Fractional condensation of bio-oil vapors from pyrolysis of various sawdust wastes in a bench-scale bubbling fluidized bed reactor.

The use of lignocellulosic waste as an energy source for substituting fossil fuels has attracted lots of attention, and pyrolysis has been established as an effective technology for this purpose. However, the utilization of bio-oil derived from non-catalytic pyrolysis faces certain constraints, making it impractical for direct application in advanced sectors. This study has focused on overcoming these challenges by employing fractional condensation of pyrolytic vapors at distinct temperatures. The potential of five types of sawdust for producing high-quality bio-oil through pyrolysis conducted with a bench-scale bubbling fluidized bed reactor was investigated for the first time. The highest yield of bio-oil (61.94 wt%) was produced using sample 3 (damaged timber). Remarkably, phenolic compounds were majorly gathered in the 1st and 2nd condensers at temperatures of 200 °C and 150 °C, respectively, attributing to their higher boiling points. Whereas, carboxylic acid, ketones, and furans were mainly collected in the 3rd (-5 °C) and 4th (-20 °C) condensers, having high water content in the range of 35.33%-65.09%. The separation of acidic nature compounds such as acetic acid in the 3rd and 4th was evidenced by its low pH in the range of 4-5, while the pH of liquid collected in the 1st and 2nd condensers exhibited higher pH (6-7). The well-separated bio-oil derived from biomass pyrolysis facilitates its wide usage in various applications, proposing a unique approach toward carbon neutrality. In particular, achieving efficient separation of phenolic compounds in bio-oil is important, as these compounds can undergo further upgrading to generate hydrocarbons and diesel fuel.

Layer-Selective Synthesis of MoS2 and WS2 Structures under Ambient Conditions for Customized Electronics.

Transition metal dichalcogenides (TMDs) have attracted significant interest as one of the key materials in future electronics such as logic devices, optoelectrical devices, and wearable electronics. However, a complicated synthesis method and multistep processes for device fabrication pose major hurdles for their practical applications. Here, we introduce a direct and rapid method for layer-selective synthesis of MoS2 and WS2 structures in wafer-scale using a pulsed laser annealing system (λ = 1.06 µm, pulse duration ∼100 ps) in ambient conditions. The precursor layer of each TMD, which has at least 3 orders of magnitude higher absorption coefficient than those of neighboring layers, rigorously absorbed the incoming energy of the laser pulse and rapidly pyrolyzed in a few nanoseconds, enabling the generation of a MoS2 or WS2 layer without damaging the adjacent layers of SiO2 or polymer substrate. Through experimental and theoretical studies, we establish the underlying principles of selective synthesis and optimize the laser annealing conditions, such as laser wavelength, output power, and scribing speed, under ambient condition. As a result, individual homostructures of patterned MoS2 and WS2 layers were directly synthesized on a 4 in. wafer. Moreover, a consecutive synthesis of the second layer on top of the first synthesized layer realized a vertically stacked WS2/MoS2 heterojunction structure, which can be treated as a cornerstone of electronic devices. As a proof of concept, we demonstrated the behavior of a MoS2-based field-effect transistor, a skin-attachable motion sensor, and a MoS2/WS2-based heterojunction diode in this study. The ultrafast and selective synthesis of the TMDs suggests an approach to the large-area/mass production of functional heterostructure-based electronics.

Ag flake/silicone rubber composite with high stability and stretching speed insensitive resistance via conductive bridge formation.

High stability, stretchable speed insensitive properties, high stretchability, and electrical conductivity are key characteristics for the realisation of wearable devices. However, conventional research is mainly focused on achieving only high stretchability and electrical conductivity. Studies on the stability and stretching speed insensitive properties generally require complex fabrication processes, which are in need of further improvement. In this study, we propose a facile formation of a conductive bridge in composites by using surface damage and the viscoelastic property of the polymer. Surface cracks due to repeated stretching cycles formed conductive bridges via stress relaxation of the viscoelastic polymer matrix. The conductive bridge resulted in the conductor having highly stable resistance values at target strains and stretching speed insensitive resistance, even at stretching speeds that were 20 times faster than the minimum.

Two-in-One Device with Versatile Compatible Electrical Switching or Data Storage Functions Controlled by the Ferroelectricity of P(VDF-TrFE) via Photocrosslinking.

Organic electronics demand new platforms that can make integrated circuits and undergo mass production while maintaining diverse functions with high performance. The field-effect transistor has great potential to be a multifunctional device capable of sensing, data processing, data storage, and display. Currently, transistor-based devices cannot be considered intrinsic multifunctional devices because all installed functions are mutually coupled. Such incompatibilities are a crucial barrier to developing an all-in-one multifunctional device capable of driving each function individually. In this study, we focus on the decoupling of electric switching and data storage functions in an organic ferroelectric memory transistor. To overcome the incompatibility of each function, the high permittivity needed for electrical switching and the ferroelectricity needed for data storage become compatible by restricting the motion of poly(vinylidene fluoride-trifluoroethylene) via photocrosslinking with bis-perfluorobenzoazide. The two-in-one device consisting of a photocrosslinked ferroelectric layer exhibits reversible and individual dual-functional operation as a typical transistor with nonvolatile memory. Moreover, a p-MOS depletion load inverter composed of the two transistors with different threshold voltages is also demonstrated by simply changing only one of the threshold voltages by polarization switching. We believe that the two-in-one device will be considered a potential component of integrated organic logic circuits, including memory, in the future.

Low-Voltage Organic Transistor Memory Fiber with a Nanograined Organic Ferroelectric Film.

Wearable technology offers new ways to be more proactive about our health and surroundings in real time. For next-generation wearable systems, robust storage and recording media are required to monitor and process the essential electrical signals generated under various unpredictable strain conditions. Here, we report the first fibriform organic transistor memory integrated on a thin and flexible metal wire. A capillary tube coating system allows the formation of a thin and nanograined organic ferroelectric film on the wire. The uniform morphology imparts excellent switching stability (∼100 cycles), quasi-permanent retention (over 5 × 104 s), and low-voltage operation (below 5 V) to the fiber-shaped memory devices. When sewn in a stretchable textile fabric, the memory fiber achieves long retention time of more than 104 s with negligible degradation of memory window even under a constant diagonal strain of 100% that exhibits reliable data storage under tough environments. These results illustrate the possibility of the practical, wearable fiber memory for recording electronic signals in smart garment applications.

Light sintering of ultra-smooth and robust silver nanowire networks embedded in poly(vinyl-butyral) for flexible OLED.

A conductive, uniform, and ultra-smooth flexible transparent composite film is produced by embedding silver nanowires (AgNWs) into poly(vinyl-butyral) (PVB) without pressure or high-temperature annealing. The adhesion of AgNWs was greatly improved by embedding them in PVB, and surface roughness and sheet resistance (Rs) improvements were achieved through the use of the intense pulsed light (IPL) method, which welds the interconnections among AgNWs in a short time without heat or pressure treatment. The sheet resistance of PVB/AgNWs with the IPL(PAI) composite film reaches 12.6 ohm/sq with a transmittance of 85.7% (at 550 nm); no clear changes in the sheet resistance are observed after a substrate bending and tape test, suggesting excellent flexibility. In the case of PAI, the change in sheet resistance was only 2.6% after a 2,000-bend test, and the resulting bending radius was less than 1 mm. When IPL was exposed to PVB/AgNWs, the figure of merit was 2.36 times higher than that without exposure. Finally, flexible OLEDs using PAI exhibited comparable or higher electroluminescent characteristics than other devices with well-known flexible electrodes-including indium-zinc-oxide on polymer plastic-which is a promising discovery for flexible optoelectronic applications.

Ultrastretchable Conductor Fabricated on Skin-Like Hydrogel-Elastomer Hybrid Substrates for Skin Electronics.

Printing technology can be used for manufacturing stretchable electrodes, which represent essential parts of wearable devices requiring relatively high degrees of stretchability and conductivity. In this work, a strategy for fabricating printable and highly stretchable conductors are proposed by transferring printed Ag ink onto stretchable substrates comprising Ecoflex elastomer and tough hydrogel layers using a water-soluble tape. The elastic modulus of the produced hybrid film is close to that of the hydrogel layer, since the thickness of Ecoflex elastomer film coated on hydrogel is very thin (30 µm). Moreover, the fabricated conductor on hybrid film is stretched up to 1780% strain. The described transfer method is simpler than other techniques utilizing elastomer stamps or sacrificial layers and enables application of printable electronics to the substrates with low elastic moduli (such as hydrogels). The integration of printed electronics with skin-like low-modulus substrates can be applied to make wearable devices more comfortable for human skin.

Flash-induced nanowelding of silver nanowire networks for transparent stretchable electrochromic devices.

Electrochromic devices (ECDs) are emerging as a novel technology for various applications like commercialized smart window glasses, and auto-dimming rear-view mirrors. Recently, the development of low-power, lightweight, flexible, and stretchable devices has been accelerated to meet the growing demand in the new wearable devices market. Silver nanowires (AgNWs) can become new primary transparent conducting electrode (TCE) materials to replace indium tin oxide (ITO) for ECDs. However, issues such as substrate adhesion, delamination, and higher resistance still exist with AgNWs. Herein, we report a high-performance stretchable flash-induced AgNW-network-based TCE on surface-treated polydimethylsiloxane (PDMS) substrates. A Xe flash light method was used to create nanowelded networks of AgNWs. Surface silane treatments increased the adhesion and durability of the films as well. Finally, ECDs were fabricated under the optimal conditions and examined under strained conditions to demonstrate the resistance and mechanical behaviours of the devices. Results showed a flexible and durable film maintaining a high level of conductivity and reversible resistance behaviour, beyond those currently achievable with standard ITO/PET flexible TCEs.

Switching Mechanisms of Nonvolatile Memory Devices Fabricated with a Polydopamine Layer.

Nonvolatile memory devices based on a polydopamine (PDA) layer were fabricated by using a dip-coating process. Atomic force microscopy images revealed that the PDA layer had a conformal surface. The energy dispersive X-ray data showed the atomic stoichiometry of nitrogen and carbon in the PDA layer. The capacitance-voltage (C-V) curves of the Al/PDA/n-Si memory devices at 300 K showed a hysteresis with a large flat band shift, indicating that the incomplete PDA layer acted as a charge storage in the memory device. The switching mechanisms for the writing and erasing processes for the Al/PDA/n-Si devices are described on the basis of the C-V results and the energy band diagrams.

Intense pulsed light induced crystallization of a liquid-crystalline polymer semiconductor for efficient production of flexible thin-film transistors.

Here we demonstrated the split-second crystallization of a liquid-crystalline conjugated polymer semiconductor induced by irradiation with intense pulsed white light (IPWL) for the efficient improvement of electrical properties of flexible thin film transistors. A few seconds of IPWL irradiation of poly(didodecylquaterthiophene-alt-didodecylbithiazole) (PQTBTz-C12) thin films generated heat energy through the photo-thermal effect, leading to the crystallization of PQTBTz-C12 and formation of nodule-like nanostructures. The IPWL-induced crystallization of PQTBTz-C12 resulted in a threefold improvement in the field-effect mobility of thin film transistors compared to as-prepared devices. The conformational change of the PQTBTz-C12 chains was found to be strongly related to the irradiation fluence. As a proof-of-concept, the IPWL treatment was successfully applied to the PQTBTz-C12 layer in flexible transistors based on plastic substrates. The performance of these flexible devices was significantly improved after only 0.6 s of IPWL treatment, without deformation of the plastic substrate.

Split-second nanostructure control of a polymer:fullerene photoactive layer using intensely pulsed white light for highly efficient production of polymer solar cells.

Intensely pulsed white light (IPWL) treatment was tested as an ultrafast, large-area processable optical technique for the control of the nanostructure of a polymeric bulk-heterojunction photoactive layer to improve the efficiencies of polymer solar cells. Only 2 s of IPWL irradiation of a polymer:fullerene photoactive layer under ambient conditions was found to enhance significantly the power conversion efficiencies of the tested polymer solar cells to values approaching that of typical devices treated with thermal annealing. Consecutive white-light pulses from the xenon lamp induce the self-organization of the polymeric donor into an ordered structure and result in the optimized phase segregation of the polymeric donor and the fullerene acceptor in the photoactive layer, which enhances the light absorption and hole mobility and results in efficient photocurrent generation. The effects of varying the pulse conditions on device performance, including the irradiation fluence, pulse duration time, and number of pulses, were systematically investigated. Finally, it was successfully demonstrated that the IPWL treatment produces flexible polymer solar cells. The proposed IPWL process is suitable for the efficient industrial roll-to-roll production of polymer solar cells.

Porous polyimide membranes prepared by wet phase inversion for use in low dielectric applications.

A wet phase inversion process of polyamic acid (PAA) allowed fabrication of a porous membrane of polyimide (PI) with the combination of a low dielectric constant (1.7) and reasonable mechanical properties (Tensile strain: 8.04%, toughness: 3.4 MJ/m3, tensile stress: 39.17 MPa, and young modulus: 1.13 GPa), with further thermal imidization process of PAA. PAA was simply synthesized from purified pyromellitic dianhydride (PMDA) and 4,4-oxydianiline (ODA) in two different reaction solvents such as γ-butyrolactone (GBL) and N-methyl-2-pyrrolidinone (NMP), which produce Mw/PDI of 630,000/1.45 and 280,000/2.0, respectively. The porous PAA membrane was fabricated by the wet phase inversion process based on a solvent/non-solvent system via tailored composition between GBL and NMP. The porosity of PI, indicative of a low electric constant, decreased with increasing concentration of GBL, which was caused by sponge-like formation. However, due to interplay between the low electric constant (structural formation) and the mechanical properties, GBL was employed for further exploration, using toluene and acetone vs. DI-water as a coagulation media. Non-solvents influenced determination of the PAA membrane size and porosity. With this approach, insight into the interplay between dielectric properties and mechanical properties will inform a wide range of potential low-k material applications.

J-aggregation induced low bandgap anthracene-based conjugated molecule for solution-processed solar cells.

A new anthracene-based X-shaped conjugated molecule, HBTATHT, was synthesized. Thin film transistors based on unannealed HBTATHT showed a carrier mobility of 0.15 cm(2) V(-1) s(-1) (I(on/off) = 7.9 × 10(6)). Further, a solution processed solar cell made of HBTATHT exhibited promising power conversion efficiencies of 4.84% and 4.70% with PC(61)BM (1:0.8 wt ratio) and PC(71)BM (1:0.6 wt ratio), respectively.

Formation of a polymer particle monolayer by continuous self-assembly from a colloidal solution.

The preparation of two-dimensional monolayers of polymer particles over a large area was demonstrated via a facile solution process. Polymer microspheres were continuously self-assembled into a close-packed monolayer from a colloidal solution confined between two plates such that the top plate was carefully dragged at a constant velocity in the direction opposite that of the monolayer growth. In situ direct observation of the particle movement during the coating process confirmed that particle transport was directed toward the contact line of the solution meniscus by evaporation-induced convective flow. Sliding of the top plate apparently effectively counterbalanced the convective flow to provide the particles with a contact line for growth of a monolayer particle array. The influence of particle concentration, sliding speed of the top plate, and surface wettability of the bottom substrate were investigated and optimized. Monolayer particle arrays were successfully demonstrated as a template for the preparation of ZnO films with ordered hollow hemispherical structures. This approach is applicable to the fabrication of ordered structures of monodispersed particles composed of various materials over large areas.

Multi-pulsed white light sintering of printed Cu nanoinks.

Pulse management of white light to maximize the sintering efficiency of a rapid (msec) and substrate-protective method, intense pulsed light (IPL), was studied systematically with a printable Cu nanoink. An excessive pulse energy that induces deleterious defects on the Cu film along with damage on a plastic substrate was dissipated into multiple sub-pulses while maintaining a total energy budget over the threshold level for successful Cu sintering. Electrical properties of the metal layers were analyzed in conjunction with pulse formation factors such as average energy, pulse duration, peak power and pulse number to determine their respective effects on IPL sintering. In the quantitative results, the optimized sintering conditions of copper nanoparticles with a mean diameter of 30 nm and a fixed total irradiated pulse energy of 32 J cm(-2) were a pulse number and pulse width of > 4 and < 3 msec, respectively.

Hollow ZnO nanofibers fabricated using electrospun polymer templates and their electronic transport properties.

Thin (0.5 to 1 microm) layers of nonaligned or quasi-aligned hollow ZnO fibers were prepared by sputtering ZnO onto sacrificial templates comprising polyvinyl-acetate (PVAc) fibers deposited by electrospinning on silicon or alumina substrates. Subsequently, the ZnO/PVAc composite fibers were calcined to remove the organic components and crystallize the ZnO overlayer, resulting in hollow fibers comprising nanocrystalline ZnO shells with an average grain size of 23 nm. The inner diameter of the hollow fibers ranged between 100 and 400 nm and their wall thickness varied from 100 to 40 nm from top to bottom. The electronic transport and gas sensing properties were examined using DC conductivity and AC impedance spectroscopy measurements under exposure to residual concentrations (2-10 ppm) of NO(2) in air at elevated temperatures (200-400 degrees C). The inner and outer surface regions of the hollow ZnO fibers were depleted of mobile charge carriers, presumably due to electron localization at O(-) adions, constricting the current to flow through their less resistive cores. The overall impedance comprised interfacial and bulk contributions. Both contributions increased upon exposure to electronegative gases such as NO(2) but the bulk contribution was more sensitive than the interfacial one. The hollow ZnO fibers were much more sensitive compared to reference ZnO thin film specimens, displaying even larger sensitivity enhancement than the 2-fold increase in their surface to volume ratio. The quasi-aligned fibers were more sensitive than their nonaligned counterparts.

Thin film fabrication of PMMA/MEH-PPV immiscible blends by corona discharge coating and its application to polymer light emitting diodes.

We introduce a new and facile process, corona discharge coating (CDC), to fabricate thin polymer films of the immiscible poly[2-methoxy-5-(2'-ethylhexyloxy)-p-phenylenevinylene] (MEH-PPV) and poly(methyl methacrylate) (PMMA) blends. The method is based on utilizing directional electric flow, known as electric wind, of the charged unipolar particles generated by corona discharge between a metallic needle and a bottom plate under high electric field (5-10 kV/cm). The electric flow rapidly spreads out the polymer solution on the bottom plate and subsequently forms a smooth and flat thin film over a large area within a few seconds. The method is found to be effective for fabricating uniform thin polymer films with areas larger than approximately 30 mm2. The thin films obtained by CDC exhibit unique microstructures where well-defined spherical and cylindrical domains of approximately 50 nm in diameter coexist. These nanosized domains are found to be much smaller than those in films made by conventional spin coating, which suggests that CDC is beneficial for fabricating phase-separated thin film structures with significantly increased interfacial areas. The effects of the applied voltage, tip-to-plate distance, and substrates on the film formation as well as the resulting microstructure are investigated. Furthermore, the light emitting performance of a device prepared by CDC is compared with one made by spin coating.

Organic-inorganic hybrid nanomaterial as a new fluorescent chemosensor and adsorbent for copper ion.

Functionalized silica nanotube (FSNT) possessing the phenanthroline moiety as a fluorescent receptor was fabricated by solgel reaction, and the binding ability of FSNT with metal ions was evaluated by fluorophotometry.