(651d) Salt Transport of Phenyl Acrylate-Based Anion Exchange Membrane with Different Crosslinkers for Artificial Photosynthesis | AIChE

(651d) Salt Transport of Phenyl Acrylate-Based Anion Exchange Membrane with Different Crosslinkers for Artificial Photosynthesis

Authors 

Lin, Y. H. - Presenter, Auburn University
Beckingham, B., Auburn University
Clinch, M., University of Kentucky
Anion exchange membranes (AEMs) are crucial components in artificial photosynthesis devices that use photoelectrochemistry to convert CO2 into valuable products. These membranes facilitate the movement of charge carriers between electrodes while restricting the transport of CO2 reduction products such as formate and acetate. Despite their importance, there is a scarcity of studies on the fundamental transport mechanisms in AEMs used in artificial photosynthesis. In this work, we present the development of a phenyl acrylate-based membrane that is functionalized with (3-acrylamidopropyl) trimethylammonium chloride (APTA) and crosslinked using two different crosslinkers: poly(ethylene glycol) diacrylate (PEDGA) and N,N'-methylenebisacrylamide (MBAA). By varying the crosslinkers and APTA content, we were able to modify the membrane's water volume fraction and control its transport propertie. The water volume fraction of a membrane has a direct impact on its salt permeability and ionic conductivity. As a result, membranes with higher ionic conductivity tend to have higher salt permeability, creating a trade-off between desirable transport properties for artificial photosynthesis applications. According to our observations, Young's modulus rises with increasing crosslinker content due to higher crosslink density, and MBAA-contained films exhibit higher yield strength than PEGDA-contained films. Additionally, decreasing permeabilities to solutes with increasing fixed charge density is caused by decreasing water volume fraction, and these permeabilities are in the following order: NH4Cl> KCl> KOFm> KOAc> NaOFm> NaOAc, most likely because of variations in hydration diameters.