Department of Physical Chemistry

Nanostructured Model Catalysts

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Thin Film Model Systems of Complex Oxides, Metal-Oxide Systems and Intermetallic Phases

This part of research is very unique as it exploits a characteristic facet of the NaCl structure, namely (001), to grow well-ordered thin films of oxides, metal-oxide and intermetallic-oxide films. The reason for preparation of such a system lies in the still existing pressure and material’s gap in catalysis, which is schematically shown below. In short, model systems (such as the discussed thin films) are necessary, since structurally highly complex materials employed in most technological applications can normally not be used in mechanistic studies of chemical or catalytical reactions. These materials usually exhibit structurally and electronically different sites with varying sizes and morphologies (“material’s gap”). To gain mechanistic insight, however, uniformity with respect to structure of active sites is required. The thin film model systems allow to bridge this gap, since they are well-ordered, but still complex enough to mimic technologically relevant materials. A second advantage lies in the ability to also bridge the so-called “pressure gap”, meaning that model systems can only be studied in pressure regimes (usually UHV conditions with p < 10-10 mbar) that are far away from those used in catalysis technology (bar-regime). Thin films can be studied under realistic conditions using a dedicated kientic microreactor setup. Generally, due to their high ordering and small film thicknesses, the films are perfect and dedicated samples for electron microscopy investigations.

Figure 1: Briding the materials and pressure gaps.
Figure 1: Briding the materials and pressure gaps.

The variety of systems that can be prepared is extraordinarily widespread and encompasses binary and more complex oxides, metal-oxide systems or intermetallic-oxide systems. Table 1 gives an overview just of oxidic materials that have recently been prepared, characterized and tested. Especially for the metal-oxide systems, the model systems unfolds its particular strenghts: it usually creates a large metal-oxide interface, which is particular useful in catalysis (see Research Area 3).

Figure 2: Prepratation process of the thin film model catalysts as well as exemplary transmission electron micrographs and results from catalytical testing.
Figure 2: Prepratation process of the thin film model catalysts as well as exemplary transmission electron micrographs and results from catalytical testing.
Table 1: Overview of pure oxidic thin films that have been prepared in the past.
Table 1: Overview of pure oxidic thin films that have been
prepared in the past.

 

References:

[1] Silicide formation on a Pt/SiO2 model catalyst studied by TEM, EELS, and EDXS
Wang, D.; Penner, S.; Su, D.; Rupprechter, G.; Hayek, K.; Schlögl, R., Journal of Catalysis 2003, 219 (2), 434-441
[2] Growth and stability of Ga2O3 nanospheres
Penner, S.; Klötzer, B.; Jenewein, B.; Klauser, F.; Liu, X.; Bertel, E., Thin Solid Films 2008, 516 (15), 4742-4749
[3] A New Preparation Pathway to Well-Defined In2O3 Nanoparticles at Low Substrate Temperatures
Lorenz, H.; Stöger-Pollach, M.; Schwarz, S.; Pfaller, K.; Klötzer, B.; Bernardi, J.; Penner, S., J. Phys. Chem. C 2008, 112 (4), 918-925
[4] The structure and composition of oxidized and reduced tungsten oxide thin films
Penner, S.; Liu, X.; Klötzer, B.; Klauser, F.; Jenewein, B.; Bertel, E., Thin Solid Films 2008, 516 (10), 2829-2836
[5] Growth and decomposition of aligned and ordered PdO nanoparticles
Penner, S.; Wang, D.; Jenewein, B.; Gabasch, H.; Klötzer, B.; Knop-Gericke, A.; Schlögl, R.; Hayek, K., J. Chem. Phys. 2006, 125 (9), 094703-
[6] Growth and structural stability of well-ordered PdZn alloy nanoparticles
Penner, S.; Jenewein, B.; Gabasch, .; Klötzer, B.; Wang, D.; Knop-Gericke, A.; Schlögl, R.; Hayek, K., J. Catal. 2006, 241 (1), 14-19
[7] The catalytic properties of thin film Pd-rich GaPd2 in methanol steam reforming
Mayr, L.; Lorenz, H.; Armbrüster, M.; Villaseca, S.; Luo, Y.; Cardoso, R.; Burkhardt, U.; Zemlyanov, D.; Haevecker, M.; Blume, R.; Knop-Gericke, A.; Klötzer, B.; Penner, S., J. Catal. 2014, 309, 231-240
[8] Metal–Support Interaction in Pt/VOx and Pd/VOx Systems: A Comparative (HR)TEM Study
Penner, S.; Stöger-Pollach, M.; Thalinger, R., Catal. Lett. 2014, 144 (1), 87-96