4.7 Article

Combustion-synthesized Ru-Al2O3 composites as anode catalyst layer of a solid oxide fuel cell operating on methane

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 36, Issue 1, Pages 755-764

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2010.09.048

Keywords

Solid-oxide fuel cells; Ruthenium-alumina; Catalyst layer; Methane; Carbon deposition

Funding

  1. National Natural Science Foundation of China [20676061, 20703024]
  2. National 863 Program [2007AA05Z133]
  3. National Basic Research Program of China [2007CB209704]

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Ru-Al2O3 composites with varied Ru contents were synthesized by a glycine nitrate combustion technique. Their potential application as anode catalyst functional layer of a solid oxide fuel cell operating on methane fuel was investigated. Catalytic tests demonstrated the 3-7 wt.% Ru-Al2O3 composites had high catalytic activity for methane partial oxidation and CO2/H2O reforming reactions, while 1 wt.% Ru-Al2O3 had insufficient activity. The 3 wt.% Ru-Al2O3 catalyst also showed excellent operation stability and good thermal mechanical compatibility with Ni-YSZ anode. H-2-TPR and TEM results indicated there was strong interaction between RuOx and Al2O3 in the as-synthesized catalysts, which may account for the good catalytic stability of 3 wt.% Ru-Al2O3 catalyst. O-2-TPO results demonstrated Ru-Al2O3 also had excellent coking resistance. Furthermore, the carbon deposited over Ru-Al2O3 had lower graphitization degree than that deposited over Ni-Al2O3, suggesting the easier elimination of potential carbon deposited over the Ru-Al2O3 catalysts. A cell with 3 wt.% Ru-Al2O3 catalyst functional layer was prepared, wh-ich delivered peak power densities of 1006, 952 and 929 mW cm(-2) at 850 degrees C, operating on methane-O-2, methane-H2O and methane-CO2 gas mixtures, respectively, comparable to that operating on hydrogen fuel. It highly promised 3 wt.% Ru-Al2O3 as a coking resistant catalyst layer for solid oxide fuel cells. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.

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