TY - JOUR
T1 - Isoindolinium Groups as Stable Anion Conductors for Anion-Exchange Membrane Fuel Cells and Electrolyzers
AU - Aggarwal, Kanika
AU - Gjineci, Nansi
AU - Kaushansky, Alexander
AU - Bsoul, Saja
AU - Douglin, John C.
AU - Li, Songlin
AU - Salam, Ihtasham
AU - Aharonovich, Sinai
AU - Varcoe, John R.
AU - Dekel, Dario R.
AU - Diesendruck, Charles E.
N1 - Publisher Copyright:
© 2022 The Authors. Published by American Chemical Society.
PY - 2022/5/11
Y1 - 2022/5/11
N2 - Anion-exchange membrane (AEM) fuel cells (AEMFCs) and water electrolyzers (AEMWEs) have gained strong attention of the scientific community as an alternative to expensive mainstream fuel cell and electrolysis technologies. However, in the high pH environment of the AEMFCs and AEMWEs, especially at low hydration levels, the molecular structure of most anion-conducting polymers breaks down because of the strong reactivity of the hydroxide anions with the quaternary ammonium (QA) cation functional groups that are commonly used in the AEMs and ionomers. Therefore, new highly stable QAs are needed to withstand the strong alkaline environment of these electrochemical devices. In this study, a series of isoindolinium salts with different substituents is prepared and investigated for their stability under dry alkaline conditions. We show that by modifying isoindolinium salts, steric effects could be added to change the degradation kinetics and impart significant improvement in the alkaline stability, reaching an order of magnitude improvement when all the aromatic positions are substituted. Density functional theory (DFT) calculations are provided in support of the high kinetic stability found in these substituted isoindolinium salts. This is the first time that this class of QAs has been investigated. We believe that these novel isoindolinium groups can be a good alternative in the chemical design of AEMs to overcome material stability challenges in advanced electrochemical systems.
AB - Anion-exchange membrane (AEM) fuel cells (AEMFCs) and water electrolyzers (AEMWEs) have gained strong attention of the scientific community as an alternative to expensive mainstream fuel cell and electrolysis technologies. However, in the high pH environment of the AEMFCs and AEMWEs, especially at low hydration levels, the molecular structure of most anion-conducting polymers breaks down because of the strong reactivity of the hydroxide anions with the quaternary ammonium (QA) cation functional groups that are commonly used in the AEMs and ionomers. Therefore, new highly stable QAs are needed to withstand the strong alkaline environment of these electrochemical devices. In this study, a series of isoindolinium salts with different substituents is prepared and investigated for their stability under dry alkaline conditions. We show that by modifying isoindolinium salts, steric effects could be added to change the degradation kinetics and impart significant improvement in the alkaline stability, reaching an order of magnitude improvement when all the aromatic positions are substituted. Density functional theory (DFT) calculations are provided in support of the high kinetic stability found in these substituted isoindolinium salts. This is the first time that this class of QAs has been investigated. We believe that these novel isoindolinium groups can be a good alternative in the chemical design of AEMs to overcome material stability challenges in advanced electrochemical systems.
KW - anion-exchange membranes
KW - electrolyzers
KW - fuel cells
KW - isoindolinium
KW - quaternary ammoniums
UR - https://www.scopus.com/pages/publications/85127160733
U2 - 10.1021/acsmaterialsau.2c00002
DO - 10.1021/acsmaterialsau.2c00002
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AN - SCOPUS:85127160733
VL - 2
SP - 367
EP - 373
JO - ACS Materials Au
JF - ACS Materials Au
IS - 3
ER -