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Demonstrates enhanced electronic and ionic conductivity in a new covalent organic framework, indicating improved performance for electronic devices.
Developing efficient mixed electronic‐ionic (MEI) conductors remains a critical challenge for next‐generation electronic devices. While covalent organic frameworks (COFs), with their tunable functionalities and ordered porosity, present a promising platform, only a limited number of COFs demonstrate dual conduction pathways. In this work, we integrate the MEI characteristics of PEDOT:PSS polymers into a COF architecture. A quinoline‐linked COF (PSS_COF) with sulfonate‐lined pore walls was synthesized via a one‐pot Povarov reaction. Subsequent in‐situ oxidative polymerization of PEDOT, electrostatically anchored to the sulfonated framework, yielded PEDOT:PSS_COF. Electron microscopy revealed ordered structure, with well‐defined reflections in the SAED patterns distinctly indexed to the modeled crystal structure. Ultraviolet photoelectron spectroscopy (UPS) showed a 1.31 eV elevation in the valence band maximum of PEDOT:PSS_COF relative to PSS_COF, with a higher DOS near the Fermi level. This enhances electronic conductivity, from ∼10 −8 to 10 −2 Scm −1 . The elevated HOMO level and strong EPR signal suggest the formation of polaronic species on the PEDOT chains. Electrochemical impedance spectroscopy (EIS) revealed a humidity‐dependent ionic conductivity, reaching 4.6 × 10 −5 Scm −1 at 95% RH and 303K, suggesting a protonic conductivity. The work demonstrates a strategy for developing high‐performance MEI‐conductive frameworks, by homing electronic carriers into anionic frameworks to achieve mixed‐ion conduction.
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Jain et al. (2026) studied this question.
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