高等学校化学学报 ›› 2014, Vol. 35 ›› Issue (12): 2688.doi: 10.7503/cjcu20140188

• 物理化学 • 上一篇    下一篇

(PtAuPt)HN/GC的制备及对甲酸氧化的电催化性能

商中瑾1, 颜亮亮1, 饶贵仕1, 熊婷1, 田伟1, 林旋1, 钟起玲1(), 任斌2   

  1. 1. 江西师范大学化学化工学院, 南昌 330022
    2. 厦门大学化学化工学院化学系, 固体表面物理化学国家重点实验室, 厦门 361005
  • 收稿日期:2014-03-07 出版日期:2014-12-10 发布日期:2014-11-29
  • 作者简介:联系人简介: 钟起玲, 男, 教授, 主要从事表/界面电化学、 光谱电化学和纳米电化学研究. E-mail:zhqiling@163.com
  • 基金资助:
    国家自然科学基金(批准号: 20663002)和厦门大学固体表面物理化学国家重点实验室基金(批准号: 200511)资助

Preparation of (PtAuPt)HN/GC and Its Electrocatalytic Performance for Formic Acid Oxidation

SHANG Zhongjin1, YAN Liangliang1, RAO Guishi1, XIONG Ting1, TIAN Wei1, LIN Xuan1, ZHONG Qiling1,*(), REN Bin2   

  1. 1. College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, China
    2. State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry,College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China
  • Received:2014-03-07 Online:2014-12-10 Published:2014-11-29
  • Contact: ZHONG Qiling E-mail:zhqiling@163.com
  • Supported by:
    † Supported by the National Natural Science Foundation of China(No.20663002) and the Foundation of State Key Laboratory of Physical Chemistry of Solid Surfaces, Xiamen University, China(No.200511)

摘要:

以Se溶胶为模板, 合成了多层核壳结构的Se@Pt@Au@Pt实心纳米粒子; 采用化学与电化学相结合的除硒方法制得了(PtAuPt)HN/GC, 并表征了(PtAuPt-Se)HN的表面形貌、 结构与组成; 以甲酸为探针分子, 比较了(PtAuPt)HN/GC和Pt/C/GC对甲酸氧化的电催化行为, 发现(PtAuPt)HN/GC催化甲酸氧化只有1个氧化峰, 峰电位和峰电流分别约为0.35 V和1.22 mA/cm2, 而Pt/C/GC则有2个氧化峰, 在 0.35 V时所对应的电流密度仅约为0.30 mA/cm2, 前者在该电位时的电流密度是后者的4倍; 在0.30 mA/cm2的电流密度下, (PtAuPt)HN /GC对应的电极电位为0.01 V, 比Pt/C/GC负移了340 mV; 在600 s时的计时电流分别为0.06和0.02 mA/cm2. (PtAuPt)HN对甲酸氧化的电催化活性不但比Pt/C高, 而且具有一定的抗CO中毒性能.

关键词: 铂-金-铂纳米空球, 电极, 电催化, 甲酸氧化

Abstract:

Se@Pt@Au@Pt multilayer core-shell nanoparticles were synthesized in bulk using selenium colloids as template. After removing the selenium template by chemical method, Pt-Au-Pt hollow nanospheres[(PtAuPt-Se)HN], which containing a small amount of residual selenium, were synthesized and used to modify GC electrode. After the residual selenium were removed from (PtAuPt-Se)HN/GC by electrochemical method, (PtAuPt)HN/GC was obtained. Scanning electron microscopy(SEM), transmission electron microscopy(TEM), energy dispersive X-ray spectrocopy(EDS) and X-ray diffraction(XRD) were used to characterize their surface morphologies, structures and compositions. The electrocatalytic oxidation activity of (PtAuPt)HN/GC and Pt/C/GC were measured by using formic acid as a probe molecule. Cyclic voltammogram(CV) reveals that the current density of the formic acid oxidation on (PtAuPt)HN/GC was four times as large as that of the latter when the potential was 0.35 V. The potential of (PtAuPt)HN/GC was shifted negatively about 340 mV compared to the Pt/C/GC when the current density was 0.30 mA/cm2. The chronoamperometry of (PtAuPt)HN/GC and Pt/C/GC was 0.06 and 0.02 mA/cm2 respectively after 600 s. The results show that the electrocatalytic activity of (PtAuPt)HN for formic acid oxidation was significantly higher than that of Pt/C.

Key words: Pt-Au-Pt hollow nanospheres, Electrode, Electrocatalysis, Oxidation of formic acid

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