Active Lattice Oxygen in Co-doped SrTiO3 on CO Oxidation Based on Mars-van Krevelen Mechanism
Abstract
Currently, most commercial environmental catalysts depend on large amounts of platinum-group metals (PGMs) to achieve high purification efficiency against environmental pollutants such as CO and NO. However, such catalysts are not readily available and have high cost, while PGMs exhibit significant price volatility. Toward the development of PGM-free environmental catalysts, we focus on the Mars-van Krevelen mechanism in which lattice oxygen constituting transition metal oxide participates in catalytic reaction. This study demonstrates the contribution of the lattice oxygen constituting SrTi1-xCoxO3 perovskite to the CO oxidation activity. The catalytic activity of SrTi1-xCoxO3 increased with increasing Co substitution and reached a maximum at x = 0.2. By contrast, Co substitution at x ≥ 0.4 resulted in decreased CO oxidation activity. H2 temperature-programmed reduction and in situ X-ray diffraction (XRD) in a H2 atmosphere suggested that the catalytic activity of SrTi1-xCoxO3 corresponded well with the lattice oxygen release behavior; that is, among the SrTi1-xCoxO3 samples, Ti-rich SrTi0.8Co0.2O3 released lattice oxygen at the lowest temperature in the H2 atmosphere. As the amount of substituted Co increased, the lattice oxygen release temperature increased, indicating that the Co-O-Ti bond was more reactive than the Co-O-Co bond. The states of the lattice oxygen in SrTi1-xCoxO3 were investigated in detail through synchrotron XRD and O K-edge X-ray absorption spectroscopy. Notably, in the samples with x ≥ 0.4, which had a large amount of Co-O-Co bonds, partial electron donation from lattice oxygen to Co species occurred, suggesting the strengthening of the Co-O-Co bonds. These results indicate that lattice oxygen, which forms relatively weak Co-O-Ti bonds in SrTi1-xCoxO3, acts as an effective active site for CO oxidation, providing valuable guidance for the rational design of PGM-free oxide catalysts.
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