Diffusion controlled analytical performances of hydrogen peroxide sensors: Towards the sensor with the largest dynamic range

被引:30
作者
Karyakin, Arkady A. [1 ]
Kuritsyna, Elena A. [1 ]
Karyakina, Elena E. [1 ]
Sukhanov, Vladislav L. [2 ]
机构
[1] Moscow MV Lomonosov State Univ, Fac Chem, Moscow 119991, Russia
[2] RAS, AF Ioffe Physicotech Inst, St Petersburg 194021, Russia
关键词
Hydrogen peroxide; Prussian Blue; Diffusion; Ultramicroelectrode; Nano-electrode array; Dynamic range; PRUSSIAN-BLUE; FLOW; CHRONOPOTENTIOMETRY; CHRONOAMPEROMETRY; ELECTRODES; BIOSENSORS; FILMS; MODEL;
D O I
10.1016/j.electacta.2008.11.049
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Analytical performances of chronoamperometric sensors are limited by mass transport of analyte, specifically by its diffusion within Nernst's layer. Limiting performance characteristics of hydrogen peroxide sensors are achieved using the most advantageous electrocatalyst for its reduction - Prussian Blue. We report on improvement of sensitivity and detection limits of H(2)O(2) sensors by substituting conventional electrode with ultramicroelectrode and with nano-electrode array. Prussian Blue based microelectrodes displayed improved sensitivity in hydrogen peroxide detection, which is close to be inversely proportional to electrode radius. To form nano-electrode arrays we used nano-structuring of the electrocatalyst on inert electrode support. Hydrogen peroxide sensor made by deposition of Prussian Blue through sol template based on vinyltriethoxysilane (nano-structuring was confirmed by AFM) displayed linear calibration range prolonged over seven orders of magnitude of H(2)O(2) concentration, which is record in electroanalysis. The two to three orders of magnitude prolonged linear calibration range without loss of sensitivity seems to be at the limiting level for sensor improvement by forming micro- or nano-electrode arrays. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5048 / 5052
页数:5
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