Insight into the effect of exposed crystal facets of anatase TiO2 on HCHO catalytic oxidation of Mn-Ce/TiO2.

ABSTRACT

Indoor formaldehyde pollution seriously jeopardizes human health. The development of efficient and stable non-precious metal catalysts for low-temperature catalytic degradation of formaldehyde is a promising approach. In this study, TiO2 {001} and {101} supports were loaded with different ratios of Mn and Ce active components, and the effects of the ratios of the active components on the catalytic activity were investigated. The elemental oxidation states, redox capacities, active oxygen mobilities and acid site distributions of the catalysts were determined using characterization techniques such as XPS, H2-TPR, O2-TPD, and NH3-TPD. In situ infrared spectroscopy was utilized to reveal the differences in the two-step dehydrogenation reactions of dioxymethylene (DOM) in 5Mn1Ce/Ti-NS and 5Mn1Ce/Ti-NP. Density-functional theory was used to investigate the differences in the catalytic steps and maximum energy barriers of Mn-Ce/Ti-NS and Mn-Ce/Ti-NP for HCHO. The differences in catalytic activity due to the influence of the manganese and cerium active components on the {001} and {101} crystal faces of anatase titanium dioxide are comprehensively revealed. Exposure of the supported crystalline surfaces alters the catalytic activity centers and reaction pathways at the molecular level. This study provides experimental and theoretical guidance for the selection of exposed crystalline surfaces for loaded catalysts.