Journal
LANGMUIR
Volume 26, Issue 10, Pages 7437-7443Publisher
AMER CHEMICAL SOC
DOI: 10.1021/la9041474
Keywords
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Funding
- Ph.D. Programs Foundation of University of Jinan
- National Science Foundation of China [20928003, 20906045, 90923011]
- Natural Science Foundation of Shandong Province [Y2007B33]
- Chinese Ministry of Education [108078]
- SEM-NCET
- Independent Innovation Foundation of Shandong University (IIFSDU)
- Shandong Natural Science Fund for Distinguished Young Scholars
- Foundation of Key Laboratory for Liquid Solid Structural Evolution and Processing of Materials, Ministry of Education, Shandong University
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We describe a facile route to the straightforward fabrication of nanoporous (NP) PtRu alloys with predetermined bimetallic compositions. Electron microscopy and X-ray diffraction characterizations demonstrate that selective etching of Al from ternary PtRuAl source alloys generates three-dimensional bicontinuous NP-PtRu alloy c with a single-phase face-centered-cubic crystalline structure. X-ray photoelectron spectroscopy shows a slight electronic structure modification of Pt by alloying with Ru as well as uniform surface and bulk bimetallic ratio. With characteristic structural dimensions less than 5 nm, these high surface area bimetallic nanostructures show distinct electrocatalytic performance as the Ru content varies within the structure. Among all samples, NP-Pt70Ru30 shows the highest specific activity as well as the most negative onset potential toward methanol oxidation reaction. NP-Pt50Ru50 was found to possess a similar specific activity to the commercial E-TEK Pt50Ru50/C catalyst, but its onset and peak potentials are about 70 mV more negative. CO stripping experiments demonstrate that the adsorption of CO is the weakest on NP-Pt70Ru30, and further increasing the Ru content actually shifts the CO stripping peak to a more positive potential. Thus, the overall sequence for CO-tolerance is NP-Pt70Ru30 > NP-Pt50Ru50 approximate to Pt50Ru50/C > NP-Pt30Ru70 > Pt/C.
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