Method for optimally charging an electrochemical battery

Abstract

Method for charging an electrochemical accumulator, comprising a step (E10) of determining the initial state of the electrochemical accumulator, characterized in that it comprises a step (E11) of determining the regime of charge of the electrochemical accumulator by optimizing the product of a charging time saving and an energy saving as a function of the initial state of the electrochemical accumulator.

Claims

1. Method for charging an electrochemical accumulator comprising the following: (a) determining the initial state; (b) searching for an optimum charging regime determined by: (i) carrying out a phase of calibrating the electrochemical accumulator, making it possible to know its charging time as a function of different charging regimes for different electrochemical accumulator initial state values; (ii) defining two quantities called time saving and energy saving and respectively representing a sensitivity to the charging time of an accumulator and a sensitivity to the energy efficiency; and (iii) calculating for an initial state of the electrochemical accumulator, a charging regime for the electrochemical accumulator which maximizes the product of the time saving and of the energy saving defined in (ii); for an initial state of the accumulator corresponding to that determined in (a) and (c) charging the electrochemical accumulator with the charging regime defined in (b).

2. The method of claim 1, wherein the electrochemical accumulator calibration phase comprises carrying out nm charging phases for n different charging regimes and m initial states of charge of the electrochemical accumulator.

3. The method of claim 2, wherein n is between 5 and 10 inclusive and/or m is between 4 and 8 inclusive.

4. The method of claim 2, wherein the first electrochemical accumulator calibration phase comprises the iteration of the following steps E1 to E4 for each of the n charging regimes (I.sub.chi), for i varying from 1 to n, and of the m initial states of charge (SOC.sub.0j), for j varying from 1 to m: E1: charging the accumulator to full charge in nominal conditions; E2: discharging the accumulator in nominal conditions, to a state of charge of the electrochemical accumulator at the SOC.sub.0j value sought; E3: fully charging the accumulator at a charging regime (I.sub.chi); E4: completely discharging the accumulator in nominal conditions.

5. The method of claim 4, wherein the step of fully charging the accumulator at a charging regime (I.sub.chi) comprises the following substeps: E33: measuring and storing the total charging time (t.sub.chij) obtained; E34: measuring and storing the total quantity (A.sub.chij) of ampere-hours injected for this charge and/or of the energy (W.sub.hij) injected into the accumulator.

6. The method of claim 1, wherein the electrochemical accumulator calibration phase also comprises an iteration of a number of charging phases for different temperatures.

7. Method for charging an electrochemical accumulator according to claim 1, wherein the step of determining the initial state of the electrochemical accumulator comprises the calculation of its initial state of charge (SOC.sub.0) or of its initial state of energy (SOE.sub.0).

8. Method for charging an electrochemical accumulator according to claim 1, wherein the step of determining the charging regime of the electrochemical accumulator comprises maximizing the product G.sub.t(I.sub.ch)G.sub.wh(I.sub.ch) where G.sub.t(I.sub.ch) is the charging time saving, which is calculated as the ratio between the charging time saved for a considered charging regime (I.sub.ch) relative to a reference slow charging time, to the charging time of this slow regime, and where G.sub.wh(I.sub.ch) is the energy saving, which is defined as the ratio between the reduction of energy injected into the accumulator at the considered charging regime (I.sub.ch) relative to the energy injected at a reference slow regime, to the energy injected into the accumulator at the slow regime.

9. Method for charging an electrochemical accumulator according to claim 1, wherein it comprises a step of charging the electrochemical accumulator comprising a charging period with constant current (Ich) whose value is determined to maximize the product of a charging time saving and an energy saving.

10. Method for charging an electrochemical accumulator according to claim 9, wherein the charging step comprises a charging period with constant current up to a voltage threshold value, then a charging period with constant voltage at this threshold value.

Description

(1) These objects, features and advantages of the present invention will be explained in detail in the following description of a particular embodiment given as a nonlimiting example in relation to the attached figures in which:

(2) FIG. 1 represents the trend of the charging current and voltage as a function of time according to an IU charging algorithm for an electrochemical accumulator of the prior art.

(3) FIG. 2 illustrates a few curves representing the charging time of an accumulator as a function of the charging regime, for different initial states of charge, according to the embodiment of the invention.

(4) FIG. 3 represents the time saving as a function of the energy saving, for different initial state of charge SOC.sub.0 values according to the embodiment of the invention.

(5) FIG. 4 represents the product of the time saving as a function of the energy saving, for different initial state of charge SOC.sub.0 values according to the embodiment of the invention.

(6) FIG. 5 represents an algorithm of the charging method according to the embodiment of the invention.

(7) According to the embodiment, the invention relies on a method for charging an electrochemical accumulator, the algorithm of which is illustrated in FIG. 5, which comprises a first phase of calibrating this electrochemical accumulator or an accumulator representative of the electrochemical technology used.

(8) This first calibration phase consists in determining the charging time needed to fully charge an accumulator and the effectiveness of said charge, from a number of initial states of the accumulator and from a number of charging regimes. This calibration thus makes it possible to define a table of values or chart, which will serve as a reference in optimizing the charging of an accumulator, which will be explained hereinbelow.

(9) According to the embodiment, the calibration is obtained for a number of accumulator charging regimes, that is to say for a number of electrical conditions I, U. For this, it is, for example, possible to define a number of charging current values I.sub.ch in the case of the use of an IU algorithm as shown with reference to FIG. 1. It should be noted that this same principle remains valid for any charging algorithm for an electrochemical accumulator, regardless of the electrical algorithm used. For simplicity, the IU algorithm will be considered hereinbelow.

(10) These different charging regime values include the nominal regime, that is to say the value recommended by the manufacturer, and the charging performance is truly tested for each of these charging regimes. A number n of different charging current values between 5 and 10 represents a good trade-off. These n values can be chosen, uniformly distributed or not, over a range of use of the accumulator, and/or for high or low regimes.

(11) Then, the calibration is also performed for different initial states of charge SOC.sub.0 of the accumulator. It should be noted that the state of charge of the accumulator, commonly referred to as simply SOC, represents the available capacity of the accumulator over a scale from 0 to 1, the values of 0 and 1 respectively representing the fully discharged and fully charged states of the accumulator. This calibration is performed over m state of charge values, m advantageously being between 4 and 8.

(12) It should be noted that the state of energy, referred to as SOE, defined as the ratio between the energy E.sub.d/PN available assuming an energy discharge in nominal conditions of the accumulator and the nominal energy E.sub.N, therefore defined by the formula SOE=E.sub.d/PN/E.sub.N, can be substituted for the SOC parameter mentioned above. This SOE value is, likewise, between 0 and 1, the value equal to 1 corresponding to a fully charged state of energy of the accumulator and the value equal to 0 corresponding to a fully discharged state.

(13) The calibration phase therefore relies on carrying out nm charging phases on an electrochemical accumulator by varying the regime and the initial state of charge of the accumulator, as described above. These nm charging conditions are chosen in such as way as not to cause any abnormal degradation or ageing of the accumulator. They remain within the ranges of values that are considered to be acceptable by the accumulator. For these different charging cycles, the ambient temperature remains constant, preferably between 20 and 25 C. For an aqueous electrochemical accumulator, water is regularly added to maintain its performance throughout the calibration phase.

(14) According to the embodiment of the invention, this calibration phase finally comprises the following steps, repeated in succession for each of the n values of I.sub.ch, (for i varying from 1 to n) and of the m SOC.sub.0j values (for j varying from 1 to m):

(15) E1: charging the accumulator to full charge in nominal conditions, for a charging regime comprising a phase with constant current Ichn, at the nominal value, then a phase with constant voltage Uthresh, as represented in FIG. 1;

(16) E2: discharging in nominal conditions, for a discharging current I.sub.dch equal to the nominal value I.sub.dchn. It should be noted that the latter is defined within a discharging band recommended by the manufacturer, and to be as reproducible as possible to obtain the most reliable calibration possible. For example, the discharging regime that makes it possible to achieve the full discharge in one hour is acceptable for the lithium-ion technology. This discharge is continued until the quantity of ampere/hours restored (Ah) is equal to (1-SOC.sub.c0j)C.sub.n, where C.sub.n represents the nominal capacity of the accumulator, the total number of Ah restored in a total discharge in nominal conditions. Such a discharge makes it possible to position the electrochemical accumulator in a state of charge at the SOC.sub.0j value sought;
E3: fully charging the accumulator at a regime i, defined by a charging current I.sub.ch=I.sub.chi. This step comprises the following substeps: E31: charging in phase I with constant current I.sub.chi up to the voltage threshold value U.sub.thresh; E32: charging in phase U at constant voltage with the value U.sub.thresh until the current drops below its threshold value I.sub.thresh;
It should be noted that these two substeps E31 and E32 will be adapted to any other charging algorithm depending on the accumulator technology being calibrated. Then, in parallel with the two substeps E31 and E32, the following substeps are carried out: E33: measuring and storing the total charging time t.sub.chij obtained from the conditions of regime I.sub.chi and of initial state of charge SOC.sub.0j; E34: measuring and storing the total quantity A.sub.chij of ampere-hours injected for this charge and/or the energy W.sub.hij injected into the accumulator, from the conditions of regime I.sub.chi and of initial state of charge SOC.sub.0j.

(17) E4: new total discharge in the nominal conditions of the battery.

(18) A pause is inserted between these different steps E1-E4, for a sufficient relaxation time, for example between 10 and 60 minutes.

(19) According to a variant embodiment, the calibration is also performed by varying the temperature. For this, p temperature values are chosen, within a range of, for example, 0 to 40 C. The preceding steps E1 to E4 are then reiterated for the nmp values considered, in a table with three entries instead of two.

(20) When this calibration is done, it is possible to deduce laws between all the values used, notably between the charging time, the initial state of charge and the charging regime of the electrochemical accumulator. It is quite simply possible to extrapolate the values not directly measured by the iteration steps explained previously from actual measurements performed. The calibration phase may thus comprise a final step E5 of determining all the values from the nm (or nmp) actual measurements obtained. The results of this calibration phase are stored for analysis.

(21) FIG. 2 illustrates, by way of example, some curves representing the charging time of an accumulator as as function of the charging regime, for different initial states of charge. More specifically, the curves 11, 12, 13, 14, 15, 16, 17 correspond respectively to an initial state of charge of 0%, 20%, 40%, 60%, 80%, 90% and 95%.

(22) As a variant, the calibration described above can be replaced by a theoretical calculation, based, for example, on a physical modelling of the accumulator, or by any other method making it possible to provide as output the values of the table mentioned previously.

(23) Then, the method for charging an electrochemical accumulator comprises a second charging phase, comprising determining the conditions of charge of a certain accumulator, which relies on finding an optimum trade-off between reducing the charging time and its efficiency or increasing the charging energy injected.

(24) According to the embodiment, the following two quantities are considered for measuring the two criteria mentioned above:

(25) G.sub.t(I.sub.ch): this is a time saving, which is calculated as the ratio between the charging time t.sub.ch saved for a charging regime I.sub.ch relative to a slow charging time (slow regime I.sub.I), to the charging time of this slow regime.

(26) This saving is therefore defined by the following formula:
G.sub.t(I.sub.ch)=(t.sub.ch(I.sub.ch)t.sub.ch(I.sub.I))/t.sub.ch(I.sub.I)

(27) G.sub.wh(I.sub.ch): this is the energy saving, which is defined as the ratio between the reduction of energy injected into the accumulator at the fast charging regime I.sub.ch relative to that injected at a reference slow regime I.sub.I, to the energy injected into the accumulator at the slow regime.

(28) This saving is therefore defined by the following formula:
G.sub.wh(I.sub.ch)=(W.sub.h(I.sub.ch)W.sub.h(I.sub.I))/W.sub.h(I.sub.I)

(29) It should be noted that the above savings have been used by way of example, but there are other possibilities for defining quantities that make it possible to represent the time saving and the energy saving in an equivalent manner. These saving terms will therefore be understood to cover all quantities in the wide sense which respectively represent a sensitivity to the charging time of an electrochemical accumulator and a sensitivity to the energy efficiency of the charging of an electrochemical accumulator.

(30) FIG. 3 represents the time saving as a function of the energy saving, for different initial state of charge SOC.sub.0 values. More specifically, the curves 21, 22, 23, 24, 25 respectively represent these curves for initial state of charge values of 0%, 20%, 40%, 60% and 80%. They clearly show that, for a zero time saving, the energy efficiency is maximum, and that, when the time saving increases, the energy efficiency decreases, to tend towards zero for a time saving between 75 and 90%. It should be noted that the plotting of these curves is made possible by virtue of the calibration data obtained in the first phase, as explained previously.

(31) According to the embodiment, the optimum trade-off of the conditions of charge of the electrochemical accumulator is defined by considering the product G.sub.t(I.sub.ch)G.sub.wh(I.sub.ch) between the two savings defined above and by maximizing this product. Thus, the method comprises a step of searching for the charging regime (here the charging current I.sub.ch) which makes it possible to maximize this product.

(32) FIG. 4 represents this product as a function of the energy saving, for different initial state of charge SOC.sub.0 values. More specifically, the curves 31, 32, 33, 34, 35 respectively represent these curves for initial state of charge values of 0%, 20%, 40%, 60% and 80%. The points 41, 42, 43, 44, 45 represent the optimum situations.

(33) Thus, the method for charging an electrochemical accumulator comprises a step E10 of determining the state of charge SOC.sub.0 of the accumulator, or an equivalent value like a state of energy SOE.sub.0. It thus generally comprises a step E10 of determining the initial state of the electrochemical accumulator. The implementation of this step makes it possible, for example, to determine which curve out of the curves 31 to 35 of FIG. 4 is relevant in light of the state of the accumulator that is to be charged.

(34) Then, it comprises a step E11 of searching for the optimum charging regime, which maximizes the product of the savings explained above. Its possible implementation consists in choosing the maximum point 41 to 45 of the curve identified 31 to 35 above. This point makes it possible to get up to the value of the current I.sub.ch of the corresponding charging regime, by virtue of the calibration data. Then, the charging as such is performed in a step E12, based on the usual IU algorithm, by using the determined current value I.sub.ch for the phase I of this charge, the second phase U remaining standard, up to the end of the charge according to any predefined criteria.

(35) Naturally, the identification of the maximum product between the two savings considered can be done as a variant by any other mathematical calculation means than the use of the curves of FIG. 4.

(36) Furthermore, this principle is applicable for any predefined charging algorithm, like the constant current algorithms generally used for NiMH-type accumulators, or the algorithms of IUi type. It is also applicable to any other algorithm. The concept of the invention is thus suited to any electrochemical accumulator, whatever its electrochemical technology used, such as lithium, nickel or lead.

(37) The invention also relates to a device for charging such an electrochemical accumulator, which implements the charging method described above.

(38) It also relates to a system comprising a device powered by an electrochemical accumulator and a device for charging this accumulator, which implements the charging method described above. For this, the system can use software and/or hardware means, comprising, for example, a memory incorporating the calibration data defined by the calibration phase described previously, and a computer for accurately knowing the state of the accumulator, in real time or not, and for implementing the above calculations.