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Uniform Pt nanoparticles supported on urchin-like mesoporous TiO hollow spheres as stable electrocatalysts for the oxygen reduction reaction. | LitMetric

AI Article Synopsis

  • The development of high-performance Pt-based electrocatalysts for the oxygen reduction reaction (ORR) is crucial for advancing proton exchange membrane fuel cells.
  • Researchers designed urchin-like mesoporous TiO hollow spheres (UMTHS) as effective supports for dispersing Pt nanoparticles, achieving uniform sizes of around 3.2 nm after heat treatment.
  • The resulting Pt/UMTHS demonstrated higher electrochemical performance and stability compared to conventional Pt/C, attributed to UMTHS's large surface area, strong metal support interaction, and its structural features that enhance stability during long-term cycling.

Article Abstract

In order to promote the commercial application of proton exchange membrane fuel cells, it is of great importance to develop Pt-based electrocatalysts with high activity and stability for the oxygen reduction reaction (ORR). Here, urchin-like mesoporous TiO hollow spheres (UMTHS) with a high specific surface area (167.1 m g) and improved conductivity were designed and applied as supports to disperse Pt nanoparticles (NPs) for the first time. Uniform Pt NPs (∼3.2 nm) on the surface of nanothorns were obtained after heat treatment. The as-prepared product (Pt/UMTHS) exhibited a more positive half-wave potential (E) than that of the reference sample Pt@C without UMTHS (0.867 V vs. 0.829 V). The improved performance can be ascribed to the high specific surface area of UMTHS. The Pt/UMTHS also exhibited a much better ORR stability than the commercial Pt/C after long-term cycling at 0.6-1.0 V according to the comparison of E, mass activity and electrochemical surface area with Pt/C. The enhanced stability of Pt/UMTHS was mainly derived from the strong metal support interaction between Pt NPs and UMTHS, together with the spatial restriction and the anti-restriction provided by UMTHS.

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Source
http://dx.doi.org/10.1039/c9nr10890dDOI Listing

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