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Modern diesel emission control systems often use Urea Selective Catalytic Reduction (Urea-SCR) for NOx control. One of the most active SCR catalysts is based on Cu-zeolite, specifically Cu-Chabazite (Cu-CHA), also known as Cu-SSZ-13. The Cu-SCR catalyst exhibits high NOx control performance and has a high thermal durability. However, its catalytic performance deteriorates upon long-term exposure to sulfur. This work describes our efforts to investigate the detailed mechanism of poisoning of the catalyst by sulfur, the optimum conditions required for de-sulfation, and the recovery of catalytic activity. Density functional theory (DFT) calculations were performed to locate the sulfur adsorption site within the Cu-zeolite structure. Analytical characterization of the sulfur-poisoned catalyst was performed using Extreme Ultraviolet Photoelectron Spectroscopy (EUPS) and Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS).

Commercial three way catalysts (TWC) are designed to eliminate HC, CO and NOx pollutants emitted from gasoline powered internal combustion engines. TWC have been optimized over many years to meet ever more stringent emission regulations. It has long been speculated that surface electrical conductivity may be a key parameter in controlling catalytic activity, however until now it has not been possible to reliably measure this physical parameter on a catalytic surface. In this study, the surface electrical conductivity of catalyst powders, such as Rh/ CeO1-x-ZrxO2, Rh/ZrO2 and Rh/Al2O3, were measured by EUPS (Extreme Ultraviolet excited Photoelectron Spectroscopy). Then the measured electrical conductivity was compared with catalyst performance from CO-NO and water gas shift reactions which are important for controlling automobile exhaust emissions from gasoline vehicles.