Method for the in-situ recalibration of a comparison electrode incorporated into an electrochemical system

Patent metadata

Field	Value
Publication number	US-10067086-B2
Application number	US-201415038192-A
Country	US
Kind code	B2
Filing date	Nov 14, 2014
Priority date	Nov 21, 2013
Publication date	Sep 4, 2018
Grant date	Sep 4, 2018

Abstract

A method recalibrates in situ a comparison electrode integrated into an electrochemical system. The electrochemical system includes a working electrode, a counter electrode, and an electrolyte. The method includes verifying a potential of the comparison electrode relative to the working electrode or to the counter electrode in situ, detecting whether there is a drift in the potential of the comparison electrode relative to a potential plateau for which the comparison electrode was functionalized or designed, and when the drift is detected, recalibrating the comparison electrode in situ.

First claim

The invention claimed is:

1. A method for recalibrating in situ a comparison electrode integrated into an electrochemical system including a working electrode, a counter electrode, and an electrolyte, the method comprising:
connecting the comparison electrode to the working electrode or the counter electrode;
verifying a potential of the comparison electrode relative to the working electrode or to the counter electrode in situ by
measuring the potential of the comparison electrode, then
applying a verification positive current of a first duration, then
measuring a first variation in the potential of the comparison electrode, then
applying a verification negative current of a second duration, then
measuring a second variation in the potential of the comparison electrode, and then
determining a voltage measurement depending on the first variation in the potential and the second variation in the potential;

detecting whether there is a drift in the potential of the comparison electrode relative to a potential plateau for which the comparison electrode was functionalized or designed when either the first variation in the potential of the comparison electrode or the second variation in the potential of the comparison electrode is greater than a plateau voltage for which the comparison electrode was functionalized or designed increased, for a given temperature, by a shift voltage value; and
when the drift is not detected, reconnecting the comparison electrode to the working electrode or the counter electrode so that the electrochemical system can be charged and discharged,
when the drift is detected, recalibrating the comparison electrode in situ by
applying a recalibration negative current until the first variation in the potential, then
memorizing a potential value obtained by lower bound, then
applying a recalibration positive current until the second variation in the potential, then
memorizing the potential value obtained by upper bound, then
determining a capacity of the comparison electrode depending on the lower bound, the upper bound, and applied currents, and then
determining a state of ageing of the comparison electrode from an initial capacity and the determined capacity, and

when the state of ageing is not above a threshold, applying the negative current to obtain a state of charge, and reconnecting the comparison electrode to the working electrode or the counter electrode so that the electrochemical system can be charge and discharged, and
when the state of ageing is above a threshold, determining that the comparison electrode has failed.

2. The method as claimed in, claim 1 , wherein the shift voltage value is at least equal to 20 mV±5 mV.

3. The method as claimed in claim 1 , wherein the potential of the comparison electrode is verified and drift in the potential of the comparison electrode detected periodically, depending on a time period that has passed since a last functionalization.

4. The method as claimed in claim 1 , wherein the potential of the comparison electrode is verified during a time period consecutive to a complete recharge, no current circulating through the electrochemical system during said time period.

5. The method as claimed in claim 1 , wherein a product of an amplitude of recalibration currents multiplied by a duration of application of recalibration currents is higher than one fifth of a total charge of the comparison electrode.

6. The method as claimed in claim 1 , further comprising:
limiting intensities of the verification positive current and the first duration so that the product of an amplitude of the verification positive current multiplied by the first duration is between one tenth of the maximum charge of the comparison electrode and the maximum charge of the comparison electrode.

7. The method as claimed in claim 1 , further comprising:
limiting intensities of the verification negative current and the second duration so that the product of an amplitude of the verification negative current multiplied by the second duration is between one tenth of the maximum charge of the comparison electrode and the maximum charge of the comparison electrode.

Assignees

• Renault Sas

Inventors

• Genies Sylvie
• Alias Melanie
• Leirens Sylvain
• Kirchev Angel Zhivkov

Classifications

• H01M10/48 Primary

  Accumulators combined with arrangements for measuring, testing or indicating the condition of cells, e.g. the level or density of the electrolyte (constructional details of current conducting connections for detecting conditions inside cells or batteries, e.g. details of voltage sensing terminals, H01M50/569) · CPC title

• H01M6/5005

  Auxiliary electrodes · CPC title

• H01M2010/4271

  Battery management systems including electronic circuits, e.g. control of current or voltage to keep battery in healthy state, cell balancing · CPC title

• G01N27/4163 Primary

  checking the operation of, or calibrating, the measuring apparatus (G01N27/3274, G01N27/4175 and G01N33/0006 take precedence) · CPC title

• G01N27/301

  Reference electrodes · CPC title