147 research outputs found
Low-dimensional hybrid perovskites containing an organic cation with an extended conjugated system : tuning the excitonic absorption features
Low-dimensional hybrid perovskites are receiving increased attention. One of the advantages of the low-dimensional hybrids over their 3D counterparts is their greater structural flexibility towards the incorporation of bigger, more complex, organic cations. In this communication, we introduce a pyrene derivative as an organic cation containing an extended pi-system for use in a variety of low-dimensional hybrids. We show that materials with different excitonic absorption features can be obtained by tuning the iodide/lead ratio in the precursor solutions, using the same pyrene cation. In this way, hybrids with optical characteristics corresponding to 2D, 1D and 0D hybrid perovskites are obtained. The formation and thermal stability of the different hybrids is analysed and compared
Tin-lead-metal halide perovskite solar cells with enhanced crystallinity and efficiency by addition of fluorinated long organic cation
Highly performing mixed Sn/Pb-metal halide perovskite solar cells (PSCs) are among the most promising options to reduce Pb content in perovskite devices and enable, owing to their reduced bandgap, the fabrication of all-perovskite tandem solar cells. Whereas pure-Pb perovskite devices exhibit efficiency up to 25.5%, alongside a high open-circuit voltage (≈1.2 V), Sn-Pb PSCs still show lower performances (22.2%) due to higher open-circuit voltage losses. Here, we introduced 2,3,4,5,6-pentafluorophenethylammonium cations in a perovskite active layer of composition (FASnI3)0.5(MAPbI3)0.5 to obtain highly oriented films with improved thermal stability. The treated films exhibit merged grains with no evidence of 2D structures, which could help to reduce the trap state density at the surface and grain boundaries. Solar cells fabricated with the fluorinated cation added to the active layer displayed reduced trap-assisted recombination losses and lower background carrier density, which leads to enhanced open-circuit voltages with respect to the reference samples and the active layers incorporating unfluorinated phenethylammonium cations. The best device reached an efficiency of 19.13%, with an open-circuit voltage of 0.84 V, which is substantially improved with respect to the reference sample showing 17.47% efficiency and 0.77 V open-circuit voltage. More importantly, the fluorinated cations' addition is instrumental to improve the device's thermal stability; 90.3% of the solar cell initial efficiency is maintained after 90 min of thermal stress at 85 °C in a nitrogen atmosphere
Facile synthesis of well-defined MDMO-PPV containing (tri)block-copolymers via controlled radical polymerization and CuAAC conjugation
A systematic investigation into the chain transfer polymerization of the so-called radical precursor polymerization of poly(p-phenylene vinylene) (PPV) materials is presented. Polymerizations are characterized by systematic variation of chain transfer agent (CTA) concentration and reaction temperature. For the chain transfer constant, a negative activation energy of −12.8 kJ·mol−1 was deduced. Good control over molecular weight is achieved for both the sulfinyl and the dithiocarbamate route (DTC). PPVs with molecular weights ranging from thousands to ten thousands g·mol−1 were obtained. To allow for a meaningful analysis of the CTA influence, Mark–Houwink–Kuhn–Sakurada (MHKS) parameters were determined for conjugated MDMO-PPV ([2-methoxy-5-(3',7'-dimethyloctyloxy)]-1,4-phenylenevinylene) to α = 0.809 and k = 0.00002 mL·g−1. Further, high-endgroup fidelity of the CBr4-derived PPVs was proven via chain extension experiments. MDMO-PPV-Br was successfully used as macroinitiator in atom transfer radical polymerization (ATRP) with acrylates and styrene. A more polar PPV counterpart was chain extended by an acrylate in single-electron transfer living radical polymerization (SET-LRP). In a last step, copper-catalyzed azide alkyne cycloaddition (CuAAC) was used to synthesize block copolymer structures. Direct azidation followed by macromolecular conjugation showed only partial success, while the successive chain extension via ATRP followed by CuAAC afforded triblock copolymers of the poly(p-phenylene vinylene)-block-poly(tert-butyl acrylate)-block-poly(ethylene glycol) (PPV-b-PtBuA-b-PEG)
Difluorodithieno[3,2-a:2′,3′-c]phenazine as a strong acceptor for materials displaying thermally activated delayed fluorescence or room temperature phosphorescence
A novel strong electron-acceptor unit, 9,10-difluorodithieno[3,2-a:2′,3′-c]phenazine (DTPz), is synthesized and applied in the design of two donor-acceptor type emitters displaying long-lived delayed emission. Using either 9,9-dimethyl-9,10-dihydroacridine (DMAC) or triisopropyl-substituted benzo[1,2-b:4,5-b']dithiophene (BDT-TIPS) as the donor component, push-pull type chromophores exhibiting charge-transfer emission are obtained and found to afford either thermally activated delayed fluorescence (TADF) for DMAC or room temperature phosphorescence (RTP) for BDT-TIPS
The effect of halogenation on PBDTT-TQxT based non-fullerene polymer solar cells – Chlorination vs fluorination
2D layered perovskite containing functionalised benzothieno-benzothiophene molecules : formation, degradation, optical properties and photoconductivity
2D layered hybrid perovskites are currently in the spotlight for applications such as solar cells, light-emitting diodes, transistors and photodetectors. The structural freedom of 2D layered perovskites allows for the incorporation of organic cations that can potentially possess properties contributing to the performance of the hybrid as a whole. In this study, we incorporated a benzothieno[3,2-b]benzothiophene (BTBT) alkylammonium cation into the organic layer of a 2D layered lead iodide perovskite. The formation and degradation of this material are discussed in detail. It is shown that the use of a solvent vapour annealing method significantly enhances the absorption, emission and crystallinity of films of this 2D layered perovskite as compared to regular thermal annealing. The photoconductivity of the films was determined using time-resolved microwave conductivity (TRMC) as well as in a device. In both cases, the solvent vapour annealed films show markedly higher photoconductivity than the films obtained using the regular thermal annealing approach
Extending the functionality of low-dimensional hybrid perovskites through the incorporation of charge-transfer complexes
Synthesis and characterization of poly(methylphenylsilylene) poly(methyl methacrylate) block copolymers
Block copolymers of poly(methylphenylsilylene) and poly(methyl methacrylate) have been synthesized by condensation of alpha,omega-dichloropoly(methylphenylsilylene) with poly(methyl methacrylate)-lithium. The alpha,omega-dichloropoly(methylphenylsilylene) was synthesized by the Wurtz-type reductive coupling of dichloromethylphenylsilane using sodium in boiling toluene and poly(methyl methacrylate)-lithium was prepared by anionic polymerization of methyl methacrylate in tetrahydrofuran initiated by alpha-methylstyrene-lithium/LiCl. The structures of the block copolymers have been confirmed using size exclusion chromatography and NMR spectroscopy. (C) 1998 SCI
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