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Understanding the nature of active sites on metal oxide catalysts in the selective catalytic reduction (SCR) of NO by NH 3 (NH 3 -SCR) is a crucial prerequisite for the development of novel efficient NH 3 -SCR catalysts. In this work, two CeO 2 -based SCR catalyst systems with diverse acidic metal oxides-CeO 2 interfaces, i.e., Nb 2 O 5 -CeO 2 (Nb 2 O 5 /CeO 2 and CeO 2 /Nb 2 O 5) and WO 3 -CeO 2 (WO 3 /CeO 2 and CeO 2 /WO 3), were prepared and used to reveal the relationship between NH 3 -SCR activity and surface acidity/redox properties. In combination with the results of the NH 3 -SCR activity test and various characterizations, it was found that the NH 3 -SCR performance of Nb 2 O 5 -CeO 2 and WO 3 -CeO 2 catalysts was highly dependent on the strong interactions between the redox component (CeO 2) and acidic component (Nb 2 O 5 or WO 3), as well as the amount of paired redox-acid sites. From a quantitative perspective, an activity-surface acidity/redox property relationship was proposed. For both Nb 2 O 5 -CeO 2 and WO 3 -CeO 2 catalysts systems operated at the more concerned low-temperature range (200 °C), the NH 3 -SCR activity in low NO x conversion region (< 40%) was mainly dominated by the surface acidity of catalysts, while the NH 3 -SCR activity in high NO x conversion region (> 40%) was more determined by redox properties. [Display omitted] • Nb 2 O 5 -CeO 2 and WO 3 -CeO 2 catalysts with tuned redox-acid property were synthesized. • Paired redox-acid sites formed through strong interaction between Nb 2 O 5 /WO 3 and CeO 2. • NH 3 -SCR activity was well controlled by the paired redox-acid sites. • Surface acidity and redox property were investigated from a quantitative perspective. • A clear surface acidity/redox property-activity relationship was established. [ABSTRACT FROM AUTHOR]

[Display omitted] • A novel hybrid strategy is employed to design catalysts with superior K resistance. • The main reason for CeMn deactivation is cut-off of L-H mechanism resulting from the formation of stable nitrates. • The addition of ZSM-5 can re-activate the inert nitrates. • Alkali metals poisoned catalysts can be regenerated by ZSM-5 hybridization. The application of cerium-manganese oxides (CeMn) in controlling exhaust gas from biomass combustion is greatly inhibited due to poor resistance to alkali metals. Herein, we report a smart strategy to circumvent the K poisoning problem of CeMn by physically coupling with ZSM-5, which exhibited almost no activity loss even under a high loading of 2 wt % K 2 O. Results showed that in contrast to the conventionally believed disturbance of redox property and reduction of acid sites, the dominant effect from K loading on the deactivation of CeMn catalysts lies on the formation of chemically inert nitrates, which significantly restrains the reaction cycle via Langmuir-Hinshelwood route. With ZSM-5 hybridization, the stable nitrates over CeMn can be facilely activated and consumed by NH 4 + species introduced by ZSM-5, thus transforming poisoning sites into active sites and ensuring superior catalytic performance. The study presenting here not only provides an efficient strategy for fabricating NH 3 -SCR catalysts with superior K resistance but also sheds new light on the deactivation mechanism of K over CeMn catalysts. [ABSTRACT FROM AUTHOR]