Study of CO Oxidation on Polycrystalline Pt Electrodes in Acidic Solution by ATR-SEIRAS

Adsorption and electro-oxidation of CO on a polycrystalline Pt electrode in acidic solutions were systematically revisited by in situ attenuated-total-reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) in conjunction with related Gram–Schmidt response analysis. CO was either adsorbed in the double-layer region, i.e., 0.45 V (RHE) (denoted as CO @DL ) or in the hydrogen underpotential deposition region, i.e., 0.1 V (RHE) (denoted as CO @UPD ). The results indicate that the CO @UPD and H 2 O free coexisted structure (or simply costructure) forms only at a sufficiently high global CO coverage (H 2 O free denotes hydrogen-bonding-broken water); In contrast, the CO @DL and H 2 O free costructure forms in an earlier adsorption phase, less dependent on the global CO coverage. The partial oxidation of CO from solution and weakly adsorbed CO L at the active sites is suggested to yield a prepeak that occurs with the relaxation of the CO ad -H 2 O free costructure and the disorganization of the outer water net layers. In the main oxidation process, the oxidation of CO @UPD tends to proceed via the “mean-field approximation” kinetics due to the high CO ad mobility resulting from the oxidation prepeak. The oxidation process of CO @DL is, however, likely via the “nucleation and growth” kinetics due to the good stability of the local CO @DL and H 2 O free costructured islands. The H 2 O free can be better assigned to the “probe” of the local CO ad coverage rather than the main oxygenated species for CO ad oxidation according to the spectral results for both CO @UPD and CO @DL .