Combined spatially resolved operando spectroscopy: New insights into kinetic oscillations of CO oxidation on Pd/γ-Al2O3

被引:24
作者
Dann, Ellie K. [1 ,2 ]
Gibson, Emma K. [2 ,3 ]
Catlow, C. Richard A. [1 ,2 ,4 ]
Celorrio, Veronica [1 ,2 ]
Collier, Paul [5 ]
Eralp, Tugce [5 ]
Amboage, Monica [6 ]
Hardacre, Christopher [2 ,7 ]
Stere, Cristina [2 ,7 ]
Kroner, Anna [6 ]
Raj, Agnes [5 ]
Rogers, Scott [1 ,2 ]
Goguet, Alexandre [2 ,8 ]
Wells, Peter P. [2 ,6 ,9 ]
机构
[1] UCL, Dept Chem, 20 Gordon St, London WC1H 0AJ, England
[2] Rutherford Appleton Lab, UK Catalysis Hub, Res Complex Harwell, Didcot OX11 0FA, Oxon, England
[3] Univ Glasgow, Sch Chem, Joseph Black Bldg, Glasgow G12 8QQ, Lanark, Scotland
[4] Cardiff Univ, Sch Chem, Cardiff Catalysis Inst, Main Bldg,Pk Pl, Cardiff CF10 3AT, S Glam, Wales
[5] Johnson Matthey Technol Ctr, Blounts Court Rd, Reading RG4 9NH, Berks, England
[6] Diamond Light Source Ltd, Harwell Sci & Innovat Campus, Didcot OX11 0DE, Oxon, England
[7] Univ Manchester, Sch Chem, Oxford Rd, Manchester M13 9PL, Lancs, England
[8] Queens Univ Belfast, Sch Chem, David Keir Bldg,Stranmillis Rd, Belfast BT9 5AG, Antrim, North Ireland
[9] Univ Southampton, Sch Chem, Univ Rd, Southampton SO17 1BJ, Hants, England
基金
英国工程与自然科学研究理事会;
关键词
XAFS; DRIFTS; CO oxidation; Pd/Al2O3; Operando spectroscopy; RAY-ABSORPTION SPECTROSCOPY; HIGH-ENERGY-RESOLUTION; IN-SITU; CARBON-MONOXIDE; CATALYTIC-OXIDATION; SELF-ORGANIZATION; MOLECULAR-BEAM; PD; PLATINUM; IR;
D O I
10.1016/j.jcat.2019.03.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Spatially resolved, combined energy dispersive EXAFS (EDE) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) measurements have been performed over a fixed catalyst bed of Pd/gamma-Al2O3 during kinetic oscillations of CO oxidation. The kinetic oscillations of CO oxidation over Pd (or for that matter Pt or Rh) catalysts are a complicated phenomenon that require characterisation techniques with high time resolution and spatial resolution in order to make links between catalyst structure and surface reactivity. By measuring the extent of Pd oxidation at the nanoparticle surface, from Pd K-edge EDE, and matching this with the CO coverage, from DRIFTS spectra, at multiple positions of the fixed bed reactor it is found that the majority of the catalyst undergoes a sharp transition from the CO poisoned catalyst to the highly active, oxidised Pd surface. This transition occurs initially at the end of the catalyst bed, nearest the outlet, and propagates upstream with increasing temperature of the reactor. The oscillations in Pd surface oxide formation and CO coverage are observed only in the first similar to 1 mm of the bed, which gives rise to oscillations in CO2 and O-2 concentrations observed by end-pipe mass spectrometry after the light-off temperature. The catalyst initially exists as less active, CO poisoned metallic Pd nanoparticles before light-off which transition to a highly active state after light-off when the Pd nanoparticle surface becomes dominated by chemisorbed oxygen. Kinetic oscillations only occur at the front of the catalyst bed where there is sufficient concentration of CO in the gas phase to compete with O-2 for adsorption sites at the catalyst surface. We demonstrate the complex nature of the evolving catalyst structure and surface reactivity during catalytic operation and the need for spatially resolved operando methods for understanding and optimising catalyst technologies. (C) 2019 The Authors. Published by Elsevier Inc.
引用
收藏
页码:201 / 208
页数:8
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