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A new random copolymer consisting of similarly shaped donor-acceptor building blocks of diketopyrrolopyrrole-selenophene-vinylene-selenophene (DPP-SVS) and DPP-thiophene-vinylene-thiophene (DPP-TVT) is designed and synthesized. The resulting P-DPP-SVS(5)-TVT(5) with an equal molecular ratio of the two building blocks produced significantly enhanced solubility when compared to that of the two homopolymers, PDPP-SVS and PDPP-TVT. More importantly, despite the maximum segmental randomness of the PDPP-SVS(5)-TVT(5) copolymer, its crystalline perfectness and preferential orientation are outstanding, even similar to those of the homopolymers thanks to the similarity of the two building blocks. This unique property produces a high charge carrier mobility of 1.23 cm2 V-1 s-1 of PDPP-SVS(5)-TVT(5), as determined from polymer field-effect transistor (PFET) measurements. The high solubility of PDPP-SVS(5)-TVT(5) promotes formulation of high-viscosity solutions which could be successfully processed to fabricate large-areal PFETs onto hydrophobically treated 4 in. wafers. A total of 269 individual PFETs are fabricated. These devices exhibit extremely narrow device-to-device deviations without a single failure and demonstrate an average charge carrier mobility of 0.66 cm2 V-1 s-1 with a standard deviation of 0.064. This is the first study to report on successfully realizing large-areal reproducibility of high-mobility polymeric semiconductors.

A conjugated polymer, poly(9,9-bis(6-bromohexyl)-9H-fluorene-alt-1,4-phenylene), is synthesized, converted to nanoparticles via a nanoprecipitation process, and utilized to fabricate thin films including conjugated polymer nanoparticles. The nanoparticles with surface bromides can be conjugated with an amine-functionalized dendrimer via a nucleophilic coupling reaction. Thus, when microliter solutions of the particulates are dragged at a constant velocity on substrates alternately in a layer-by-layer manner, thin films composed of the nanoparticles and dendrimers can be successfully built up on the substrates. Our results suggest a methodology to control the deposition of thin films bearing conjugated polymer nanoparticles while minimizing processing time and decreasing material consumption.

In this work, a whole manufacturing process of the curved copper nanowires (CCNs) based flexible transparent conductive electrode (FTCE) is reported with all solution processes, including synthesis, coating, and networking. The CCNs with high purity and good quality are designed and synthesized by a binary polyol coreduction method. In this reaction, volume ratio and reaction time are the significant factors for the successful synthesis. These nanowires have an average 50 nm in width and 25-40 μm range in length with curved structure and high softness. Furthermore, a meniscus-dragging deposition (MDD) method is used to uniformly coat the well-dispersed CCNs on the glass or polyethylene terephthalate substrate with a simple process. The optoelectrical property of the CCNs thin films is precisely controlled by applying the MDD method. The FTCE is fabricated by networking of CCNs using solvent-dipped annealing method with vacuum-free, transfer-free, and low-temperature conditions. To remove the natural oxide layer, the CCNs thin films are reduced by glycerol or NaBH4 solution at low temperature. As a highly robust FTCE, the CCNs thin film exhibits excellent optoelectrical performance (T = 86.62%, R(s) = 99.14 Ω ◻(-1)), flexibility, and durability (R/R(0) < 1.05 at 2000 bending, 5 mm of bending radius).

This study presents a new DEP manipulation technique using a movable liquid electrode, which allows manipulation of particles by actively controlling the locations of electrodes and applying on-off electric input signals. This DEP system consists of mercury as a movable liquid electrode, indium tin oxide (ITO)-coated glass, SU-8-based microchannels for electrode passages, and a PDMS medium chamber. A simple squeezing method was introduced to build a thin PDMS layer at the bottom of the medium chamber to create a contactless DEP system. To determine the operating conditions, the DEP force and the friction force were analytically compared for a single cell. In addition, an appropriate frequency range for effective DEP manipulation was chosen based on an estimation of the Clausius-Mossotti factor and the effective complex permittivity of the yeast cell using the concentric shell model. With this system, we demonstrated the active manipulation of yeast cells, and measured the collection efficiency and the dielectrophoretic velocity of cells for different AC electric field strengths and applied frequencies. The experimental results showed that the maximum collection efficiency reached was approximately 90%, and the dielectrophoretic velocity increased with increasing frequency and attained the maximum value of 10.85 ± 0.95 μm/s at 100 kHz, above which it decreased.