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电化学(中英文) ›› 2016, Vol. 22 ›› Issue (2): 123-128.  doi: 10.13208/j.electrochem.151153

• 燃料电池电化学催化与催化剂近期研究专辑(重庆大学 魏子栋教授主编) • 上一篇    下一篇

碳纸负载高指数晶面铂纳米粒子的制备及其在直接甲酸燃料电池中的催化性能研究

黄龙1,詹梅1,王宇成1,林燕芬1,刘硕1,袁婷2,杨辉2,孙世刚1*   

  1. 1厦门大学固体表面物理化学国家重点实验室, 化学化工学院化学系,福建厦门 361005  2 中国科学院上海高等研究院,上海 201210
  • 收稿日期:2016-01-12 修回日期:2016-03-23 出版日期:2016-04-28 发布日期:2016-04-28
  • 通讯作者: 孙世刚 E-mail:sgsun@xmu. edu. cn
  • 基金资助:

    国家自然科学基金创新研究群体项目(No.21321061)、NSFC(海外及港澳学者合作研究基金)延续资助项目(No.21229301)、NSFC-IUPAC(国际(地区)合作与交流项目)(No. 21361140374)资助

Syntheses of Carbon Paper Supported High-index Faceted Pt Nanoparticles and their Performance in Direct Formic Acid Fuel Cells

HUANG Long1,ZHAN Mei1,WANG Yu-cheng1, LIN Yan-fen1, LIU Shuo1, YUAN Ting2, YANG Hui2, SUN Shi-gang 1*   

  1. 1. State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian, China;2. Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, China
  • Received:2016-01-12 Revised:2016-03-23 Published:2016-04-28 Online:2016-04-28
  • Contact: SUN Shi-gang E-mail:sgsun@xmu. edu. cn

摘要:

直接甲酸燃料电池(DFAFCs)是一种很有前景的可用于移动电子设备的电源. 钯对甲酸电催化氧化有很高的活性,但稳定性较差,容易失活;铂对甲酸电催化氧化的活性低于钯,但稳定性好. 前期研究表明,高指数晶面铂纳米粒子对甲酸的电催化氧化活性显著高于低指数晶面铂纳米粒子. 本文以碳纸为载体,应用方波电位法生长高指数晶面铂纳米粒子(HIF-Pt/C-paper),通过改变方波上下限电位,合成出不同粒径的二十四面体和偏方三八面体铂纳米粒子. 进一步在碳纸上修饰一层碳黑微孔层并优化电沉积条件,制备出粒径约10 nm,载量0.069 mg•cm-2的HIF-Pt/C-paper作为DFAFCs的阳极催化剂.在甲酸浓度为3M时,测得30℃下单电池最大功率密度10.6 mW•cm-2,最大质量功率密度153.5 mW•mg-1Pt,是以1 mg•cm-2 载量的商业60 wt% Pt/C为阳极催化剂的电池的8.4倍. HIF-Pt/C-paper阳极DFAFCs在20 mA•cm-2条件下运行50 h,电压保持率为95%,显示出很好的稳定性.

关键词: 碳纸, 铂纳米粒子, 高指数晶面, 电沉积, 直接甲酸燃料电池

Abstract:

Direct formic acid fuel fuels (DFAFCs) are promising energy source for portable electronic devices. Palladium (Pd) is more active than platinum (Pt) for the formic acid electrooxidation. However, the stability of Pd is much poorer than that of Pt. Unfortunately, the ultra-low natural abundance of the Pt makes it extremely expensive and limits its application as a fuel cell catalyst. Boosting both the activity and stability of Pt nanoparticles to enhance their efficiency is urgent. As previous works illustrated, nanoparticles enclosed with high-index facets usually bare a higher activity toward fuel cell related reactions than those nanoparticles with low-index facet. We adopted in this study the square-wave potential (SWP) method to electrochemically synthesize high-index faceted Pt nanoparticles on carbon paper support (HIF-Pt/C-paper). By carefully tuning the deposition conditions such as upper potential limit (EU) and lower potential limit (EL) of the SWP, we successfully synthesized the tetrahexahedral Pt nanoparticles and trapezohedral Pt nanoparticles with different sizes ranging from 40 ~ 200 nm. Furthermore, when the electrodeposition was carried out on the XC-72 modified carbon paper, the high-index faceted Pt nanoparticles of ~ 10 nm in size with high density can be synthesize by delicately adjusting the electrodeposition conditions, the Pt loading on this electrode was determined to be 0.069 mg•cm-2 by ICP-MS. Using the HIF-Pt/C-paper as the anode of DFAFCs and 3 mol•L-1 formic acid as the fuel, the maximum power density of single cell was 10.6 mW•cm-2 under 30 °C, and 95% of the cell voltage had been maintained after 50 h test with current density equal to 20 mA•cm-2, which demonstrates a reasonable stability under the test condition. The Pt mass normalized maximum power density was 153.5 mW•mg-1Pt, which is 8.4 times as high as that of the DFAFCs using commercial 60% (by mass) Pt/C as the anode catalyst (Pt loading of 1 mg•cm-2). The enhanced mass activity of the as-synthesized HIF-Pt/C-paper is mainly attributed to the ultralow loading of the Pt and the unique distribution of Pt nanoparticles, and to the electrodeposition method that generates the Pt nanoparticles mainly locating at the boundary site between the carbon support and the Nafion membrane.

Key words: carbon paper, Pt nanoparticles, high-index facet, electrodeposition, Direct formic acid fuel cells.

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