Morphology-dependent selective hydrogenation catalysis of hollow AuCu bimetallic nanostructures

被引:22
作者
Doan Van Thuan [1 ,2 ]
Nguyen Tri Khoa [1 ,2 ]
Kim, Soon Wook [1 ,2 ]
Kim, Eui Jung [3 ]
Hahn, Sung Hong [1 ,2 ]
机构
[1] Univ Ulsan, Dept Phys, Ulsan 680749, South Korea
[2] Univ Ulsan, Energy Harvest Storage Res Ctr, Ulsan 680749, South Korea
[3] Univ Ulsan, Dept Chem Engn, Ulsan 680749, South Korea
基金
新加坡国家研究基金会;
关键词
Hollow structure; Bimetallic; Hydrogenation reduction; Catalysis; AuCu; GOLD NANOPARTICLES; SIZE; PD; PERFORMANCE; FABRICATION; KIRKENDALL; ADSORPTION; REDUCTION; NANOTUBES; EVOLUTION;
D O I
10.1016/j.jcat.2015.05.001
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
We synthesized hollow AuCu bimetallic nanostructures using a Cu2O template and evaluated their hydrogen dissociation performance. The formation of a superstructural bimetallic and well-inherited shape was confirmed using transmission electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The AuCu bimetallic nanostructures were tested for the catalytic reduction of o-nitroaniline to 1,2-benzenediamine, and they showed much better catalytic activity than pure Au. The hollow AuCu cubic structure exhibited superior catalytic efficiency (reaction rate constant = 0.33 min(-1)) compared with other structures such as a cuboctahedral structure (0.08 min(-1)), an octahedral structure (0.17 min(-1)), and pure Au (0.06 min(-1)). Furthermore, we examined the dependence of o-nitroaniline reduction activity of the hollow AuCu hybrids on NaBH4 concentration. The reaction rate constant became saturated at a lower NaBH4 concentration for Au nanoparticles, while its saturation occurred at a higher NaBH4 concentration in the case of hollow AuCu nanostructures. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:144 / 150
页数:7
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