Au-Modified Pd catalyst exhibits improved activity and stability for NO direct decomposition. Issue 8 (3rd March 2021)

• Record Type: Journal Article
• Authors: Elgayyar, Taha; Schnee, Josefine; Tuel, Alain; Burel, Laurence; Bosselet, Francoise; Schuurman, Yves; Meunier, Frederic C.; Delannoy, Laurent; Thomas, Cyril
• Is Part Of: Catalysis science & technology. Volume 11:Issue 8(2021)
• Page Start: 2908
• Page End: 2914
• Publication Date: 2021-03-03
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/d1cy00301a
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : The promotion of a Pd catalyst with Au leads to higher and stable activity for the direct decomposition of NO, due to improved oxygen desorption. Abstract : The direct decomposition of NO x at moderate temperatures is a challenge because of the poisoning of the surface of noble metals by oxygen, yet the modification of Pd with Au enables obtaining a highly stable catalyst under an O2 -free feed at 450 °C. Care was taken to ensure that the reaction was not due to the reduction of NO x with carbonaceous residues by monitoring CO2 evolution. Pd–Au alloyed domains with a wide range of compositions were evidenced by in situ and ex situ XRD, the Pd content of which decreased with the increasing oxidising nature of the feed due to phase segregation giving rise to PdO and an Au-rich alloy. Under air, the limiting alloy composition was Pd0.2 Au0.8 . The catalyst was yet inactive in the presence of 5% O2 .