Journal
SENSORS AND ACTUATORS B-CHEMICAL
Volume 204, Issue -, Pages 629-636Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2014.08.022
Keywords
One-dimensional MgO nanostructures; Ascorbic acid; Dopamine; Uric acid; Simultaneous detection
Funding
- Hi-tech Research and Development Program of China (863 Program) [2013AA030801]
- National Nature Science Foundation of China [61301045, 61401306]
- Natural Science Foundation of Tianjin [13JCZDJC36000]
- Excellent Young Teachers Program of Tianjin
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One-dimensional (1D) MgO nanostructures of various morphologies including tadpole-like nanobelts (tadpoles), nanobelts, and nanorods were synthesized via direct current (DC) arc plasma jet chemical vapor deposition (CVD). The effect of morphology on the biosensing properties of the nanostructures was investigated by comparing their electrochemical properties. Compared with tadpoles and nanorods, the MgO nanobelts had excellent electrocatalytic activity toward ascorbic acid (AA), dopamine (DA) and uric acid (UA). The response of the MgO nanobelts to the analytes was twice that of the tadpoles. A MgO nanobelt-modified electrode was thus fabricated for the simultaneous determination of AA, DA, and UA. The peak separations between AA and DA, DA and UA, and AA and UA for this electrode were 111, 161, and 272 mV, respectively. The linear response ranges of the electrodes were 2.5-15 and 25-150 mu M for AA, 0.125-7.5 mu M for DA, and 0.5-3 and 5-30 p,M for UA. The calculated detection limits were 0.2, 0.05, and 0.04 mu M (SIN = 3), respectively. The excellent electrocatalytic activity of the MgO nanobelts can be attributed to various surface defects such as low-coordination anions (O-5c(2-) and O-4(C2-) at the terrace and edge sites, and O-3C(2-) at the corner and kink sites). Additionally, electron tunneling between these surface defects is possible. These defects have a strong adsorption capacity toward AA, DA, and UA. This affinity improves sensitivity and decreases the detection limits of the MgO nanobelt electrodes. (C) 2014 Elsevier B.V. All rights reserved.
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