Search

Τhe fabrication of organic light-emitting diodes (OLEDs) from solution involves the major problem of stack integrity, setting the determination of the composition and the characteristics of the resulting interfaces prerequisite for the optimization of the growth processes and the achievement of high devices' performance. In this work, a poly(9,9-dioctylfluorene) (F8) and poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT) blend is used for the emissive layer (EML), poly-3,4-ethylene dioxythiophene; poly-styrene sulfonate (PEDOT:PSS) is used for a hole transport layer (HTL), and Poly(9,9-bis(3′-(N,N-dimethyl)-N-ethylammoinium-propyl-2,7-fluorene)-alt-2,7-(9,9-dioctylfluore-ne))dibromide (PFN-Br) for an electron transport layer (ETL) to produce the OLED device. All the layers are developed using the slot-die process, onto indium tin oxide (ITO)-coated polyethylene terephthalate (PET) flexible substrates, whereas Ag cathode was formed by ink-jet printing under ambient conditions. Spectroscopic ellipsometry measurements were performed upon completion of the successive films' growth, in sequential steps, for the multilayer OLED development. Ellipsometry analysis using different models demonstrate the degree of intermixing within the layers and provide information about the interfaces. These interfacial properties are correlated with the emission characteristics as well as the final performance of the OLED devices. [ABSTRACT FROM AUTHOR]

Obtaining white light from organic LEDs is a considerable challenge and, to realize white light emission, many studies have been conducted, primarily addressing two- or three-color blend systems as a promising strategy. In this work, pristine films, grown by spin coating, consisting of commercial blue Poly(9,9-di-n-octylfluorenyl-2,7-diyl) (PFO), green Poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT), and red spiro-copolymer (SPR) light-emitting materials, were studied as reference materials. Afterward, binary (SPR doped in host PFO) and ternary (SPR and F8BT doped in host PFO) thin films were successfully prepared with various ratios. The characterization of the as-grown and thermally-treated blend films was focused on their optical and photophysical properties. After, the fabrication of OLED devices on glass substrates was carried out for the evaluation of a blend's composition and annealing in terms of the devices' electrical characteristics and electro-emission properties in order to achieve white light emission. Their analysis provided insights into the energy transfer mechanisms between the constituent materials, which were correlated to host–guest interactions as well as to the structural changes originated by thermal treatment, leading to the crystallization of PFO. Finally, the OLEDs based on ternary blends approach the white light emission with (x, y) of (0.272, 0.346). These fabricated devices also exhibit turn-on voltages as low as 3 V, accompanied by remarkable luminance values above 3000 cd/m2. [ABSTRACT FROM AUTHOR]

In this study, fully aromatic polyether sulfones were developed, bearing blue, yellow, and orange–red π-conjugated semiconducting units. Carbazole-, anthracene-, and benzothiadiazole-based fluorophores are copolymerized with a diphenylsulfone moiety. A diphenylpyridine comonomer was additionally utilized, acting as both a solubilizing unit and a weak blue fluorescent group. Using this rationale, fluorescent polyarylethers with high molecular weights, up to 70 kDa, were developed, showing film formation ability and high thermal stability, while preserving excellent solubility in common organic, nonvolatile, and nonchlorinated solvents. Fine-tuning of the emission color was achieved through subtle changes of the comonomers' type and ratio. Single-chromophore-bearing copolymers emitted in the blue or the yellow region of the visible spectrum, while the dual-chromophore-bearing terpolymers emitted throughout the visible spectrum, resulting in white light emission. Solutions of 20 wt% in polar aprotic solvents at ambient conditions allowed the deposition of fluorescent copolyethers and printing from non-chlorinated solvents. All polyethers were evaluated for their structural and optoelectronic properties, and selected copolymers were successfully used in the emitting layer (EML) of organic light-emitting diode (OLED) devices, using either rigid or flexible substrates. Remarkable color stability was displayed in all cases for up to 15 V of bias voltage. The Commission Internationale de L'Eclairage (CIE) of the fabricated devices is located in the blue (0.16, 0.16), yellow (0.44, 0.50), or white region of the visible spectrum (0.33, 0.38) with minimal changes according to the ratio of the comonomers. The versatile methodology toward semiconducting polyethersulfones for polymer light-emitting diodes (PLEDs) developed herein led to the scaled-up production of luminescent polymers of up to 25 g of high-molecular-weight single batches, demonstrating the effectiveness of this approach as a straightforward tool to facilitate the synthesis of flexible and printable EMLs for large-area PLED coverage. [ABSTRACT FROM AUTHOR]

Titanium nitride (TiN) is a candidate material for several plasmonic applications, and pulsed laser ablation in liquids (PLAL) represents a rapid, scalable, and environmentally friendly approach for the large-scale production of nanomaterials with customized properties. In this work, the nanosecond PLAL process is developed, and we provide a concise understanding of the process parameters, such as the solvent and the laser fluence and pulse wavelength, to the size and structure of the produced TiN nanoparticles (NPs). TiN films of a 0.6 μm thickness developed by direct-current (DC) magnetron sputtering were used as the ablation targets. All laser process parameters lead to the fabrication of spherical NPs, while the laser pulse fluence was used to control the NPs' size. High laser pulse fluence values result in larger TiN NPs (diameter around 42 nm for 5 mJ and 25 nm for 1 mJ), as measured from scanning electron microscopy (SEM). On the other hand, the wavelength of the laser pulse does not affect the mean size of the TiN NPs (24, 26, and 25 nm for 355, 532, and 1064 nm wavelengths, respectively). However, the wavelength plays a vital role in the quality of the produced TiN NPs. Shorter wavelengths result in NPs with fewer defects, as indicated by Raman spectra and XPS analysis. The solvent type also significantly affects the size of the NPs. In aqueous solutions, strong oxidation of the NPs is evident, while organic solvents such as acetone, carbides, and oxides cover the TiN NPs. [ABSTRACT FROM AUTHOR]

White Organic Light‐Emitting Diodes (WOLEDs) have attracted an enormous interest because they can be implemented in numerous lighting applications as next‐generation light sources. Several device setups such as multilayer, blends, or single layers of polymer nanomaterials have been proposed to achieve white light emission. In this work, novel copolymers bearing blue, yellow, and red chromophores, are used for the fabrication of WOLED systems including single emissive layer. These terpolymers provide easy tuning of white color emission by selecting the appropriate ratios between the chromophores while being solution processable from typical organic solvents, like chlorobenzene (CB), o‐dichlorobenzene (o‐DCB), etc. The chromophores can be directly excited by capturing charge carriers or through energy transfer from the other chromophores. Incomplete energy transfer between the chromophores is necessary to get white light as combined emission from all of them. The opto‐electronic and electro‐optical characterization is carried out by NIR–Vis–far UV spectroscopic ellipsometry, photoluminescence, and electroluminescence, to provide valuable information toward the optimization and functionalization of these WOLED devices. Novel copolymers bearing blue, yellow, and red chromophores, are used for the fabrication of white organic light‐emitting diode (WOLED) systems including single emissive layer. These terpolymers provide easy tuning of white colour emission by selecting the appropriate ratios between the chromophores while being solution processable. The opto‐electronic and electro‐optical characterization is carried out by NIR–Vis–far UV spectroscopic ellipsometry, photoluminescence, and electroluminescence. [ABSTRACT FROM AUTHOR]

Extensive research has been dedicated to the solution-processable white organic light-emitting diodes (WOLEDs), which can potentially influence future solid-state lighting and full-color flat-panel displays. The proposed strategy based on WOLEDs involves blending two or more emitting polymers or copolymerizing two or more emitting chromophores with different doping concentrations to produce white light emission from a single layer. Toward this direction, the development of blends was conducted using commercial blue poly(9,9-di-n-octylfluorenyl2,7-diyl) (PFO), green poly(9,9-dioctylfluorenealt-benzothiadiazole) (F8BT), and red spiro-copolymer (SPR) light-emitting materials, whereas the synthesized copolymers were based on different chromophores, namely distyryllanthracene, distyrylcarbazole, and distyrylbenzothiadiazole, as yellow, blue, and orange–red emitters, respectively. A comparative study between the two approaches was carried out to examine the main challenge for these doping systems, which is ensuring the proper balance of emissions from all the units to span the entire visible range. The emission characteristics of fabricated WOLEDs will be explored in terms of controlling the emission from each emitter, which depends on two possible mechanisms: energy transfer and carrier trapping. The aim of this work is to achieve pure white emission through the color mixing from different emitters based on different doping concentrations, as well as color stability during the device operation. According to these aspects, the WOLED devices based on the copolymers of two chromophores exhibit the most encouraging results regarding white color emission coordinates (0.28, 0.31) with a CRI value of 82. [ABSTRACT FROM AUTHOR]

A commercial TCAD tool (Silvaco-Atlas) is used for the simulation of organic field-effect transistor (OFET) devices based on sprayed 6,13-bis(triisopropylsilylethynyl)-pentacene (TIPS-Pentacene) organic semiconductor and polystyrene (PS) insulating polymer blends (0.8:0.2 w/w). The simulation results are validated and improved after systematic comparison with experimental data. Shallow donor-like bulk and interface traps density of states (DOS) are taken into account for better convergence with the experimental data. Also, the necessity to include negative interface charge density was revealed. Furthermore, the constant low-field mobility model as well as the band-to-band tunneling model were selected, while their parameters were properly adjusted. Simulated electrical characteristics and experimental data demonstrate a very good agreement but necessitate further improvement. The important physical quantity of root-mean-square (RMS) roughness at the TIPS-Pentacene/PS interface is also included in the simulation considering various patterns. Different levels of RMS roughness at the active interface and different patterns are considered. Also, the TIPS-Pentacene thickness non-uniformity was examined, and the simulation results suggest that it is more significant when the TIPS-Pentacene thickness is thinner near the drain electrode side. Finally, the effects of non-uniformity on the device's overall electrical behavior are systematically investigated. [Display omitted] • TCAD simulation of the spray-coated TIPS-PEN:PS blend OFETs. • Inherent variability of the real devices demands different simulation parameters. • Need to include interface roughness and active channel thickness non-uniformity. • Improved fitting between simulated and experimental input and output I–V curves. • TIPS-PEN non-uniformity is more critical when it is thinner near the drain side. [ABSTRACT FROM AUTHOR]

[Display omitted] • Design of hybrid materials for photonic applications. • Structural and optical properties of hybrid materials. • Hybrid materials self-assembly in bulk vs. thin film. • Effect of gold nanoparticles in block copolymer self-assembly. We introduce the preparation as well as the structural and optical properties of hybrid materials consisting of diblock copolymer matrices with gold nanoparticles. Anionically synthesized diblock copolymers of the PS- b -P4VP sequence, where PS: polystyrene and P4VP: poly(4-vinylpyridine) with well-defined characteristics were utilized as the polymer matrices. The specific pyridine-containing copolymers were selected due to their susceptibility to post-polymerization chemical modification reactions. Basic tertiary amines can be easily modified due to the presence of the nitrogen atom (N) in the 4-position (-para) of the aromatic ring in the monomeric units of poly(4-vinylpyridine). In this manner, the addition of either atoms or whole compounds as ion pairs is enabled. We report that the role of noble metal atoms in polymer matrices is dual. Firstly, microphase separation in the presence of heteroatoms occurs even in cases of extremely low molecular characteristics due to the increased repulsion between the components and secondly the excitation of plasmon resonance at the polymer/nanoparticle interface is induced. We believe that our work sheds light on the driving forces of self-assembly on the studied modified copolymers. The results strongly suggest that the hybrid materials can adopt well-defined morphologies even in very low molecular weights, a fact that renders them promising candidates for photonic applications. [ABSTRACT FROM AUTHOR]

To study the development, characterisation, and drug release of one‐ and two‐layered thin films based on organic polymers [poly(D,L‐lactide‐co ‐glycolide) lactide:glycolide (65:35), poly(D,L‐lactide‐co ‐glycolide) lactide:glycolide (75:25), and polycaprolactone] and dexamethasone. To examine their applicability for intraocular lenses (IOLs) and function in intraocular drug delivery systems. Four series of thin films, single and double‐layer, were prepared by the spin‐coating method on a silicon substrate. The films were studied using atomic force microscopy and spectroscopic ellipsometry. The release rate of dexamethasone was studied for a period of ten weeks. Series A and C demonstrated the formation of large dexamethasone aggregates. The monolayer films of series C and D formed pores, in agreement with previous findings. The spectroscopic ellipsometry study demonstrated that the samples were transparent. The drug release study demonstrated that dexamethasone was released during the first 6 weeks at a desirable rate. The films exhibited properties suitable for use in intraocular drug delivery systems. The single‐layer thin films demonstrated a sufficient encapsulation of dexamethasone and appropriate release of the therapeutic substance. Further studies are necessary to investigate the possibility of developing the films directly on the surface of the IOL. [ABSTRACT FROM AUTHOR]

To study the development, characterisation, and drug release of one- and two-layered thin films based on organic polymers [poly(D,L-lactide-co-glycolide) lactide:glycolide (65:35), poly(D,L-lactide-co-glycolide) lactide:glycolide (75:25), and polycaprolactone] and dexamethasone. To examine their applicability for intraocular lenses (IOLs) and function in intraocular drug delivery systems. Four series of thin films, single and double-layer, were prepared by the spin-coating method on a silicon substrate. The films were studied using atomic force microscopy and spectroscopic ellipsometry. The release rate of dexamethasone was studied for a period of ten weeks. Series A and C demonstrated the formation of large dexamethasone aggregates. The monolayer films of series C and D formed pores, in agreement with previous findings. The spectroscopic ellipsometry study demonstrated that the samples were transparent. The drug release study demonstrated that dexamethasone was released during the first 6 weeks at a desirable rate. The films exhibited properties suitable for use in intraocular drug delivery systems. The single-layer thin films demonstrated a sufficient encapsulation of dexamethasone and appropriate release of the therapeutic substance. Further studies are necessary to investigate the possibility of developing the films directly on the surface of the IOL. [ABSTRACT FROM AUTHOR]

In this study, novel copolymers consisting of blue and red chromophores are presented to induce emission tuning, enabling the definition of white light emission in a single polymeric layer. These aromatic polyether sulfones exhibit high molecular weights, excellent solubility and processability via solution deposition techniques. In addition, by carefully controlling the molar ratios of chromophores composition, the energy transfer mechanism, from blue to red chromophores, takes place enabling us to define properly the emission covering the entire range of the visible spectrum. The optical and photophysical properties of the monomers and copolymers were thoroughly investigated via NIR-Vis-far UV Spectroscopic Ellipsometry (SE), Absorbance and Photoluminescence (PL). These copolymers are used as an emissive layer and applied in solution-processed WOLED devices. The fabricated WOLED devices have been subsequently studied and characterized in terms of their electroluminescence properties. Finally, the WOLED devices possess high color stability and demonstrate CIE Coordinates (0.33, 0.38), which approach closely the pure white light CIE coordinates. [ABSTRACT FROM AUTHOR]