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Updated: Jan 13, 2026

Self-Assembly of Hybrid Lipid Membranes Doped with Hydrophobic Organic Molecules at the Water/Air Interface
Published on: May 1, 2020
Interfacial Engineering with Hydrophobic Self-Assembled Monolayers Boosting Ionic and Electronic Conduction in N-Type
Yunong Peng1, Xuejiao Wu1, Shuo Yang1
1College of Chemistry and Chemical Engineering, State Key Laboratory of Chemo and Biosensing, Hunan University, Changsha 410082, China.
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Interface engineering has proven to be an effective strategy for improving the performance of thin-film optoelectronic devices. However, in bioelectronic devices, especially in organic electrochemical transistors (OECTs) using mixed ionic-electronic conductors as the active layer, the influence of self-assembled monolayers (SAMs) at the substrate-semiconductor interface remains comparatively underexplored. In this study, four different silane-based hydrophobic SAMs were systematically investigated on glass substrates, offering a novel approach to enhancing the performance of n-type OECTs. It was demonstrated that these SAM-modified interfaces not only effectively promote the crystallization of conjugated Homo-gDPP polymer films but also trigger the spontaneous formation of porous microstructures, overall yielding significant improvements in n-type device characteristics. Upon the SAM's incorporation, we observed a nearly doubled mobility-volumetric capacitance (μC*) (from 49.4 to 89.7 F·cm-1·V-1·s-1) and a 2.5-fold increase in normalized transconductance (gm,norm). These notable enhancements can be attributed to facilitated ion penetration and improved electronic transport within the semiconducting layer, likely stemming from reduced lateral ionic impedance, interface trap density, and elevated charge conductivity. Furthermore, the hydrophobic SAM-treated OECTs exhibit greater operational stability and an accelerated temporal response, highlighting the potential of interfacial modification as a versatile and scalable approach for advancing high-performance bioelectronic devices.

