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- George, Zandra, 1985, et al.
(författare)
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Improved performance and life time of inverted organic photovoltaics by using polymer interfacial materials
- 2015
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Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248. ; 133, s. 99-104
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Tidskriftsartikel (refereegranskat)abstract
- A previously published fluorene based interlayer polymer is here compared to three similar polymers where the fluorene monomer has been exchanged with monomers that have been reported to have a higher photo-chemical stability. The polymer interlayers have been studied in terms of their influence on device performance and stability on inverted devices with an active layer of P3HT:PC61BM. By acting as a hole-blocking layer the polymers are able to increase the efficiency of the devices with similar to 50% compared to devices with an ITO cathode. In addition, the polymers also improve the photo-stability of the devices, mainly as an effect of a reduced decrease in open-circuit voltage and fill factor. This indicates that solution processable polymer interlayers could be a way towards both higher efficiency and improved stability of inverted organic solar cells.
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| 3. |
- Kroon, Renee, 1982, et al.
(författare)
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New quinoxaline and pyridopyrazine-based polymers for solution-processable photovoltaics
- 2012
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Ingår i: Solar Energy Materials and Solar Cells. - : Elsevier BV. - 0927-0248 .- 1879-3398. ; 105, s. 280-286
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Tidskriftsartikel (refereegranskat)abstract
- The recently published quinoxaline/thiophene-based polymer TQ1 has been modified on its acceptor unit, either altering the acceptor strength by incorporating a pyridopyrazine, substitution of the acceptor-hydrogens by fluorine, or substitution of the alkoxy side chain by alkyl. The changes in physical, electronic and device properties are discussed. For the polymers incorporating the stronger acceptors a decreased performance is found, where in both cases the current in the devices is compromised. Incorporation of the pyridopyrazine-based acceptor seems to result in more severe or additional loss mechanisms compared to the polymer that incorporates the fluorine atoms. A similar performing material is obtained when changing the alkoxy side chain in TQ1 to an alkyl, where the solar cell performance is mainly improved on the fill factor. It is demonstrated that the standard TQ1 structure is easily modified in a number of ways, showing the versatility and robustness of the standard TQ1 structure and synthesis.
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| 4. |
- Vesce, Luigi, et al.
(författare)
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Hysteresis-Free Planar Perovskite Solar Module with 19.1% Efficiency by Interfacial Defects Passivation
- 2022
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Ingår i: Solar RRL. - : John Wiley & Sons. - 2367-198X. ; 6:7
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Tidskriftsartikel (refereegranskat)abstract
- In few years, perovskite solar devices have reached high efficiency on lab scale cells. Upscaling to module size, effective perovskite recipe and posttreatment are of paramount importance to the breakthrough of the technology. Herein this work, the development of a low-temperature planar n-i-p perovskite module (11 cm(2) aperture area, 91% geometrical fill factor) is reported on, exploiting the defect passivation strategy to achieve an efficiency of 19.1% (2% losses stabilized) with near-zero hysteresis, that is the most unsolved issue in the perovskite photovoltaic technology. The I/Br (iodine/bromide) halide ion ratio of the triple-cation perovskite formulation and deposition procedure are optimized to move from small area to module device and to avoid the detrimental effect of dimethyl sulfoxide (DMSO) solvent. The organic halide salt phenethylammonium iodide (PEAI) is adopted as surface passivation material on module size to suppress perovskite defects. Finally, homogeneous and defect-free layers from cell to module with only 8% relative efficiency losses, high reproducibility, and optimized interconnections are scaled by laser ablation methods. The homogeneity of the perovskite layers and of the full stack was assessed by optical, morphological, and light beam-induced current (LBIC) mapping characterizations.
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