| 1. |
- Lindqvist, Camilla, 1985, et al.
(författare)
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Fullerene Nucleating Agents: A Route Towards Thermally Stable Photovoltaic Blends
- 2014
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Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6840 .- 1614-6832. ; 4:9, s. 1301437-
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Tidskriftsartikel (refereegranskat)abstract
- The bulk-heterojunction nanostructure of non-crystalline polymer: fullerene blends has the tendency to rapidly coarsen when heated above its glass transition temperature, which represents an important degradation mechanism. We demonstrate that fullerene nucleating agents can be used to thermally arrest the nanostructure of photovoltaic blends that comprise a non-crystalline thiophene-quinoxaline copolymer and the widely used fullerene derivative [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM). To this end, C-60 fullerene is employed to efficiently nucleate PCBM crystallization. Sub-micrometer-sized fullerene crystals are formed when as little as 2 wt% C-60 with respect to PCBM is added to the blend. These reach an average size of only 200 nanometers upon introduction of more than 8 wt% C-60. Solar cells based on C-60-nucleated blends indicate significantly improved thermal stability of the bulk-heterojunction nanostructure even after annealing at an elevated temperature of 130 degrees C, which lies above the glass transition temperature of the blend. Moreover, we find that various other compounds, including C-70 fullerene, single-walled carbon nanotubes, and sodium benzoate, as well as a number of commercial nucleating agents-commonly used to clarify isotactic polypropylene-permit to control crystallization of the fullerene phase.
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| 2. |
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| 3. |
- Dyson, M., et al.
(författare)
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Structure/Property/Processing Relationships for Organic Solar Cells
- 2018
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Ingår i: RSC Nanoscience and Nanotechnology. - : The Royal Society of Chemistry. - 1757-7136. - 9781782626749 ; 2018-January:45, s. 182-225
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Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
- Rapid developments in the field of organic solar cells have been driven by this technology's potentially advantageous traits: the environmentally friendly, low-cost generation of energy with the possibility of large area manufacturing of flexible, lightweight, semi-transparent devices, with predicted low energy payback times. Major step changes leading to vastly improved devices with ever-increasing performance have been achieved through new insights into materials design and an improved understanding of the often complex microstructure and phase morphology of organic solar cell systems. This chapter summarises the advances in synthesis, concentrating on the relevant structure/property relations and how the chemical structure affects processing and the microstructure. This is followed by a detailed discussion of classical materials science approaches that assist in gaining insights into complex materials systems, such as organic solar cell blends from the molecular to the micrometre scale, with a focus on polymer-based systems and how to apply this knowledge to future larger area processing of organic photovoltaic architectures.
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| 4. |
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| 5. |
- Koch, Felix Peter Vinzenz, et al.
(författare)
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The impact of molecular weight on microstructure and charge transport in semicrystalline polymer semiconductors–poly(3-hexylthiophene), a model study
- 2013
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Ingår i: Progress in Polymer Science. - : Elsevier BV. - 0079-6700. ; 38:12, s. 1978-1989
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Tidskriftsartikel (refereegranskat)abstract
- Electronic properties of organic semiconductors are often critically dependent upon their ability to order from the molecular level to the macro-scale, as is true for many other materials attributes of macromolecular matter such as mechanical characteristics. Therefore, understanding of the molecular assembly process and the resulting solid-state short- and long-range order is critical to further advance the field of organic electronics. Here, we will discuss the structure development as a function of molecular weight in thin films of a model conjugated polymer, poly(3-hexylthiophene) (P3HT), when processed from solution and the melt. While focus is on the microstructural manipulation and characterization, we also treat the influence of molecular arrangement and order on electronic processes such as charge transport and show, based on classical polymer science arguments, how accounting for the structural complexity of polymers can provide a basis for establishing relevant processing/structure/property-interrelationships to explain some of their electronic features. Such relationships can assist with the design of new materials and definition of processing protocols that account for the molecular length, chain rigidity and propensity to order of a given system.
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| 6. |
- Yu, Liyang, 1986, et al.
(författare)
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Conjugated Polymer Mesocrystals with Structural and Optoelectronic Coherence and Anisotropy in Three Dimensions
- 2022
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Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 34:1
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Tidskriftsartikel (refereegranskat)abstract
- Semiconducting mesocrystalline bulk polymer specimens that exhibit near-intrinsic properties using channel-die pressing are demonstrated. A predominant edge-on orientation is obtained for poly(3-hexylthiophene-2,5-diyl) (P3HT) throughout 2 mm-thick/wide samples. This persistent mesocrystalline arrangement at macroscopic scales allows reliable evaluation of the electronic charge-transport anisotropy along all three crystallographic axes, with high mobilities found along the π-stacking. Indeed, charge-carrier mobilities of up to 2.3 cm2 V−1 s−1 are measured along the π-stack, which are some of the highest mobilities reported for polymers at low charge-carrier densities (drop-cast films display mobilities of maximum ≈10−3 cm2 V−1 s−1). The structural coherence also leads to an unusually well-defined photoluminescence line-shape characteristic of an H-aggregate (measured from the surface perpendicular to the materials flow), rather than the typical HJ-aggregate feature usually found for P3HT. The approach is widely applicable: to electrical conductors and materials used in n-type devices, such as poly{[N,N′-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-(2,2′-bithiophene)} (N2200) where the mesocrystalline structure leads to high electron transport along the polymer backbones (≈1.3 cm2 V−1 s−1). This versatility and the broad applicability of channel-die pressing signifies its promise as a straightforward, readily scalable method to fabricate bulk semiconducting polymer structures at macroscopic scales with properties typically accessible only by the tedious growth of single crystals.
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