Water promoting effect in CO oxidation over N-doped Co3O4/Pt nanocatalysts by tailoring metal-support interfaces

Summary The interfacial sites of metal-support catalysts are crucial for catalytic reactions. Herein, we designed well-defined N-Co 3 O 4 /Pt catalysts with N-tailoring metal-support interfaces to promote catalytic activity toward CO oxidation under humid environments. A series of N-Co 3 O 4 /Pt catalysts were fabricated using ZIF-67 nanocubes as self-sacrificing templates, which showed exceptionally high catalytic activity in low-temperature CO oxidation. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) study indicates that H 2 O molecules undergo dissociative adsorption to form active –OH species (Co 3+ –OH–Pt). Isotopic labeling technique indicates that H 2 O molecules (or –OH groups) contribute to ∼65% of CO 2 production in CO oxidation. Moreover, the amount of N dopant that stabilized the Co 3+ –OH–Pt species was highly dependent on the H 2 O-soaking conditions of ZIF-67/Pt. Density functional theory (DFT) calculations suggest that the COOH ∗ pathway of CO oxidation over the N-Co 3 O 4 /Pt interface is energetically favorable in humid conditions. In particular, the N doping could stabilize the Co 3+ –OH–Pt interface and simultaneously reduce the energy barrier of CO 2 formation from COOH ∗ intermediates.