| 11. |
- Krebs, Frederik C, et al.
(författare)
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A round robin study of flexible large-area roll-to-roll processed polymer solar cell modules
- 2009
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Ingår i: SOLAR ENERGY MATERIALS AND SOLAR CELLS. - : Elsevier BV. - 0927-0248. ; 93:11, s. 1968-1977
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Tidskriftsartikel (refereegranskat)abstract
- A round robin for the performance of roll-to-roll coated flexible large-area polymer solar-cell modules involving 18 different laboratories in Northern America, Europe and Middle East is presented. The study involved the performance measurement of the devices at one location (Riso DTU) followed by transportation to a participating laboratory for performance measurement and return to the starting location (Riso DTU) for re-measurement of the performance. It was found possible to package polymer solar-cell modules using a flexible plastic barrier material in such a manner that degradation of the devices played a relatively small role in the experiment that has taken place over 4 months. The method of transportation followed both air-mail and surface-mail paths.
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| 12. |
- Li, Weiwei, et al.
(författare)
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The Effect of additive on performance and shelf-stability of HSX-1/PCBM photovoltaic devices
- 2011
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Ingår i: Organic electronics. - : Elsevier Science B.V., Amsterdam.. - 1566-1199 .- 1878-5530. ; 12:9, s. 1544-1551
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Tidskriftsartikel (refereegranskat)abstract
- How 1,8-diiodooctane (DIO) enhances performance of polymer solar cells based on polymer HXS-1 and fullerene [6,6]-phenyl C(71)-butyric acid methyl ester (PC(71)BM) from 3.6% to 5.4% is scrutinized with several techniques by comparing devices or blend films spin-coated from dichlorobenzene (DCB) to those from DCB/DIO (97.5:2.5 v/v). Morphology of blend films is examined with atomic force microscopy (AFM), transmission electron microscopy (TEM) and electron tomography (3-D TEM), respectively. Charge generation and recombination is studied with photoluminescence, and charge transport with field effect transistors. The morphology with domain size in 10-20 nm and vertical elongated clusters formed in DIO system is supposed to facilitate charge transport and minimize charge carrier recombination, which are the main reasons for enhancing power conversion efficiency (PCE) from 3.6% (without DIO) to 5.4% (with DIO). Furthermore, a two year inspection shows no significant impact of DIO on the shelf-stability of the solar cells. No visible degradation in the second year indicates that the morphology of the active layers in the devices is relatively stable after initial relaxation in the first year.
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| 13. |
- Müller, Christian, et al.
(författare)
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Influence of Molecular Weight on the Performance of Organic Solar Cells Based on a Fluorene Derivative
- 2010
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Ingår i: Advanced Materials for Optics and Electronics. - : Wiley. - 1616-301X .- 1616-3028. ; 20:13, s. 2124-2131
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Tidskriftsartikel (refereegranskat)abstract
- The performance of organic photovoltaic (OPV) bulk-heterojunction blends comprising a liquid-crystalline fluorene derivative and a small-molecular fullerene is found to increase asymptotically with the degree of polymerization of the former. Similar to various thermodynamic transition temperatures as well as the light absorbance of the fluorene moiety, the photocurrent extracted from OPV devices is found to strongly vary with increasing oligomer size up to a number average molecular weight, M-n approximate to 10 kg mol(-1), but is rendered less chain-length dependent for higher M-n as the fluorene derivative gradually adopts polymeric behavior.
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| 14. |
- Müller, Christian, et al.
(författare)
-
Phase behaviour of liquid-crystalline polymer/fullerene organic photovoltaic blends : thermal stability and miscibility
- 2011
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Ingår i: Journal of Materials Chemistry. - : RSC Publishing. - 0959-9428 .- 1364-5501. ; 21, s. 10676-10684
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Tidskriftsartikel (refereegranskat)abstract
- The thermal behaviour of an organic photovoltaic (OPV) binary system comprised of a liquidcrystalline fluorene-based polymer and a fullerene derivative is investigated. We employ variabletemperature ellipsometry complemented by photo- and electroluminescence spectroscopy as well as optical microscopy and scanning force nanoscopy to explore phase transitions of blend thin films. The high glass transition temperature correlates with the good thermal stability of solar cells based on these materials. Furthermore, we observe partial miscibility of the donor and acceptor together with the tendency of excess fullerene derivative to segregate into exceedingly large domains. Thus, for charge generation less adequate bulk-heterojunction nanostructures are poised to develop if this mixture is exposed to more elevated temperatures. Gratifyingly, the solubility of the fullerene derivative in the polymer phase is found to decrease if a higher molecular-weight polymer fraction is employed, which offers routes towards improving the photovoltaic performance of non-crystalline OPV blends.
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| 15. |
- O Reese, Matthew, et al.
(författare)
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Consensus stability testing protocols for organic photovoltaic materials and devices
- 2011
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Ingår i: SOLAR ENERGY MATERIALS AND SOLAR CELLS. - : Elsevier Science B.V., Amsterdam.. - 0927-0248. ; 95:5, s. 1253-1267
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Tidskriftsartikel (refereegranskat)abstract
- Procedures for testing organic solar cell devices and modules with respect to stability and operational lifetime are described. The descriptions represent a consensus of the discussion and conclusions reached during the first 3 years of the international summit on OPV stability (ISOS). The procedures include directions for shelf life testing, outdoor testing, laboratory weathering testing and thermal cycling testing, as well as guidelines for reporting data. These procedures are not meant to be qualification tests, but rather generally agreed test conditions and practices to allow ready comparison between laboratories and to help improving the reliability of reported values. Failure mechanisms and detailed degradation mechanisms are not covered in this report.
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| 16. |
- Tang, Zheng, et al.
(författare)
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Interlayer for Modified Cathode in Highly Efficient Inverted ITO-Free Organic Solar Cells
- 2012
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Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 24:4, s. 554-
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Tidskriftsartikel (refereegranskat)abstract
- Inverted polymer solar cells with a bottom metal cathode modified by a conjugated polymer interlayer show considerable improvement of photocurrent and fill factor, which is due to hole blocking at the interlayer, and a modified surface energy which affects the nanostructure in the TQ1/[70]PCBM blend.
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| 17. |
- Tang, Zheng, et al.
(författare)
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Semi-Transparent Tandem Organic Solar Cells with 90% Internal Quantum Efficiency
- 2012
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Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6840 .- 1614-6832. ; 2:12, s. 1467-1476
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Tidskriftsartikel (refereegranskat)abstract
- Semi-transparent (ST) organic solar cells with potential application as power generating windows are studied. The main challenge is to find proper transparent electrodes with desired electrical and optical properties. In this work, this is addressed by employing an amphiphilic conjugated polymer PFPA-1 modified ITO coated glass substrate as the ohmic electron-collecting cathode and PEDOT:PSS PH1000 as the hole-collecting anode. For active layers based on different donor polymers, considerably lower reflection and parasitic absorption are found in the ST solar cells as compared to solar cells in the standard geometry with an ITO/PEDOT:PSS anode and a LiF/Al cathode. The ST solar cells have remarkably high internal quantum efficiency at short circuit condition (similar to 90%) and high transmittance (similar to 50%). Hence, efficient ST tandem solar cells with enhanced power conversion efficiency (PCE) compared to a single ST solar cell can be constructed by connecting the stacked two ST sub-cells in parallel. The total loss of photons by reflection, parasitic absorption and transmission in the ST tandem solar cell can be smaller than the loss in a standard solar cell based on the same active materials. We demonstrate this by stacking five separately prepared ST cells on top of each other, to obtain a higher photocurrent than in an optimized standard solar cell.
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| 18. |
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| 19. |
- 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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| 20. |
- Tvingstedt, Kristofer, 1976-, et al.
(författare)
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Folded reflective tandem polymer solar cell doubles efficiency
- 2007
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 91:12, s. 123514-
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Tidskriftsartikel (refereegranskat)abstract
- Conjugated polymers are promising materials for the production of inexpensive and flexible photovoltaic cells. Organic materials display tunable optical absorption within a large spectral range. This enables the construction of organic tandem photovoltaic cells. The authors here demonstrate a reflective tandem cell where single cells are reflecting the nonabsorbed light upon another adjacent cell. By folding two planar but spectrally different cells toward each other, spectral broadening and light trapping are combined to give an enhancement of power conversion efficiency of a factor of 1.8±0.3.
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