Electrophoresis Assisted Printing: A Method To Control the Morphology in Organic Thin Films.

A major advantage of organic solar cells (OSC) is the processability out of solution allowing for advanced printing methods toward large-scale production. Controlling the blend morphology of solution coated active layers is a key challenge to optimize their power conversion efficiency. We have derived a printing procedure from an industrial coating process that facilitates tuning the nanomorphology of a blend of poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as model system for OSCs. Applying an electric field during printing and the film drying process modifies the vertical film composition of the photoactive layer and optimizes the polymer crystal orientation. The choice of chloroform as solvent allows us to obtain material transport within the wet film, due to an induced electrophoretic mobility. Tailoring the morphology improves the power conversion efficiency of the OSCs by up to 25%. Our findings indicate that electrophoresis assisted printing provides an efficient approach to optimize the active layer for various material and solvent combinations that exhibit an electrophoretic mobility.

Ionic-Liquid Doping Enables High Transconductance, Fast Response Time, and High Ion Sensitivity in Organic Electrochemical Transistors.

Organic electrochemical transistors (OECTs) are highly attractive for applications ranging from circuit elements and neuromorphic devices to transducers for biological sensing, and the archetypal channel material is poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate), PEDOT:PSS. The operation of OECTs involves the doping and dedoping of a conjugated polymer due to ion intercalation under the application of a gate voltage. However, the challenge is the trade-off in morphology for mixed conduction since good electronic charge transport requires a high degree of ordering among PEDOT chains, while efficient ion uptake and volumetric doping necessitates open and loose packing of the polymer chains. Ionic-liquid-doped PEDOT:PSS that overcomes this limitation is demonstrated. Ionic-liquid-doped OECTs show high transconductance, fast transient response, and high device stability over 3600 switching cycles. The OECTs are further capable of having good ion sensitivity and robust toward physical deformation. These findings pave the way for higher performance bioelectronics and flexible/wearable electronics.