TY - JOUR
T1 - Initialization of a methane-fueled single-chamber solid-oxide fuel cell with NiO + SDC anode and BSCF + SDC cathode
AU - Zhang, Chunming
AU - Zheng, Yao
AU - Ran, Ran
AU - Shao, Zongping
AU - Jin, Wanqin
AU - Xu, Nanping
AU - Ahn, Jeongmin
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China under contract, Nos. 20646002 and 20676061, and National Basic Research Program of China under contract No. 2007CB209704.
PY - 2008/5/1
Y1 - 2008/5/1
N2 - The initialization of an anode-supported single-chamber solid-oxide fuel cell, with NiO + Sm0.2Ce0.8O1.9 anode and Ba0.5Sr0.5Co0.8Fe0.2O3-δ + Sm0.2Ce0.8O1.9 cathode, was investigated. The initialization process had significant impact on the observed performance of the fuel cell. The in situ reduction of the anode by a methane-air mixture failed. Although pure methane did reduce the nickel oxide, it also resulted in severe carbon coking over the anode and serious distortion of the fuel cell. In situ initialization by hydrogen led to simultaneous reduction of both the anode and cathode; however, the cell still delivered a maximum power density of ∼350 mW cm-2, attributed to the re-formation of the BSCF phase under the methane-air atmosphere at high temperatures. The ex situ reduction method appeared to be the most promising. The activated fuel cell showed a peak power density of ∼570 mW cm-2 at a furnace temperature of 600 °C, with the main polarization resistance contributed from the electrolyte.
AB - The initialization of an anode-supported single-chamber solid-oxide fuel cell, with NiO + Sm0.2Ce0.8O1.9 anode and Ba0.5Sr0.5Co0.8Fe0.2O3-δ + Sm0.2Ce0.8O1.9 cathode, was investigated. The initialization process had significant impact on the observed performance of the fuel cell. The in situ reduction of the anode by a methane-air mixture failed. Although pure methane did reduce the nickel oxide, it also resulted in severe carbon coking over the anode and serious distortion of the fuel cell. In situ initialization by hydrogen led to simultaneous reduction of both the anode and cathode; however, the cell still delivered a maximum power density of ∼350 mW cm-2, attributed to the re-formation of the BSCF phase under the methane-air atmosphere at high temperatures. The ex situ reduction method appeared to be the most promising. The activated fuel cell showed a peak power density of ∼570 mW cm-2 at a furnace temperature of 600 °C, with the main polarization resistance contributed from the electrolyte.
KW - BaSrCoFeO
KW - Methane
KW - Single chamber
KW - Solid-oxide fuel cell (SOFC)
UR - http://www.scopus.com/inward/record.url?scp=40849130021&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=40849130021&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2008.01.030
DO - 10.1016/j.jpowsour.2008.01.030
M3 - Article
AN - SCOPUS:40849130021
SN - 0378-7753
VL - 179
SP - 640
EP - 648
JO - Journal of Power Sources
JF - Journal of Power Sources
IS - 2
ER -