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Preparation and characterization of PtSn/C anode electrocatalysts for direct ethanol fuel cell

机译:preparation and characterization of ptsn/C anode electrocatalysts for direct ethanol fuel cell

摘要

Highly active PtSn/C catalyst was prepared by a polyol method. The catalyst was reduced in H-2/Ar atmosphere at 600 degreesC for 2 h in order to obtain different metallic phase. TEM images show uniform dispersion of spherical metal nanoparticles with average diameters of 1.8 and 3.9 nm for the as-prepared and treated catalysts, respectively. UV-vis spectrophotometry is employed to monitor the preparation process and the results indicate that Pt-Sn complex formed once the precursors of Pt and Sn were mixed together. The structure properties of the samples were characterized using X-ray diffraction. The results show that after reduction, the catalyst tends to form PtSn alloy. TPR experiment results show that Sn exists in multivalent state in the as-prepared sample while only zero-valence Sn was detected in the treated sample, while it could not be excluded that the multivalent tin existed in the treated sample. Cyclic voltammetry (CV) technique and single direct ethanol fuel cell (DEFC) tests indicate that the as-prepared catalyst possesses superior catalytic activity for ethanol oxidation to the treated sample. The results suggest that Pt and multivalent Sn are the active species for ethanol oxidation. (C) 2004 Elsevier B.V. All rights reserved.
机译:通过多元醇法制备高活性的PtSn / C催化剂。为了获得不同的金属相,将催化剂在H-2 / Ar气氛中在600℃下还原2小时。 TEM图像显示了分别制备和处理的催化剂的平均直径分别为1.8和3.9 nm的球形金属纳米颗粒的均匀分散。紫外可见分光光度法用于监测制备过程,结果表明,一旦将Pt和Sn的前体混合在一起,就会形成Pt-Sn络合物。样品的结构性质使用X射线衍射表征。结果表明,还原后,催化剂趋于形成PtSn合金。 TPR实验结果表明,制得的样品中Sn以多价态存在,而处理后的样品中仅检测到零价Sn,而不能排除多价锡存在于处理后的样品中。循环伏安法(CV)技术和单直接乙醇燃料电池(DEFC)测试表明,所制备的催化剂对乙醇氧化的催化活性优于处理后的样品。结果表明,Pt和多价Sn是乙醇氧化的活性物种。 (C)2004 Elsevier B.V.保留所有权利。

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