Multisine electrochemical impedance spectroscopy for Li-ion battery characterisation
Abstract
Electrochemical impedance spectroscopy (EIS) is a valuable tool for non-invasive battery characterisation, providing a compact representation of physical processes over a wide range of time scales. Commonly, sinusoids at different frequencies are injected sequentially (single-sines). Alternatively, a multisine excitation (a sum of sines) is advantageous for reducing experiment time and allowing impedance to be measured during operation. In this work, we demonstrate high-fidelity multisine EIS measurements on Li-ion cells over a wide frequency range (20 mHz to 1 kHz), taken with a commercial potentiostat modified to give access to the underlying current and voltage time-series data, and compare these to single-sine EIS. We show how this allows the conditions of linearity and stationarity to be verified directly, which is not possible with impedance data alone. We then measure broadband impedance during charging and discharging, temperature change, and relaxation. Because impedance is a linearisation of the response about an operating point, each of these conditions probes a state that classical EIS excludes by definition: kinetics linearised about a non-zero current, thermally activated reaction rates, and relaxing concentration gradients, respectively. Operando multisine EIS is therefore not simply a faster measurement approach, but one that resolves behaviour that steady-state EIS cannot.
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BibTeX
@misc{hallemans2026multisine,
title = {{Multisine electrochemical impedance spectroscopy for Li-ion battery characterisation}},
author = {Noël Hallemans and Heiko Seel-Mayer and Peter Keil and Stephen R. Duncan and David A. Howey},
howpublished = {arXiv},
year = {2026},
month = sep,
doi = {10.48550/arxiv.2607.17832},
eprint = {2607.17832},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2607.17832},
}
RIS
TY - UNPB
TI - Multisine electrochemical impedance spectroscopy for Li-ion battery characterisation
AU - Noël Hallemans
AU - Heiko Seel-Mayer
AU - Peter Keil
AU - Stephen R. Duncan
AU - David A. Howey
PY - 2026
DA - 2026/09/11
PB - arXiv
DO - 10.48550/arxiv.2607.17832
UR - https://arxiv.org/abs/2607.17832
AB - Electrochemical impedance spectroscopy (EIS) is a valuable tool for non-invasive battery characterisation, providing a compact representation of physical processes over a wide range of time scales. Commonly, sinusoids at different frequencies are injected sequentially (single-sines). Alternatively, a multisine excitation (a sum of sines) is advantageous for reducing experiment time and allowing impedance to be measured during operation. In this work, we demonstrate high-fidelity multisine EIS measurements on Li-ion cells over a wide frequency range (20 mHz to 1 kHz), taken with a commercial potentiostat modified to give access to the underlying current and voltage time-series data, and compare these to single-sine EIS. We show how this allows the conditions of linearity and stationarity to be verified directly, which is not possible with impedance data alone. We then measure broadband impedance during charging and discharging, temperature change, and relaxation. Because impedance is a linearisation of the response about an operating point, each of these conditions probes a state that classical EIS excludes by definition: kinetics linearised about a non-zero current, thermally activated reaction rates, and relaxing concentration gradients, respectively. Operando multisine EIS is therefore not simply a faster measurement approach, but one that resolves behaviour that steady-state EIS cannot.
ER -