Improvements in electrical and electrochemical properties of Nb-doped SnO sub(2- delta ) supports for fuel cell cathodes due to aggregation and Pt loading
We found that Nb-doped SnO sub(2- delta ) nanoparticles were improved in their electrical conductivity by more than two orders of magnitude by the aggregation of the particles, including the fusion of nearest-neighbor particles to form a random branching structure, and the formation of a porous aggl...
Gespeichert in:
Veröffentlicht in: | RSC advances 2014-07, Vol.4 (61), p.32180-32188 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | We found that Nb-doped SnO sub(2- delta ) nanoparticles were improved in their electrical conductivity by more than two orders of magnitude by the aggregation of the particles, including the fusion of nearest-neighbor particles to form a random branching structure, and the formation of a porous agglomerated structure similar to that of conventional carbon blacks. The electrical conductivity was increased by an additional two orders of magnitude as a result of the loading of Pt nanoparticles to produce an electrocatalyst (Pt/Nb-doped SnO sub(2- delta )) for fuel cell applications. We also found that the specific activities of Pt/Sn sub(0.96)Nb sub(0.04)O sub(2- delta ) (16 wt% Pt loading) for the oxygen reduction reaction increased with increasing electrical conductivity of the support and exceeded that of a conventional Pt catalyst supported on carbon black (Pt/CB). Since the tin oxide supports are much more stable than CB supports to the exposure to positive potentials (0.9 similar to 1.3 V) during the start/stop operation of fuel cells, Pt or Pt alloy catalysts supported on oxide supports with such a chain-like, necked structure, as developed in this work, become superior candidates as robust cathode catalysts for the fuel cell vehicle application. |
---|---|
ISSN: | 2046-2069 |
DOI: | 10.1039/c4ra03988b |