Polymer electrolyte membrane fuel cells (PEMFCs) are promising alternative power sources for stationary and automotive applications due to their low exhaust emissions and quick start-up and load response. However, the widespread commercialization of PEMFCs is still challenging to meet the cost and durability. Therefore, enhancing the durability of the PEMFC stack is the most important aspect of recent studies through improving the electrochemical and mechanical stability of major components such as polymer electrolyte membranes (PEM). The main factors contributing to the durability deterioration of PEM are chemical and mechanical degradation caused by the inescapable generation of hydroxyl and hydroperoxyl radical species through gas crossover during PEMFC operation.1 Several studies have proven using the cerium ions as radical scavengers effectively mitigates the chemical degradation of PEMs to solve these problems. Although cerium is an effective radical scavenger, it can be combined with sulfonic acid groups to lower the proton conductivity during cell operation.2 In this study, we aimed to mitigate the polymer electrolyte membrane chemical degradation and minimize proton conductivity deterioration by introducing an organic ligand group to cerium-based radical scavengers. The cerium-based radical scavengers were incorporated into the catalyst ink at different concentrations, and membrane electrode assemblies (MEAs) were subsequently fabricated by spray-coating onto perfluorosulfonic acid membranes using the prepared catalyst inks. The chemical stability of the MEAs including radical scavengers was evaluated by open circuit voltage (OCV) decay and electrochemical gas crossover at high temperatures and with low relative humidity (RH) reactant gases. The fuel cell performance was also conducted using the polarization curve, impedance, cyclic voltammetry, and linear sweep voltammetry at 80 °C and 100% RH conditions. The Cerium-based radical scavenger incorporated PFSA membrane showed significantly extended lifetimes during the steady-state OCV test as compared with a non-stabilized PFSA membrane. The MEA performance tests confirmed that the cerium-based radical scavenger dramatically mitigates degradation effects, which improves MEA chemical durability and minimizes performance losses.
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