Title of article :
Physically mixed LiLaNi–Al2O3 and copper as conductive anode catalysts in a solid oxide fuel cell for methane internal reforming and partial oxidation
Author/Authors :
Wang، نويسنده , , Wei and Su، نويسنده , , Chao and Ran، نويسنده , , Ran and Park، نويسنده , , Hee Jung and Kwak، نويسنده , , Chan and Shao، نويسنده , , Zongping، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
12
From page :
5632
To page :
5643
Abstract :
Different concentrations of copper are added to LiLaNi–Al2O3 to improve the electronic conductivity property for application as the materials of the anode catalyst layer for solid oxide fuel cells operating on methane. Their catalytic activity for the methane partial oxidation, steam and CO2 reforming reactions at 600–850 °C is systematically investigated. Among the three catalysts, the LiLaNi–Al2O3/Cu (50:50, by weight) catalyst presents the best catalytic activity. Thus, the catalytic stability, carbon deposition and surface conductivity of the LiLaNi–Al2O3/Cu catalyst are further studied in detail. O2-TPO results indicate that the coking resistance of LiLaNi–Al2O3/Cu is satisfactory and comparable to that of LiLaNi–Al2O3. The surface conductivity tests demonstrate it is extremely improved for LiLaNi–Al2O3 catalyst due to the addition of 50 wt.% copper. A cell with LiLaNi–Al2O3/Cu (50:50) catalyst layer is operated on mixtures of methane–O2, methane–H2O and methane–CO2, and peak power densities of 1081, 1036 and 988 mW cm−2 are obtained at 850 °C, respectively, comparable to the cell with LiLaNi–Al2O3 catalyst layer. In summary, the results of the present study indicate that LiLaNi–Al2O3/Cu (50:50) catalysts are highly coking resistant and conductive catalyst layers for solid oxide fuel cells.
Keywords :
Carbon deposition , Surface conductivity , solid oxide fuel cells , catalyst layer , Methane
Journal title :
International Journal of Hydrogen Energy
Serial Year :
2011
Journal title :
International Journal of Hydrogen Energy
Record number :
1665492
Link To Document :
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