Monodispersed porous flowerlike PtAu nanocrystals as effective electrocatalysts for ethanol oxidation

被引:17
|
作者
Li, Shumin [1 ]
Xu, Hui [1 ]
Xiong, Zhiping [1 ]
Zhang, Ke [1 ]
Wang, Caiqin [2 ]
Yan, Bo [1 ]
Guo, Jun [3 ]
Du, Yukou [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Univ Toronto, Chem Dept, Toronto, ON M5S 3H4, Canada
[3] Soochow Univ, Testing & Anal Ctr, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Shape-controlled; PtAu nanoflowers; Direct fuel cells; Electrocatalytic oxidation; REDUCED GRAPHENE OXIDE; FORMIC-ACID ELECTROOXIDATION; CORE-SHELL CATALYSTS; METHANOL ELECTROOXIDATION; FACILE SYNTHESIS; ETHYLENE-GLYCOL; NANOPARTICLES; NANOSHEETS; NANOWIRES; PALLADIUM;
D O I
10.1016/j.apsusc.2017.05.246
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
Designing and tuning the bimetallic nanoparticles with desirable morphology and structure can embody them with greatly enhanced electrocatalytic activity and stability towards liquid fuel oxidation. We herein reported a facile one-pot method for the controlled synthesis of monodispersed binary PtAu nanoflowers with abundant exposed surface area. Owing to its fantastic structure, synergistic and electronic effect, such as-prepared PtAu nanoflowers exhibited outstandingly high electrocatalytic activity with the mass activity of 6482 mA mg(-1) towards ethanol oxidation, which is 28.3 times higher than that of commercial Pt/C (227 mA mg(-1)). More interesting, the present PtAu nanoflower catalysts are more stable for the ethanol oxidation reaction in the alkaline with lower current density decay and retained a much higher current density after successive CVs of 500 cycles than that of commercial Pt/C. This work may open a new way for maximizing the catalytic performance of electrocatalysts towards ethanol oxidation by synthesizing shape-controlled alloy nanoparticles with more surface active sites to enhance the performances of direct fuel cells reaction, chemical conversion, and beyond. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:172 / 178
页数:7
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