Amperometric sensing of hydrogen peroxide via an ITO electrode modified with gold nanoparticles electrodeposited on a CoMn-layered double hydroxide

被引:29
作者
Xu, Liang [1 ]
Lian, Meiling [1 ]
Chen, Xu [1 ]
Lu, Yanluo [1 ]
Yang, Wensheng [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Binary transition metals; Multicomponent active support; Nanocomposite; Synergetic effect; Nonenzymatic sensor; Electrocatalytic oxidation; GLASSY-CARBON ELECTRODE; REDUCED GRAPHENE OXIDE; SILVER NANOPARTICLES; OXIDATION; COPPER; NANOCOMPOSITES; COMPOSITES; GLUCOSE; FILMS; H2O2;
D O I
10.1007/s00604-017-2428-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An electrochemical sensor for hydrogen peroxide (H2O2) has been fabricated by electrodepositing gold nanoparticles (AuNPs) on an indium tin oxide (ITO) electrode modified with cobalt and manganese-layered double hydroxides (CoMn-LDHs). Scanning electron microscopy images reveal well-dispersed AuNPs with a typical size of 12 nm on the surface of the layered double hydroxides. Electrochemical characterizations show that the introduction of the LDH support significantly enhances the voltammetric response to H2O2. This is underpinned by a comparative study that uses single transition metal-LDHs (CoAl-LDHs or MgMn-LDHs) as supports. The results indicate that the presence of binary transition metals in the LDH layer may result in multiple interaction and interfacial effects between AuNPs and the support. At an optimal working voltage of +0.55 V (vs. Ag/AgCl), the sensor displays a wide linear range (0.1 mu M to 1.27 mM), low detection limit (0.06 mu M) and high sensitivity (125.0 mu A.mM(-1).cm(-2)), which are characteristics superior to those of most previously reported AuNP-based composite-modified electrodes. The sensor has good reproducibility and storage stability. In our view, this sensor represents a valuable tool for advanced sensing of H2O2.
引用
收藏
页码:3989 / 3996
页数:8
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