Abstract
The impact of the electrolyte's pH on the catalytic activity of platinum group metal-free (PGM-free) catalysts toward the oxygen reduction reaction (ORR) was studied. The results indicate that the ORR mechanism is determined by the affinity of protons and hydroxyls toward multiple functional groups present on the surface of the PGM-free catalyst. It was shown that the ORR is limited by the proton-coupled electron transfer at pH values below 10.5. At higher pH values (>10.5), the reaction occurs in the outer Helmholtz plane (OHP), favoring hydrogen peroxide production. Using a novel approach, the changes in the surface chemistry of PGM-free catalyst in a full pH range were studied by X-ray photoelectron spectroscopy (XPS). The variations in the surface concentration of nitrogen and carbon species are correlated with the electron transfer process and overall kinetics. This study establishes the critical role of the multitude of surface functional groups, presented as moieties or defects in the carbonaceous "backbone" of the catalyst, in mechanism of oxygen reduction reaction. Understanding the pH-dependent mechanism of ORR provides the basis for rational design of PGM-free catalysts for operation across pH ranges or at a specific pH of interest. This investigation also provides the guidelines for developing and selecting ionomers used as "locally-confined electrolytes", by taking into account affinities and possible interactions of specific functional groups of the PGM-free catalysts with protons or hydroxyls facilitating the overall ORR kinetics.
Original language | English |
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Pages (from-to) | 3041-3053 |
Number of pages | 13 |
Journal | ACS Catalysis |
Volume | 8 |
Issue number | 4 |
DOIs | |
State | Published - Apr 6 2018 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2018 American Chemical Society.
Keywords
- Oxygen reduction reaction
- PGM-free catalysts
- XPS
- mechanism
- pH-dependent activity