4.7 Article

Catalytic decomposition of hydrous hydrazine to hydrogen over oxide catalysts at ambient conditions for PEMFCs

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 37, Issue 1, Pages 1133-1139

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2011.02.076

Keywords

Hydrous hydrazine; Catalytic activity; Hydrogen selectivity; Proton exchange membrane fuel cells

Funding

  1. National Natural Science Foundation of China [20703024]
  2. National Basic Research Program of China [2007CB209704]
  3. Outstanding Young Scholar Grant at Jiangsu Province [2008023]
  4. program for New Century Excellent Talents
  5. Fok Ying Tung Education Foundation [111073]

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Hydrous hydrazine is a hydrogen carrier in liquid state at room temperature, having high hydrogen content, and free of CO and other carbon-containing gases. In this study, the effects of oxides properties on the initial catalytic activity towards hydrous hydrazine decomposition as hydrogen source for proton exchange membrane fuel cells (PEMFCs) were systematically investigated. The results showed that the perovskite structure, cobalt ion and oxygen nonstoichiometry of oxides have important influence on the catalytic decomposition of hydrous hydrazine. The hydrogen selectivity of Ba0.5Sr0.5Co0.8Fe0.2O3 (-)delta (BSCF), SrCoO3-delta (SC) and La0.2Sr0.8CoO3-delta (LSC2) catalysts with KOH promoter for hydrous hydrazine decomposition was compared at 55 C, which indicated that hydrogen selectivity of BSCF and LSC2 could reach 100%. The performance of a PEMFC operating on the decomposition products from hydrous hydrazine was also studied and compared with that operating on pure hydrogen. The cell delivered a peak power density of 510 mW cm(-2) at 50 degrees C by operating on the gaseous decomposition products of hydrous hydrazine, which was only slightly lower than that of a similar cell with pure hydrogen as fuel, due to the diluting effect of nitrogen. It highly promises hydrous hydrazine as a indirect fuel of PEMFCs for portable application. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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