Synthesis of highly active and stable Au-PtCu core-shell nanoparticles for oxygen reduction reaction

被引:42
|
作者
Hsu, Chiajen [1 ]
Huang, Chienwen [1 ]
Hao, Yaowu [1 ]
Liu, Fuqiang [1 ]
机构
[1] Univ Texas Arlington, Dept Mat Sci & Engn, Arlington, TX 76019 USA
基金
美国国家科学基金会;
关键词
FUEL-CELLS; ELECTRONIC-STRUCTURE; ORR ACTIVITY; FE ALLOYS; ELECTROCATALYSTS; PLATINUM; STABILIZATION; ALKALINE; SURFACES; METAL;
D O I
10.1039/c2cp42716h
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
Au-PtCu core-shell nanoparticles were successfully synthesized via galvanic replacement of Cu by Pt on hollow Au nano-spheres. Characterizations of the nanoparticles were conducted by X-ray diffraction (XRD), transmission electron microscopy (TEM), and electrochemical measurements. Results indicate 2-2.5 times higher specific activity and mass activity of the Au-PtCu catalysts than commercial Pt black and Pt/C in oxygen reduction reaction (ORR), measured in a rotating disk electrode system. Besides, thinner PtCu coating (25 nm thick, deposition time of 20 min) on the hollow Au nano-spheres demonstrated a pronounced CO oxidation peak shift (by 0.13 V) and long-term durability probably due to the unique core-shell structure and strong electronic coupling between the Au core and the PtCu shell.
引用
收藏
页码:14696 / 14701
页数:6
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