کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1278308 1497546 2012 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Catalyst loading for Pt-nanowire thin film electrodes in PEFCs
موضوعات مرتبط
مهندسی و علوم پایه شیمی الکتروشیمی
پیش نمایش صفحه اول مقاله
Catalyst loading for Pt-nanowire thin film electrodes in PEFCs
چکیده انگلیسی

Among electrocatalysts with novel nanostructures in low temperature polymer electrolyte fuel cells (PEFCs), Pt nanowires (Pt-NWs), as one-dimensional (1-D) nanomaterials, are recognized as promising candidates. It has also been reported that the excellent catalytic performance of the nanostructure benefited from their unique 1-D features, but also bring unusual shapes and bulky specific volumes, which make Pt-NWs difficult to fabricate into fuel cell electrodes by any conventional procedures. To understand the effect of catalyst loading on the Pt-NW electrode structure, Pt-NW thin film electrodes of various catalyst loadings were examined towards the oxygen reduction reaction (ORR) ability at the cathode side in low temperature PEFCs. SEM, XRD and electrochemical impedance spectroscopy (EIS) measurements were performed to help understanding and elucidating the electrode role under ‘real’ conditions. The results showed a similar optimal catalyst loading as compared with conventional GDEs with spherical electrocatalysts, but exhibiting a different electrode structure with increasing Pt-NW loading, although a similar larger mass transfer resistance was observed at high Pt-NW loading. The mechanism is further discussed in this paper.


► Study catalyst loading in Pt-nanowire thin film catalyst electrodes in PEFCs.
► Electrodes have thickness only hundreds nanometers with different Pt-nanowire loadings.
► A high loading leads to dense and large size Pt nanowires in electrodes.
► Similar optimal loading to conventional electrodes with spherical nanocatalysts.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Hydrogen Energy - Volume 37, Issue 23, December 2012, Pages 17892–17898
نویسندگان
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