کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
188423 459659 2012 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Palygorskite promoted PtSn/carbon catalysts and their intrinsic catalytic activity for ethanol oxidation
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Palygorskite promoted PtSn/carbon catalysts and their intrinsic catalytic activity for ethanol oxidation
چکیده انگلیسی

PtSn nanoparticles deposited on a stable electrocatalytic support containing conventional carbon and palygorskite are prepared using pre-treated palygorskite and are evaluated by ethanol oxidation. The electrocatalysts are characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). TEM and XRD show that the pre-treatment has an effective impact on the morphology of palygorskite, but does not destroy its architecture. XPS results imply that introduction of palygorskite can facilitate the formation of Sn oxides on the surface of catalyst. Sn oxides increase the amount of surface oxygen-containing species and in turn facilitate to oxidize CO-like species adsorbed on Pt active sites, which has been proved by CO stripping voltammetry. Cyclic voltammetry (CV) measurements show that the addition of palygorskite into the carbon as support improves the electrocatalytic activity in ethanol oxidation. The developed new composite support is catalytically more active for ethanol electrooxidation than the conventional carbon support and shows good stability, offering great potential for widespread application of palygorskite as support for electrocatalysis.


► Palygorskite (PLS) is firstly used to improve the performance of C support.
► Tube-like porous PLS facilitates diffusion of ethanol.
► PtSn/PLS–C has a good catalytic activity for oxidation of ethanol.
► Introduction of PLS can facilitate the formation of Sn oxides.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 70, 30 May 2012, Pages 394–401
نویسندگان
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