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Updated: Jun 17, 2026

Electroactive Polymer Nanoparticles Exhibiting Photothermal Properties
Published on: January 8, 2016
Iodine-mediated proton-coupled electron transfer enables selective polymerization of organic pollutants in an
Zexiao Zheng1, Jin Zhang2, Jonathan J Calvillo Solís1
1Department of Civil and Environmental Engineering, The Hong Kong University of Science and Technology, Hong Kong, China.
Abstract:
Organic polymerization offers a sustainable water treatment approach that enables resource recovery, yet current oxidant-involved practices suffer from poor selectivity. We present an oxidant-free electrocatalytic system for phenolic pollutant polymerization via iodine-mediated proton-coupled electron transfer (PCET) with an iodine-enriched bismuth-oxyiodide-coated carbon cloth (I-BiOI@CC) anode, achieving 97.1% polymerization selectivity by converting pollutants into insoluble polymerized products. Mechanistic investigations demonstrate that I-BiOI@CC provides reversible redox mediation (3I⁻ ⇆ I₃⁻), enhancing pollutant-electrode interaction and accelerating interfacial charge transfer to facilitate PCET-oxidation of phenols to phenolic radicals that undergo polymerization through thermodynamically favored ortho C-O coupling. Polymerization kinetics depend on proton and electron transfer energetics, wherein phenols with stronger electron-donating capacity and weaker O-H bond strength promote the PCET process. The electrocatalytic system exhibits high energy and cost efficiency, demonstrates negligible biotoxicity, and shows excellent practicality. This work offers a promising proof-of-concept for future development of green and selective electrocatalytic processes for water decontamination.
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