Evolution of the Structure and Chemical State of Pd Nanoparticles during the in Situ Catalytic Reduction of NO with H-2

    Authors

    K. Paredis; L. K. Ono; F. Behafarid; Z. F. Zhang; J. C. Yang; A. I. Frenkel;B. R. Cuenya

    Comments

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    Abbreviated Journal Title

    J. Am. Chem. Soc.

    Keywords

    X-RAY-ABSORPTION; LEAN-BURN CONDITIONS; ENVIRONMENTAL; ELECTRON-MICROSCOPY; NITRIC-OXIDE REDUCTION; NOBLE-METAL CATALYSTS; NITROGEN-OXIDES; SELECTIVE REDUCTION; FINE-STRUCTURE; PARTICLE-SIZE; PALLADIUM CATALYSTS; Chemistry, Multidisciplinary

    Abstract

    An in-depth understanding of the fundamental structure of catalysts during operation is indispensable for tailoring future efficient and selective catalysts. We report the evolution of the structure and oxidation state of ZrO2-supported Pd nanocatalysts (similar to 5 nm) during the in situ reduction of NO with H-2 using X-ray absorption fine-structure spectroscopy and X-ray photoelectron spectroscopy. Prior to the onset of the reaction ( < = 120 degrees C), a NO-induced redispersion of our initial metallic Pd nanoparticles over the ZrO2 support was observed, and Pd delta+ species were detected. This process parallels the high production of N2O observed at the onset of the reaction ( > 120 degrees C), while at higher temperatures ( > = 150 degrees C) the selectivity shifts mainly toward N-2 (similar to 80%). Concomitant with the onset of N-2 production, the Pd atoms aggregate again into large (6.5 nm) metallic Pd nanoparticles, which were found to constitute the active phase for the H-2-reduction of NO. Throughout the entire reaction cycle, the formation and stabilization of PdOx was not detected. Our results highlight the importance of in situ reactivity studies to unravel the microscopic processes governing catalytic reactivity.

    Journal Title

    Journal of the American Chemical Society

    Volume

    133

    Issue/Number

    34

    Publication Date

    1-1-2011

    Document Type

    Article

    Language

    English

    First Page

    13455

    Last Page

    13464

    WOS Identifier

    WOS:000295551600045

    ISSN

    0002-7863

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