(673b) Silver Single Atom Catalysts on Different Supports with Distinct Catalytic Performance for the Selective Oxidation of Ammonia | AIChE

(673b) Silver Single Atom Catalysts on Different Supports with Distinct Catalytic Performance for the Selective Oxidation of Ammonia

Authors 

Ye, K. - Presenter, University of Central Florida
Liu, F. - Presenter, University of Central Florida
Xie, S., University of Central Florida
Campbell, T., University of Central Florida
Le, D., University of Central Florida
Rahman, T. S., University of Central Florida
The selective catalytic oxidation of NH3 (NH3-SCO) is an efficient route to remove NH3 from the NH3 slip of vehicle emission control. Supported metal catalysts such as Pt, Pd and Cu catalysts are widely reported, but the high cost and high N2O yield limited their application [1]. Ag, with relatively low price and superior catalytic activity, recently attracted great attention and showed high potential for NH3-SCO reaction. However, to date, very few works have reported the preparation and application of Ag single atom catalysts (Ag1 SACs) for NH3-SCO reaction, particularly the effect of supports on Ag coordination environments and catalytic performance.

We herein report the preparation and application of Ag catalysts with 1wt.% Ag loading on three different supports including CeO2, Al2O3 and ZrO2 for NH3-SCO reaction. By means of TEM, UV-vis DRS and EXAFS, it was verified that Ag is present as single atom phase within all the three catalysts. Under different testing conditions with or without H2O, NH3-SCO activity on the catalysts decreased by the order of Ag1/CeO2 > Ag1/ZrO2 > Ag1/Al2O3 (Figure 1), with the Ag1/CeO2 catalyst performing the best. H2-temperature programed reduction (H2-TPR) results indicated that Ag1/CeO2 exhibited the best low-temperature reducibility. In accompanying density functional theory-based calculation, we believe that the greatest advantage offered by the Ag SACs on CeO2 is the formation of hydrogen bonds between NH3 and surface oxygen atoms, providing a drastically smaller activation energy barrier corresponding to shorter distances required for the hydrogen to dissociate.

References:

[1]. G.Y. Xu, Y. Zhang, J.G. Lin, Y.B. Wang, X.Y. Shi, Y.B. Yu, and H. He. ACS Catalysis 11(9): 5506-5516, 2021.

Topics