AI Article Synopsis

  • Research is focused on enhancing Pt-based catalysts for better performance and durability in energy conversion systems, especially in fuel cells.
  • While efforts are made to increase the electroactive surface area and activity for oxygen reduction reactions (ORR), most findings are limited to laboratory setups (like rotating disk electrodes) rather than practical applications in full-cell systems.
  • The review aims to compare catalyst performance in laboratory vs. real-world fuel cells, address durability issues, and provide new strategic design ideas for improving full-cell device efficiency.

Article Abstract

A substantial amount of research effort has been directed toward the development of Pt-based catalysts with higher performance and durability than conventional polycrystalline Pt nanoparticles to achieve high-power and innovative energy conversion systems. Currently, attention has been paid toward expanding the electrochemically active surface area (ECSA) of catalysts and increase their intrinsic activity in the oxygen reduction reaction (ORR). However, despite innumerable efforts having been carried out to explore this possibility, most of these achievements have focused on the rotating disk electrode (RDE) in half-cells, and relatively few results have been adaptable to membrane electrode assemblies (MEAs) in full-cells, which is the actual operating condition of fuel cells. Thus, it is uncertain whether these advanced catalysts can be used as a substitute in practical fuel cell applications, and an improvement in the catalytic performance in real-life fuel cells is still necessary. Therefore, from a more practical and industrial point of view, the goal of this review is to compare the ORR catalyst performance and durability in half- and full-cells, providing a differentiated approach to the durability concerns in half- and full-cells, and share new perspectives for strategic designs used to induce additional performance in full-cell devices.

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Source
http://dx.doi.org/10.1021/acs.chemrev.0c01337DOI Listing

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