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Model studies on heterogeneous catalysts at the atomic scale: From supported metal particles to two-dimensional zeolites

MPS-Authors
http://pubman.mpdl.mpg.de/cone/persons/resource/persons21524

Freund,  Hans-Joachim
Chemical Physics, Fritz Haber Institute, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons21628

Heyde,  Markus
Chemical Physics, Fritz Haber Institute, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons21916

Nilius,  Niklas
Chemical Physics, Fritz Haber Institute, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons22062

Schauermann,  Swetlana
Chemical Physics, Fritz Haber Institute, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons22106

Shaikhutdinov,  Shamil K.
Chemical Physics, Fritz Haber Institute, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons22140

Sterrer,  Martin
Chemical Physics, Fritz Haber Institute, Max Planck Society;

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JCatal.pdf
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Citation

Freund, H.-J., Heyde, M., Nilius, N., Schauermann, S., Shaikhutdinov, S. K., & Sterrer, M. (2013). Model studies on heterogeneous catalysts at the atomic scale: From supported metal particles to two-dimensional zeolites. Journal of Catalysis, 308, 154-167. doi:10.1016/j.jcat.2013.06.007.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0014-61C5-0
Abstract
After a general introduction to model studies in catalysis, results from different research areas are presented: (a) adsorption and reaction on nanoparticles supported on thin oxide films. It is shown that carbonaceous deposits on specific nanoparticle sites influence hydrogenation reactions through control of hydrogen surface–subsurface diffusion. (b) 2D-3D-morphology, geometric, and electronic structure of supported metal nanoparticles partially in relation to doping of the support. We learn how dopants, as electron sources, even if they are well beneath the active surface influence nanoparticle morphology on surfaces. (c) Strong metal–support interaction (SMSI). Ultrathin oxide films are proven to become chemically active in CO oxidation as they form on deposited nanoparticles dependent on the oxygen chemical potential in the gas phase. (d) Adsorption and reaction on two-dimensional silicates and alumino silicates in ordered and vitreous phases. Bilayer silica films on Ru(0 0 0 1) are transformed by Al doping into 2D-aluminosilicates and shown to exhibit binding hydroxyl with an acidity close to 3D-zeolites, such as chabazite.