| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 43059 | Applied Catalysis A: General | 2008 | 8 Pages |
Chalcogenide (S, Se, and Te)-modified ruthenium catalysts prepared by a wet impregnation method demonstrated the electrocatalytic activities in the order of Ru–Te > Ru–Se > Ru–S for the oxygen reduction reaction (ORR) in acidic media. The ORR activity of Ru–Te supported on carbon black (Ru–Te/C) significantly depends on the initial Te/Ru atomic ratio. The catalyst obtained at a Te/Ru = 2 produced the maximum value current density, the reaction was confirmed to form a RuTe2 intermetallic compound, based on the XRD. The TEM image of RuTe2/C shows that the loaded RuTe2 particles consist of well-crystallized plate-like particles with diameters of about 10 nm. Rotating ring disk electrode (RRDE) measurements indicated that RuTe2/C generates about 4% H2O2 during the ORR, preferentially proceeding via the four-electron charge transfer pathway to form H2O. RuTe2/C showed a comparable activity with regard to the cathodic current to that of the conventional Pt/C catalyst at the same metal loading. Unfortunately, the onset electrode potential for oxygen reduction by RuTe2/C was more negative than that catalyzed by the commercial Pt/C by about 0.2 V.
Graphical abstractChalcogenide (S, Se, and Te)-modified ruthenium catalysts demonstrated the electrocatalytic activities in the order of Ru–Te > Ru–Se > Ru–S for the oxygen reduction reaction (ORR) in acidic media. The catalyst obtained at a Te/Ru = 2 produced the maximum value current density, the reaction was confirmed to form a RuTe2 intermetallic compound. RuTe2/C showed a comparable activity with regard to the cathodic current to that of the conventional Pt/C catalyst at the same metal loading. Figure optionsDownload full-size imageDownload as PowerPoint slide
