کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1274758 1497550 2012 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A strategy for easy synthesis of carbon supported Co@Pt core–shell configuration as highly active catalyst for oxygen reduction reaction
موضوعات مرتبط
مهندسی و علوم پایه شیمی الکتروشیمی
پیش نمایش صفحه اول مقاله
A strategy for easy synthesis of carbon supported Co@Pt core–shell configuration as highly active catalyst for oxygen reduction reaction
چکیده انگلیسی

An oxygen-mediated galvanic battery reaction strategy has been developed to one-step synthesize carbon-supported Co@Pt core–shell nanostructures. Relying on this strategy, a structural evolution of 3-D Pt-on-Co bimetallic nanodendrites into Co@Pt core–shell configuration is readily achieved in our study. These well-supported and low-Pt-content nanostructures show superior electrocatalytic activities to oxygen reduction reaction. Especially, the supported Co@Pt core–shell electrocatalyst for oxygen reduction reaction shows a high activity with the maximal Pt-mass activity of 465 mA mg−1 Pt at 0.9 V (vs. RHE). The present investigation clearly demonstrates that the design and synthesis of the core–shell nanostructures is a viable route for building Pt-based electrocatalysts with optimized utilization efficiency and higher cost performance.

The supported Pt nanodendrites can transfer into core–shell nanosturctures by restraining the galvanic reaction on support, which shows a significantly high activity for oxygen reduction reaction.Figure optionsDownload as PowerPoint slideHighlights
► Oxygen-mediated galvanic battery reaction leads to one-step synthesis of supported core–shell nanostructures.
► Supported core–shell electrocatalyst affords high activity and stability for oxygen reduction reaction.
► Design of core–shell nanostructures is a viable route for building high performance electrocatalysts.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Hydrogen Energy - Volume 37, Issue 19, October 2012, Pages 14152–14160
نویسندگان
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