Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-11-14T17:57:01.123Z Has data issue: false hasContentIssue false

Advance in Nanostructural Electrochemical Reactors for NOX Treatment in the Presence of Oxygen.

Published online by Cambridge University Press:  01 February 2011

Koichi Hamamoto
Affiliation:
Advanced Manufacturing Research Institute, AIST, Shimo-Shidami, Moriyama-ku, Nagoya 463–8687, Japan
Yoshinobu Fujishiro
Affiliation:
Advanced Manufacturing Research Institute, AIST, Shimo-Shidami, Moriyama-ku, Nagoya 463–8687, Japan
Masanobu Awano
Affiliation:
Advanced Manufacturing Research Institute, AIST, Shimo-Shidami, Moriyama-ku, Nagoya 463–8687, Japan
Shingo Katayama
Affiliation:
Synergy Ceramics Laboratory, FCRA, Shimo-Shidami, Moriyama-ku, Nagoya 463–8687, Japan
Sergei Bredikhin
Affiliation:
Institute of Solid State Physics Russian Academy of Science, 142432 Chernogolovka, Russia
Get access

Abstract

Dramatic improvement in the selective separation and purification of NOX in exhaust gases by an electrochemical reactor with a catalytic electrode has been achieved. The novel electrochemical cells for NOX decomposition were developed by nano-scale control of penetrating pores from the catalytic electrode surface to the bottom of the catalytic electrode layer. The penetration pores and nano-size Ni grains are self-assembled at NiO/YSZ interfaces in the catalytic electrode by oxidization-reduction reaction of the NiO during the cell operation. In order to use reduced Ni for NOX decomposition reaction efficiently, we successfully designed a functional multilayer catalytic electrode. By multilayering of the catalytic electrode, adsorption and decomposition of coexisting oxygen in exhaust gases was suppressed and the selectivity of NOX decomposition reaction is improved. Structural change of the catalytic electrode as a result of the electrochemical processes was investigated and correlated with the NO decomposition properties of the cell.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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

REFERENCES

1. Lerdau, Manuel T., William Munger, J., and Jacob, Daniel J., Science 289, 22912293 (2000).Google Scholar
2. Finlayson-Pitts, Barbara J. and Pitts, James N. Jr, Science 276, 10451051 (1997).Google Scholar
3. Pancharatnam, S., Huggins, R.A., Mason, D.M., J. Electrochem. Soc. 122, 1067 (1975).Google Scholar
4. Gur, T.M., Huggins, R.A., J. Electrochem. Soc. 126, 869 (1979).Google Scholar
5. Hibino, T., Chem.Lett. 5, 927931 (1994).Google Scholar
6. Nakatani, J., Ozeki, Y., Sakamoto, K., Iwayama, K., Chem. Lett., 4, 315319 (1996).Google Scholar
7. Washman, Eric D., Palitha Jayaweera, Gopala Krishnan, Angel Sanjurjo, Solid State Ionics 136–137, 775782 (2000).Google Scholar
8. Bredikhin, S., Maeda, K. and Awano, M., Journal of Ionics, 7, 109115 (2001).Google Scholar
9. Bredikhin, S., Maeda, K. and Awano, M., Solid State Ionics 144, 19 (2001).Google Scholar
10. Bredikhin, S., Maeda, K. and Awano, M., Journal of the Electrochemical Society 148, D133D138, (10) (2001).Google Scholar
11. Matsuda, K., Bredikhin, S., Maeda, K. and Awano, M., Solid State Ionics, 156, 223231 (2003).Google Scholar
12. Bredikhin, S., Matsuda, K., Maeda, K. and Awano, M., Solid State Ionics 149, 327333 (2002).Google Scholar
13. Lindsay, R., Theobald, A., Gieβel, T., Schaff, O., Bradshaw, A. M., Booth, N. A. and Woodruff, D. P., Surface Science 405, L566L572 (1998).Google Scholar
14. Rickardsson, I., Jönsson, L. and Nyberg, C., Surface Science 414, 389395 (1998).Google Scholar