Increasing the Alkaline Stability of N,N-Diaryl Carbazolium Salts Using Substituent Electronic Effects

[Image: see text] Anion-exchange membrane fuel cells (AEMFCs) have attracted the attention of the scientific community during the past years, mostly because of the potential for eliminating the need for using costly platinum catalysts in the cells. However, the broad commercialization of AEMFCs is hampered by the low chemical stability of the cationic functional groups in the anion-conducting membranes required for the transportation of hydroxide ions in the cell. Improving the stability of these groups is directly connected with the ability to recognize the different mechanisms of the OH(–) attack. In this work, we have synthesized eight different carbazolium cationic model molecules and investigated their alkaline stability as a function of their electronic substituent properties. Given that N,N-diaryl carbazolium salts decompose through a single-electron-transfer mechanism, the change in carbazolium electron density leads to a very significant impact on their chemical stability. Substituents with very negative Hammett parameters demonstrate unparalleled stability toward dry hydroxide. This study provides guidelines for a different approach to develop stable quaternary ammonium salts for AEMFCs, making use of the unique parameters of this decomposition mechanism.