapor phase polymerised PEDOT (VPP PEDOT) of conductivity 102–103 S/cm. The cathode is supported on an elastomeric substrate, and forms a conformal contact to the APFO-3/PCBM blend. Transparent solar cells are useful for building multilayer and tandem solar cells.
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| 14. |
- Gadisa, Abay, et al.
(författare)
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Transparent polymer cathode for organic photovoltaic devices
- 2006
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Ingår i: Synthetic Metals. ; 156:16-17, s. 1102-1107
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Tidskriftsartikel (refereegranskat)abstract
- A prototype solar cell with a transparent polymer cathode and an ITO/poly(3,4-ethylene dioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS) anode was fabricated. As an active layer, a thin film of a bulk heterojunction of polyfluorene copolymer, poly[2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (APFO-3) and an electron acceptor mol. [6,6]-phenyl-C61-butyric acid Me ester (PCBM) (1:4 by wt.) was sandwiched between the 2 transparent polymer electrodes. The cathode is another form of PEDOT formed by vapor phase polymd. PEDOT (VPP PEDOT) with a cond. 102-103 S/cm. The cathode is supported on an elastomeric substrate and forms a conformal contact to the APFO-3/PCBM blend. Transparent solar cells are useful for building multilayer and tandem solar cells. [on SciFinder (R)]
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| 15. |
- Inganaes, Olle, et al.
(författare)
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Alternating fluorene copolymer-fullerene blend solar cells
- 2005
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Ingår i: Optical Science and Engineering. ; 99, s. 387-402
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Tidskriftsartikel (refereegranskat)abstract
- We present a new class of alternating fluorene copolymers, which can be combined with a fullerene acceptor, to make polymer blends suitable for photovoltaic energy conversion. By choice of comonomers in the polymer, it is possible to engineer the optical absorption spectrum and to cover the wavelength range down to 900 nm. The transport properties of the polymers investigated so far are competitive with other polymers used in polymer solar cells and the mixing of polymers with acceptors in the form of fullerenes is extensive. These polymers are therefore of interest in the future developments of high-performance polymer solar cells. [on SciFinder (R)]
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| 16. |
- Inganäs, Olle, 1951-, et al.
(författare)
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Alternating fluorene copolymer/fullerene blend solar cells
- 2005. - 1
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Ingår i: Organic Photovoltaics. - Boca Raton, FL, USA : CRC Press. - 082475963X - 9780824759636 ; , s. 387-402
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Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
- Recently developed organic photovoltaics (OPVs) show distinct advantages over their inorganic counterparts due to their lighter weight, flexible shape, versatile materials synthesis and device fabrication schemes, and low cost in large-scale industrial production. Although many books currently exist on general concepts of PV and inorganic PV materials and devices, few are available that offer a comprehensive overview of recently fast developing organic and polymeric PV materials and devices.Organic Photovoltaics: Mechanisms, Materials, and Devicesfills this gap. The book provides an international perspective on the latest research in this rapidly expanding field with contributions from top experts around the world. It presents a unified approach comprising three sections: General Overviews; Mechanisms and Modeling; and Materials and Devices. Discussions include sunlight capture, exciton diffusion and dissociation, interface properties, charge recombination and migration, and a variety of currently developing OPV materials/devices. The book also includes two forewords: one by Nobel Laureate Dr. Alan J. Heeger, and the other by Drs. Aloysius Hepp and Sheila Bailey of NASA Glenn Research Center.Organic Photovoltaics equips students, researchers, and engineers with knowledge of the mechanisms, materials, devices, and applications of OPVs necessary to develop cheaper, lighter, and cleaner renewable energy throughout the coming decades.
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| 17. |
- Inganäs, Olle, et al.
(författare)
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Low bandgap alternating polyfluorene copolymers in plastic photodiodes and solar cells
- 2004
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Ingår i: Applied Physics A. - : Springer Science and Business Media LLC. - 0947-8396 .- 1432-0630. ; 79:1, s. 31-35
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Tidskriftsartikel (refereegranskat)abstract
- We report a comparative study of plastic photodiodes using four different copolymers of fluorene, with a variation of alkyl side chain length and chemical structure. Photodiode materials are formed by blending the polymers with a fullerene derivative and spincoating the blend solution. A photovoltage of 1 V is obtained in devices, where the anode is a doped polymer and the cathode is LiF/Al. Monochromatic quantum efficiencies are better than 40% over most of the absorption range, and under solar light AM 1.5 simulation, we reach energy efficiencies beyond 2%. The high fill factors obtained in some of the devices indicate that these are of interest for more elaborate optimisation. Reasons for the benign electrical transport are discussed. © Springer-Verlag 2004.
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| 18. |
- Jespersen, Kim, et al.
(författare)
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Charge formation and transport in bulk-heterojunction solar cells based on alternating polyfluorene copolymers blended with fullerenes
- 2006
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Ingår i: Organic Electronics. - : Elsevier BV. - 1566-1199 .- 1878-5530. ; 7:4, s. 235-242
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Tidskriftsartikel (refereegranskat)abstract
- We investigate charge formation in bulk-heterojunction solar cells based on conjugated polymers in the form of alternating polyfluorene copolymers and the methanofullerene PCBM. Using transient absorption spectroscopy we show that optimal charge formation is obtained with 20-50 wt% PCBM. This is in contrast to the maximum short circuit current density obtained at similar to 80 wt% PCBM as determined by steady state current density-voltage characterization. Hence, we show explicitly that the solar cell performance of these interpenetrating polymer networks containing PCBM is limited by charge transport rather than by formation of charges. (c) 2006 Elsevier B.V. All rights reserved.
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| 19. |
- Mammo, W., et al.
(författare)
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New low band gap alternating polyfluorene copolymer-based photovoltaic cells
- 2007
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Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248 .- 1879-3398. ; 91:11, s. 1010-1018
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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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| 20. |
- Mammo, Wendimagegn, 1954, et al.
(författare)
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New low band gap alternating polyfluorene copolymer-based photovoltaic cells
- 2007
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Ingår i: Sol. Energy Mater. Sol. Cells FIELD Full Journal Title:Solar Energy Materials & Solar Cells. ; 91:11, s. 1010-1018
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Tidskriftsartikel (refereegranskat)abstract
- New low band gap alternating polyfluorene copolymers were synthesized for use in plastic solar cells and their optical, electrochem., and photovoltaic characteristics 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 HOMO-LUMO values were estd. from electrochem. 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 detd. 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 prepn. 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. [on SciFinder (R)]
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| 21. |
- Tvingstedt, Kristofer, et al.
(författare)
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Electroluminescence from Charge Transfer States in Polymer Solar Cells
- 2009
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Ingår i: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 131:33, s. 11819-11824
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Tidskriftsartikel (refereegranskat)abstract
- In this article we report the weak but omnipresent electroluminescence (EL) from several types of organic polymer:fullerene bulk heterojunction solar cells biased in the forward direction. The light emitted from blends of Some commonly used polymers and the fullerene molecule is significantly different from that of any of the pure materials comprising the blend. The lower energy of the blend EL is found to correlate with both the voltage onset of emission and the open-circuit voltage of the photovoltaic cell under solar illumination. WE., accordingly interpret the emission to originate from interfacial charge transfer state recombination and emphasize EL as a very valuable tool to characterize the charge transfer state present in donor/acceptor organic photovoltaic (OPV) cells.
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| 22. |
- Vandewal, Koen, et al.
(författare)
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On the origin of the open-circuit voltage of polymer-fullerene solar cells
- 2009
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Ingår i: NATURE MATERIALS. - : Springer Science and Business Media LLC. - 1476-1122 .- 1476-4660. ; 8:11, s. 904-909
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Tidskriftsartikel (refereegranskat)abstract
- The increasing amount of research on solution-processable, organic donor-acceptor bulk heterojunction photovoltaic systems, based on blends of conjugated polymers and fullerenes has resulted in devices with an overall power-conversion efficiency of 6%. For the best devices, absorbed photon-to-electron quantum efficiencies approaching 100% have been shown. Besides the produced current, the overall efficiency depends critically on the generated photovoltage. Therefore, understanding and optimization of the open-circuit voltage (V-oc) of organic solar cells is of high importance. Here, we demonstrate that charge-transfer absorption and emission are shown to be related to each other and V-oc in accordance with the assumptions of the detailed balance and quasi-equilibrium theory. We underline the importance of the weak ground-state interaction between the polymer and the fullerene and we confirm that V-oc is determined by the formation of these states. Our work further suggests alternative pathways to improve V-oc of donor-acceptor devices.
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| 23. |
- Vandewal, Koen, et al.
(författare)
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Relating the open-circuit voltage to interface molecular properties of donor:acceptor bulk heterojunction solar cells
- 2010
-
Ingår i: PHYSICAL REVIEW B. - : American Physical Society. - 1098-0121. ; 81:12, s. 125204-
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Tidskriftsartikel (refereegranskat)abstract
- The open-circuit voltage (V-oc) of polymer:fullerene bulk heterojunction solar cells is determined by the interfacial charge-transfer (CT) states between polymer and fullerene. Fourier-transform photocurrent spectroscopy and electroluminescence spectra of several polymer:fullerene blends are used to extract the relevant interfacial molecular parameters. An analytical expression linking these properties to V-oc is deduced and shown to be valid for photovoltaic devices comprising three commonly used conjugated polymers blended with the fullerene derivative [6,6]-phenyl-C61-butyric acid methyl ester (PCBM). V-oc is proportional to the energy of the CT states E-CT. The energetic loss q Delta V between E-CT and qV(oc) vanishes when approaching 0 K. It depends linearly on T and logarithmically on illumination intensity. Furthermore q Delta V can be reduced by decreasing the electronic coupling between polymer and fullerene or by reducing the nonradiative recombination rate. For the investigated devices we find a loss q Delta V of similar to 0.6 eV at room temperature and under solar illumination conditions, of which similar to 0.25 eV is due to radiative recombination via the CT state and similar to 0.35 eV is due to nonradiative recombination.
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| 24. |
- Zhang, Fengling, et al.
(författare)
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Influence of buffer layers on the performance of polymer solar cells
- 2004
-
Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 84:19, s. 3906-3908
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Tidskriftsartikel (refereegranskat)abstract
- The study of the influence of different anode buffer layers on the performance of solar cells based on blends of polyfluorene copolymers, acting as electron donor, and [6,6]-phenyl-C61-butyric acid methylester (PCBM), acting as electron acceptor was presented. The construction of buffer later was done from different forms of poly(3, 4-ethylenedioxythiophene) poly-(styrenesulfonate) (PEDOT-PSS). Variations in open-circuit voltage, short-circuit current and fill factor were also observed. The anode buffer layer influences the photovoltage of polymer solar cells by controlling the conditions for charge injection at the anode.
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