摘要
For traditional strategies to construct SO 2 and H 2 O co-resistant systems in low-temperature NH 3 selective catalytic reduction (NH 3 -SCR) catalysts, the primary challenge lies in mitigating the partial loss of redox activity at active sites. Herein, we present an approach to construct a protective system based on interface engineering principles, effectively safeguarding Cu active sites in ZnO/FeCu-SSZ-13 under SO 2 and H 2 O exposure. The core innovation stems from the creation of a strong interface effect originated from Zn-O-Al bonds formed between ZnO and the framework Al on the FeCu-SSZ-13 surface. This interface effect can regulate the electronic structure of Zn O bonds on ZnO component, producing abundant basic sites around the Cu active sites, enabling the preferential adsorption of SO 2 and its oxidation into ZnSO 4 , thereby virtually eliminating the redox ability loss of Cu active sites. As a result, ZnO/FeCu-SSZ-13 achieves exceptional low-temperature NH 3 -SCR performance, maintaining over 90 % NO x conversion even in the presence of SO 2 and H 2 O. Our work opens a new avenue for developing low-temperature NH 3 -SCR catalysts with desired SO 2 and H 2 O resistance, offering valuable insights for advancing catalytic performance in challenging reaction conditions.
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