Characterization of hydrogen generation for fuel cells via borane hydrolysis using an electroless-deposited Co–P/Ni foam catalyst
The effect of an electroless-deposited Co–P/Ni foam catalyst on H 2 generation kinetics in ammonia borane (NH 3BH 3) solution and the cyclic behaviour (durability) of the catalyst are investigated. The electroless-deposited Co–P is composed of an inner flat layer and outer layer that consists of an...
Saved in:
Published in: | Journal of power sources Vol. 195; no. 9; pp. 2830 - 2834 |
---|---|
Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
01-05-2010
Elsevier |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The effect of an electroless-deposited Co–P/Ni foam catalyst on H
2 generation kinetics in ammonia borane (NH
3BH
3) solution and the cyclic behaviour (durability) of the catalyst are investigated. The electroless-deposited Co–P is composed of an inner flat layer and outer layer that consists of an aggregate of spherical particles. The H
2 generation rate/projected area of the Co–P/Ni foam catalyst is much higher than that of a Co–P/Cu sheet catalyst. The activation energy (
E
a) for the hydrolysis of NH
3BH
3 using the Co–P/Ni foam catalyst is calculated to be 48
kJ
mol
−1. After the first cycle, the H
2 generation rate decreases dramatically, i.e., by 16%, due to a decrease in surface area caused by the partial separation of spherical Co–P particles. Between the first and sixth cycles, the H
2 generation rate decreases gradually (by 14%) on account of a decrease in the number of P atoms that create active metallic Co sites on catalytic surface. After six cycles, about 70% of the initial H
2 generation rate remains constant. The study reveals a promising means of hydrogen generation for polymer electrolyte membrane fuel cells. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2009.11.084 |