TY - JOUR
T1 - Fabrication of bilayered YSZ/SDC electrolyte film by electrophoretic deposition for reduced-temperature operating anode-supported SOFC
AU - Matsuda, Motohide
AU - Hosomi, Takushi
AU - Murata, Kenji
AU - Fukui, Takehisa
AU - Miyake, Michihiro
N1 - Funding Information:
This work was supported financially by a Grant-in-Aid for Scientific Research (B) (No. 16360331) from the Japan Society for the Promotion of Science (JSPS). This work was also supported in part by a Grant-in-Aid for Scientific Research (B) (No. 17350101) from JSPS and by the Okayama University 21st Century COE Program.
PY - 2007/2/25
Y1 - 2007/2/25
N2 - Bilayered Y2O3-stabilized ZrO2 (YSZ)/Sm2O3-doped CeO2 (SDC) electrolyte films were successfully fabricated on porous NiO-YSZ composite substrates by electrophoretic deposition (EPD) based on electrophoretic filtration followed by co-firing with the substrates. In EPD, positively charged YSZ and SDC powders were deposited directly on the substrates, layer by layer from ethanol-based suspensions. Delamination between YSZ and SDC films was avoided by reducing the SDC films' thickness to ca. 1 μm. A single cell was constructed on the bilayered electrolyte films composed of ca. 4 μm-thick YSZ and ca. 1 μm-thick SDC films. As a cathode in the cell, La0.6Sr0.4Co0.2Fe0.8O3-x (LSCF) was used. Maximum output power densities greater than 0.6 W cm-2 were obtained at 700 °C for the bilayered YSZ/SDC electrolyte cells thus constructed.
AB - Bilayered Y2O3-stabilized ZrO2 (YSZ)/Sm2O3-doped CeO2 (SDC) electrolyte films were successfully fabricated on porous NiO-YSZ composite substrates by electrophoretic deposition (EPD) based on electrophoretic filtration followed by co-firing with the substrates. In EPD, positively charged YSZ and SDC powders were deposited directly on the substrates, layer by layer from ethanol-based suspensions. Delamination between YSZ and SDC films was avoided by reducing the SDC films' thickness to ca. 1 μm. A single cell was constructed on the bilayered electrolyte films composed of ca. 4 μm-thick YSZ and ca. 1 μm-thick SDC films. As a cathode in the cell, La0.6Sr0.4Co0.2Fe0.8O3-x (LSCF) was used. Maximum output power densities greater than 0.6 W cm-2 were obtained at 700 °C for the bilayered YSZ/SDC electrolyte cells thus constructed.
KW - Ceramic processing
KW - Electrolyte film
KW - Electrophoretic deposition
KW - Solid oxide fuel cell
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U2 - 10.1016/j.jpowsour.2006.11.087
DO - 10.1016/j.jpowsour.2006.11.087
M3 - Article
AN - SCOPUS:33846811548
VL - 165
SP - 102
EP - 107
JO - Journal of Power Sources
JF - Journal of Power Sources
SN - 0378-7753
IS - 1
ER -