Tandem Reaction on Ru/Cu-CHA Catalysts for Ammonia Elimination with Enhanced Activity and Selectivity

Environ Sci Technol. 2025 Jan 17. doi: 10.1021/acs.est.4c10396. Online ahead of print.

Abstract

Ammonia emissions from vehicles and power plants cause severe environmental issues, including haze pollution and nitrogen deposition. Selective catalytic oxidation (SCO) is a promising technology for ammonia abatement, but current catalysts often struggle with insufficient activity and poor nitrogen selectivity, leading to the formation of secondary pollutants. In this study, we developed a bifunctional Ru/Cu-CHA zeolite catalyst for ammonia oxidation, incorporating both SCO sites (Ru) and selective catalytic reduction sites (SCR, Cu). Various characterizations, including HAADF-STEM, XAFS, and H2-TPR, revealed that Cu2+ cations are dispersed within the CHA zeolite, while RuOx clusters and nanoparticles are present both inside and on the surface of the zeolite. Operando DRIFTS-MS, in situ Raman spectroscopy, and DFT calculations confirmed that NH3 adsorbed on Cu2+ Lewis acid sites efficiently reduced RuO2 with a lower energy barrier, significantly enhancing the low-temperature activity of the Ru/Cu-CHA catalyst. Additionally, Cu2+ cations further facilitated the elimination of byproducts (NOx) via the tandem SCR reaction, thus greatly improving the nitrogen selectivity. This synergistic effect contributed to high catalytic activity (>94% at 200 °C) and excellent nitrogen selectivity (>90% even at high temperatures above 325 °C) for Ru2.5/Cu-CHA during practical ammonia elimination in the presence of NOx and water vapor.

Keywords: DFT calculations; Ru/Cu-CHA; ammonia abatement; operando DRIFTS-MS; synergistic effect; tandem reaction.