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Fe对Pt-Fe/C催化剂电催化氧还原反应活性的影响
引用本文:王彦恩,唐亚文,周益明,高颖,刘长鹏,陆天虹.Fe对Pt-Fe/C催化剂电催化氧还原反应活性的影响[J].高等学校化学学报,2007,28(4):743-746.
作者姓名:王彦恩  唐亚文  周益明  高颖  刘长鹏  陆天虹
作者单位:1. 南京师范大学化学与环境科学学院,南京,210097
2. 哈尔滨师范大学理化学院化学系,哈尔滨,150080
3. 中国科学院长春应用化学研究所,长春,130022
4. 南京师范大学化学与环境科学学院,南京,210097;中国科学院长春应用化学研究所,长春,130022
基金项目:国家自然科学基金 , 江苏省高校自然科学基金
摘    要:制备了用作直接甲醇燃料电池的碳载Pt-Fe(Pt-Fe/C)阴极催化剂, X射线能量色散谱(EDX)、X射线衍射谱和电化学测量的结果表明, 在Pt-Fe/C催化剂中, Fe以3种形式存在. 质量分数大约为20%的Fe进入Pt的晶格, 形成Pt-Fe合金, 质量分数大约为80%的Fe没有进入Pt的晶格而以Fe和Fe2O3的形式单独存在. 该催化剂经酸处理后, 非合金化Fe和Fe2O3被溶解, 而使Pt-Fe/C催化剂的电化学活性比表面积要比未经酸处理前的增加约30%左右, 导致Pt-Fe/C催化剂对氧还原的电催化活性优于未经酸处理前的Pt-Fe/C催化剂. 研究结果表明, Pt-Fe/C催化剂的电化学活性比表面积对氧还原的电催化活性起重要的作用, 另外, 只有与Pt形成合金的Fe能提高Pt对氧还原的电催化活性, 而非合金化的Fe对Pt催化剂对氧还原的电催化活性基本没有影响.

关 键 词:碳载Pt-Fe催化剂  氧还原  电化学活性比表面积  电催化活性
文章编号:0251-0790(2007)04-0743-04
收稿时间:2006-05-13
修稿时间:2006-05-13

Effect of Fe on Electrocatalytic Activity of Pt-Fe/C Catalyst for Oxygen Reduction
WANG Yan-En,TANG Ya-Wen,ZHOU Yi-Ming,GAO Ying,LIU Chang-Peng,LU Tian-Hong.Effect of Fe on Electrocatalytic Activity of Pt-Fe/C Catalyst for Oxygen Reduction[J].Chemical Research In Chinese Universities,2007,28(4):743-746.
Authors:WANG Yan-En  TANG Ya-Wen  ZHOU Yi-Ming  GAO Ying  LIU Chang-Peng  LU Tian-Hong
Institution:1. College of Chemistry and Environmental Science, Nanjing Normal University, Nanjing 210097, China; 2. Department of Chemistry, College of Sciences, Harbin Normal University, Harbin 150080, China; 3. Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
Abstract:In this paper, the carbon supported Pt-Fe(Pt-Fe/C) cathodic catalyst in the direct methanol fuel cell was prepared. The results of the energy dispersive X-ray(EDX) analysis, X-ray reflection spectroscopy(XRD) and electrochemical measurements indicate that in the Pt-Fe/C catalyst, Fe exists as the three forms. About 20%(mass fraction) Fe enters the crystal lattice of Pt, forming the alloy with Pt. About 80%(mass fraction) Fe does not enter the crystal lattice of Pt and exists as Fe and Fe2O3. After the Pt-Fe/C catalyst being treated with acid , non-alloying Fe and Fe2O3 in the catalyst are dissolved. Therefore, the electrochemically active specific surface area of the Pt-Fe particles in the Pt-Fe/C catalyst after the acid treatment is 30% larger than that of the Pt-Fe/C catalyst before the acid treatment. Thus, the electrocatalytic activity of the Pt-Fe/C catalyst after the acid treatment for the oxygen reduction is higher than that of the Pt-Fe/C catalyst before the acid treatment. It illustrates that the electrochemically active specific surface area of the Pt-Fe particles in the Pt-Fe/C catalyst can significantly affects the electrocatalytic activity of the Pt-Fe/C catalyst for the oxygen reduction. In addition, it also demonstrates that only alloying Fe can increase the electrocatalytic activity of the Pt for the oxygen reduction and non-alloying Fe has no such effect.
Keywords:Carbon supported Pt-Fe catalyst  Oxygen reduction  Electrochemically active specific surface area  Electrocatalytic activity
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