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High-pressure X-ray photoelectron spectroscopy of palladium model hydrogenation catalysts. Part 1: Effect of gas ambient and temperature

MPS-Authors
/persons/resource/persons22163

Teschner,  Detre
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21951

Pestryakov,  Alexeij
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21730

Kleimenov,  Evgueni
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21590

Hävecker,  Michael
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21376

Bluhm,  Hendrik
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22051

Sauer,  Hermann
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21743

Knop-Gericke,  Axel
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22071

Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Teschner, D., Pestryakov, A., Kleimenov, E., Hävecker, M., Bluhm, H., Sauer, H., et al. (2005). High-pressure X-ray photoelectron spectroscopy of palladium model hydrogenation catalysts. Part 1: Effect of gas ambient and temperature. Journal of Catalysis, 230(1), 186-194. doi:10.1016/j.jcat.2004.11.036.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-0A22-7
Abstract
In light of accumulating evidence highlighting the major effect of operational conditions (gas composition, pressure, temperature) on the surface/bulk structure of catalytic materials, their characterization should involve more and more in situ methods. We constructed a synchrotron-based high-pressure X-ray photoelectron spectroscopic (XPS) instrument, allowing us to investigate the surface and near-surface state of a catalyst in the mbar pressure range. We discuss here the surface characteristics of palladium samples as a function of gas phase (hydrogen, oxygen) and temperature. We demonstrate that the surface region of catalytic materials behaves dynamically in its composition,
always reflecting its environment. For example, surface oxide can be formed on Pd(111) in oxygen, which decomposes rapidly when the gas supply is switched off. The chemical nature of carbonaceous deposits also depends strongly on the operational conditions (gas-phase hydrogen, temperature). This is the first time that an XPS investigation of palladium β-hydride was performed at RT. The possible drawbacks of using a non-UHV setup (e.g., fast carbon accumulation) are also discussed.