| 1. |
- Hohn, Nuri, et al.
(författare)
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Impact of Catalytic Additive on Spray Deposited and Nanoporous Titania in Films Observed via in Situ X-ray Scattering : Implications for hanced Photovoltaics
- 2018
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Ingår i: ACS Applied Nano Materials. - : American Chemical Society (ACS). - 2574-0970. ; 1:8, s. 4227-4235
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Tidskriftsartikel (refereegranskat)abstract
- With the aim of obtaining nanostructured titania thin films for the tential use in hybrid or dye sensitized solar cells, the amphiphilic block copolymer polystyrene-b-poly(ethylene oxide) is employed as a ructure directing template in combination with solgel chemistry. For sy upscaling, spraying is used as a deposition technique. In situ azing incidence small-angle X-ray scattering (GISAXS) measurements are rformed during spraying and show that most titania structures are ready formed within the solution prior to deposition. However, ructural rearrangement is enabled during the deposition period when all amounts of hydrochloric acid (HCl) are used as a catalytic ditive to the spray solution. This behavior is ascribed to an altering the reaction dynamics and phase separation in the presence of HCl, ich significantly improves the templating effect of the employed block copolymer. With HCl as an additive the final nanoscale rphologies exhibit smaller pore sizes and strongly enhanced order as mpared to thin films sprayed from solutions that do not contain HCl as antified with atomic force microscopy, scanning electron microscopy, d GISAXS.
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| 2. |
- Jiang, Xinyu, et al.
(författare)
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Film Formation Kinetics of Polymer Donor and Nonfullerene Acceptor Active Layers During Printing Out of 1,2,4-Trimethylbenzene in Ambient Conditions
- 2023
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Ingår i: Solar RRL. - : Wiley. - 2367-198X. ; 7:6
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Tidskriftsartikel (refereegranskat)abstract
- Slot-die coating is a promising upscaling fabrication method to promote commercialization in the field of organic solar cells. Herein, the nonfullerene active layer blend of a conjugated polymer PffBT4T-2OD and a small molecule acceptor EH-IDTBR, which is printed out of the nonhalogenated solvent 1,2,4-trimethylbenzene, is studied. The film formation kinetics of the active layer PffBT4T-2OD:EH-IDTBR is probed in terms of the temporal evolutions in morphology as well as molecular conformation and aggregation as revealed by in situ grazing-incidence small angle X-ray scattering and UV–vis spectroscopy during the film printing process. A five-regime mesoscale domain growth process is observed in the active layer from the liquid state to the final dry state. The solvent evaporation-induced domain growth is accompanied with molecular stacking in a distinct J-type aggregation of the acceptor and a slight H-type aggregation of the donor molecules. The printed active layers exhibit an edge-on dominated PffBT4T-2OD and a face-on dominated EH-IDTBR crystallite structure. Compared to the neat PffBT4T-2OD and EH-IDTBR films, in the active layer, the crystallite structure deviates slightly in lattice spacing.
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| 3. |
- Reb, Lennart K., et al.
(författare)
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Space‐ and Post‐Flight Characterizations of Perovskite and Organic Solar Cells
- 2023
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Ingår i: Solar RRL. - : Wiley. - 2367-198X. ; 7:9
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Tidskriftsartikel (refereegranskat)abstract
- Perovskite and organic solar cells are promising for space applications for enabling higher specific powers or alternative deployment systems. However, terrestrial tests can only mimic space conditions to a certain extent. Herein, a detailed analysis of irradiation-dependent photovoltaic parameters of perovskite and organic solar cells exposed to space conditions during a suborbital flight is presented. In orbital altitudes, perovskite and organic solar cells reach power-conversion efficiencies of more than 13% and 6%, respectively. Based on postflight grazing-incidence small-angle and wide-angle X-ray scattering, the active layer morphology and crystalline structure of the returned space solar cells are studied and compared to those of reference solar cells that stayed in an inert atmosphere. Minor changes in the active layer morphology are induced by the sole transport, without causing significant performance loss. For the space solar cells, morphological changes are attributed to the flight experiment that includes rocket launch, spaceflight, and reentry, as well as short-terrestrial environment exposure before and after launch. In contrast, no significant changes to the crystalline phase are observed. The notable performance during flight and high active layer stability, especially of perovskite solar cells, are promising results for further steps toward an orbital demonstration.
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| 4. |
- Wang, Kun, et al.
(författare)
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Comparison of UV Irradiation and Sintering on Mesoporous Spongelike ZnO lms Prepared from PS-b-P4VP Templated Sol-Gel Synthesis
- 2018
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Ingår i: ACS Applied Nano Materials. - : American Chemical Society (ACS). - 2574-0970. ; 1:12, s. 7139-7148
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Tidskriftsartikel (refereegranskat)abstract
- Mesoporous ZnO films with large surface-area-to-volume ratio show great omise in multiple applications, among which solid-state dye-sensitized lar cells (ssDSSCs) have attracted great attention in the field of otovoltaics. An appropriate mesopore size in the nanostructured ZnO lms significantly plays an indispensable role in improving the device ficiency that resulted from an efficient penetration of dye molecules d solid hole transport material. In the present work, mesoporous ongelike ZnO films are prepared using sol-gel synthesis templated by a block copolymer polystyrene-block-poly(4-vinylpyridine). Two different mplate removal techniques, ultraviolet (UV) irradiation and gh-temperature sintering, are used to compare their respective impact the pore sizes of the final ZnO thin films. Both the surface rphology and the inner morphology show that mesopores obtained via UV radiation are smaller as compared to their sintered counterparts. reover, increasing the template-to-ZnO precursor ratio is found to rther enlarge present mesopores. Accordingly, a strong correlation tween the pore sizes of sol-gel synthesized ZnO films and photovoltaic rformance of fabricated ssDSSCs is demonstrated. In contrast with the vices fabricated from the UV-irradiated ZnO films, those obtained from ntered samples show >2 times higher efficiency.
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| 5. |
- Wienhold, Kerstin S., et al.
(författare)
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Effect of Solvent Additives on the Morphology and Device Performance of Printed Nonfullerene Acceptor Based Organic Solar Cells
- 2019
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 11:45, s. 42313-42321
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Tidskriftsartikel (refereegranskat)abstract
- Printing of active layers of high-efficiency organic solar cells and morphology control by processing with varying solvent additive concentrations are important to realize real-world use of bulk-heterojunction photovoltaics as it enables both up-scaling and optimization of the device performance. In this work, active layers of the conjugated polymer with benzodithio-phene units PBDB-T-SF and the nonfullerene small molecule acceptor IT-4F are printed using meniscus guided slot-die coating. 1,8-Diiodooctane (DIO) is added to optimize the power conversion efficiency (PCE). The effect on the inner nanostructure and surface morphology of the material is studied for different solvent additive concentrations with grazing incidence small-angle X-ray scattering (GISAXS), grazing incidence wide-angle X-ray scattering (GIWAXS), scanning electron microscopy (SEM), and atomic force microscopy (AFM). Optical properties are studied with photoluminescence (PL), UV/vis absorption spectroscopy, and external quantum efficiency (EQE) measurements and correlated to the corresponding PCEs. The addition of 0.25 vol % DIO enhances the average PCE from 3.5 to 7.9%, whereas at higher concentrations the positive effect is less pronounced. A solar cell performance of 8.95% is obtained for the best printed device processed with an optimum solvent additive concentration. Thus, with the large-scale preparation method printing similarly well working solar cells can be realized as with the spin-coating method.
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| 6. |
- Xia, Senlin, et al.
(författare)
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Spray-Coating Magnetic Thin Hybrid Films of PS-b-PNIPAM and Magnetite Nanoparticles
- 2019
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Ingår i: Advanced Functional Materials. - : WILEY-V C H VERLAG GMBH. - 1616-301X .- 1616-3028. ; 29:15
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Tidskriftsartikel (refereegranskat)abstract
- Spray coating is employed to fabricate magnetic thin films composed of the diblock copolymer polystyrene-block-poly(N-isopropylacrylamide) and Fe3O4 magnetic nanoparticles (MNPs) functionalized with hydrophobic coatings. The kinetics of structure formation of the hybrid films is followed in situ with grazing incidence small angle X-ray scattering during the spray deposition. To gain a better understanding of the influence of MNPs on the overall structure formation, the pure polymer film is also deposited as a reference via an identical spray protocol. At the initial spraying stage, the hybrid film (containing 2 wt% of MNPs) exhibits a faster formation process of a complete film as compared to the reference. The existence of MNPs depresses the dewetting behavior of polymer films on the substrate at macroscale and simultaneously alters the polymer microphase separation structure orientation from parallel to vertical. As spraying proceeds, MNPs aggregate into agglomerates with increasing sizes. After the spray deposition is finished, both samples gradually reach an equilibrium state and magnetic films with stable structures are achieved in the end. Superconducting quantum interference device investigation reveals the superparamagnetic property of the sprayed hybrid film. Consequently, potential application of sprayed films in fields such as magnetic sensors or data storage appears highly promising.
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