Direct separation of faradaic and double layer charging current in potential step voltammetry

被引:17
作者
Tu, Jiarun [1 ,2 ]
Cai, Wensheng [1 ,2 ]
Shao, Xueguang [1 ,2 ]
机构
[1] Nankai Univ, Coll Chem, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Chem, Res Ctr Analyt Sci, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Capacitance current; Faradaic current; ITTFA; NPV; Potential step; TRANSFORMATION FACTOR-ANALYSIS; CURRENT CYCLIC VOLTAMMETRY; MULTIVARIATE CALIBRATION; SINUSOIDAL VOLTAMMETRY; STAIRCASE VOLTAMMETRY; PULSE POLAROGRAPHY; FOURIER-TRANSFORM; ELECTRODES; SCAN; CHEMOMETRICS;
D O I
10.1016/j.talanta.2013.07.021
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Double layer charging current in electrochemical systems has been a challenging problem in the last several decades because it causes interference to the accurate measurement of faradaic current. A method for extracting faradaic current and double layer charging current directly from the measured total current in potential step voltammetry is developed by using iterative target transformation factor analysis (ITTFA). The method constructs initial target vectors based on the theoretical formulae of faradaic and charging current, and then calculates the weights of faradaic and charging current in the measured signal via the iterative transformation of the initial vectors. Therefore, the two currents in one experiment can be obtained simultaneously without any assumption. The potential step voltammetric signals of potassium ferricyanide, copper sulfate and paracetamol were analyzed with the proposed method. The results show that the shape of the obtained voltammogram is an ideal sigmoid curve with horizontal straight baseline and plateaus, and the intensity of the signal is greatly enhanced. Therefore, the method provides a new way to measure the pure faradic current in the potential step voltammetric experiment, and may provide an alternative for improving the sensitivity of quantitative analysis. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:575 / 580
页数:6
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