Ultrafast aqueous electric double layer dynamics

The electric double layer (EDL) is critical in electrochemical capacitors and transistors, on-water chemistry, and bioelectric technologies. Ion dynamics within the EDL define the limits for charging and discharging processes. Classical EDL models struggle at high electrolyte concentrations, and observing EDL dynamics has been challenging. In this study, an all-optical technique allowed real-time monitoring of EDL dynamics at arbitrary concentration by quasi-instantaneously changing the surface propensity of protons (H<sub>3</sub>O<sup>+</sup>) adsorbed at the air-aqueous electrolyte solution interface and by subsequently tracking EDL relaxation with femtosecond time-resolved spectroscopy. EDL reorganization occurred on picosecond timescales and was strongly concentration dependent. Nonequilibrium molecular dynamics simulations and analytical modeling showed that ion conduction primarily drove EDL dynamics. This research quantified EDL dynamics and identified its primary driver, providing insights for optimization of electrochemical applications.

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Publication Details

Journal
Science
Published
2025-04-24
DOI
https://doi.org/10.1126/science.adu5781
Citations
37
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
46.13
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article

Ultrafast aqueous electric double layer dynamics

Johannes Hunger, Mischa Bonn, Yuki Nagata, Sho Imoto et al.
37 citations
Science
Spectroscopy and Quantum Chemical Studies
46.13
article

Ultrafast aqueous electric double layer dynamics

Johannes Hunger, Mischa Bonn, Yuki Nagata, Sho Imoto, Ellen H. G. Backus, Alessandro Greco
article en
37 citations

Abstract

The electric double layer (EDL) is critical in electrochemical capacitors and transistors, on-water chemistry, and bioelectric technologies. Ion dynamics within the EDL define the limits for charging and discharging processes. Classical EDL models struggle at high electrolyte concentrations, and observing EDL dynamics has been challenging. In this study, an all-optical technique allowed real-time monitoring of EDL dynamics at arbitrary concentration by quasi-instantaneously changing the surface propensity of protons (H<sub>3</sub>O<sup>+</sup>) adsorbed at the air-aqueous electrolyte solution interface and by subsequently tracking EDL relaxation with femtosecond time-resolved spectroscopy. EDL reorganization occurred on picosecond timescales and was strongly concentration dependent. Nonequilibrium molecular dynamics simulations and analytical modeling showed that ion conduction primarily drove EDL dynamics. This research quantified EDL dynamics and identified its primary driver, providing insights for optimization of electrochemical applications.

ScienceVol. 388(6745)
University of Vienna (AT), Max Planck Institute for Polymer Research (DE)
Clean water and sanitation
Openalex Percentile: Top 0%
Spectroscopy and Quantum Chemical Studies
46.13
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