Resistance Breakdown of a Membraneless Hydrogen-Bromine Redox Flow Battery

Journal Article (2022)
Author(s)

Daniel Alfisi (Technion Israel Institute of Technology)

Amit N. Shocron (Technion Israel Institute of Technology)

Robert Gloukhovski (Technion Israel Institute of Technology)

DA Vermaas (TU Delft - ChemE/Transport Phenomena)

Matthew E. Suss (Technion Israel Institute of Technology)

Research Group
ChemE/Transport Phenomena
Copyright
© 2022 Daniel Alfisi, Amit N. Shocron, Robert Gloukhovski, D.A. Vermaas, Matthew E. Suss
DOI related publication
https://doi.org/10.1021/acssuschemeng.2c02169
More Info
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Publication Year
2022
Language
English
Copyright
© 2022 Daniel Alfisi, Amit N. Shocron, Robert Gloukhovski, D.A. Vermaas, Matthew E. Suss
Research Group
ChemE/Transport Phenomena
Issue number
39
Volume number
10
Pages (from-to)
12985-12992
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Abstract

A key bottleneck to society's transition to renewable energy is the lack of cost-effective energy storage systems. Hydrogen-bromine redox flow batteries are seen as a promising solution, due to the use of low-cost reactants and highly conductive electrolytes, but market penetration is prevented due to high capital costs, for example due to costly membranes to prevent bromine crossover. Membraneless hydrogen-bromine cells relying on colaminar flows have thus been investigated, showing high power density nearing 1 W/cm2. However, no detailed breakdown of resistance losses has been performed to-date, a knowledge gap which impedes further progress. Here, we characterize such a battery, showing the main sources of loss are the porous cathode, due to both Faradaic and Ohmic losses, followed by Ohmic losses in the electrolyte channel, with all other sources relatively minor contributors. We further develop and fit analytical expressions for the impedance of porous electrodes in high power density electrochemical cells to impedance measurements from our battery, which enabled the detailed cell resistance breakdown and determination of important electrode parameters such as volumetric exchange current density and specific capacitance. The insights developed here will enable improved engineering designs to unlock exceptionally high-power density membraneless flow batteries.