Water-soluble Au nanocages for enzyme-free H2O2 sensor and 4-nitrophenol reduction

被引:14
|
作者
Li, Houshen [1 ]
Li, Yijing [2 ]
Wang, Shengqing [3 ]
机构
[1] Shandong Agr Univ, Coll Chem & Mat Sci, Tai An 271018, Shandong, Peoples R China
[2] Shandong Univ, State Key Lab Crystal Mat, Jinan 250100, Peoples R China
[3] Linyi Engn Consulting Inst, Linyi 276000, Shandong, Peoples R China
来源
CRYSTENGCOMM | 2015年 / 17卷 / 11期
关键词
CORE-SHELL NANOPARTICLES; HYDROGEN-PEROXIDE SENSOR; DIRECT ELECTROCHEMISTRY; HORSERADISH-PEROXIDASE; METAL NANOSTRUCTURES; REPLACEMENT REACTION; CATALYTIC-PROPERTIES; HOLLOW INTERIORS; CARBON ELECTRODE; PERFORMANCE;
D O I
10.1039/c4ce02455a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this paper, water-soluble, high yield and quality, quasi-spherical Au nanocages have been successfully prepared via a galvanic replacement reaction with HAuCl4 in water at room temperature, where monodisperse, quasi-spherical Ag nanocrystals are used as sacrificial templates. Quasi-spherical Au nanocages were employed as both an enzyme-free electrochemical sensor and in catalytic application, which showed superior performance compared to solid and nanocrystals with other structures. In the enzyme-free H2O2 detection, the quasi-spherical Au nanocages based biosensor exhibited long linearity, a low detection limit, high stability and good selectivity. The enzyme-free H2O2 sensor also exhibited excellent selectivity for H2O2 in comparison to other normally co-existing electroactive species, such as ascorbic acid, uric acid and glucose. Furthermore, Au nanocages were also found to serve as a more effective catalyst for the reduction of 4-nitrophenol to 4-aminophenol in the presence of NaBH4 than Au nanocrystals with other structures. The reduction has an activity parameter of 4000 s(-1) g(-1), which is also significantly higher than other Au or Ag based nanomaterials in previous research.
引用
收藏
页码:2368 / 2375
页数:8
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