TY - JOUR
T1 - On the suitability of hydrous ruthenium oxide supports to enhance intrinsic proton conductivity in DMFC anodes
AU - Scheiba, F.
AU - Scholz, M.
AU - Cao, L.
AU - Schafranek, R.
AU - Roth, C.
AU - Cremers, C.
AU - Qiu, X.
AU - Stimming, U.
AU - Fuess, H.
PY - 2006/12
Y1 - 2006/12
N2 - Hydrous ruthenium oxides have been investigated as novel support materials for fuel cell electrocatalysts for use in DMFC applications. These oxides were chosen in particular due to their potential intrinsic proton conductivity. Pt nanoparticles have been deposited onto the new support, and the resulting catalysts characterized both structurally and electrochemically. The Pt nanoparticles are sized between 3-4 nm and are highly dispersed on the support. Transmission electron micrographs show that the individual Pt nanoparticles are covered by an amorphous coating layer - probably hydrous ruthenium oxide, in good agreement with the XPS data. Electrochemical measurements on model electrodes indicate that proton conductivity of the supporting material is strongly affected by interdiffusion of methanol. Nevertheless, initial tests on membrane electrode assemblies (MEAs) showed improved performance, particularly with respect to internal resistance, when compared to Pt-Ru black. The catalyst showed very high activity in CO stripping experiments performed on a full MEA, suggesting high catalyst utilization, despite the comparatively low Nafion® content used in the electrode layer.
AB - Hydrous ruthenium oxides have been investigated as novel support materials for fuel cell electrocatalysts for use in DMFC applications. These oxides were chosen in particular due to their potential intrinsic proton conductivity. Pt nanoparticles have been deposited onto the new support, and the resulting catalysts characterized both structurally and electrochemically. The Pt nanoparticles are sized between 3-4 nm and are highly dispersed on the support. Transmission electron micrographs show that the individual Pt nanoparticles are covered by an amorphous coating layer - probably hydrous ruthenium oxide, in good agreement with the XPS data. Electrochemical measurements on model electrodes indicate that proton conductivity of the supporting material is strongly affected by interdiffusion of methanol. Nevertheless, initial tests on membrane electrode assemblies (MEAs) showed improved performance, particularly with respect to internal resistance, when compared to Pt-Ru black. The catalyst showed very high activity in CO stripping experiments performed on a full MEA, suggesting high catalyst utilization, despite the comparatively low Nafion® content used in the electrode layer.
KW - DMFC
KW - Hydrous ruthenium oxide
KW - Intrinsic proton conductivity
KW - Percolation theory
KW - Support
KW - Three-phase boundary
UR - http://www.scopus.com/inward/record.url?scp=33846253666&partnerID=8YFLogxK
U2 - 10.1002/fuce.200500238
DO - 10.1002/fuce.200500238
M3 - Article
AN - SCOPUS:33846253666
SN - 1615-6846
VL - 6
SP - 439
EP - 446
JO - Fuel Cells
JF - Fuel Cells
IS - 6
ER -