Solution Processing Techniques Research Articles

Achieving Record External Quantum Efficiency of 11.5 % in Solution-Processable Deep-Blue Organic Light-Emitting Diodes Utilizing Hot Exciton Mechanism.

High performance solution-processable deep-blue emitters with a Commission International de l'Eclairage (CIE) coordinate of CIEy≤0.08 are highly desired in ultrahigh-definition display. Although, deep-blue materials with hybridized local and charge-transfer (HLCT) excited-state feature are promising candidates, their rigidity and planar molecular structures limit their application in solution-processing technique. Herein, four novel deep-blue solution-processable HLCT emitters were first proposed by attaching rigid imide aliphatic rings as functional units onto the HLCT emitting core. The functional units not only improve solubility, enhance thermal properties and morphological stability of the emitting core, but also promote photoluminescence efficiency, balance charge carrier transport, and inhibit aggregation-caused quenching effect due to the weak electron-withdrawing property as well as steric hindrance. The corresponding solution-processable organic light-emitting diodes (OLEDs) substantiate an unprecedented maximum external quantum efficiency (EQEmax) of 11.5 % with an emission peak at 456 nm and excellent colour purity (full width at half maximum=56 nm and CIEy=0.09). These efficiencies represent the state-of-the-art device performance among the solution-processable blue OLEDs based on the "hot exciton" mechanism. This simple strategy opens up a new avenue for designing highly efficient solution-processable deep-blue organic luminescent materials.

Optimized Incorporation of Furan into Diketopyrrolopyrrole-Based Conjugated Polymers for Organic Field-Effect Transistors.

Flexible electronics have received considerable attention in the past decades due to their promising application in rollable display screens, wearable devices, implantable devices, and other electronic applications. In particular, conjugated polymers are favored for flexible electronics due to their mechanical flexibility and potential for solution-processed fabrication techniques, such as blade-coating, roll-to-roll printing, and high-throughput printing allowing for high-performance transistor devices. Thiophene is the prevailing conjugated unit to construct these conjugated polymers due to its favorable electronic properties. On the other hand, furans are among the few conjugated moieties that are easily derived from bio renewable resources. To promote sustainability, we selectively introduced furan into the conjugated backbone of a high-mobility polymer scaffold and systematically studied the effect on the microstructure and charge transport. We show that partially and selectively replacing thiophene units with furan can yield nearly comparable performance compared to the all-thiophene polymer. This strategy offers an improvement in the sustainability of the polymer by incorporating bio-sourced furan without sacrificing the high-performance characteristics. Meanwhile, polymers with incorrect or complete furan incorporation show reduced mobilities. This work serves to develop coherent structure-morphology-performance relationships; such knowledge will establish guidelines for the future development of sustainable, furan-based conjugated materials.

Growth Processing and Strategies: A Way to Improve the Gas Sensing Performance of Nickel Oxide-Based Devices

The review paper provides a comprehensive analysis of nickel oxide (NiO) as an emerging material in environmental monitoring by surveying recent developments primarily within the last three years and reports the growth processing and strategies employed to enhance NiO sensing performance. It covers synthesis methods for pristine NiO, including vapor-phase, liquid-phase, and solution-processing techniques, highlighting advantages and limitations. The growth mechanisms of NiO nanostructures are explored, with a focus on the most recent research studies. Additionally, different strategies to improve the gas sensing performance of NiO are discussed (i.e., surface functionalization by metallic nanoparticles, heterostructure formation, carbon-based nanomaterials, and conducting polymers). The influence of these strategies on selectivity, sensitivity, response time, and stability of NiO-based sensors is thoroughly examined. Finally, the challenges and future directions that may lead to the successful development of highly efficient NiO-based gas sensors for environmental monitoring are introduced in this review.

Stretchable Device for Simultaneous Measurements of Contractility and Electrophysiology of Neuromuscular Tissue in the Gastrointestinal Tract.

Devices interfacing with biological tissues can provide valuable insights into function, disease, and metabolism through electrical and mechanical signals. However, certain neuromuscular tissues, like those in the gastrointestinal tract, undergo significant strains of up to 40%. Conventional inextensible devices cannot capture the dynamic responses in these tissues. This study introduces electrodes made from poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and polydimethylsiloxane (PDMS) that enable simultaneous monitoring of electrical and mechanical responses of gut tissue. The soft PDMS layers conform to tissue surfaces during gastrointestinal movement. Dopants, including Capstone FS-30 and polyethylene glycol, are explored to enhance the conductivity, electrical sensitivity to strain, and stability of the PEDOT:PSS. The devices are fabricated using shadow masks and solution-processing techniques, providing a faster and simpler process than traditional clean-room-based lithography. Tested on ex vivo mouse colon and human stomach, the device recorded voltage changes of up to 300 µV during contraction and distension consistent with muscle activity, while simultaneously recording resistance changes of up to 150% due to mechanical strain. These devices detect and respond to chemical stimulants and blockers, and can induce contractions through electrical stimulation. They hold great potential for studying and treating complex disorders like irritable bowel syndrome and gastroparesis.

Uniform Nanoscale Ion-Selective Membrane Prepared by Precision Control of Solution Spreading and Evaporation.

Ion-selective membrane has broad application in various fields, while the present solution-processed techniques can only prepare uniform membrane with microscale thickness. Herein, a high-quality polymer membrane with nanoscale thickness and uniformity is precisely prepared by controlling solution spreading and solvent evaporation stability/rate. With the arrayed capillaries, the stable spreading of polymer solution with volume of microliter induces the formation of solution film with micrometers thickness. Moreover, the fast increase of solution dynamic viscosity during solvent evaporation inhibits nonuniform Marangoni flow and capillary flow in solution film. Consequently, the uniform Nafion-Li membranes with ∼200 nm thickness are prepared, while their Li+ conductivity is 2 orders of magnitude higher than that of commercially Nafion-117 membrane. Taking lithium-sulfur battery as a model device, the cells (capacities of 8-10 mAh cm-2) can stably operate for 150 cycles at a S loading of 12 mg cm-2 and an electrolyte/sulfur ratio of ∼7.

Design and optimization of the performance of PbS quantum dot based vertical photodetector

Abstract Quantum dots (QDS) are widely used as photoactive materials for various optoelectronic applications, such as light-emitting diodes, photodetectors, lasers, and solar cells, because of their unique and outstanding physical properties for fabricating devices via solution-processing techniques and for varying the sizes of QD to modulate the band gap. In this study, we constructed a numerical model of a vertical photodetector using lead sulfide (PbS) quantum dot layer undergoing ligand exchange treatment with tetrabutylammonium iodide (TBAI) as the light absorption layer to obtain an optimized high-performance photodetector using 1D-Solar Cell Capacitance Simulator (SCAPS) software. For the hole transport layer (HTL) and electron transport layer (ETL), a PbS quantum dot layer that employs an ethanedithiol (EDT) ligand exchange scheme and a zinc oxide (ZnO) layer were utilized, respectively, with gold (Au) and indium tin oxide (ITO) as the bottom and upper electrodes, respectively. After optimizing the thickness and doping concentration of the absorption layer, we obtained a maximum responsivity of 0.4675 A W−1 and detectivity of 2.44 * 10 13 Jones at a reverse bias of 0.5 volts after optimizing of thickness and doping concentration of absorption layer showing an improvement of 19% and 87.7% respectively compared to the initial structure whose parameters originated from studies of PbS quantum dot solar cells with the same structure and materials, although optimization of other transport layers do not provide as great performance enhancement as absorption layer. This study demonstrates that the structural parameters of solar cells are not always applicable to photodetectors, and that photodetectors have great potential for numerical optimization. Ethical Compliance: All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Solution processing of crystalline porous material based membranes for CO2 separation.

The carbon emission problem is a significant challenge in today's society, which has led to severe global climate issues. Membrane-based separation technology has gained considerable interest in CO2 separation due to its simplicity, environmental friendliness, and energy efficiency. Crystalline porous materials (CPMs), such as zeolites, metal-organic frameworks, covalent organic frameworks, hydrogen-bonded organic frameworks, and porous organic cages, hold great promise for advanced CO2 separation membranes because of their ordered and customizable pore structures. However, the preparation of defect-free and large-area crystalline porous material (CPM)-based membranes remains challenging, limiting their practical use in CO2 separation. To address this challenge, the solution-processing method, commonly employed in commercial polymer preparation, has been adapted for CPM membranes in recent years. Nanosheets, spheres, molecular cages, and even organic monomers, depending on the CPM type, are dissolved in suitable solvents and processed into continuous membranes for CO2 separation. This feature article provides an overview of the recent advancements in the solution processing of CPM membranes. It summarizes the differences among the solution-processing methods used for forming various CPM membranes, highlighting the key factors for achieving continuous membranes. The article also summarizes and discusses the CO2 separation performance of these membranes. Furthermore, it addresses the current issues and proposes future research directions in this field. Overall, this feature article aims to shed light on the development of solution-processing techniques for CPM membranes, facilitating their practical application in CO2 separation.

Characterization of nanoscale morphology and mechanical properties of conjugated polymer thin films dynamically exposed to a secondary solvent

Solution processing techniques are often used to enhance intra and interchain order in semiconducting conjugated polymer thin films used in the active layer of organic optoelectronic devices. While there has been extensive research into the impact of solution processing on the local structural and electronic properties of these films, the nanomechanical properties of the films are less well understood and are challenging to characterize. We investigate the nanomechanical properties of conjugated polymer thin films arising from solution processing techniques. Our study relies on dynamic secondary solvent dripping to induce subtle changes to the film morphology. We examine thin films of P3HT, PCDTBT, PTB7, and PBDB-T-SF conjugated polymers, commonly used in organic photovoltaics, with the bimodal amplitude modulation-frequency modulation (AM-FM) imaging mode of the atomic force microscopy (AFM) viscoelastic method to probe their local physical and mechanical properties. We find that Young's Modulus data measured by AM-FM AFM can detect additional changes in film properties not discernible by other commonly used bulk thin-film characterization techniques. For PBDB-T-SF, we detect an increase in molecular order that is not noticable by UV–visible absorption spectroscopy, X-ray diffraction or nanoindentation. PCDTBT, the most amorphous of the polymers studied, shows no changes in absorption or X-ray diffraction data, yet clear changes in Young's Modulus were detected by AFM. On the other hand, increases in P3HT order that occurred due to dynamic secondary solvent dripping are detected in both the bulk and AFM measurements. Our study demonstrates the applicability of nanomechanical measurements for characterizing local structural variations in conjugated polymer films. This work is relevant to ongoing efforts to control and understand the complex structure-property-processing relationships of conjugated polymer thin films.

Bilayered graded phase homojunction FA0.15MA0.85PbI3-based organic-inorganic hybrid perovskite solar cells crossing 22 % efficiency

Making highly efficient and stable perovskite solar cells (PSCs) are often based on the processing techniques, band gap of the material and effective interface charge separation. The efficiency of PSCs can be enhanced through several methods including the utilization of a solar-friendly absorber, interface passivation and the implementation of multi-junction spectrally matched absorbers or bilayered phase homojunction (BPHJ) consisting of identical absorbers. Here, we demonstrated BPHJ concept by stacking identical compositions of highly efficient and stable FA0.15MA0.85PbI3 perovskite absorbers adopting solution process (SP) and thermal evaporation (TEV) techniques. We successfully achieved FA0.15MA0.85PbI3 (SP)/FA0.15MA0.85PbI3-(TEV) based BPHJ normal n-i-p devices, which significantly crossing 22.% PCE. These improvement stems from effective deposition method for achieving high-quality FA0.15MA0.85PbI3-based BPHJ enabling smooth charge transfer at the interfaces. The resulting BPHJ-based champion device achieve a 22.13 % PCE and retain >95 % its original efficiency over 1000 hours.

Constructing thermally activated delayed fluorescence dendrimers for solution processable blue OLEDs by molecular engineering of peripheral dendrons

Thermally activated delayed fluorescence (TADF) dendrimers with definite chemical structure are ideal candidate to fabricate high-efficiency organic light emitting diodes (OLEDs) using lower-cost solution processing techniques. Nevertheless, there still remains a challenge to construct molecular architectures of dendrimer-based TADF emitters that show easily controlled photophysical properties and superior carrier transporting capability simultaneously. Herein, we integrate peripheral dendrons possessing bipolar transmission capability with donor-acceptor skeleton through spiro junction to construct newly designed dendritic TADF emitters, TrzSpiroAc-tmCP and TrzSpiroAc-tmCPCN. By precisely regulating peripheral dendrons in these newly designed molecules, the lifetime and proportion of delayed components for TrzSpiroAc-tmCPCN are meticulously modulated to be 3.1 μs and 26.0 %, respectively, and thus exhibiting enhanced reverse intersystem crossing process with rate constant of 3.2 × 105 s−1 and excellent photoluminescence quantum yield over 70 %. Solution processable OLEDs based on TrzSpiroAc-tmCPCN with blue emission are achieved, and the external quantum efficiency value can exceed 10 %. Overall, this work manifests a valid strategy to tackle the imperative need for further exploring high-efficiency TADF dendrimers by integrating molecular engineering of peripheral dendritic units with constructing spiro junction between emission core and dendritic units.

Large area inkjet-printed OLED fabrication with solution-processed TADF ink

This work demonstrates successful large area inkjet printing of a thermally activated delayed fluorescence (TADF) material as the emitting layer of organic light-emitting diodes (OLEDs). TADF materials enable efficient light emission without relying on heavy metals such as platinum or iridium. However, low-cost manufacturing of large-scale TADF OLEDs has been restricted due to their incompatibility with solution processing techniques. In this study, we develop ink formulation for a TADF material and show successful ink jet printing of intricate patterns over a large area (6400 mm2) without the use of any lithography. The stable ink is successfully achieved using a non-chlorinated binary solvent mixture for a solution processable TADF material, 3‐(9,9‐dimethylacridin‐10(9H)‐yl)‐9H‐xanthen‐9‐one dispersed in 4,4’-bis-(N-carbazolyl)-1,1’-biphenyl host. Using this ink, large area ink jet printed OLEDs with performance comparable to the control spin coated OLEDs are successfully achieved. In this work, we also show the impact of ink viscosity, density, and surface tension on the droplet formation and film quality as well as its potential for large-area roll-to-roll printing on a flexible substrate. The results represent a major step towards the use of TADF materials for large-area OLEDs without employing any lithography.

Impact of the series resistance on reverse current of solution-processed Schottky-Barrier-Diodes based on ZnO-rods

In the last years, the implementation of solution-processing techniques, as well as the use of nanostructured oxide semiconductors, have pursued the development of large-area electronic systems. However, the proper understanding of the electrical characteristics of this type of devices is needed with the aim to properly implement potential applications. In general, the diode behaviour at forward condition has been analysed in the literature, but at reverse condition further research is required. Therefore, in this work, the fabrication and electrical characterization at reverse condition of solution-processed Schottky-Barrier-Diodes based on ZnO-rods is presented. Two different conduction mechanisms with a transition occurring at around –2 V were observed. Also, numerical solutions of the diode reverse current characteristic, which includes the series resistance (R s ) for both conduction mechanisms, were implemented and the impact of the series resistance was addressed. Finally, a numerical optimization strategy was used to determine the diode parameters which best fit the experimental current.

Asymmetrically Functionalized Electron-Deficient π-Conjugated System for Printed Single-Crystalline Organic Electronics.

Large-area single-crystalline thin films of n-type organic semiconductors (OSCs) fabricated via solution-processed techniques are urgently demanded for high-end electronics. However, the lack of molecular designs that concomitantly offer excellent charge-carrier transport, solution-processability, and chemical/thermal robustness for n-type OSCs limits the understanding of fundamental charge-transport properties and impedes the realization of large-area electronics. The benzo[de]isoquinolino[1,8-gh]quinolinetetracarboxylic diimide (BQQDI) π-electron system with phenethyl substituents (PhC2 -BQQDI) demonstrates high electron mobility and robustness but its strong aggregation results in unsatisfactory solubility and solution-processability. In this work, an asymmetric molecular design approach is reported that harnesses the favorable charge transport of PhC2 -BQQDI, while introducing alkyl chains to improve the solubility and solution-processability. An effective synthetic strategy is developed to obtain the target asymmetric BQQDI (PhC2 -BQQDI-Cn ). Interestingly, linear alkyl chains of PhC2 -BQQDI-Cn (n = 5-7) exhibit an unusual molecular mimicry geometry with a gauche conformation and resilience to dynamic disorders. Asymmetric PhC2 -BQQDI-C5 demonstrates excellent electron mobility and centimeter-scale continuous single-crystalline thin films, which are two orders of magnitude larger than that of PhC2 -BQQDI, allowing for the investigation ofelectron transport anisotropy and applicable electronics.

Air-Stable Semiconducting Ionic Polymers for Thermoelectric Applications

Thermoelectric (TE) devices that interconvert heat and electricity are the promising tools to harvest waste heat and solve energy problems. The current TE market is dominated by inorganic materials such as Bi2Te3 due to their excellent TE performance; however, the issues of inorganics that involve material toxicity, rigidity, heavy weight and energy-intensive processing techniques are limiting the wide applications of TE devices. Choosing organic materials that are light weight, mechanically flexible, abundant and require low-temperature processing, as in our research focus, is paving the path to sustainability and opening up opportunities for a variety of applications such as electronic wearables and sensors.In our study, we aim to design and develop sensors that can detect high electric-field utilizing air-stable ionic polymer TE systems, a novel type of organic semiconductors, via a facile, solution-processing technique. We selected two n-type chloride-based ionic polymers, MADQUAT and PDADMAC as our starting materials because they have relatively low yet reliable ionic conductivities and intrinsically high Seebeck Coefficients under dry condition. The key challenge was that chloride-based polymers were extremely unstable due to their sensitivity to air/moisture and polymer relaxation. We adopted a solution-processable anion exchange technique and successfully created new systems with the same cationic polymer chain but various anions such as tetrafluoroborate (BF4 -) and hexafluorophosphate (PF6 -), that are more hydrophobic, increasing the system stability. Currently, we are investigating our stable ionic polymer TE performance by applying high voltages (500V-2000V) laterally across the samples through a pair of electrodes thermally evaporated on top. The change in TE properties after the high E-field application will help us probe further into the ionic movement of the polymeric systems thermodynamically and kinetically and understand what determines the p/n-type behavior. The thermoelectric sensor for high E-field detection can be incorporated into devices that can detect planetary objects in the outer space as well as microscale biological systems.

(Invited) emerging Designs for Organic Infrared Photodetectors and Energy Storage

The shortwave infrared spectral region (SWIR: 1-3 mm) is particularly powerful for health and environmental monitoring, enabling greater penetration depth and improved resolution in comparison to visible light. However, conventional SWIR sensors are limited by complex die transfer and bonding processing. This presentation will discuss the advances made in organic infrared detectors to overcome the issues in conventional SWIR detectors. The organic devices show photo-response spanning from the visible to 1.7 micron, using a new generation of semiconducting polymers that are processed by solution processing techniques and allow simple direct deposition. We will discuss the recent progress in identifying avenues that will improve sensor detector, such as understanding the origin of efficiency losses and materials optimization. Several demonstrations will show the various potential applications of organic infrared imagers, particularly for an up-conversion structure that combine photo-sensing and display in a compact structure without the need for pixilation. The imaging active area of 2 cm2 enabled concurrent recording of blood vessel location and blood flow pulses.In addition to visualisation of infrared radiation, we are also developing the integration of redox polymers into supercapacitor structures to serve as energy supplies for wireless electronics. A new Faradaic electrode material comprised of a narrow bandgap donor−acceptor conjugated enhanced charge delocalization and thus improved stability dramatically. The supercapacitors were patterned by electrodeposition and showed a high areal power density of 227 mW/cm2, enabling rapid charging and high power output. The capacitance retention was 84% after 11,000 full redox cycles, offering the critical benefit of long cycle life. This work demonstrated the application of a new class of stable redox-active materials suitable to meet the energy storage needs for short-range wireless electronics.

Thin Film Transistors Incorporating Ultrapure Semiconducting Single-Walled Carbon Nanotubes and Green Dielectrics

Printed electronics is a burgeoning field that has received intense research interest and is beginning to experience commercial successes. Single-walled carbon nanotubes (SWNTs) are a unique and promising building block for incorporation into next generation superfast electronic devices. SWNTs have very high carrier mobilites, with band gaps compatible for integration into logic circuits. Their excellent mechanical flexibility allows for potential incorporation into flexible printed electronics, enabling fully-printed transistors and circuits with performances that support low cost, large area fabrication. Progress in incorporating SWNTs into commercial devices has been hindered by the presence of metallic SWNTs, which are produced alongside semiconducting SWNTs during synthesis, and negatively impact device performance. Fabrication of ambipolar SWNT organic thin film transistors (OTFTs) with high carrier mobilities and high on/off ratios remains particularly challenging; many examples in the literature required high temperature, expensive and energy-demanding processes.Since the initial discovery of conjugated polymer-assisted dispersion and purification of SWNTs in 2008, several polymer families have been successfully shown to selectively disperse semiconducting SWNTs. However, only a relatively small number of these supramolecular complexes have been incorporated into OTFTs. We used a novel conjugated polymer to exclusively disperse semiconducting SWNTs. The dispersal procedure requires a simple sonication and centrifugation, during which the metallic SWNTs sediment out. Solution purity was evaluated using UVVis- NIR and Raman spectroscopies. The resulting dispersions are amenable to solution processing techniques such drop casting and spin coating, allowing for the potential for large area device fabrication at room temperature. Ambipolar OTFTs were fabricated under ambient conditions using this solution and tested in both air and under inert atmosphere. The presence of excess conjugated polymer, solution deposition techniques, SWNT density, surface treatment, and post-fabrication treatment were all investigated to determine which parameters facilitated the production of OTFTs with high mobilities (>20 cm2V-1s-1), high on/off ratios (10^6-10^8), negligeble hysteresis, controlled threshold voltages, and high bias stability.[1] Protocols for sorting and dispersing ultrapure sc-SWNTs with conjugated polymers for thin-film transistor (TFT) applications have been well refined. Conventional wisdom dictates that removal of excess unbound polymer through filtration or centrifugation is necessary to produce high- erformance TFTs. However, this is time-consuming, wasteful, and resource-intensive. We challenge this paradigm and demonstrate that excess unbound polymer during semiconductor film fabrication is not necessarily detrimental to device performance.[2] With focus on further improving device performance, we look to green, compostable dielectrics to pair with SWCNTs. We report a tri-layer dielectric using poly (lactic acid) (PLA), poly(vinyl alcohol)/cellulose nanocrystals (PVAc) and toluene diisocyanate terminated poly(caprolactone) (TPCL) which we integrated into SWCNT based TFTs in a top gate bottom contact architecture. The PVA provides a high dielectric constant due to the hydroxy groups, the cellulose is used to optimize the viscosity, the TPCL layer provides a robust hydrophobic surface[3], and the PLA eliminates the interfacial charge traps present in the PVAc. This leads to a decrease in leakage currents and reduced the polarity at the dielectric/semiconductor interface. The TFTs fabricated using tri-layer dielectrics led to air stable and balanced hole and electron mobilities which was not observed for the PVAc/TPCL bilayer systems with supressed hole mobility. These TFTs were then used to study the impact of electrochemical doping on the performance of sc-SWCNT TFTs when switching from n-type, where an electrical double layer is formed, to p-type, where the TFSI anions are free to interact with the sc-SWCNTs.[4]The following presentation will focus on the engineering of sc-SWNTs based electronic devices. The choice of conjugated wrapping polymer, dielectric and processing conditions on film formation and the TFT device performance.

Influence of Excess Conjugated Wrapping Polymer in Semiconducting Single-Walled Carbon Nanotube Dispersions

Single-walled carbon nanotubes (SWNTs) are promising nanomaterials for incorporation into organic electronic devices (OEDs), with the potential to fabricate flexible devices while exploiting inexpensive solution-processing techniques. As-synthesized SWNTs are insoluble and comprised of a mixture of metallic and semiconducting SWNTs (sc-SWNTs), necessitating dispersal and purification before integration into OEDs. Refinement of conjugated polymer extraction techniques has allowed for the isolation of sc-SWNTs from metallic in a reproducible and scalable manner. The availability of highly-pure sc-SWNT materials has facilitated the production of thin-film transistors (TFTs) with very high charge carrier mobilities, outperforming organic small molecule and polymer semiconductors. However, the realization of commercial OED applications of polymer-sorted sc-SWNTs have not yet been achieved, partially due to the prohibitive time and materials costs associated with purifying sc-SWNTs.Current protocols for dispersing sc-SWNTs with conjugated polymers involve three broad steps: (1) dispersion of bulk SWNT material, (2) removal of non-dispersed carbonaceous materials, and (3) removal of excess polymer through filtration or centrifugation. The final step of removal of excess polymer is time-consuming and wasteful, but viewed as necessary for preparing high-performing TFTs, as the conjugated polymer has much lower performance compared to SWNTs.In this study we performed the first systematic investigation of the effect of excess polymer on SWNT TFT performance. Three SWNT concentrations were investigated, with varying ratios of excess polymer added to each. TFT device performance was monitored using several metrics, including: mobility, threshold voltage, on/off ratios and hysteresis. Characterization of large numbers of replicate TFT devices determined that below a threshold amount of excess polymer the presence of excess polymer did not have a negative impact on device performance. Detailed analysis of the sc-SWNT films through Raman spectroscopy and atomic force microscopy (AFM) confirmed that a simple rinsing step was sufficient to remove all the unbound conjugated polymer from the substrate surface without affecting the sc-SWNT network. The volume of solvent required for the rinsing step was substantially lower than that required for filtration or centrifugation steps. Furthermore, at higher SWNT concentrations the excess polymer prevented nanotube bundling, resulting in moderate improvements in both mobility and on/off ratios. Our results were reproducible for two different conjugated polymer sc-SWNT systems, demonstrating the versatility of this procedure.

A novel binuclear iridium complex with bis β-diketone and carbazole groups for efficient solution-processed yellow PLEDs

In this paper, we synthesized a novel binuclear Ir complex [(Dfppy)4Ir2(ecbtpd)] with a bis β-diketone substituted carbazole derivative as the auxiliary ligand and 2-(2-fluoro-4-methylphenyl) pyridine as the main ligand. The thermal stability, UV–vis absorption spectra, photoluminescence spectra, phosphorescent lifetime, electrochemistry, and luminescent mechanism of this Ir complex were investigated as well as the device fabricated in phosphorescent PLEDs through solution-process technique. The devices show yellow emissions with maximum current efficiency and maximum external quantum efficiency of 23.67 cd/A and 8.44%, respectively.

Effect of Rubidium Fluoride on Grain Sintering and Optoelectronic Properties of Nanostructured CuInSe2 Thin Films Obtained by Solution Processing

Chalcopyrite CuInSe2 (CISe) and Cu(In, Ga)(S, Se)2 (CIGS) absorber layers, have emerged as promising alternatives in the solar cell field due to their unique properties such as power conversion efficiencies (PCEs) above 20 %, direct bandgap, and high absorption coefficient. This enables the making of high-quality PV devices with absorbers from 2 μm thick, significantly reducing the use of raw materials. Additionally, the CISe absorber layer is a desirable material for Perovskite/CIS tandem configuration with a narrow band gap at the bottom that has demonstrated PCEs close to 25 %, and potential applications in lightweight and/or flexible substrates. Recently, the addition of alkali elements such as sodium, potassium, rubidium, and cesium via post-deposition techniques (PDTs) has demonstrated an improvement in CIGS-based solar cells’ performance. In this study, 10, 20, and 30 nm thick layers of rubidium fluoride were post-deposited on CISe-films made by solution processing techniques and then selenized under a selenium-argon atmosphere to improve the CISe photoelectronic properties such as the number of charge carriers collected and grain growth, critical characteristics to ensure useful photovoltaic devices. Thus, the effect of rubidium fluorine on CISe-based solar cells was analyzed using several characterization techniques. According to the results, thin films made by an amine-thiol mixture with uniform atomic composition were obtained. The crystallinity and grain growth improved with an increase in rubidium fluoride addition. Moreover, with 10 nm of rubidium fluoride, an improvement in the lifetime of the charge carrier, photoluminescence intensity, and the number of carriers collected by the solar cells was obtained.

Developing Solution-Processed Distributed Bragg Reflectors for Microcavity Polariton Applications.

Improving the performance of organic optoelectronics has been under vigorous research for decades. Recently, polaritonics has been introduced as a technology that has the potential to improve the optical, electrical, and chemical properties of materials and devices. However, polaritons have been mainly studied in optical microcavities that are made by vacuum deposition processes, which are costly, unavailable to many, and incompatible with printed optoelectronics methods. Efforts toward the fabrication of polariton microcavities with solution-processed techniques have been utterly absent. Herein, we demonstrate for the first time strong light-matter coupling and polariton photoluminescence in an organic microcavity consisting of an aluminum mirror and a distributed Bragg reflector (DBR) made by sequential dip coating of titanium hydroxide/poly(vinyl alcohol) (TiOH/PVA) and Nafion films. To fabricate and develop the solution-processed DBRs and microcavities, we automatized a dip-coating device that allowed us to produce sub-100 nm films consistently over many dip-coating cycles. Owning to the solution-based nature of our DBRs, our results pave the way to the realization of polariton optoelectronic devices beyond physical deposition methods.