<em>(Invited)</em> Anion Exchange Membrane and Ionomer Development for Electrochemical CO<sub>2</sub> Reduction

Holdcroft, Steven

Recent developments have proven the economic potential of electrochemical reduction of CO₂ to value added chemicals, where single cells are now capable of achieving high energetic efficiencies at industrially relevant current densities. ¹ These advances are in no small part due to the increased ionic conductivity, hydroxide stability and commercial availability of anion exchange membranes (AEMs). However, there currently exists little understanding as to how these materials affect the efficiency of CO₂ conversion devices because the research community is only now beginning to understand the variety and complexity of the transport processes involved. ² In collaboration with Ionomr Innovations Inc. and the National Research Council of Canada, and as part of the Energy for Clean Materials Challenge Program, we have made advances in the understanding of how AEM properties affect device performance and how we can develop materials tailor-made for CO₂ electrolyser technology.

Here, we demonstrate the development of a zero-gap single cell design, utilizing first generation Aemion® materials for the conversion of CO₂ to CO with an energetic efficiency of 40% at 200 mA cm^-2. ³ Despite the initially high energetic efficiency, we demonstrate how the crossover of carbonate dianions results in the reduction of anolyte pH and deconvolute how this results in a diminished cell efficiency over extended operation. From this, we show how functionalization of the polymer electrolyte structure can reduce this degradation mechanism while retaining high energetic efficiencies.

In addition, we demonstrate how under milder electrolysis conditions, the total cell efficiency has a significant dependency on the flux of alkali metal cationic species from the supporting anolyte to the cathode. We show that due to the large promotion effect of cations for the electrochemical CO₂ reduction, AEM design not only influences ohmic resistances in the cell, but also greatly affects the charge transfer resistance (R_CT) of the cathode to a much greater extent than other electrochemical conversion devices. We thus make correlations between water permeability and perm-selectivity of AEMs to the overall CO₂ conversion efficiency.

We then discuss the incorporation of anion exchange ionomers in the cathode catalyst layer of CO₂ electrolysis cells and how the ionomer parameters define the efficiency and selectivity of Ag catalysts towards electrochemical CO₂ reduction. Through this work, we demonstrate the influencing factors of AEM and ionomer materials on the efficiency of electrochemical CO₂ conversion and conclude that further advances are paramount for the adoption of this promising technology, which is integral in closing the carbon loop of the petrochemical industry and meeting our wider climate change targets.

References:

P. De Luna et al., Science, 364, eaav3506 (2019).
D. Salvatore, C. Gabardo, A. Reyes, and S. Holdcroft, Nat. Energy, 6, 339–348 (2021).
P. Mardle, S. Cassegrain, F. Habibzadeh, Z. Shi, and S. Holdcroft, J. Phys. Chem. C, 125, 25446–25454 (2021).

1767 (Invited) Anion Exchange Membrane and Ionomer Development for Electrochemical CO2 Reduction

1767
(Invited) Anion Exchange Membrane and Ionomer Development for Electrochemical CO₂ Reduction