TY - JOUR
T1 - Combustion-synthesized Ru-Al2O3 composites as anode catalyst layer of a solid oxide fuel cell operating on methane
AU - Wang, Wei
AU - Ran, Ran
AU - Shao, Zongping
PY - 2011/1
Y1 - 2011/1
N2 - 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-Al 2O3 catalyst. O2-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-Al 2O3 catalyst functional layer was prepared, wh-ich delivered peak power densities of 1006, 952 and 929 mW cm-2 at 850 °C, operating on methane-O2, 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.
AB - 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-Al 2O3 catalyst. O2-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-Al 2O3 catalyst functional layer was prepared, wh-ich delivered peak power densities of 1006, 952 and 929 mW cm-2 at 850 °C, operating on methane-O2, 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.
KW - Carbon deposition
KW - Catalyst layer
KW - Methane
KW - Ruthenium-alumina
KW - Solid-oxide fuel cells
UR - http://www.scopus.com/inward/record.url?scp=79251639210&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2010.09.048
DO - 10.1016/j.ijhydene.2010.09.048
M3 - 文章
AN - SCOPUS:79251639210
SN - 0360-3199
VL - 36
SP - 755
EP - 764
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 1
ER -