| 1. |
|
|
| 2. |
- Andersson, Lars Mattias, et al.
(författare)
-
Bipolar transport observed through extraction currents on organic photovoltaic blend materials
- 2006
-
Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 89, s. 142111-
-
Tidskriftsartikel (refereegranskat)abstract
- Both electron and hole mobilities have been simultaneously measured through charge extraction by linearly increasing voltage on polymer heterojunction solar cells with varying stoichiometry of polymer and acceptor. The polymer is a low band gap copolymer of fluorene, thiophene, and electron accepting groups named APFO-Green 5, and the acceptor is [6,6]-phenyl-C61-butyric acid methylester. Results are correlated to field effect transistor measurements on the same material system. A monotonous increase in mobility for both carrier types is observed with increased acceptor loading.
|
|
| 3. |
- 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.
|
|
| 4. |
- 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.
|
|
| 5. |
|
|
| 6. |
|
|
| 7. |
- Barrau, Sophie, et al.
(författare)
-
Nanomorphology of Bulk Heterojunction Organic Solar Cells in 2D and 3D Correlated to Photovoltaic Performance
- 2009
-
Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 42:13, s. 4646-4650
-
Tidskriftsartikel (refereegranskat)abstract
- Control of the nanoscale morphology of the donor-acceptor material blends inorganic solar Cells is critical for optimizing the photovoltaic performances. The influence of intrinsic (acceptor materials) and extrinsic (donor:acceptor weight ratio, substrate, solvent) parameters was investigated, by atomic force microscopy (AFM) and electron tomography (ET), on the nanoscale phase separation of blends of a low-band-gap alternating polyfluorene copolymers (APFO-Green9) with [6,6]-phenyl-C-71-butyric acid methyl ester ([70]PCBM). The photovoltaic performances display an optimal efficiency for the device elaborated with a 1:3 APFO-Green polymer:[70][PCBM weight ratio and spin-coated from chloroform solution. The associated active layer morphology presents small phase-separated domains which is a good balance between as a large interfacial donor-acceptor area and Continuous paths of the donor and acceptor phases to the electrodes.
|
|
| 8. |
- Bjorstrom, Cecilia M., et al.
(författare)
-
Influence of solvents and substrates on the morphology and the performance of low-bandgap polyfluorene: PCBM photovoltaic devices - art. no. 61921X
- 2006
-
Ingår i: Proceedings of SPIE, the International Society for Optical Engineering. - : International Society for Optical Engineering; 1999. - 0277-786X .- 1996-756X. ; 6192, s. X1921-X1921
-
Tidskriftsartikel (refereegranskat)abstract
- Spin-coated thin films of poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-5,5-(4,7-di-2-thienyl-2,1,3-benzothiadiazole)] (APFO-3) blended with [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM) are used as the active material in polymer photovoltaic cells. Such blends are known for their tendency to phase separate during film formation. Tuning the morphology of the blend in a controlled way is one possible road towards higher efficiency. We studied the effect of adding chlorobenzene to chloroform-based blend solutions before spin-coating on the conversion efficiency of APFO-3:PCBM photodiodes, and related that to the lateral and vertical morphology of thin films of the blend. The lateral morphology is imaged by atomic force microscopy (AFM) and the vertical compositional profile is obtained by dynamic secondary ion mass spectrometry (SIMS). The profiles reveal compositional variations consisting of multilayers of alternating polymer-rich and PCBM-rich domains in the blend film spin-coated from chloroform. The vertical compositional variations are caused by surface-directed spinodal waves and are frozen in during the rapid evaporation of a highly volatile solvent. With addition of the low-vapour pressure solvent chlorobenzene, a more homogeneous vertical composition is found. The conversion efficiency for solar cells of this blend was found to be optimal for chloroform: chlorobenzene mixtures with a volume-ratio of 80:1. We have also investigated the role of the substrate on the morphology. We found that blend films spin-coated from chloroform solutions on PEDOT:PSS-coated ITO show a similar compositional structure as the films on silicon, and that changing the substrate from silicon to gold only affects the vertical phase separation in a region close to the substrate interface.
|
|
| 9. |
|
|
| 10. |
- Björström, Cecilia M., et al.
(författare)
-
Influence of solvents and substrates on the morphology and the performance of low-bandgap polyfluorene:PCBM photovoltaic devices
- 2006
-
Ingår i: Proceedings of SPIE, the International Society for Optical Engineering. - Cardiff : SPIE - International Society for Optical Engineering. - 0277-786X .- 1996-756X. ; 6192, s. 61921X-
-
Tidskriftsartikel (refereegranskat)abstract
- Spin-coated thin films of poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (APFO-3) blended with [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) are used as the active material in polymer photovoltaic cells. Such blends are known for their tendency to phase separate during film formation. Tuning the morphology of the blend in a controlled way is one possible road towards higher efficiency. We studied the effect of adding chlorobenzene to chloroform-based blend solutions before spin-coating on the conversion efficiency of APFO-3:PCBM photodiodes, and related that to the lateral and vertical morphology of thin films of the blend. The lateral morphology is imaged by atomic force microscopy (AFM) and the vertical compositional profile is obtained by dynamic secondary ion mass spectrometry (SIMS). The profiles reveal compositional variations consisting of multilayers of alternating polymer-rich and PCBM-rich domains in the blend film spin-coated from chloroform. The vertical compositional variations are caused by surface-directed spinodal waves and are frozen in during the rapid evaporation of a highly volatile solvent. With addition of the low-vapour pressure solvent chlorobenzene, a more homogeneous vertical composition is found. The conversion efficiency for solar cells of this blend was found to be optimal for chloroform:chlorobenzene mixtures with a volume-ratio of 80:1. We have also investigated the role of the substrate on the morphology. We found that blend films spin-coated from chloroform solutions on PEDOT:PSS-coated ITO show a similar compositional structure as the films on silicon, and that changing the substrate from silicon to gold only affects the vertical phase separation in a region close to the substrate interface
|
|
