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A comprehensive experimental and theoretical study of the CO + NO reaction catalyzed by Au/Ni nanoparticles

DOI: 10.1021/acscatal.8b05154 DOI Help

Authors: Georgios Kyriakou (European Bioenergy Research Institute, Aston University; University of Patras) , Antonio M. Márquez (Universidad de Sevilla) , Juan P Holgado (Instituto de Ciencia de Materiales de Sevilla (CSIC-University of Seville)) , Martin J. Taylor (European Bioenergy Research Institute, Aston University) , Andrew E. H. Wheatley (Cambridge University) , Joshua P. Mehta (Cambridge University) , Javier Fernández Sanz (Universidad de Sevilla) , Simon K. Beaumont (University of Durham) , Richard M. Lambert (Cambridge University)
Co-authored by industrial partner: No

Type: Journal Paper
Journal: Acs Catalysis

State: Published (Approved)
Published: April 2019
Diamond Proposal Number(s): 9577

Abstract: The catalytic and structural properties of five different nanoparticle catalysts with varying Au/Ni composition were studied by six different methods, including in situ XAS and DFT calculations. The as-prepared materials contained substantial amounts of residual capping agent arising from the commonly used synthetic procedure. Thorough removal of this material by oxidation was essential for the acquisition of valid catalytic data. All catalysts were highly selective towards N2 formation, with 50-50 Au:Ni material best of all. In situ XANES showed that although Au acted to moderate the oxidation state of Ni, there was no clear correlation between catalytic activity and nickel oxidation state. However, in situ EXAFS showed a good correlation between Au-Ni coordination number—highest for Ni50Au50—and catalytic activity. Importantly, these measurements also demonstrated substantial and reversible Au/Ni intermixing as a function of temperature between 550 °C (reaction temperature) and 150 °C, underlining the importance of in situ methods to the correct interpretation of reaction data. DFT calculations on smooth, stepped, monometallic and bimetallic surfaces showed that N+N recombination rather than NO dissociation was always rate-determining and that the activation barrier to recombination reaction decreased with increased Au content, thus accounting for the experimental observations. Across the entire composition range the oxidation state of Ni did not correlate with activity, in disagreement with earlier work, and theory showed that that NiO itself should be catalytically inert. Au-Ni interactions were of paramount importance in promoting N+N recombination, the rate-limiting step.

Journal Keywords: Bimetallic catalysts; in situ measurements; DFT; active species; effect of Au; reaction mechanism

Subject Areas: Chemistry

Instruments: B18-Core EXAFS