Demonstrating Pressure Jumping as a Tool to Address the Pressure Gap in High Pressure Photoelectron Spectroscopy of CO and CO2 Hydrogenation on Rh(211)

Author:

Degerman David1ORCID,Goodwin Christopher M.12ORCID,Lömker Patrick1ORCID,García‐Martínez Fernando3ORCID,Shipilin Mikhail1ORCID,Gloskovskii Andrei3ORCID,Nilsson Anders1ORCID

Affiliation:

1. Department of Physics Stockholm University AlbaNova University Center Roslagstullsbacken 21 114 21 Stockholm Sweden

2. Present Address: ALBA Synchrotron Light Facility Carrer de la Llum 2, 26 08290 Cerdanyola del Vallés Spain

3. Deutsches Elektronen Synchrotron DESY Notkestraße 85 226 07 Hamburg Germany

Abstract

AbstractOperando probing by x‐ray photoelectron spectroscopy (XPS) of certain hydrogenation reactions are often limited by the scattering of photoelectrons in the gas phase. This work describes a method designed to partially circumvent this so called pressure gap. By performing a rapid switch from a high pressure (where acquisition is impossible) to a lower pressure we can for a short while probe a “remnant” of the high pressure surface as well as the time dynamics during the re‐equilibration to the new pressure. This methodology is demonstrated using the CO2 and the CO hydrogenation reaction over Rh(211). In the CO2 hydrogenation reaction, the remnant surface of a 2 bar pressure shows an adsorbate distribution which favors chemisorbed CHx adsorbates over chemisorbed CO. This contrasts against previous static operando spectra acquired at lower pressures. Furthermore, the pressure jumping method yields a faster acquisition and more detailed spectra than static operando measurements above 1 bar. In the CO hydrogenation reaction, we observe that CHx accumulated faster during the 275 mbar low pressure regime, and different hypotheses are presented regarding this observation.

Funder

Knut och Alice Wallenbergs Stiftelse

Vetenskapsrådet

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,Atomic and Molecular Physics, and Optics

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