Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-29T07:46:35.180Z Has data issue: false hasContentIssue false

Microstructure and Hydrogen Absorption/Desorption Behavior of Nanoporous Pd Thin Films

Published online by Cambridge University Press:  01 February 2011

Wen-Chung Li
Affiliation:
[email protected], University of Kentucky, Chemical and Materials Engineering, 700 Woodland Ave. Apt. A-8, Lexington, KY, 40508, United States, 859-797-9539, 859-323-1929
Simone C. Schendel
Affiliation:
[email protected], University of Kentucky, Chemical and Materials Engineering, 177 F. Paul Anderson Tower, Lexington, KY, 40506-0046, United States
T. John Balk
Affiliation:
[email protected], University of Kentucky, Chemical and Materials Engineering, 177 F. Paul Anderson Tower, Lexington, KY, 40506-0046, United States
Get access

Abstract

Nanoporous Pd (np-Pd) prepared from Pd-Ni alloy films on Si substrates was studied to understand hydriding/dehydriding processes in nanoscale Pd. Porous structures of the np-Pd thin films can be changed under different dealloying conditions. Stress measurement of the np-Pd showed that the np-Pd thin films can survive hydrogen pressures from 0 to 1 atm with no blistering, although this problem often occurs in dense Pd films in actual, high-pressure hydrogen environments. These tests indicated that hydrogen atoms can be stored in the np-Pd for much longer times than in fully dense Pd films subjected to ambient conditions. It is proposed that the stress distribution in np-Pd and the small pore size (<10 nm) inhibit hydrogen diffusion to free surfaces and thus prevent hydrogen degassing from the nanoporous structure. Moreover, phase transformation of Pd hydrides and effect of hydrogen trapping are also considered as possible reasons for the slow release of hydrogen.

Keywords

Type
Research Article
Copyright
Copyright © Materials Research Society 2008

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] Berube, V., Radtke, G., Dresselhaus, M., and Chen, G., “Size effects on the hydrogen storage properties of nanostructured metal hydrides: A review,” International Journal of Energy Research, vol. 31, pp. 637663, May 2007.Google Scholar
[2] Dornheim, M., Eigen, N., Barkhordarian, G., Klassen, T., and Bormann, R., “Tailoring hydrogen storage materials towards application,” Advanced Engineering Materials, vol. 8, pp. 377385, May 2006.Google Scholar
[3] Seayad, A. M. and Antonelli, D. M., “Recent advances in hydrogen storage in metal-containing inorganic nanostructures and related materials,” Advanced Materials, vol. 16, pp. 765777, May 17 2004.Google Scholar
[4] Flanagan, T. B. and Oates, W. A., “The Palladium-Hydrogen System,” Annual Review of Materials Science, vol. 21, pp. 269304, 1991.Google Scholar
[5] Rather, S. U., Zacharia, R., Hwang, S. W., Naik, M. U., and Nahm, K. S., “Hyperstoichiometric hydrogen storage in monodispersed palladium nanoparticles,” Chemical Physics Letters, vol. 438, pp. 7884, Apr 11 2007.Google Scholar
[6] Sachs, C., Pundt, A., Kirchheim, R., Winter, M., Reetz, M. T., and Fritsch, D., “Solubility of hydrogen in single-sized palladium clusters,” Physical Review B, vol. 64, pp. -, Aug 15 2001.Google Scholar
[7] Erlebacher, J., “An atomistic description of dealloying - Porosity evolution, the critical potential, and rate-limiting behavior,” Journal of the Electrochemical Society, vol. 151, pp. C614–C626, 2004.Google Scholar
[8] Schirber, J. E. and Morosin, B., “Lattice-Constants of Beta-Pdhx and Beta-Pddx with X near 1.0,” Physical Review B, vol. 12, pp. 117118, 1975.Google Scholar
[9] Krenn, C. R., “Continuum modelling of transformation hysteresis in a metal hydride system,” Modelling and Simulation in Materials Science and Engineering, vol. 12, pp. S415–S424, Jul 2004.Google Scholar