کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1288234 1498003 2013 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Catalytic activities of PtBi nanoparticles toward methanol electrooxidation in acid and alkaline media
موضوعات مرتبط
مهندسی و علوم پایه شیمی الکتروشیمی
پیش نمایش صفحه اول مقاله
Catalytic activities of PtBi nanoparticles toward methanol electrooxidation in acid and alkaline media
چکیده انگلیسی

Spherical PtBi nanoparticles are electrodeposited from aqueous solution according to the preset composition. Their catalytic activities toward methanol electrooxidation are examined by cyclic voltammetry and chronoamperometry in acid media and first in alkaline media. Experimental results show that, methanol electrooxidation has lower onset potentials on PtBi than on Pt in either acid or alkaline media. The improved catalytic activities are due to the electronic effects of bismuth in PtBi. At higher overpotentials, the electrolyte acidity has produced different influences on the kinetics of methanol electrooxidation on PtBi and Pt. In acid media, PtBi is inferior to Pt for methanol oxidation at above 0.460 V, because that fewer continuous Pt sites on PtBi are not enough for the adsorption and dehydrogenation of methanol molecules. In alkaline media, the oxidation current on PtBi becomes much higher than that on Pt at above 0.768 V. The raised current can be credited to the bifunctional mechanism. Bi2O5 sites on PtBi surface serve for OHad adsorption and Pt sites for methanol dehydrogenation. The better catalytic activity of PtBi nanoparticles in alkaline media suggests their promising application in alkaline direct alcohol fuel cells.

Figure optionsDownload as PowerPoint slideHighlights
► PtBi nanoparticles are prepared by a simple potentiostatic deposition.
► These nanoparticles have a spherical shape and a preset composition.
► They have a good catalysis toward methanol electrooxidation in alkaline media.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Power Sources - Volume 229, 1 May 2013, Pages 42–47
نویسندگان
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