Synergistic Utilization of a CeO2-Anchored Bifunctionalized Metal–Organic Framework in a Polymer Nanocomposite toward Achieving High Power Density and Durability of PEMFC

Abstract

The free radicals produced during the long-term operation of fuel cells can accelerate the chemical degradation of the proton exchange membrane (PEM). In the present work, the widely used free radical scavenger CeO2 was anchored on amino-functionalized metal–organic frameworks, and flexible alkyl sulfonic acid side chains were tethered onto the surface of inorganic nanoparticles. The prepared CeO2-anchored bifunctionalized metal–organic framework (CeO2-MNCS) was used as a promising synergistic filler to modify the Nafion matrix for addressing the detrimental effect of pristine CeO2 on the performance and durability of PEMs, including decreased proton conductivity and the migration problem of CeO2. The obtained hybrid membranes exhibited a high proton conductivity up to 0.239 S cm–1, enabling them to achieve a high power density of 591.47 mW cm–2 in a H2/air PEMFC single cell, almost 1.59 times higher than that of recast Nafion. After 115 h of acceleration testing, the OCV decay ratio of the hybrid membrane was decreased to 0.54 mV h–1, which was significantly lower than that of recast Nafion (2.18 mV h–1). The hybrid membrane still maintained high power density, low hydrogen crossover, and unabated catalytic activity of the catalyst layer after the durability test. This study provides an effective one-stone-two-birds strategy to develop highly durable PEMs by immobilizing CeO2 without sacrificing proton conductivity, allowing for the realization of improvement on the performance and sustained durability of PEMFC simultaneously.