Enhancing stability of octahedral PtNi nanoparticles for oxygen reduction reaction by halide treatment

被引:42
|
作者
Choi, Juhyuk [1 ]
Lee, Youhan [1 ]
Kim, Jihan [1 ]
Lee, Hyunjoo [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
Oxygen reduction reaction; PtNi nanoparticles; Alloys; Stability; Leaching; Halides; FORMIC-ACID OXIDATION; PEM FUEL-CELLS; ALLOY NANOPARTICLES; CATALYTIC-ACTIVITY; GOLD NANOCRYSTALS; SHAPE EVOLUTION; IN-SITU; ELECTROCATALYSTS; PLATINUM; NI;
D O I
10.1016/j.jpowsour.2016.01.063
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
Because a reduction in the amount of Pt catalysts is essential for the commercialization of fuel cells, various approaches have been tested to maximize the mass activity of Pt-based catalysts. Among these, the most successful results so far were obtained using shaped PtNi alloy nanoparticles, preferably with PtNi(111) facets. However, these nanoparticles typically suffer from much lower activity after the durability tests due to the leaching out of the surface Ni during the oxygen reduction reaction (ORR), which leads to the disappearance of the activity-enhancing effect caused by electronic structure modification. Here, we showed that halide treatment of the octahedral PtNi nanoparticles could significantly enhance their durability. Halides are adsorbed on surface Ni more strongly than on surface Pt, and the surface halides are found to preserve the surface Ni that induces the ORR activity enhancement. Especially, Br can preserve the surface Ni effectively. Durability testing by repeating cyclic voltammetry 10,000 times in the 0.6-1.1 V range showed that the mass activity decreased by 52.6% for the as prepared PtNi octahedral nanoparticles, whereas the mass activity decreased by only 15.0% for the Br-treated PtNi nanoparticles. The simple treatment significantly enhanced the long-term stability of the highly active PtNi alloy nano-octahedra. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:883 / 890
页数:8
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