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Improving time-resolution and sensitivity of X-ray photoelectron spectroscopy of a powder catalyst by modulated excitation

Ambient pressure X-ray photoelectron spectroscopy (APXPS) is a powerful tool to characterize the surface structure of heterogeneous catalysts in situ . In order to improve the time resolution and the signal-to-noise (S/N) ratio of photoemission spectra, we collected consecutive APXP spectra during t...

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Bibliographic Details
Published in:Chemical science (Cambridge) 2023-07, Vol.14 (27), p.7482-7491
Main Authors: Roger, M, Artiglia, L, Boucly, A, Buttignol, F, Agote-Arán, M, van Bokhoven, J. A, Kröcher, O, Ferri, D
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Summary:Ambient pressure X-ray photoelectron spectroscopy (APXPS) is a powerful tool to characterize the surface structure of heterogeneous catalysts in situ . In order to improve the time resolution and the signal-to-noise (S/N) ratio of photoemission spectra, we collected consecutive APXP spectra during the periodic perturbation of a powder Pd/Al 2 O 3 catalyst away from its equilibrium state according to the modulated excitation approach (ME). Averaging of the spectra along the alternate pulses of O 2 and CO improved the S/N ratio demonstrating that the time resolution of the measurement can be limited solely to the acquisition time of one spectrum. Through phase sensitive analysis of the averaged time-resolved spectra, the formation/consumption dynamics of three oxidic species, two metal species, adsorbed CO on Pd 0 as well as Pd n + ( n > 2) was followed along the gas switches. Pd n + and 2-fold surface PdO species were recognised as most reactive to the gas switches. Our approach demonstrates that phase sensitive detection of time-resolved XPS data allows following the dynamics of reactive species at the solid-gas interface under different reaction environments with unprecedented precision. Modulated excitation experiments coupled to time-resolved NAP-XPS allow following the dynamics of reactive species on a powder Pd/Al 2 O 3 catalyst with unprecedented precision..
ISSN:2041-6520
2041-6539
DOI:10.1039/d3sc01274c