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Solution Processing (solution + processing)
Selected AbstractsFlexible Fullerene Field-Effect Transistors Fabricated Through Solution ProcessingADVANCED MATERIALS, Issue 47 2009Chao-Feng Sung C60-based thin-film transistors are fabricated through solution processing. On rigid indium tin oxide glass, the transistors display electron mobilities as high as 0.21,cm2 V,1 s,1 and a threshold voltage of 0.7,V, only slightly lower than those of organic thin-film transistors prepared through vacuum deposition. On ITO-coated PET substrates, the mobilities in the flexible devices (see image) are approximately one order of magnitude lower than those of devices prepared on rigid glass substrates. [source] Solution Processing of Chalcogenide Semiconductors via Dimensional ReductionADVANCED MATERIALS, Issue 31 2009David B. Mitzi Abstract The quest to develop thin-film solution processing approaches that offer low-cost and preferably low-temperature deposition, while simultaneously providing quality semiconductor characteristics, has become an important thrust within the materials community. While inorganic compounds offer the potential for outstanding electronic properties relative to organic systems, the very nature of these materials rendering them good electronic materials,namely strong covalent bonding,also leads to poor solubility. This review presents a "dimensional reduction" approach to improving the solubility of metal chalcogenide semiconductors, which generally involves breaking the extended framework up into discrete metal chalcogenide anions separated by small and volatile cationic species. The resulting soluble precursor may be solution-processed into thin-film form and thermally decomposed to yield the desired semiconductor. Several applications of this principle to the solution deposition of high-performance active layers for transistors (channel mobility >10,cm2 V,1 s,1), solar cells (power conversion efficiency of as high as 12%), and fundamental materials study will be presented using hydrazine as the deposition solvent. [source] Photocurable Organic Gate Insulator for the Fabrication of High-Field Effect Mobility Organic Transistors by Low Temperature and Solution Processing,ADVANCED MATERIALS, Issue 18 2007T.-W. Lee A new organic gate insulator in OTFT devices, which satisfies the requirements for the fabrication of a practical TFT array, such as a good chemical resistance, a low moisture uptake, a low temperature process, and a good film surface smoothness, is introduced. Since this gate insulator film is formed by photo-curing after spincasting on the top of the gate electrode, the process does not require high temperatures. [source] Cathode Properties of Nanocrystalline Manganese Oxide Synthesized Through Soft Solution Processing.CHEMINFORM, Issue 2 2006Takashi Watanabe Abstract For Abstract see ChemInform Abstract in Full Text. [source] Conjugated-Polymer-Based Lateral Heterostructures Defined by High-Resolution PhotolithographyADVANCED FUNCTIONAL MATERIALS, Issue 17 2010Jui-Fen Chang Abstract Solution processing of polymer semiconductors provides a new paradigm for large-area electronics manufacturing on flexible substrates, but it also severely restricts the realization of interesting advanced device architectures, such as lateral heterostructures with defined interfaces, which are easily accessible with inorganic materials using photolithography. This is because polymer semiconductors degrade, swell, or dissolve during conventional photoresist processing. Here a versatile, high-resolution photolithographic method is demonstrated for patterning of polymer semiconductors and exemplify this with high-performance p-type and n-type field-effect transistors (FETs) in both bottom- and top-gate architectures, as well as ambipolar light-emitting field-effect transistors (LEFETs), in which the recombination zone can be pinned at a photolithographically defined lateral heterojunction between two semiconducting polymers. The technique therefore enables the realization of a broad range of novel device architectures while retaining optimum materials performance. [source] An Alternative Approach to Constructing Solution Processable Multifunctional Materials: Their Structure, Properties, and Application in High-Performance Organic Light-Emitting DiodesADVANCED FUNCTIONAL MATERIALS, Issue 18 2010Shanghui Ye Abstract A new series of full hydrocarbons, namely 4,4,-(9,9,-(1,3-phenylene)bis(9H -fluorene-9,9-diyl))bis(N,N -diphenylaniline) (DTPAFB), N,N,-(4,4,-(9,9,-(1,3-phenylene)bis(9H -fluorene-9,9-diyl))bis(4,1-phenylene))bis(N -phenylnaphthalen-1-amine) (DNPAFB), 1,3-bis(9-(4-(9H -carbazol-9-yl)phenyl)-9H -fluoren-9-yl)benzene, and 1,3-bis(9-(4-(3,6-di- tert -butyl-9H -carbazol-9-yl)phenyl)-9H -fluoren-9-yl)benzene, featuring a highly twisted tetrahedral conformation, are designed and synthesized. Organic light-emitting diodes (OLEDs) comprising DNPAFB and DTPAFB as hole transporting layers and tris(quinolin-8-yloxy)aluminum as an emitter are made either by vacuum deposition or by solution processing, and show much higher maximum efficiencies than the commonly used N,N,-di(naphthalen-1-yl)- N,N,-diphenylbiphenyl-4,4,-diamine device (3.6 cd A,1) of 7.0 cd A,1 and 6.9 cd A,1, respectively. In addition, the solution processed blue phosphorescent OLEDs employing the synthesized materials as hosts and iridium (III) bis[(4,6-di-fluorophenyl)-pyridinato-N, C2] picolinate (FIrpic) phosphor as an emitter present exciting results. For example, the DTPAFB device exhibits a brightness of 47 902 cd m,2, a maximum luminescent efficiency of 24.3 cd A,1, and a power efficiency of 13.0 lm W,1. These results show that the devices are among the best solution processable blue phosphorescent OLEDs based on small molecules. Moreover, a new approach to constructing solution processable small molecules is proposed based on rigid and bulky fluorene and carbazole moieties combined in a highly twisted configuration, resulting in excellent solubility as well as chemical miscibility, without the need to introduce any solubilizing group such as an alkyl or alkoxy chain. [source] Electroluminescence: (Highly Emitting Neutral Dinuclear Rhenium Complexes as Phosphorescent Dopants for Electroluminescent Devices) Adv.ADVANCED FUNCTIONAL MATERIALS, Issue 16 2009Funct. Neutral, dinuclear, highly luminescent rhenium(I) complexes are prepared and their photophysical and electrochemical properties investigated by Professor Luisa De Cola and co-workers. For the first time, electroluminescent devices, using a rhenium complex as dopant, obtained by sublimation and by solution processing are described. [source] Photocrosslinkable Polythiophenes for Efficient, Thermally Stable, Organic PhotovoltaicsADVANCED FUNCTIONAL MATERIALS, Issue 14 2009Bumjoon J. Kim Abstract Photocrosslinkable bromine-functionalized poly(3-hexylthiophene) (P3HT-Br) copolymers designed for application in solution-processed organic photovoltaics are prepared by copolymerization of 2-bromo-3-(6-bromohexyl) thiophene and 2-bromo-3-hexylthiophene. The monomer ratio is carefully controlled to achieve a UV photocrosslinkable layer while retaining the ,,, stacking feature of the conjugated polymers. The new materials are used as electron donors in both bulk heterojunction (BHJ) and bilayer type photovoltaic devices. Unlike devices prepared from either P3HT:PCBM blend or P3HT-Br:PCBM blend without UV treatment, photocrosslinked P3HT-Br:PCBM devices are stable even when annealed for two days at the elevated temperature of 150,°C as the nanophase separated morphology of the bulk heterojunction is stabilized as confirmed by optical microscopy and grazing incidence wide angle X-ray scattering (GIWAXS). When applied to solution-processed bilayer devices, the photocrosslinkable materials show high power conversion efficiencies (,2%) and excellent thermal stability (3 days at 150,°C). Such performance, one of the highest obtained for a bilayer device fabricated by solution processing, is achieved as crosslinking does not disturb the ,,, stacking of the polymer as confirmed by GIWAXS measurements. These novel photocrosslinkable materials provide ready access to efficient bilayer devices thus enabling the fundamental study of photophysical characteristics, charge generation, and transport across a well-defined interface. [source] Control of the Morphology and Structural Development of Solution-Processed Functionalized Acenes for High-Performance Organic TransistorsADVANCED FUNCTIONAL MATERIALS, Issue 10 2009Jung Ah Lim Abstract Solution-processable functionalized acenes have received special attention as promising organic semiconductors in recent years because of their superior intermolecular interactions and solution-processability, and provide useful benchmarks for organic field-effect transistors (OFETs). Charge-carrier transport in organic semiconductor thin films is governed by their morphologies and molecular orientation, so self-assembly of these functionalized acenes during solution processing is an important challenge. This article discusses the charge-carrier transport characteristics of solution-processed functionalized acene transistors and, in particular, focuses on the fine control of the films' morphologies and structural evolution during film-deposition processes such as inkjet printing and post-deposition annealing. We discuss strategies for controlling morphologies and crystalline microstructure of soluble acenes with a view to fabricating high-performance OFETs. [source] Characteristics of Solution-Processed Small-Molecule Organic Films and Light-Emitting Diodes Compared with their Vacuum-Deposited CounterpartsADVANCED FUNCTIONAL MATERIALS, Issue 10 2009Tae-Woo Lee Abstract Although significant progress has been made in the development of vacuum-deposited small-molecule organic light-emitting diodes (OLEDs), one of the most desired research goals is still to produce flexible displays by low-cost solution processing. The development of solution-processed OLEDs based on small molecules could potentially be a good approach but no intensive studies on this topic have been conducted so far. To fabricate high-performance devices based on solution-processed small molecules, the underlying nature of the produced films and devices must be elucidated. Here, the distinctive characteristics of solution-processed small-molecule films and devices compared to their vacuum-deposited counterparts are reported. Solution-processed blue OLEDs show a very high luminous efficiency (of about 8.9,cd A,1) despite their simplified structure. A better hole-blocking and electron-transporting layer is essential for achieving high-efficiency solution-processed devices because the solution-processed emitting layer gives the devices a better hole-transporting capability and more electron traps than the vacuum-deposited layer. It is found that the lower density of the solution-processed films (compared to the vacuum-deposited films) can be a major cause for the short lifetimes observed for the corresponding devices. [source] Multifunctional Crosslinkable Iridium Complexes as Hole Transporting/Electron Blocking and Emitting Materials for Solution-Processed Multilayer Organic Light-Emitting DiodesADVANCED FUNCTIONAL MATERIALS, Issue 7 2009Biwu Ma Abstract Here, a new series of crosslinkable heteroleptic iridium (III) complexes for use in solution processed phosphorescent organic light emitting diodes (OLEDs) is reported. These iridium compounds have the general formula of (PPZ-VB)2Ir(C,N), where PPZ-VB is phenylpyrazole (PPZ) vinyl benzyl (VB) ether; and the C,N ligands represent a family of four different cyclometallating ligands including 1-phenylpyrazolyl (PPZ) (1), 2-(4,6-difluorophenyl)pyridyl (DFPPY) (2), 2-(p-tolyl)pyridyl (TPY) (3), and 2-phenylquinolyl (PQ) (4). With the incorporation of two crosslinkable VB ether groups, these compounds can be fully crosslinked after heating at 180,°C for 30,min. The crosslinked films exhibit excellent solvent resistance and film smoothness which enables fabrication of high-performance multilayer OLEDs by sequential solution processing of multiple layers. Furthermore, the photophysical properties of these compounds can be easily controlled by simply changing the cyclometallating C,N ligand in order to tune the triplet energy within the range of 3.0,2.2,eV. This diversity makes these materials not only suitable for use in hole transporting and electron blocking but also as emissive layers of several colors. Therefore, these compounds are applied as effective materials for all-solution processed OLEDs with (PPZ-VB)2IrPPZ (1) acting as hole transporting and electron blocking layer and host material, as well as three other compounds, (PPZ-VB)2IrDFPPY (2), (PPZ-VB)2IrTPY(3), and (PPZ-VB)2IrPQ(4), used as crosslinkable phosphorescent emitters. [source] Solution-Processable Carbazole-Based Conjugated Dendritic Hosts for Power-Efficient Blue-Electrophosphorescent DevicesADVANCED MATERIALS, Issue 48 2009Junqiao Ding A novel class of hosts suitable for solution processing has been developed based on a conjugated dendritic scaffold. By increasing the dendron generation, the highest occupied molecular orbital (HOMO) energy level can be tuned to facilitate hole injection, while the triplet energy remains at a high level, sufficient to host high-energy-triplet emitters. A power-efficient blue-electrophosphorescent device based on H2 (see figure) is presented. [source] Flexible Fullerene Field-Effect Transistors Fabricated Through Solution ProcessingADVANCED MATERIALS, Issue 47 2009Chao-Feng Sung C60-based thin-film transistors are fabricated through solution processing. On rigid indium tin oxide glass, the transistors display electron mobilities as high as 0.21,cm2 V,1 s,1 and a threshold voltage of 0.7,V, only slightly lower than those of organic thin-film transistors prepared through vacuum deposition. On ITO-coated PET substrates, the mobilities in the flexible devices (see image) are approximately one order of magnitude lower than those of devices prepared on rigid glass substrates. [source] Highly Efficient and Color-Stable Deep-Blue Organic Light-Emitting Diodes Based on a Solution-Processible DendrimerADVANCED MATERIALS, Issue 47 2009Lei Wang A color-stable blue organic light-emitting diode is obtained utilizing a solution-processible fluorescent , -conjugated dendrimerG0 (see image), with a maximum luminance efficiency of 5.3,cd A,1. Efficient green, red, and white OLEDs are also demonstrated by doping G0 with phosphorescent dyes. Combining high device efficiency with solution processibility, G0 becomes one of the best blue-emitting materials for fabricating flat-panel displays and white-light lighting panels via solution processing. [source] Cover Picture: Multilayer Polymer Light-Emitting Diodes: White-Light Emission with High Efficiency (Adv. Mater.ADVANCED MATERIALS, Issue 17 200517/2005) Abstract White-light-emitting polymer diodes can be fabricated by solution processing using a blend of luminescent semiconducting polymers and organometallic complexes as the emission layer, and water-soluble (or ethanol-soluble) polymers and/or small molecules as the hole-injection/transport layer (HIL/HTL) and the electron injection/transport layer (EIL/ETL), as reported on p.,2053 by Gong, Bazan, Heeger and co-workers. Illumination-quality light is obtained from these multilayer, high-performance devices, with stable CIE coordinates, color temperatures, and high color-rendering indices all close to those of "pure" white light. The cover illustration envisages the incorporation of the fabrication technique with low-cost manufacturing technology in order to produce large areas of high-quality white light. [source] Template-directed synthesis of hybrid nanowires and nanorodsPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 10 2010Jiayin Yuan Abstract Recently, one-dimensional (1D) nanostructures, such as wires, rods, tubes, etc., have attracted considerable attention due to their unique shape- and size-dependant properties and many potential applications. Template-directed synthesis is a powerful and widely used method to prepare 1D objects. As robust unimolecular template, cylindrical polymer brushes have been exploited for the fabrication of various hybrid nanowires and nanorods, for instance, ,-Fe2O3, CdS, CdSe, TiO2, silica, Au, Te, etc. As a key advantage of this polymeric templating, the obtained 1D hybrid nanostructures are colloidally stable in solution, facilitating their further solution processing. Cryo-TEM image of organo-silica hybrid nanowires in aqueous solution (the inset shows a cartoon of the structure). [source] The morphology and thermal properties of multi-walled carbon nanotube and poly(hydroxybutyrate- co -hydroxyvalerate) compositePOLYMER INTERNATIONAL, Issue 10 2004Mingfang Lai Abstract Nanocomposites based on poly(hydroxybutyrate- co -hydroxyvalerate) (PHBV) and multi-walled carbon nanotubes (MWNTs) were prepared by solution processing. Ultrasonic energy was used to uniformly disperse MWNTs in solutions and to incorporate them into composites. Microscopic observation reveals that polymer-coated MWNTs dispersed homogenously in the PHBV matrix. The thermal properties and the crystallization behavior of the composites were characterized by thermogravimetric analysis, differential scanning calorimetry and wide-angle X-ray diffraction, the nucleant effect of MWNTs on the crystallization of PHBV was confirmed, and carbon nanotubes were found to enhanced the thermal stability of PHBV in nitrogen. Copyright © 2004 Society of Chemical Industry [source] Reactive doping of PAni,CSA and its use in microwave absorbing materialsPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 1 2009R. S. Biscaro Abstract Conductive coatings have been studied for static dissipation and as microwave absorbing materials. The doping process of polyaniline (PAni), which makes it conductive, is an important stage that determines the coating performance. For this purpose, polyaniline was doped by reactive processing in a torque rheometer using different molar ratios between PAni and acid (PAni:CSA) at three different temperatures (80, 90, and 100°C). Aqueous solution doping was also used in the ratio of 1:2 of PAni/CSA, with the aim to investigate the influence of different methods of PAni doping on its characteristics and, consequently, on the performance of coatings. Thermal analyses of the processed materials showed that PAni doped by both routes, reactive and solution processing, showed similar behaviors. X-ray diffraction analyses showed a semicrystalline structure for the PAni,CSA doped by reactive processing using high CSA concentrations and temperature. It was also observed that the doping process affects the dispersion of the components into the conductive coatings. Microwave absorption measurements (8,12,GHz) of PU-doped PAni blends showed the dependence of the doping type, the PAni,CSA concentration, and the mixing conditions of the components on the coating performance; it was found up to 99% of attenuation of the incident radiation for some composites in a narrow frequency range. The microwave absorption efficiency of the coating samples prepared by using the reactive doping process indicates the advantage of this methodology over solution doping. Moreover, the reactive process addresses the environmental requirements. Copyright © 2008 John Wiley & Sons, Ltd. [source] | ||||||||||