Hilbert transform of voltammetric data

被引:9
作者
Arundell, M
Patel, BA
Yeoman, MS
Parker, KH
O'Hare, D
机构
[1] Univ London Imperial Coll Sci & Technol, PFSG, Dept Bioengn, London SW7 2AZ, England
[2] Univ Brighton, Sch Pharm & Biomol Sci, Brighton BN2 4GJ, E Sussex, England
基金
英国工程与自然科学研究理事会;
关键词
Hilbert transform; sinusoidal perturbations; 5-hydroxytryptamine (5-HT); non-linear; non-stationary; instantaneous frequency;
D O I
10.1016/j.elecom.2004.02.003
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The use of the fast Fourier transform (FFT) assumes stationarity and, in many applications, linearity; assumptions that are often invalid in the analysis of voltammetric data. Empirical mode decomposition followed by the Hilbert transform offers an alternative mode of analysis that can overcome these difficulties. The validity of the Hilbert transform for the analysis of non-linear signals merits application to electrochemistry which, to our knowledge, has not been carried out before. Preliminary results, for three well-characterised redox processes: (i) a thermodynamically reversible electron transfer; (ii) formation of a passivating layer; (iii) growth of an oxide layer on an electrode surface, suggest that it can provide useful and novel insights into electrochemical processes. A less well-characterised process, the adsorption of 5-hydroxytryptamine (5-HT) oxidation products on the surface of a glassy carbon electrode, is also investigated using the Hilbert transform. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:366 / 372
页数:7
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