The present disclosure relates to a method for fast-charging an electrochemical cell. It also relates to a fast-charging system implementing this method and to fast-charging controller implemented in this system.
Many rechargeable (secondary) battery chemistries are currently produced such as: i. Lithium ion batteries (LIB), ii. Lead acid batteries (LAB), iii. Nickel-cadmium batteries (NiCd), iv. Nickel Metal Hydride batteries (NiMH), v. Redox flow batteries (RFB) and Sodium sulfur batteries (NaS). In 2016 above 450 GWh in batteries were produced worldwide; 350 GWh of which are LAB and 90 GWh are LIB. In 2016 LAB and LIB generated USD35B and US30B in revenue, respectively, out of a total market of USD69B. Other batteries generated about USD4B in revenue. The overall market of rechargeable batteries has a CAGR of 8%.
LIB is the fastest growing segment with average CAGR of 25% over the last 10 years. LIB dominate the autonomous power sources with close to 7 billion cells produced in 2016.
LIB main advantages are: 1) high energy density, 2) high power density, 3) long life, 4) wide range of operation temperatures, 5) No memory effect, 6) good safety record, 7) economical and, 8) recyclable.
LIB major applications include portable electronics, electrical vehicles and energy storage systems, the two latter are the fastest growing market segments.
Currently, most LIB are charged using the so called “CCCV” protocol. CCCV charging consists of applying a constant current (CC) until the voltage reached a preset value. A constant voltage (CV) is then applied to the cell until full charge is reached.
To ensure long cycle life under CCCV charging protocol requires a charging time typically comprised between 2 and 8 hours depending on type of LIB (energy or power design), application and on available power of the charging unit.
Fast charging with CCCV (below 30 minutes) is technically possible. However, CCCV fast charging results in premature end of life (EoL) of the cell and the battery system and may pose safety problems.
There is a strong demand to reduce the charging time in all LIB applications including in electro mobility, in mobile electronics and in energy storage systems (ASS).
Fast charge should not come at the expense of battery life and safety.
There is a crucial need to develop new fast-charging methods and systems different from current CCCV. Besides CCCV, other fast-charging methods have been reported:
Prior art fast-charging methods are, for example, disclosed in U.S. Pat. No. 9,425,646 B2 (Wang), US 2016/011898 A1 (Luo et al.), US 2015/0204625 A1 (Josephus et al.), US 2017/0256960 A1 (Shin et al.), US 2017/0229891 A1 (Lee et al.), U.S. Pat. No. 5,440,221 (Landau et al.), US 2017/0288417 A1 (Trichy), U.S. Pat. No. 9,065,292 B2 (Yazami),
U.S. Pat. No. 9,065,292 B2 discloses a method of charging an electrochemical cell, the method comprising the steps of providing the electrochemical cell and providing a time-varying charging voltage to the electrochemical cell, thereby generating a charging current resulting in charging of the electrochemical cell. The time-varying charging voltage has a non-linear time dependency provided by V=V0±k(t)t and Vm≤Vs≤Vmax; wherein V is the time-varying charging voltage, t is time, V0 is an initial voltage, k(t) is a time dependent voltage rate, Vmin is a minimum voltage and Vmax is a maximum voltage.
It is an objective to provide a battery fast-charging method and system, in order to reduce charging time down to 10 minutes and below, and to extend battery life and enhance battery reliability and safety.
This goal is achieved with a method for fast-charging an electrochemical cell, the method comprising the steps of:
wherein the step of providing a time-varying charging voltage is arranged to apply N bundles of current pulses in such a way that:
The parameters N, M, Pk, ik, ni,k·τi,k, can be selected so that:
τi,k can be comprised between 1 s and 120 s.
The M parameter can be determined as equal to 36.
The amount of SOC increase target value can be comprised in the range [20%, 100%].
Two successive current pulse ik and ik+l in a bundle can be separated by a rest time ρi,k and two successive bundles are separated by a rest time Ok.
The parameters N, M, Pk, ik, ni,k·τi,k, can be selected so that the total charge time (tcharge) computed as
t
charge=Σk=1k=NΣi=1i=P
is substantially comprised between 2 hours and 2 minutes.
The charging method according to the present disclosure can further comprise a step for determining the state of charge (SOC) of the electrochemical cell.
The SOC determination step can comprise implementing a SOC determination method among a group comprising Coulomb counting, Kalman filter, extended Kalman filter, neural networks or thermodynamics.
The SOC determination step can be at least partially implemented by an electronic circuit close to or within the electrochemical cell.
The SOC determination step can be at least partially implemented by an electronic circuit close to or within a fast-charging system implementing the charging method.
The charging method according to the present disclosure can be applied to a secondary electrochemical cell belonging, for example, to a group comprising lithium ion batteries, Sodium ion batteries, Nickel cadmium batteries, lithium polymer batteries, solid state lithium batteries, sodium-sulfur batteries, metal-air batteries, sodium-nickel chloride batteries, nickel metal hydride batteries, lead-acid batteries, or redox-flow batteries.
The metal in a metal-air battery can consist of lithium, sodium, magnesium, zinc, aluminum and a combination thereof.
According to another aspect of the present disclosure, it is proposed a system for fast-charging an electrochemical cell, comprising:
wherein the power supply is controlled to apply N bundles of current pulses in such a way that:
The charging system of the present disclosure can further comprise means for real-time determining the state of the charge (SOC) of the electrochemical cell.
The SOC-determination means can comprise an electronic circuit close to or within the electrochemical cell, and an electronic circuit close to or within the power supply.
According to another aspect of the present disclosure, it is proposed a secondary battery charging controller comprising a control circuit for controlling a charging voltage provided by a power supply for charging a secondary battery, wherein the control circuit controls the charging voltage to provide a time-varying charging voltage to the electrochemical cell, thereby generating a charging current resulting in charging of the electrochemical cell from the initial state of charge (SOCi) to a state-of-charge target value (SOCf),
wherein the charging controller is programed to apply N bundles of current pulses in such a way that:
A new charging protocol has thus been demonstrated based on intermittent current pulses (Cascade Pulse Charging Protocol: CPC). CPC enables fast charging in 10 minutes or less.
CPC applies to any rechargeable battery chemistry including LIB, NIMH, NiCd, LAB, Redoc flow, NaS, or NaNiCl2. CPC is safer than CCCV and extends battery life.
Activation polarization ηa has been measured during pulse and plotted vs. state of charge (SOC). It is found that ηa is low under CPC charging even at very high rate (12C).
CPC parameters (N, Pk, ni,k, ri,k, pi,k, Wi,k, Vcharge) are adjustable to minimize the charge time and extend the battery life.
Comparing two bundles (6C, 9C, 12C) and (12C, 9C, 6C), the later gives lower end of charge voltage Vcharge=4.65 V vs. 4.95 V for the former. Therefore, a bundle with decreasing C-rate sequence should be preferred to a one with increasing sequence.
When the C-rate in a bundle is low such as in (1C, 3C, 6C) bundle, a longer time is needed to fully charge a cell (45 minutes vs. 15 minutes).
The activation polarization ηa under CPC is low (<200 mV), therefore, there is less damage to the cell after each charge allowing for longer cycle life.
The activation polarization qa profile can be used for efficient charging under varying charging current Icharge with SOC.
A relationship between qa and Icharge can be drawn where qa and Icharge vary in reciprocal ways as function of SOC such as:
I
charge(SOC)=k(ηa(SOC))−a,a>0,k=constant>0
The charging method according to the present disclosure can be applied to any rechargeable battery chemistry, including but not limited to NiIVIEL NiCd, LAB, NaS, NaNiCl2, redox flow (ZnBr, VRB, . . . ).
Charge from any initial SOC to any final SOC (not limited to 0-100% charging). For example, the fast-charging protocol CPC according to the present disclosure can be applied to charging between 20% and 80% SOC. Initial SOC can be determined by existing methods such as those based on coulomb counting, Kalman filter, Extended Kalman Filter, Neural networks or thermodynamics.
These and other features and advantages of the present disclosure will become better understood with regards to the following description, appended claims, and accompanying drawings wherein:
With reference to
In this description, the battery 2 includes cylindrical LIB cells of about 700 mAh nominal capacity. Cells have been subjected to the following tests:
1. Cells are first cycled 3 times
2. Cells at step c) are charged using the CPC protocol.
3. Cells are discharged under C/2 rate (350 mA) to 2.5V. Discharge capacity is then determined.
During the CPC protocol; the activation polarization ηa(I,k) (mV) and activation resistance Ra(i,k) are determined for each pulse I,k using the equations:
Where e(t) is the cell voltage during pulse, to is a delay time and I (i,k) is the current in A. Ra(i,k) is in mω. Here 0.5 s<t0<2 s.
Examples: nik = 2 and ni,k = 0.33 correspond to a charge in 0.5 hour and in 3 hours, respectively. The C-rate definition applies likely to charge and to discharge rates.
A corresponding typical voltage profile during a current pulse is represented in
Current and voltage profiles during a bundle are illustrated by
The following examples are given to illustrate the CPC concept. In these examples:
CPC test data illustrated below include
A first 10-minute charging test implementing the charging method according to the present disclosure is now described with reference to
A second 10-minute charging test implementing the charging method according to the present disclosure is now described with reference to
The following table summarizes the main experimental results obtained with the two above-cited tests:
A group of experimental tests corresponding to 15 minutes charging is now described with reference to
A first 15-minute charging test has been done with the following test conditions:
A second 15-minute charging test has been done with the following test conditions:
A third 15-minute charging test has been done with the following test conditions:
A fourth 15-minute charging test has been done with the following test conditions:
The following Table summarizes the main results obtained from these four tests and illustrated by
Another group of tests has been done with the CPC method according to the present disclosure with charging times varying from about 5 hours to 20 minutes, and the main results are summarized in the table below.
The experimental tests implementing the CPC charging protocol according to the present disclosure show, in comparison with the convention CCCV protocol, that
Number | Date | Country | Kind |
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10201710301V | Dec 2017 | SG | national |
This application is a national phase entry under 35 U.S.C. § 371 of International Patent Application PCT/M2018/059705, filed Dec. 6, 2018, designating the United States of America and published as International Patent Publication WO 2019/162748 A1 on Aug. 29, 2019, which claims the benefit under Article 8 of the Patent Cooperation Treaty to Singapore Patent Application Serial No. 10201710301V, filed Dec. 6, 2017.
Filing Document | Filing Date | Country | Kind |
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PCT/IB2018/059705 | 12/6/2018 | WO | 00 |