42 research outputs found

    Low-Cost and Green Fabrication of Polymer Electronic Devices by Push-Coating of the Polymer Active Layers

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    Because of both its easy processability and compatibility with roll-to-roll processes, polymer electronics is considered to be the most promising technology for the future generation of low-cost electronic devices such as light-emitting diodes and solar cells. However, the state-of-the-art deposition technique for polymer electronics (spin-coating) generates a high volume of chlorinated solution wastes during the active layer fabrication. Here, we demonstrate that devices with similar or higher performances can be manufactured using the push-coating technique in which a poly(dimethylsiloxane) (PDMS) layer is simply laid over a very small amount of solution (less than 1μL/covered cm2), which is then left for drying. Using mm thick PDMS provides a means to control the solvent diffusion kinetics (sorption/retention) and removes the necessity for additional applied pressure to generate the desired active layer thickness. Unlike spin-coating, push-coating is a slow drying process that induces a higher degree of crystallinity in the polymer thin film without the necessity for a post-annealing step. The polymer light-emitting diodes and solar cells prepared by push-coating exhibit slightly higher performances with respect to the reference spin-coated devices, whereas at the same time reduce the amounts of active layer materials and chlorinated solvents by 50 and 20 times, respectively. These increased performances can be correlated to the higher polymer crystallinities obtained without applying a post-annealing treatment. As push-coating is a roll-to-roll compatible method, the results presented here open the path to low-cost and eco-friendly fabrication of a wide range of emerging devices based on conjugated polymer materials

    Design of Lanthanide-Based OLEDs with Remarkable Circularly Polarized Electroluminescence

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    Organic light-emitting diodes (OLEDs) able to directly emit circularly polarized (CP) electroluminescence (CP-OLEDs) are rapidly gaining much interest, due to their possible applications in displays with antiglare filters and 3D displays. Development of more efficient CP-OLEDs can open their use also in point-of-care and personalized diagnostic tools, since CP light alteration can be related to health state of irradiated tissues. In this work it is shown that the performance of chiral europium complex-based CP-OLEDs can be improved both in terms of external quantum efficiency (measured on all the Eu bands) and degree of polarization of emitted photons (as measured by the dissymmetry factor gEL), by proper active layer formulation and through a fine tuning of the architecture of the device. Polarization performances (gEL = −1) are obtained about three times higher than for any other CP-OLED reported so far. Moreover, for the first time, it is shown that the position of the recombination zone (RZ) plays a major role on the polarization outcomes. In order to rationalize these results the level of light polarization is related to the position of the RZ allied with the reflection on the cathode through a simple mathematical model. The values predicted by this model are in qualitative agreement with the experimental ones

    Benzothiadiazole-based conjugated polyelectrolytes for interfacial engineering in optoelectronic devices

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    Abstract Polar semiconducting polymers based on a conjugated polymer backbone endowed with chemically anchored polar groups on the side chains have proved to be particularly interesting as optimization layer at organic/cathode interface in optoelectronic devices. In particular, the pendant phosphonate groups impart water-alcohol solubility allowing easy solution processing, and improve electron injection thanks to both a favorable interfacial dipole of phosphonate groups and an intense coordination interaction between the phosphonate groups and Al cathode. In this work we synthesize alternating fluorene-benzothiadiazole copolymers by proposing a post-polymerization reaction to insert the phosphonate groups. Thanks to this approach it is possible to use standard Suzuki coupling conditions, simplifying the process of synthesis, purification and characterization. The polymer Poly[9,9-bis(6′-diethoxylphosphorylhexyl)-alt-benzothiadiazole] (P2), is tested in conventional organic solar cells as cathode interfacial layers showing, with respect to the control device, an increasing of all the photovoltaic parameters, with a final power conversion efficiency that reaches 5.35% starting from 4.6%. The same trend is observed for multilayered polymer light-emitting diodes with an external quantum efficiency of the P2-based PLED enhanced of 1.5 times with respect to the basic devices with bare Al cathode, and negligible roll-off efficiency. The synergic effects of energy gap modulation and of polar phosphonated pendant functionalities of P2 are compared with the corresponding fluorene-based polar homopolymer. Our results show that, not only a proper selection of side functionalities, but also the tailoring of the energy gap of cathode interfacial materials (CIMs) is a possible effective strategy to engineer cathode of different optoelectronic devices and enhance their performance

    Modular chiral Eu(iii) complexes for efficient circularly polarized OLEDs

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    Achieving both high dissymmetry factors and strong emission in circularly polarized (CP) luminescent materials and, at the same time, compatibility with manufacturing processes for organic electronic devices, is a crucial issue for reliable applications of CP emitters in many fields, such as chiral electronics and optoelectronics. In this communication, we show that the independent choice of the sensitizing and the chirality inducing ligands allows europium(III) complexes to meet the multiple requirements for solution processed efficient CP electroluminescent devices

    High-efficiency all-solution-processed light-emitting diodes based on anisotropic colloidal heterostructures with polar polymer injecting layers

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    Colloidal quantum dots (QDs) are emerging as true candidates for light-emitting diodes with ultrasaturated colors. Here, we combine CdSe/CdS dot-in-rod hetero-structures and polar/polyelectrolytic conjugated polymers to demonstrate the first example of fully solution-based quantum dot light-emitting diodes (QD-LEDs) incorporating all-organic injection/transport layers with high brightness, very limited roll-off and external quantum efficiency as high as 6.1%, which is 20 times higher than the record QD-LEDs with all-solution processed organic interlayers and exceeds by over 200% QD-LEDs embedding vacuum-deposited organic molecules

    Intellectual Property, Open Science and Research Biobanks

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    In biomedical research and translational medicine, the ancient war between exclusivity (private control over information) and access to information is proposing again on a new battlefield: research biobanks. The latter are becoming increasingly important (one of the ten ideas changing the world, according to Time magazine) since they allow to collect, store and distribute in a secure and professional way a critical mass of human biological samples for research purposes. Tissues and related data are fundamental for the development of the biomedical research and the emerging field of translational medicine: they represent the “raw material” for every kind of biomedical study. For this reason, it is crucial to understand the boundaries of Intellectual Property (IP) in this prickly context. In fact, both data sharing and collaborative research have become an imperative in contemporary open science, whose development depends inextricably on: the opportunities to access and use data, the possibility of sharing practices between communities, the cross-checking of information and results and, chiefly, interactions with experts in different fields of knowledge. Data sharing allows both to spread the costs of analytical results that researchers cannot achieve working individually and, if properly managed, to avoid the duplication of research. These advantages are crucial: access to a common pool of pre-competitive data and the possibility to endorse follow-on research projects are fundamental for the progress of biomedicine. This is why the "open movement" is also spreading in the biobank's field. After an overview of the complex interactions among the different stakeholders involved in the process of information and data production, as well as of the main obstacles to the promotion of data sharing (i.e., the appropriability of biological samples and information, the privacy of participants, the lack of interoperability), we will firstly clarify some blurring in language, in particular concerning concepts often mixed up, such as “open source” and “open access”. The aim is to understand whether and to what extent we can apply these concepts to the biomedical field. Afterwards, adopting a comparative perspective, we will analyze the main features of the open models – in particular, the Open Research Data model – which have been proposed in literature for the promotion of data sharing in the field of research biobanks. After such an analysis, we will suggest some recommendations in order to rebalance the clash between exclusivity - the paradigm characterizing the evolution of intellectual property over the last three centuries - and the actual needs for access to knowledge. We argue that the key factor in this balance may come from the right interaction between IP, social norms and contracts. In particular, we need to combine the incentives and the reward mechanisms characterizing scientific communities with data sharing imperative

    Intellectual Property, Open Science and Research Biobanks

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    Carbon Dots as a Sustainable New Platform for Organic Light Emitting Diode

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    Over the past 10 years, carbon dots (CDs) synthesized from renewable raw materials have received considerable attention in several fields for their unique photoluminescent properties. Moreover, the synthesis of CDs fully responds to the principles of circular chemistry and the concept of safe-by-design. This review will focus on the different strategies for incorporation of CDs in organic light-emitting devices (OLEDs) and on the study of the impact of CDs properties on OLED performance. The main current research outcomes and highlights are summarized to guide users towards full exploitation of these materials in optoelectronic applications

    Highly circularly polarized electroluminescence from a chiral europium complex

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    The first circularly polarized OLED (CP-OLED) based on a chiral lanthanide complex is developed. With a simple architecture, this proof-of-concept device attains the highest polarization reported so far and additionally presents the first example of a Ln-based OLED that can be turned into a CP-OLED, fully retaining the special features of Ln-based OLEDs

    Nanophase Separation in Polystyrene-Polyfluorene Block Copolymers Thin Films Prepared through the Breath Figure Procedure

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    The amphiphilic block copolymer formed by a hydrophobic body of polystyrene and a hydrophilic head of poly[9,9-di(2-(2-tetrahydropyranyl-oxy)hexyl)fluorene-alt-9,9-dioctylfluorene] was synthesized, and its solution was used to create thin films with ordered pattern of holes, by means of the breath figure technique. These porous films, after a thermal treatment, were found to show ordered aggregates of the pi-conjugated blocks in the place of the cavities. This is probably due to a preorganization of the two different blocks of the copolymer occurring during the breath figure formation, which is driven by the condensation of water microdroplets on the polymer solution, and to a following phase segregation occurring during the thermal annealing. This approach is a promising tool to be employed for the organization of organic materials at the micro and nanoscale
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