Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-09T08:44:39.559Z Has data issue: false hasContentIssue false

Microstructure and Activity of Thin Films for a Microelectronic Gas Sensor

Published online by Cambridge University Press:  15 February 2011

Sanjay V. Patel
Affiliation:
Departments of Chemical Engineering University of Michigan, Ann Arbor, MI 48190-2136, [email protected].
Michael Dibattistam
Affiliation:
Departments of Chemical Engineering University of Michigan, Ann Arbor, MI 48190-2136, [email protected].
John L. Gland
Affiliation:
Departments of Chemical Engineering Chemistryt University of Michigan, Ann Arbor, MI 48190-2136, [email protected].
Johannes W. Schwank
Affiliation:
Departments of Chemical Engineering University of Michigan, Ann Arbor, MI 48190-2136, [email protected].
Get access

Abstract

Scanning force microscopy is used to study the structure of various sensing films after chemical and thermal treatments. An example chemical modification of the sensing film can be achieved by heating a Pt/Ti sensing film in an oxygen environment. 1 With Pt acting as a catalyst, the Ti can become partially oxidized, resulting in a Pt/TiOx film which has different electronic properties than a metallic film. By further oxidizing the film, an insulating layer of TiO2 may be achieved. Or as in the case of hydrogen sensing, the Pt/TiOx film may revert to a more metallic state via the reduction of TiOx. The chemical interactions of these sensing films may be associated with large scale microstructural changes. The sensing activity and the structure of Ti, Pt/Ti, and Au/Ti films to gases such as hydrogen, and propylene has been studied. These chemical and morphological changes can be monitored by measuring the resistance of the thin sensing films. Pt/Ti films were found to have the best response to hydrogen (200 ppm) and propylene (150 ppm), while Au/Ti films showed weaker response to propylene (500 ppm) and CO (1000 ppm). The Pt/Ti films also showed shifts in temperature with changing propylene concentration possibly due to catalytic combustion.

Type
Research Article
Copyright
Copyright © Materials Research Society 1996

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

[1] Park, K. H., Kim, C. Y., Jeong, Y. W., Kwon, H. J., Kim, K. Y., Lee, J. S., and Kim, S. T., J. Mater. Res. 10, No. 7, (1995), pp. 1790-94.Google Scholar
[2] Johnson, C. L., Ph. D. Dissertation, The University of Michigan (1990), pp. 22-33.Google Scholar
[3] Johnson, C. L., Schwank, J. W., and Wise, K. D., U.S. Patent 4,935,387 (Sept. 4, 1990).Google Scholar