TY - JOUR
T1 - Mesoporous PdCo sponge-like nanostructure synthesized by electrodeposition and dealloying for oxygen reduction reaction
AU - Tominaka, Satoshi
AU - Hayashi, Tomoya
AU - Nakamura, Yusuke
AU - Osaka, Tetsuya
PY - 2010/9/14
Y1 - 2010/9/14
N2 - A mesoporous PdCo sponge-like nanostructure was successfully synthesized by the combination of electrodeposition and dealloying, and was evaluated as a catalyst for the oxygen reduction reaction of fuel cells. The synthesized film had a sponge-like mesoporosity consisting of 5-30 nm thick ligaments with pores of tens of nanometers. Its porosity was estimated to be ca. 62%, suggesting that the oxygen transport in the film was smooth. The resultant composition was Pd93Co7, whose crystalline phase was determined to be a solid solution of Pd92Co8 by X-ray diffractometry. This degree of alloying is known to induce the most desirable lattice contraction into a Pd catalyst for the oxygen reduction reaction. Actually, the mesoporous PdCo catalyst had a higher specific activity than the Pt catalyst in the potential range of <0.85 V vs. SHE, i.e., the potential range of interest for fuel cell operation. This fascinatingly higher catalytic activity was attributable to the preferable reaction mechanism, because the PdCo electrode had a lower Tafel slope (43 mV decade-1) than a typical Pt electrode (71 mV decade-1).
AB - A mesoporous PdCo sponge-like nanostructure was successfully synthesized by the combination of electrodeposition and dealloying, and was evaluated as a catalyst for the oxygen reduction reaction of fuel cells. The synthesized film had a sponge-like mesoporosity consisting of 5-30 nm thick ligaments with pores of tens of nanometers. Its porosity was estimated to be ca. 62%, suggesting that the oxygen transport in the film was smooth. The resultant composition was Pd93Co7, whose crystalline phase was determined to be a solid solution of Pd92Co8 by X-ray diffractometry. This degree of alloying is known to induce the most desirable lattice contraction into a Pd catalyst for the oxygen reduction reaction. Actually, the mesoporous PdCo catalyst had a higher specific activity than the Pt catalyst in the potential range of <0.85 V vs. SHE, i.e., the potential range of interest for fuel cell operation. This fascinatingly higher catalytic activity was attributable to the preferable reaction mechanism, because the PdCo electrode had a lower Tafel slope (43 mV decade-1) than a typical Pt electrode (71 mV decade-1).
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U2 - 10.1039/c0jm00973c
DO - 10.1039/c0jm00973c
M3 - Article
AN - SCOPUS:77955803278
SN - 0959-9428
VL - 20
SP - 7175
EP - 7182
JO - Journal of Materials Chemistry
JF - Journal of Materials Chemistry
IS - 34
ER -