METHOD FOR CHANGING THE POTENTIAL VALUE IN AN ELECTROCHEMICAL MEASUREMENT

DE602024000019T2Active Publication Date: 2025-02-26UNIV LODZKI
View PDF 0 Cites 0 Cited by

Patent Information

Application Number
DE602024000019
Authority / Receiving Office
DE · DE
Patent Type
Patents
Current Assignee / Owner
Filing Date
2024-03-14
Publication Date
2025-02-26
Estimated Expiration
2044-03-14

AI Technical Summary

Technical Problem

Existing electrochemical measurement methods are limited in their ability to efficiently characterize and differentiate substances by varying critical parameters like amplitude and frequency simultaneously during a single measurement.

Method used

A method that changes potential values during electrochemical measurements by simultaneously varying amplitude and frequency of a square wave, allowing for characterization of redox systems through multiple cycles with predefined series of amplitude and frequency values.

Benefits of technology

This method enables efficient characterization and differentiation of substances by interacting with the redox system through independent amplitude and frequency parameters, achieving cost- and time-efficient electrochemical characterization in a single measurement.

✦ Generated by Eureka AI based on patent content.
Patent Text Reader
Need to check novelty before this filing date? Find Prior Art

Description

[0001] The object of the invention is a method of changing the potential value during an electrochemical measurement as defined in claim 1.

[0002] In the method described in Electrochemical Faradaic Spectroscopy (ChemElectroChem, 2018, 5, 187-194), the authors used multiple, alternating applications of two fixed potential values, with a square waveform, at a predefined frequency. The potential values are set relative to the formal potential of the redox reaction that is being characterised in the course of the experiment so designed. The frequency with which the potential values are changed depends on the duration of the application of the potential value and is constant throughout the measurement. The current flowing through the circuit is measured each time at the end of the application of the potential. In this way, the forward values, the backward values and their difference (the resulting net current) are obtained. The number of cycles (series of two adjacent potentials) is not fixed. The end result of the measurement is the dependence of the measured current values as a function of the number of cycle changes or the duration of the experiment.

[0003] In another example presented in Multi-frequency analysis in a single square-wave chronoamperometric experiment (Electrochem. Commun., 2021, 124, 106943), the inventors used the analogous principle of alternating the application of the potential with a constant potential difference and a square waveform. In this case, however, the principle of changing frequency values during a single measurement was applied. This means that two adjacent pulses of potential (a single cycle) have the same duration, while successive cycles are already assigned different, predefined frequency values. The current flowing through the circuit is measured each time at the end of the application of the potential. In this way, the forward values, the backward values and their difference (the resulting net current) are obtained. The number of cycles (series of two adjacent potentials) is not fixed. The end result of the measurement is the dependence of the measured current values as a function of the number of cycle changes or the duration of the experiment.

[0004] In another case presented in Electrode kinetics from a single experiment: Multi-amplitude analysis in square-wave chronoamperometry; (Physical Chemistry Chemical Physics, (2022), 24, 24419-24428) the authors presented a modified method of measurement based on the reapplication of alternating potential values, this time with a fixed duration for each pulse, but varying the potential values in a predefined way. The current flowing through the circuit is measured each time at the end of the application of the potential. In this way, the forward values, the backward values and their difference (the resulting net current)) are obtained. The number of cycles (series of two adjacent potentials) is not fixed. The end result of the measurement is the dependence of the measured current values as a function of the number of shift cycles or the duration of the experiment.

[0005] CN 1740783 A discloses a solution analysis method including the following steps: applying a pulse scanning signal modulated by various constant-frequency amplitude modulation or amplitude frequency to a reference electrode and working electrode , detecting the response current signal on an auxiliary electrode to obtain the frequency-amplitude response spectrum, and analysing and processing said spectrum to obtain the result of solution characteristics.

[0006] The object of the invention is a method of changing the potential when conducting an electrochemical measurement using predefined, variable potential valuesas defined in claim 1. The method is based on the fact that in the first cycle of changing the potential value, the first potential is applied to the working electrode with the value of the formal potential of the tested redox system increased by a value of the first of the series of amplitudes. The duration of the first applied potential results from the first of the series of frequencies applied, while the value of the second return pulse results from the potential reduced by the value of the first of the series of amplitudes Then, in the second cycle of change, the value of the potential is changed analogously, but the value of the amplitude used is another of the series, while the change of the duration of the application of the potential is based on the next series of frequency values, in the next stage successive cycles of potential changes are realized analogously exhausting the previously planned series of values of amplitude and frequency. The number of positions in the series is not predefined, and the current flowing through the circuit is measured each time at the end of the duration of the applied potential values.

[0007] The principle of changing the values of these potentials is based on the simultaneous application of both changing amplitude and frequency values of the square wave. In this way, a single pair of applied potentials, the change cycle, receives one pair of frequency, duration and amplitude values, which is the difference between the applied value and the output value - determined in relation to the value of the formal potential of the redox reaction, which is subjected to characterization in such a designed measurement. In this way, the forward values, the backward values and their difference (the resulting net current) are obtained. The number of cycles, a series of two adjacent potentials, is not fixed. The end result of the measurement is the dependence of the measured current values as a function of the number of shift cycles or the duration of the experiment.

[0008] The advantage of the method according to the invention is that current values relevant only for the characterised substances are obtained, which is due to the fact that the applied potential values are changed within the influence of the electroactive substance on the recorded current close to the value of the formal potential of the given redox reaction.

[0009] The advantage of the method according to the invention is also the simultaneous influence on the recorded signal through the amplitude and frequency values changing at the same time, as parameters that provide the possibility of characterizing and differentiating the substances analysed in the measurement. The electrochemical characterisation of the substance under analysis, in terms of the electrode reaction mechanism and its kinetics, can be carried out in a single measurement, which is highly cost- and time-efficient compared with electrochemical characterisation methods known in the literature, such as cyclic voltammetry (CV) or square wave voltammetry (SWV).

[0010] An additional advantage of the method according to the invention is the use of a simultaneous change in the values of the characterizing parameters, i.e. the amplitude and frequency of a square wave in an electrochemical measurement based on the principles described for the method called electrochemical Faradaic spectroscopy. This allows interaction with the redox system under analysis through two independent parameters. In this way, it is possible to characterise the mechanism and kinetics of the electrode reaction in a single measurement, as both amplitude and frequency are triggers for the interaction of the measurement method with the redox system under analysis. None of the electrochemical analysis methods known so far allow the use of variable values of critical parameters during a single measurement.

[0011] The invention is illustrated in embodiments and figures, where fig. 1 shows a general diagram of the changes of the potential value throughout a single measurement and in fig. 2, which shows the parameters characterising the amplitude E sw , the frequency ƒ=1 / 2t p and the moment of registration of the flowing current (forward and backward, the resulting net value being the difference from adjacent pulses n and n+1 respectively).Embodiment 1

[0012] The assumed series of amplitude values are: 10, 20, 30, 40, 50, 60, 70, 80, 90 and 100 mV, while the series of frequency values are: 10, 15, 20, 30, 40, 50, 75, 100, 150 and 200 Hz. A potential (E m ) was applied to the working electrode, with the value of the formal potential of the tested redox system increased by a value of the first of the series of amplitudes, i.e. 10 mV. The duration of the applied potential is derived from the first of a series of applied frequencies, i.e. 10 Hz. The value of the potential in the second (return) pulse results from the potential (E m ) minus the value of the first in the amplitude series, i.e. 10 mV. This represents the first cycle of potential change. In the second cycle of changes, the value of the potential is changed in a similar manner, but the value of the amplitude used is the next in the series, i.e. 20 mV, while the change in the duration of application of the potential is based on the next in the series of frequency values, changed according to the series given above. Subsequent cycles of potential change were carried out in an analogous manner exhausting a pre-planned range of amplitude and frequency values. The number of positions in the ranks is not predefined. The current flowing through the circuit was measured each time at the end of the applied potential values.Embodiment 2

[0013] As in example 1, except that the frequency value is changed in a differently defined manner, e.g. every 0.1 on a logarithmic scale and similarly for the amplitude value, e.g. every 20 mV.

Claims

1. Method of changing the potential value during the electrochemical measurement, wherein in the first cycle of changing the potential value, the first potential value of a formal potential of the tested redox system is applied to the working electrode increased by a value of the first of the series of amplitudes, the duration of the first applied potential results from the first of the series of frequencies applied, the value of the second return pulse results from the potential reduced by the value of the first of the series of amplitudes, then in the second cycle of change, the value of the potential is changed analogously, but the value of the amplitude used is another of the series, while the change of the duration of the application of the potential is based on the next series of frequency values, in the next stage successive cycles of potential changes are realized analogously exhausting the previously planned series of values of amplitude and frequency, the intensity of the current flowing through the circuit is measured each time at the end of the duration of the applied values of the potential, wherein the amplitude values are selected from the range 5-250 mV and the frequency values are selected from the range 1-1000 Hz, and wherein the first value taken from those ranges are most preferably lowest or highest one, the number of cycles is from 5 to 1000, most preferably 50 and the range order is ascending or descending, independently of each other.