Fe@Pt core-shell nanoparticles as electrocatalyst for oxygen reduction reaction in acidic media

被引:12
作者
Huang, Yanli [1 ,2 ,3 ]
Tan, Zhan [1 ,2 ,3 ]
Wu, Huimin [1 ,2 ,3 ]
Feng, Chuanqi [1 ,2 ,3 ]
Ding, Yu [4 ]
机构
[1] Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Hubei, Peoples R China
[2] Hubei Univ, Key Lab Synth & Applicat Organ Funct Mol, Minist Educ, Wuhan 430062, Hubei, Peoples R China
[3] Hubei Univ, Coll Chem & Chem Engn, Wuhan 430062, Hubei, Peoples R China
[4] Hubei Engn Univ, Coll Chem & Mat Sci, Xiaogan 432000, Peoples R China
基金
中国国家自然科学基金;
关键词
Fe@Pt nanoparticles; Core-shell structure; Oxygen reduction reaction; fuel cell; FUEL-CELLS; ELECTROCHEMICAL SENSOR; HYDROGEN-PEROXIDE; CARBON NANOTUBES; CATALYSTS; ALLOY; DESIGN; CU; PD; FUNCTIONALIZATION;
D O I
10.1007/s11581-017-2186-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To settle the drawbacks of non-cost-effective and enhance the electrocatalytic performance of Pt/C, Fe@Pt core-shell nanoparticles supported by Vulcan XC-72 have been designed and synthetized successfully. The synthesized materials were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy, whereas the electrochemical analyses were obtained by electrochemical impedance spectroscopy, cyclic voltammetry, linear sweep voltammetry, and chronoamperometry. Results suggest that the onset potential of oxygen reduction reaction on the Fe@Pt/C is about 0.6 V (vs. Hg/Hg2Cl2) in O-2-saturated 0.5 M H2SO4, which shifts positively more than 30 mV compared with that of Pt/C. The corresponding electron transfer number is 4, meaning the reduction reaction mainly occurred through a 4-electron pathway. More importantly, the Fe@Pt/C has an excellent stability and better catalytic performance towards oxygen reduction reaction activity compared with Pt/C. Thus, Fe@Pt/C could be utilized as promising cathode catalysts in proton exchange membrane fuel cells.
引用
收藏
页码:229 / 236
页数:8
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