TY - JOUR
T1 - Electrodeposited Pd-Co catalyst for direct methanol fuel cell electrodes
T2 - Preparation and characterization
AU - Tominaka, Satoshi
AU - Momma, Toshiyuki
AU - Osaka, Tetsuya
N1 - Funding Information:
We thank H. Obata, S. Ohta, T. Aida, and S. Enomoto for technical supports for the measurements. This work was partly supported by Encouraging Development Strategic Research Centers Program “Establishment of Consolidated Research Institute for Advanced Science and Medical Care” from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, and partly carried out at the Global COE program of MEXT “Center for Practical Chemical Wisdom”.
PY - 2008/5/30
Y1 - 2008/5/30
N2 - Pd-Co alloy has been recently proposed as a catalyst for the cathode of direct methanol fuel cells with both excellent oxygen reduction activity and methanol tolerance, hence electrodeposition of this alloy is an attractive approach for synthesizing porous metal electrodes with high methanol tolerance in direct methanol fuel cells. In this study, we electrodeposited two types of Pd-Co films onto Au substrates by applying different current density (-10 or -200 mA cm-2); and then characterized them in terms of morphology, composition, crystal structure, and catalytic activity. Pd-Co deposited at -10 mA cm-2 was smooth and possessed smaller particles (ca. 10 nm), while that at -200 mA cm-2 was dendritic (or rough) and possessed larger particles (ca. 50 nm). Both the Pd-Co alloys were found to be almost the same structure, i.e. a solid solution of ca. Pd7Co3 with Pd-skin, and also confirmed to possess comparable activity in oxygen reduction to Pt (potential difference at 1.0 μA cm-2 was 0.05 V). As for methanol tolerance, cell-voltage was not influenced by addition of 1 mol dm-3 methanol to the oxidant solution. Our approach provides fundamental technique for synthesizing Pd-Co porous metal electrodes by electrodeposition.
AB - Pd-Co alloy has been recently proposed as a catalyst for the cathode of direct methanol fuel cells with both excellent oxygen reduction activity and methanol tolerance, hence electrodeposition of this alloy is an attractive approach for synthesizing porous metal electrodes with high methanol tolerance in direct methanol fuel cells. In this study, we electrodeposited two types of Pd-Co films onto Au substrates by applying different current density (-10 or -200 mA cm-2); and then characterized them in terms of morphology, composition, crystal structure, and catalytic activity. Pd-Co deposited at -10 mA cm-2 was smooth and possessed smaller particles (ca. 10 nm), while that at -200 mA cm-2 was dendritic (or rough) and possessed larger particles (ca. 50 nm). Both the Pd-Co alloys were found to be almost the same structure, i.e. a solid solution of ca. Pd7Co3 with Pd-skin, and also confirmed to possess comparable activity in oxygen reduction to Pt (potential difference at 1.0 μA cm-2 was 0.05 V). As for methanol tolerance, cell-voltage was not influenced by addition of 1 mol dm-3 methanol to the oxidant solution. Our approach provides fundamental technique for synthesizing Pd-Co porous metal electrodes by electrodeposition.
KW - Direct methanol fuel cells
KW - Electrodeposition
KW - Methanol tolerance
KW - Oxygen reduction catalyst
KW - Pd-Co alloy
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U2 - 10.1016/j.electacta.2008.01.069
DO - 10.1016/j.electacta.2008.01.069
M3 - Article
AN - SCOPUS:41049106690
SN - 0013-4686
VL - 53
SP - 4679
EP - 4686
JO - Electrochimica Acta
JF - Electrochimica Acta
IS - 14
ER -