Stability of Carbon Supported Pd/C Catalyst in Direct Formic Acid Fuel Cell

被引:0
|
作者
Shen Juan-Zhang [1 ]
Chen Ying [2 ]
Yang Gai-Xiu [3 ]
Tang Ya-Wen [1 ]
Lu Tian-Hong [1 ,4 ]
机构
[1] Nanjing Normal Univ, Jiangsu Key Lab New Power Batteries, Jiangsu Key Lab Biofunct Mat, Sch Chem & Environm Sci, Nanjing 210097, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Mech & Met Engn, Zhangjiagang 215600, Peoples R China
[3] Chinese Acad Sci, Key Lab Renewable Energy & Gas Hydrate, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
[4] Chinese Acad Sci, Changchun Inst Appl Chem, Changchun 130022, Peoples R China
来源
关键词
Carbon supported Pd catalyst; Formic acid oxidation; Formic acid decomposition; Dipping in formic acid; Direct formic acid fuel cell; ANODIC CATALYST; PALLADIUM NANOPARTICLES; FOMIC ACID; OXIDATION; ELECTROOXIDATION; DECOMPOSITION; PERFORMANCE; ELECTRODES; BEHAVIOR; PURE;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In order to understand the reason for the poor electrocatalytic stability of the Pd/C catalyst for formic acid oxidation, the changes in the structure and the electrocatalytic performance of the Pd/C catalyst after dipping in the formic acid solution for a certain time were investigated using X-ray diffraction spectroscopy and electrochemical methods. It is found that the relative crystallinity of the Pd particles of Pd/C catalyst increases from 1. 73 to 3. 34 and the average size decreases from 4.4 nm to 1. 8 nm after dipping in formic acid solution for 15 d. The electrocatalytic activity and stability of the Pd/C catalyst for formic acid oxidation decrease. The peak current density of formic acid oxidation decreases from 9. 3 mA/cm(2) to 6. 7 mA/cm(2). It may. be due to the certain dissolution of Pd in the Pd/C catalyst and the catalytic decomposition of formic acid at the Pd/C catalyst. This result may supply a new approach for exploring the reason for the poor electrocatalytic stability of the Pd/C catalyst for the formic acid oxidation.
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收藏
页码:2626 / 2629
页数:4
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