Abstract
Carbon-supported Pd catalysts (Pd/CBs) for oxygen reduction reaction (ORR) in polymer electrolyte fuel cells (PEFCs) were modified with transition metals to enhance their catalytic activity. Pd-M/CB(N) (M = Co, Cu, Y, and Ag) was prepared by the reduction of metal precursors with NaBH4 in the presence of ethylene glycol (EG) without heat treatment. Pd-Ag/CB(N) showed the highest catalytic activity for the ORR among all the Pd-based catalysts tested in the present study, and it had twice higher activity than Pd/CB. The Pd-Ag/CB(N) also had the higher ORR activity than the Pd-Ag/CB prepared by a conventional impregnation method (Pd-Ag/CB(I)) due to the formation of smaller Pd-Ag alloy particles with 1–2 nm diameters. Pd-Ag/CB(N) was covered with silica layers (SiO2/Pd-Ag/CB(N)) in order to improve their durability under severe cathode conditions. The SiO2/Pd-Ag/CB(N) had high catalytic activity for the ORR during the durability test because silica layers prevented the diffusion of metal species from the catalysts.
| Original language | English |
|---|---|
| Pages (from-to) | 18951-18958 |
| Number of pages | 8 |
| Journal | International Journal of Hydrogen Energy |
| Volume | 42 |
| Issue number | 30 |
| DOIs | |
| Publication status | Published - Jul 27 2017 |
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All Science Journal Classification (ASJC) codes
- Renewable Energy, Sustainability and the Environment
- Fuel Technology
- Condensed Matter Physics
- Energy Engineering and Power Technology
Cite this
Carbon-supported Pd-Ag catalysts with silica-coating layers as active and durable cathode catalysts for polymer electrolyte fuel cells. / Park, Kayoung; Matsune, Hideki; Kishida, Masahiro; Takenaka, Sakae.
In: International Journal of Hydrogen Energy, Vol. 42, No. 30, 27.07.2017, p. 18951-18958.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Carbon-supported Pd-Ag catalysts with silica-coating layers as active and durable cathode catalysts for polymer electrolyte fuel cells
AU - Park, Kayoung
AU - Matsune, Hideki
AU - Kishida, Masahiro
AU - Takenaka, Sakae
PY - 2017/7/27
Y1 - 2017/7/27
N2 - Carbon-supported Pd catalysts (Pd/CBs) for oxygen reduction reaction (ORR) in polymer electrolyte fuel cells (PEFCs) were modified with transition metals to enhance their catalytic activity. Pd-M/CB(N) (M = Co, Cu, Y, and Ag) was prepared by the reduction of metal precursors with NaBH4 in the presence of ethylene glycol (EG) without heat treatment. Pd-Ag/CB(N) showed the highest catalytic activity for the ORR among all the Pd-based catalysts tested in the present study, and it had twice higher activity than Pd/CB. The Pd-Ag/CB(N) also had the higher ORR activity than the Pd-Ag/CB prepared by a conventional impregnation method (Pd-Ag/CB(I)) due to the formation of smaller Pd-Ag alloy particles with 1–2 nm diameters. Pd-Ag/CB(N) was covered with silica layers (SiO2/Pd-Ag/CB(N)) in order to improve their durability under severe cathode conditions. The SiO2/Pd-Ag/CB(N) had high catalytic activity for the ORR during the durability test because silica layers prevented the diffusion of metal species from the catalysts.
AB - Carbon-supported Pd catalysts (Pd/CBs) for oxygen reduction reaction (ORR) in polymer electrolyte fuel cells (PEFCs) were modified with transition metals to enhance their catalytic activity. Pd-M/CB(N) (M = Co, Cu, Y, and Ag) was prepared by the reduction of metal precursors with NaBH4 in the presence of ethylene glycol (EG) without heat treatment. Pd-Ag/CB(N) showed the highest catalytic activity for the ORR among all the Pd-based catalysts tested in the present study, and it had twice higher activity than Pd/CB. The Pd-Ag/CB(N) also had the higher ORR activity than the Pd-Ag/CB prepared by a conventional impregnation method (Pd-Ag/CB(I)) due to the formation of smaller Pd-Ag alloy particles with 1–2 nm diameters. Pd-Ag/CB(N) was covered with silica layers (SiO2/Pd-Ag/CB(N)) in order to improve their durability under severe cathode conditions. The SiO2/Pd-Ag/CB(N) had high catalytic activity for the ORR during the durability test because silica layers prevented the diffusion of metal species from the catalysts.
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U2 - 10.1016/j.ijhydene.2017.06.046
DO - 10.1016/j.ijhydene.2017.06.046
M3 - Article
AN - SCOPUS:85021353642
VL - 42
SP - 18951
EP - 18958
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
SN - 0360-3199
IS - 30
ER -