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Chemical waves in the O2 + H2 reaction on a Rh(111) surface alloyed with nickel. II. Photoelectron spectroscopy and microscopy.

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Název: Chemical waves in the O2 + H2 reaction on a Rh(111) surface alloyed with nickel. II. Photoelectron spectroscopy and microscopy.
Autoři: Smolinsky, Tim, Homann, Mathias, von Boehn, Bernhard, Gregoratti, Luca, Amati, Matteo, Al-Hada, Mohamed, Sezen, Hikmet, Imbihl, Ronald
Zdroj: Journal of Chemical Physics; 4/21/2018, Vol. 148 Issue 15, p1-12, 12p
Témata: CHEMICAL reactions, RHODIUM, OXYGEN, HYDROGEN, NICKEL, PHASE separation, MICROSCOPY, PHOTOELECTRON spectroscopy
Abstrakt: Chemical waves in the H2 + O2 reaction on a Rh(111) surface alloyed with Ni [ ΘNi < 1.5 monolayers (ML)] have been investigated in the 10-7 and 10-6 mbar range at T = 773 K using scanning photoelectron microscopy and x-ray photoelectron spectroscopy as in situ methods. The local intensity variations of the O 1s and the Ni 2p signal display an anticorrelated behavior. The coincidence of a high oxygen signal with a low Ni 2p intensity, which seemingly contradicts the chemical attraction between O and Ni, has been explained with a phase separation of the oxygen covered Rh(111)/Ni surface into a 3D-Ni oxide and into a Ni poor metallic phase. Macroscopic NiO islands (≈1 μm size) formed under reaction conditions have been identified as 2D-Ni oxide. Titration experiments of the oxygen covered Rh(111)/Ni surface with H2 demonstrated that the reactivity of oxygen is decreased by an order of magnitude through the addition of 0.6 ML Ni. An excitation mechanism is proposed in which the periodic formation and reduction of NiO modulate the catalytic activity. [ABSTRACT FROM AUTHOR]
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Abstrakt:Chemical waves in the H<subscript>2</subscript> + O<subscript>2</subscript> reaction on a Rh(111) surface alloyed with Ni [ Θ<subscript>Ni</subscript> < 1.5 monolayers (ML)] have been investigated in the 10<sup>-7</sup> and 10<sup>-6</sup> mbar range at T = 773 K using scanning photoelectron microscopy and x-ray photoelectron spectroscopy as in situ methods. The local intensity variations of the O 1s and the Ni 2p signal display an anticorrelated behavior. The coincidence of a high oxygen signal with a low Ni 2p intensity, which seemingly contradicts the chemical attraction between O and Ni, has been explained with a phase separation of the oxygen covered Rh(111)/Ni surface into a 3D-Ni oxide and into a Ni poor metallic phase. Macroscopic NiO islands (≈1 μm size) formed under reaction conditions have been identified as 2D-Ni oxide. Titration experiments of the oxygen covered Rh(111)/Ni surface with H<subscript>2</subscript> demonstrated that the reactivity of oxygen is decreased by an order of magnitude through the addition of 0.6 ML Ni. An excitation mechanism is proposed in which the periodic formation and reduction of NiO modulate the catalytic activity. [ABSTRACT FROM AUTHOR]
ISSN:00219606
DOI:10.1063/1.5020372