Nanoporous PdCu alloys as highly active and methanol-tolerant oxygen reduction electrocatalysts

Nanoporous (NP) PdCu alloys with three different bimetallic ratios are fabricated by selectively dealloying PdCuAl ternary alloys in sulfuric acid solution. Electron microscopy and X-ray diffraction characterizations demonstrate that selective etching of Al from ternary PdCuAl source alloys in acid...

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Veröffentlicht in:International journal of hydrogen energy 2013-08, Vol.38 (24), p.10029-10038
Hauptverfasser: Zhang, Huan, Hao, Qin, Geng, Haoran, Xu, Caixia
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Sprache:eng
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Zusammenfassung:Nanoporous (NP) PdCu alloys with three different bimetallic ratios are fabricated by selectively dealloying PdCuAl ternary alloys in sulfuric acid solution. Electron microscopy and X-ray diffraction characterizations demonstrate that selective etching of Al from ternary PdCuAl source alloys in acid medium generates three-dimensional bicontinuous ligament-pore nanostructures with a single-phase face-centered-cubic crystalline structure. NP-PdCu alloys show superior electrocatalytic activity and structure stability toward oxygen reduction reaction (ORR) compared with the commercial Pt/C catalyst. The specific and mass activities for ORR follow the order of NP-Pd50Cu50 > NP-Pd75Cu25 > NP-Pd30Cu70 > Pt/C. It is found that among three PdCu samples NP-Pd50Cu50 exhibits the highest methanol tolerance and catalytic durability for ORR. These experimental observations indicate that incorporation of 50 at.% Cu into Pd accompanied with the network nanoarchitecture is beneficial to maximize the ORR performances of Pd. •Nanoporous (NP) PdCu alloys with three alloy ratios are fabricated by dealloying.•NP-PdCu alloys exhibit superior catalytic activity toward ORR than Pt/C catalyst.•NP-PdCu alloys show a higher selectivity for ORR in methanol-containing medium.•NP-PdCu alloys show higher catalytic durability for ORR compared with Pt/C.•NP-Pd50Cu50 shows the best specific and mass ORR activity among all catalysts.
ISSN:0360-3199
1879-3487
DOI:10.1016/j.ijhydene.2013.06.010