RESUMO
Integrated reference electrodes allow to deconvolute voltage contributions of anode and cathode and contribute to a better understanding of CO2 electrolyzers. However, in zero-gap cell configurations, this integration can be challenging and obtaining error-free data with such a setup is a non-trivial task. This study compares five different methods to integrate a reference electrode into an alkaline zero-gap CO2 electrolysis cell. Sources of error and measures to circumvent them are investigated and finite-element simulation is used to gain a better understanding of observed effects. Placing a reference electrode into the inactive area of the cell is found to be a reliable method, as long as the placement of electrodes is sufficiently controlled. Sandwiching a wire quasi-reference electrode between two membranes is especially useful for electrochemical impedance spectroscopy; however, it can affect the overall cell performance. Contacting the catalyst layer from the backside with a salt-bridge is promising for localized measurements if sufficient reproducibility can be ensured.
RESUMO
The electrochemical reduction of CO2 is a pivotal technology for the defossilization of the chemical industry. Although pilot-scale electrolyzers exist, water management and salt precipitation remain a major hurdle to long-term operation. In this work, we present high-resolution neutron imaging (6 µm) of a zero-gap CO2 electrolyzer to uncover water distribution and salt precipitation under application-relevant operating conditions (200 mA cm-2 at a cell voltage of 2.8 V with a Faraday efficiency for CO of 99%). Precipitated salts penetrating the cathode gas diffusion layer can be observed, which are believed to block the CO2 gas transport and are therefore the major cause for the commonly observed decay in Faraday efficiency. Neutron imaging further shows higher salt accumulation under the cathode channel of the flow field compared to the land.
