Electrochemically Mediated Depolymerization of Polymers Synthesized by Atom Transfer Radical Polymerization

The concept of electrochemically mediated depolymerization is introduced as a means to initiate and regulate depolymerization by efficiently switching between active and dormant species. During the chemical recycling of ATRP-synthesized polymers, high percentages of monomers are successfully regenerated by utilizing a readily available and inexpensive iron catalyst. In the absence of electrochemical means, negligible depolymerization occurs, thus enabling temporal control. Notably, under comparable conditions, electrochemical depolymerization outperforms thermal, photo, and chemical depolymerization approaches yielding higher monomer recovery and unlocking the potential of new solvents to trigger a lower-temperature depolymerization pathway. The presented approach significantly expands the chemical recycling toolbox to include an electrochemical switch as an alternative external stimulus for depolymerization.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-02-17
DOI
https://doi.org/10.1021/jacs.5c20629
Primary Topic
Advanced Polymer Synthesis and Characterization
Type
article
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article

Electrochemically Mediated Depolymerization of Polymers Synthesized by Atom Transfer Radical Polymerization

Lok Nga Poon, Victor Mougel, Victoria Lohmann, Athina Anastasaki et al.
Journal of the American Chemical Society
Advanced Polymer Synthesis and Characterization
article

Electrochemically Mediated Depolymerization of Polymers Synthesized by Atom Transfer Radical Polymerization

Lok Nga Poon, Victor Mougel, Victoria Lohmann, Athina Anastasaki, Richard Whitfield, Krzysztof Matyjaszewski
article en

Abstract

The concept of electrochemically mediated depolymerization is introduced as a means to initiate and regulate depolymerization by efficiently switching between active and dormant species. During the chemical recycling of ATRP-synthesized polymers, high percentages of monomers are successfully regenerated by utilizing a readily available and inexpensive iron catalyst. In the absence of electrochemical means, negligible depolymerization occurs, thus enabling temporal control. Notably, under comparable conditions, electrochemical depolymerization outperforms thermal, photo, and chemical depolymerization approaches yielding higher monomer recovery and unlocking the potential of new solvents to trigger a lower-temperature depolymerization pathway. The presented approach significantly expands the chemical recycling toolbox to include an electrochemical switch as an alternative external stimulus for depolymerization.

Journal of the American Chemical SocietyVol. 148(8)
ETH Zurich (CH), Carnegie Mellon University (US)
Openalex Percentile: Top 51%
Advanced Polymer Synthesis and Characterization
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