质子交换膜燃料电池
电催化剂
催化作用
化学
炭黑
电解质
氧还原反应
无机化学
氧还原
燃料电池
色散(光学)
化学工程
核化学
电化学
材料科学
电极
物理化学
有机化学
天然橡胶
工程类
物理
光学
作者
Siripong Limpattayanate,Mali Hunsom
标识
DOI:10.1016/j.renene.2013.09.014
摘要
Pt–Pd electrocatalysts supported on different types of support including domestic Hicon Black (HB), multi-walled carbon nanotubes (MWCNT) and titania (TiO2) were prepared by a combined approach of impregnation and seeding, and compared to that prepared using the commercial Vulcan XC-72 (C). Their oxygen reduction reaction (ORR) activities in an acid electrolyte (0.5 M H2SO4) and in a single proton exchange membrane (PEM) fuel cell were evaluated. The type of support was found to affect the Pt–Pd electrocatalyst morphology and ORR activity. The Pt–Pd/C electrocatalyst had the smallest Pt particle size, better catalyst dispersion and a higher Pt:Pd M ratio compared to that of other types of supported Pt–Pd electrocatalysts. However, both in the acid solution and in a single PEM fuel cell, the ORR activities of the Pt–Pd/HB and Pt–Pd/CNT electrocatalysts were comparable to that of the Pt–Pd/C one. The ORR pathway of all supported Pt–Pd electrocatalysts were close to the four-electron pathway.
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