Synergetic Evolution of Diketopyrrolopyrrole-Based Polymeric Semiconductor for High Reproducibility and Performance: Random Copolymerization of Similarly Shaped Building Blocks.

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.

Development of a new contactless dielectrophoresis system for active particle manipulation using movable liquid electrodes.

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.

Microencapsulation by pectin for multi-components carriers bearing both hydrophobic and hydrophilic active agents.

Oil/water microencapsulation by microfluidic systems has been a prominent delivery method to prepare functional microcapsules in the food, cosmetic, and pharmaceutical industries because it is an easy way to control the shape and size of structures and functionalities. We prepared biocompatible and multi-component microcapsules using the precipitation and ionic crosslinking of pectin in a poor solubility environment and with multivalent cations, respectively. When the aqueous solution (including calcium ions and ethanol) in a sheath flow met the flow of a pectin aqueous solution containing oil droplets, ethanol-gelation and ionic cross-linking occurred, enclosing the inner oil phase droplets by solidified pectin shells. Furthermore, the resulting microcapsules stabilized by pectin shells exhibited functionalities using a hydrophobic agent and nanoparticles of a hydrophilic species that were dissolved and dispersed, respectively, in the oil phase.