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An Ex-SituReactor with Anaerobic Specimen Transfer Capabilities for TEM Studies of Reactive (Catalyst) Specimens

Published online by Cambridge University Press:  02 July 2020

L. F. Allard
Affiliation:
High Temperature Materials Laboratory, Oak Ridge National Laboratory, Oak Ridge, TN
K. S. Ailey
Affiliation:
High Temperature Materials Laboratory, Oak Ridge National Laboratory, Oak Ridge, TN
A. K. Datye
Affiliation:
Dept. of Chemical and Nuclear Engineering, University of New Mexico, Albuquerque, NM
W. C. Bigelow
Affiliation:
Dept. of Materials Science and Engineering, University of Michigan, Ann Arbor, MI
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Extract

The optimization of currently available catalysts and the development of new ones requires a detailed understanding of the effects of both microstructure and composition on their function. Previous work has demonstrated that information at the atomic-scale on heterogeneous catalysts can be derived using high resolution transmission electron microscopy (TEM). Under favorable conditions, the morphology of heavy metal catalytic particles can be related to catalytic activity. It has been shown that preoxidation can disrupt the surface of small metal particles causing altered activity and selectivity in reactions such as alkane hydrogenolysis. Metals such as Pt, Rh, or Ru are noble and pick up no more than a monolayer of oxygen when exposed to air during sample preparation for microscopy. This oxygen monolayer is not imaged in the microscope, most likely because the oxygen desorbs during exposure to the high energy electron beam. However, when metals such as Fe, Co, Ni, Pd or Cu are exposed to air, there is a corrosive interaction that alters particle structure quite dramatically.

Type
In Situ Studies in Microscopy
Copyright
Copyright © Microscopy Society of America 1997

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References

1. Research sponsored by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory, managed for the Department of Energy by Lockheed Martin Energy Research Corp., under contract DE-AC05-96OR22464.Google Scholar