CPM Seminar
Scanning Tunneling Microscopy studies of model catalysts
Peter Thostrup
Department of Physics and Astronomy &
Interdisciplinary Nanoscience Center (iNANO) University of Aarhus
Data from well-controlled surface-science studies are routinely
being used to interpret and understand the behaviour of heterogeneous
catalysts. The so-called surface science approach is used to extrapolate
data obtained under ultrahigh vacuum (UHV) and at low temperature to
real industrial conditions, where catalytic reactions typically proceed
under elevated pressures and temperatures. While this approach has proven
successful in many cases, a number of recent studies seem to invalidate and
thus fundamentally undermine current practice. This on-going discussion has
led to the identification of a number of so-called gaps between surface
science and industrial catalysis, e.g. the pressure gap, the temperature
gap and the structure gap.
I will focus on the pressure gap and through example demonstrate both
qualitative and quantitative correspondence between studies performed under
UHV and elevated pressures, i.e. effectively bridge the pressure gap. The
low and high-pressure studies are performed using the same technique,
Scanning Tunneling Microscopy.
Heterogeneous catalysts typically consist of nano-sized metal
clusters supported on a metal oxide. Conventional wisdom reduced the
support material to a passive role whose only purpose is to maintain high
dispersion, thus maximizing the surface area, of the active part. Recent
studies however indicate that the support material plays an active role
in number of steps in the overall catalytic cycle. Much interest is thus
currently targeted at the chemistry of oxide surfaces.
I will discuss an important model system for low-temperature carbon
monoxide oxidation consisting of gold clusters supported on titanium dioxide
(TiO2). By the use of STM, we have unravelled a number of
important atomistic mechanisms for the interaction of water and dioxygen
with reduced TiO2.
Monday, December 5th 2005, 11:00
Ernest Rutherford Physics Building, R.E. Bell Conference Room (room 103)
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