AI Article Synopsis

  • The study investigates how particle size affects the oxygen reduction reaction (ORR) activity of platinum (Pt) in various electrolytes, noting that while the ORR rate varies with the electrolyte type, the particle size's impact remains consistent across them.
  • The specific activity (SA) for ORR decreases in a clear order: polycrystalline Pt shows the highest activity, followed by unsupported Pt black particles (~30 nm), and then high surface area (HSA) carbon supported Pt nanoparticles (1 to 5 nm).
  • Additionally, it points out that the differences in SA between HSA carbon supported catalysts of different sizes are minimal and underscores the need to further explore the stark SA contrasts between polycrystalline Pt and the other types of Pt catalysts

Article Abstract

The influence of particle size on the oxygen reduction reaction (ORR) activity of Pt was examined in three different electrolytes: two acidic solutions, with varying anionic adsorption strength (HClO(4) < H(2)SO(4)); and an alkaline solution (KOH). The experiments show that the absolute ORR rate is dependent on the supporting electrolyte; however, the relationship between activity and particle size is rather independent of the supporting electrolyte. The specific activity (SA) toward the ORR rapidly decreases in the order of polycrystalline Pt > unsupported Pt black particles (~30 nm) > high surface area (HSA) carbon supported Pt nanoparticle catalysts (of various size between 1 and 5 nm). In contrast to previous work, it is highlighted that the difference in SA between the individual HSA carbon supported catalysts (1 to 5 nm) is rather trivial and that the main challenge is to understand the significant differences in SA between the polycrystalline Pt, unsupported Pt particles, and HSA carbon supported Pt catalysts. Finally, a comparison between measured and modeled activities (based on the distribution of surface planes and their SAs) for different particle sizes indicates that such simple models do not capture all aspects of the behavior of HSA carbon supported catalysts.

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Source
http://dx.doi.org/10.1021/ja207016uDOI Listing

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