钯
催化作用
X射线光电子能谱
直接乙醇燃料电池
能量色散X射线光谱学
扫描电子显微镜
化学
无机化学
锡
材料科学
化学工程
分析化学(期刊)
脱氢
冶金
质子交换膜燃料电池
有机化学
复合材料
工程类
作者
Wenxin Du,Kayla E. Mackenzie,Daniel F. Milano,N. Aaron Deskins,Dong Su,Xiaowei Teng
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2012-01-10
卷期号:2 (2): 287-297
被引量:282
摘要
In this paper, we present a study of a series of carbon-supported Pd–Sn binary alloyed catalysts prepared through a modified Polyol method as anode electrocatalysts for direct ethanol fuel cell reactions in an alkaline medium. Transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and aberration-corrected scanning transmission electron microscopy equipped with electron energy loss spectroscopy were used to characterize the Pd–Sn/C catalysts, where homogeneous Pd–Sn alloys were determined to be present with the surface Sn being partially oxidized. Among various Pd–Sn catalysts, Pd86Sn14/C catalysts showed much enhanced current densities in cyclic voltammetric and chronoamperometric measurements, compared to commercial Pd/C (Johnson Matthey). The overall rate law of ethanol oxidation reaction for both Pd86Sn14/C and commercial Pd/C were also determined, which clearly showed that Pd86Sn14/C was more favorable in high ethanol concentration and/or high pH environment. Density functional theory calculations also confirmed Pd–Sn alloy structures would result in lower reaction energies for the dehydrogenation of ethanol, compared to the pure Pd crystal.
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