Potential-dependent infrared absorption spectroscopy of adsorbed CO and X-ray photoelectron spectroscopy of arc-melted single-phase Pt, PtRu, PtOs, PtRuOs, and Ru electrodes

The potential- and coverage-dependent infrared absorption spectroscopy (IRAS) of linearly bound CO on single-phase polycrystalline are-melted Pt, PtRu(1/1), PtRu(8/2), PtOs(8/2), PtRuOs(8/1/1), PtRuOs(65/25/ 10), and Ru electrodes in 0.5 M H2SO4 are correlated with the potential-dependent X-ray photoelectron spectroscopy (XPS) of the PtRu(l/l), PtOs(8/2), and PtRuOs(65/25/10) substrates. The CO stretching frequencies decrease as the mole fraction of Pt in the alloy is decreased. The CO oxidation onset on pure Pt at 100.0% CO coverage is 0.5 V vs a reversible hydrogen electrode and shifts negatively as the alloy mole fraction of Pt is reduced. At CO dosing conditions that yield 100% coverage on purr: Pt, the CO bandwidths increase with decreasing Pt mole fraction: on pure Pt the bandwidths increase as the CO coverage is reduced. The effects of CO coverage and bulk alloy composition on the Stark tuning rates (STRs) have been systematically examined on Pt, and a series of binary and ternary alloy surfaces. The XPS data confirm a potential-dependent surface distribution of oxides and no significant surface segregation of the alloying components. The systematic displacement, to lower frequencies, of the linear STRs as the mole fraction of Pt is reduced suggests no significant island formation on the are-melted alloy surfaces. The XPS data also suggest that the alloying metals, rather than Pt, are responsible for activation of the water required for methanol oxidation in the direct methanol fuel cell potential window.