Mixed Ionic-Electronic Transport for PEDOT:PSS-Based Zero-Gated Organic Electrochemical Transistors Using Impedance Spectroscopy and Micro-Raman Imaging

离子键合 佩多:嘘 化学物理 介电谱 拉曼光谱 材料科学 生物电子学 离子电导率 离子运输机 化学 离子 纳米技术 电化学 物理化学 电解质 有机化学 电极 生物传感器 光学 物理 图层(电子)
作者
Mariano Romero,Dominique Mombrú,Fernando Pignanelli,Ricardo Faccio,Álvaro W. Mombrú
出处
期刊:ACS applied electronic materials [American Chemical Society]
卷期号:5 (9): 4863-4874 被引量:7
标识
DOI:10.1021/acsaelm.3c00655
摘要

Recent studies are being focused on establishing a link between structural and mixed ionic-electronic transport properties based on the characterization of organic mixed ionic-electronic conductors (OMIECs) under operation conditions in organic electrochemical transistor (OECT) devices. Here, we report the simultaneous access to microstructural, chemical, and physical information using impedance spectroscopy and micro-Raman imaging techniques to address the mixed ionic-electronic transport mechanisms in PEDOT:PSS-based OMIECs working as OECT channel materials. We focused on the out-of-plane and in-plane mixed ionic-electronic transport mechanisms and complement our experimental studies with computational simulations using molecular dynamics (MD) and density functional theory (DFT) methodologies. Our studies revealed that the out-of-plane transport is based on ionic injection and diffusion mainly associated with the formation of nanopore channels in PEDOT:PSS exhibiting sulfonic groups toward the aqueous media. Thus, we also evidenced that the dedoping is not only due to the direct interaction of positive ions with PEDOT:PSS bulk region but also indirectly by the rearrangements of sulfonic groups from PSS toward the aqueous media. The in-plane transport in the OECT channel was properly described as a mixed ionic-electronic transport, with not only ionic transport of sodium (Na+) but also hydronium (H3O+) species mainly through nanopores and PEDOT:PSS bulk regions and with electronic transport mainly through the PEDOT:PSS bulk region. Although it is shown that the electronic transport monotonically declines with increasing ionic concentration, the Na+ diluted regime (1 mM) exhibits weak selectivity compared to H3O+ species, and the Na+ concentrated regime (100 mM) induces extreme porosity in PEDOT:PSS yielding to the destruction of the device. These results introduce some particular features for PEDOT:PSS-based OECT channel materials that need to be considered not only for ionic concentration and selectivity but also other related stability issues.
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