Preventing Salt Formation in Zero-Gap CO2 Electrolyzers by Quantifying Cation Accumulation

Journal Article (2025)
Author(s)

Jasper Biemolt (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Jai Singh (Student TU Delft)

G. Prats Vergel (TU Delft - ChemE/Materials for Energy Conversion and Storage)

H.M. Pelzer (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Tom Burdyny (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Research Group
ChemE/Materials for Energy Conversion and Storage
DOI related publication
https://doi.org/10.1021/acsenergylett.4c03242
More Info
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Publication Year
2025
Language
English
Research Group
ChemE/Materials for Energy Conversion and Storage
Issue number
2
Volume number
10
Pages (from-to)
807-814
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Abstract

The electrochemical CO2 reduction reaction (CO2RR) in a membrane electrode assembly (MEA) efficiently turns CO2 into a feedstock. However, unfavorable steady-state concentrations of ions in the cathode compartment result in salt formation if unaddressed, which restricts the access of CO2 and causes cell failure. Here, we systematically show the relationship between salt accumulation and four system parameters including cation species, anolyte concentration, membrane thickness, and operating temperature. To compare each metric, we quantified the cation accumulation rate at predefined operating times. Notably, we show that operating at temperatures above 50 °C with properly humidified CO2 stream fully avoids salt formation. We further show that combining separate operating conditions is also highly effective, showing operation for >144 h with no measurable salt deposition at 200 mA/cm2. Collectively, our work systematically demonstrates that salt formation is a prevalent yet surmountable CO2RR challenge that can be overcome by elevated cell temperatures or switching to more soluble alkali cations.