Mechanistic Origins of Wave Coalescence in Electrochemically Mediated CO 2 Capture: Kinetic Drill and Potential Inversion Paradigm

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Authors: Abderrahman Atifi, Michael D. Ryan
Cited by: 2
References: 60

Abstract

Electrochemically mediated carbon capture (EMCC) offers a tunable and reversible platform for CO 2 separation driven by renewable electricity. Quinones, particularly anthraquinone (AQ), are among the most studied redox-active sorbents; yet key fundamental ambiguities remain regarding the identity of the CO 2 -reactive species and the origin of voltammetric wave coalescence observed under CO 2 saturation. This study integrates cyclic voltammetry (CV), thin-layer spectroelectrochemistry (SEC), and density functional theory (DFT) to elucidate the sequence of electron transfer and CO 2 binding events in the AQ system. Among the various explored mechanisms, the ECE pathway provided a more physically consistent fit but exhibited simulation parameter non-uniqueness, with multiple possible combinations of the bound intermediate radical RAQCO 2 binding constant ( K 1 ) and its reduction potential to the DAQCO 2 complex, where DAQ is the dianion of anthraquinone. Evolving factor analysis of SEC spectra, combined with DFT, reveals the formation of the radical anion (RAQ) and the dominant accumulation of the bound dianion DAQCO 2 adduct. Complementary Butler-Volmer fitting and derivative cyclic voltabsorptometry analysis yield a second reduction wave at approximately −15 mV more negative than first reduction potential, consistent with potential compression rather than inversion. CV retrofitting across scan rates, using SEC-derived constraint, yields a RAQCO 2 binding constant K 1 less than 0.5. Despite the weak RAQ binding affinity, the overall mechanistic analysis supports ECE mechanism, with kinetically inferred formation of transient RAQCO 2 that enable immediate reduction to DAQCO 2 . This “ kinetic drill ” effect drives a substantial positive shift (∼0.6 V) and accounts for the observed wave coalescence. These results provide mechanistic resolution in reversible redox-coupled CO 2 capture-release and underscore the critical need for orthogonal constraints in rational EMCC understanding and design.

Fields of Study & Subjects

CO2 Reduction Techniques and Catalysts Carbon Dioxide Capture Technologies Ionic liquids properties and applications

Publication details

Journal / source
ACS electrochemistry.
Publisher
American Chemical Society (ACS)
Volume
2
Issue
2
Pages
541–553
Publication date
26 January 2026
Language
EN