pH-Responsive Emission of Novel Water-Soluble Polymeric Iridium(III) Complexes

The synthesis and characterization of water-soluble copolymers containing N,N-dimethylacrylamide (DMAM) and a vinylic monomer containing an Iridium(III), Ir(III), complex substituted with the quinoline-based unit 2-(pyridin-2-ylo)-6-styrene-4-phenylquinoline (VQPy) as ligand are reported. These copolymers were prepared through pre- or post-polymerization complexation of Ir(III) with the VQPy units. The first methodology led to copolymer P1 having fully complexed VQPy units, whereas the latter methodology allowed the preparation of terpolymers containing free and Ir(III)-complexed VQPy units (copolymer P2). The optical properties of the copolymers were studied in detail through UV-Vis and photoluminescence spectroscopy in aqueous solution. It is shown that the metal-to-ligand charge transfer (ΜLCT) emission is prevailing in the case of P1, regardless of pH. In contrast, in the case of terpolymer P2 the MLCT emission of the Ir(III) complex is combined with the pH-responsive emission of free VQPy units, leading to characteristic pH-responsive color changes under UV illumination in the acidic pH region

Synthesis of Polythiophene–Fullerene Hybrid Additives as Potential Compatibilizers of BHJ Active Layers

Perfluorophenyl functionalities have been introduced as side chain substituents onto regioregular poly(3-hexyl thiophene) (rr-P3HT), under various percentages. These functional groups were then converted to azides which were used to create polymeric hybrid materials with fullerene species, either C60 or C70. The P3HT–fullerene hybrids thus formed were thereafter evaluated as potential compatibilizers of BHJ active layers comprising P3HT and fullerene based acceptors. Therefore, a systematic investigation of the optical and morphological properties of the purified polymer–fullerene hybrid materials was performed, via different complementary techniques. Additionally, P3HT:PC70BM blends containing various percentages of the herein synthesized hybrid material comprising rr-P3HT and C70 were investigated via Transmission Electron Microscopy (TEM) in an effort to understand the effect of the hybrids as additives on the morphology and nanophase separation of this typically used active layer blend for OPVs

Nucleophilic Aromatic Substitution of Pentafluorophenyl-Substituted Quinoline with a Functional Perylene: A Route to the Modification of Semiconducting Polymers

A systematic study of the influence of the chemical substitution pattern of semiconducting polymers carrying side chain perylene diimide (PDI) groups is presented. Semiconducting polymers based on perflurophenyl quinoline (5FQ) were modified via a readily accessible nucleophilic substitution reaction. The perfluorophenyl group was studied as an electron-withdrawing reactive functionality on semiconducting polymers that can undergo fast nucleophilic aromatic substitution. A PDI molecule, functionalized with one phenol group on the bay area, was used for the substitution of the fluorine atom at the para position in 6-vinylphenyl-(2-perfluorophenyl)-4-phenyl quinoline. The final product was polymerized under free radical polymerization providing polymers of 5FQ incorporated with PDI side groups. Alternatively, the post-polymerization modification of the fluorine atoms at the para position of the 5FQ homopolymer with the PhOH-di-EH-PDI was also successfully tested. In this case, the PDI units were partially introduced to the perflurophenyl quinoline moieties of the homopolymer. The para-fluoro aromatic nucleophilic substitution reaction was confirmed and estimated via 1H and 19F NMR spectroscopies. The two different polymer architectures, namely, fully or partially modified with PDI units, were studied in terms of their optical and electrochemical properties, while their morphology was evaluated using TEM analysis, revealing polymers of tailor-made optoelectronic and morphological properties. This work provides a novel molecule-designing method for semiconducting materials of controlled properties

Copolymers and Hybrids Based on Carbazole Derivatives and Their Nanomorphology Investigation

Oligomers of the low-band-gap PCDTBT polymer, based on either 3,6 or 2,7 carbazole units, were modified with vinyl ω-chain end functionalities. The vinyl-functionalized oligomers were used as comonomers in free radical polymerizations with quinoline-based monomers such as 6-vinylphenyl-(2-pyridinyl)-4-phenyl-quinoline (vinyl-QPy), and 6-vinylphenyl-(2-perfluorophenyl)-4-phenyl quinoline (vinyl-5FQ). The co-polymeric materials bearing the vinyl-QPy moiety were developed as potential compatibilizers in polymer electron donor⁻fullerene acceptor blends for non-covalent interactions with the fullerene part. The co-polymeric materials bearing the vinyl-5FQ moiety were developed for the covalent attachment of carbon nanostructures; specifically, PC61BM. Both copolymers and hybrids, after thorough purification, were characterized in terms of their spectroscopic and optical properties as well as their ability to form nanophased separated films as such, or as additives at various percentages into PCDTBT: PC71BM blends

A Di-Carbazole-Based Dye as a Potential Sensitizer for Greenhouse-Integrated Dye-Sensitized Solar Cells

For the first time in dye-sensitized solar cell (DSSC) technology, a di-carbazole-based dye was synthesized and evaluated for its usage as a potential sensitizer for the development of wavelength selective semi-transparent DSSCs for greenhouses-oriented applications. The dye was designed to demonstrate a blue light absorption, allowing a high transmittance in the red region of the visible light, even after its adsorption on the anode semiconductor, which is the most important one for the photosynthetic action of the plants. The application of the new dye to DSSCs was examined using either a high-performance iodide-based electrolyte or a highly transparent iodine-free electrolyte to determine a good balance between electric power generation and device transparency. The spectral engineered DSSCs demonstrated quite promising characteristics, providing a high external quantum efficiency (higher than 70%) in the whole blue–green region of the visible light, while allowing high transparency (up to 55%) in the red region, where the second peak in the absorbance spectrum of chlorophyll is located. Finally, the derived results were discussed under the consideration of important metrics for this niche application, including the transparency of the solar cells in the region of photosynthetic active radiation and the attained crop growth factor. The present work constitutes one of the few comprehensive studies carried out up to now in the direction of the development of 3rd generation “agrivoltaics” for their possible integration as cladding materials in energy-autonomous greenhouses

Electron Transporting Perylene Diimide-Based Random Terpolymers with Variable Co-Monomer Feed Ratio: A Route to All-Polymer-Based Photodiodes

A route toward processable n-type terpolymers is presented herein based on the random donor-acceptor-donor-acceptor (D-A1)-(D-A2) molecular configuration. Carbazole is utilized as the electron donating unit (D) combined with perylene diimide (PDI) as the first electron acceptor (A1) and either one of two different benzothiadiazole (BTZ) derivatives (di-thienyl substituted-BTZ and di-3,4-ethylenedioxythienyl substituted-BTZ) as the second electron accepting unit (A2). Increasing the content of the PDI co-monomer resulted in terpolymers of higher molecular weights, enhanced solubility, and stronger n-type character. The physicochemical properties of the random PDI-Cz-BTZ derivatives are fine-tuned based on the feed ratio of the co-monomers. Photodiode devices were demonstrated, having photoactive layers composed of the rich in PDI terpolymer, namely, P4 having a 75% PDI content, and the PCE10 electron donor, under various ratios. For a range of P4 blend compositions, UV-Vis, is spectroscopy confirmed the strong absorption of the blend films across the 350-800 nm spectral region, and AFM imaging verified their low surface roughness. The study of the electro-optical device properties identified the 1:2 blending ratio as the optimum PCE10:P4 combination for maximum charge photogeneration efficiency. Despite the relatively deep LUMO energy of the n-type P4 terpolymer (ELUMO = -4.04 eV), trap-induced charge recombination losses were found to limit the PCE10:P4 photodiode performance. Unipolar devices of the P4-alone exhibited hole and electron mobility values of 2.2 × 10-4 and 6.3 × 10-5 cm2 V-1 s-1, respectively