Influence of lattice oxygen on the catalytic activity of blue titania supported Pt catalyst for CO oxidation

Despite extensive research into understanding the reaction mechanism for CO oxidation over transition metals supported on TiO2, the active species for oxidation remains controversial. Herein, the characteristics of the active oxygen species of blue TiO2 with a higher concentration of oxygen vacancies as a model catalyst with deposited nano-sized Pt toward CO oxidation are unraveled. Pt deposited on blue TiO2 showed 8.8 times higher catalytic activity than that on TiO2 at 200 degrees C. Formation of the oxygen vacancies induced electron generation, and the electrons were transferred to CO, weakening the binding strength. The ratio of lattice oxygen on the top surface of Pt/blue TiO2 decreased from 50.4% before the reaction to 6.1% during the reaction, as analyzed by near ambient pressure X-ray photoelectron spectroscopy. The results directly show that the facile reducibility of surface lattice oxygen of blue TiO2 leads to the high activity of CO oxidation.

Automated summary

The study reveals that the catalyst with Pt deposited on blue TiO2 exhibits 8.8 times higher catalytic activity than that on TiO2 for CO oxidation. The formation of oxygen vacancies on blue TiO2 promotes electron generation, leading to weakened CO binding strength. The facile reducibility of surface lattice oxygen on blue TiO2 is identified as the reason behind its high CO oxidation activity.