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

Universidad de la República; Universidad de la República; Universidad de la República; Universidad de la República; Universidad de la República
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Publisher: ACS
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Abstract AITranslate

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.

KeyWords AITranslate

mixed ionicelectronic organic electrochemical transistors impedance spectroscopy microRaman imaging modeling
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Basic Information:

DOI:https://doi.org/10.1021/acsaelm.3c00655

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Citation Information:

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.

quote

GB/T 7714-2015 [1] Mariano Romero, Dominique Mombrú, Fernando Pignanelli, et al. ACS Applied Electronic Materials, 2023(5). DOI:10.1021/acsaelm.3c00655.
MLA [1] Mariano Romero, et al., ACS Applied Electronic Materials, no. 5, 2023, https://doi.org/10.1021/acsaelm.3c00655.
APA [1] Mariano Romero, Dominique Mombrú, Fernando Pignanelli, Ricardo Faccio, & Álvaro W. Mombrú. (2023). ACS Applied Electronic Materials(5). https://doi.org/10.1021/acsaelm.3c00655
IEEE [1] Mariano Romero, Dominique Mombrú, Fernando Pignanelli, Ricardo Faccio, and Álvaro W. Mombrú, ACS Applied Electronic Materials, no. 5, 2023, doi: 10.1021/acsaelm.3c00655. keywords: {mixed ionicelectronic organic electrochemical transistors impedance spectroscopy microRaman imaging modeling}