Battery balancing

  (Redirected from Battery balancer)

Battery balancing and battery redistribution refer to techniques that improve the available capacity of a battery pack with multiple cells (usually in series) and increase each cell's longevity.[1] A battery balancer or battery regulator is an electrical device in a battery pack that performs battery balancing.[2] Balancers are often found in lithium-ion battery packs for laptop computers, electrical vehicles. etc.

Battery balancer
Contacts on a DeWalt 20V Max (18V XR in Europe) power tool battery. The C1–C4 contacts are connected to the individual cells in the battery and are used by the charger for battery balancing.

RationaleEdit

The individual cells in a battery pack naturally have somewhat different capacities, and so, over the course of charge and discharge cycles, may be at a different state of charge (SOC). Variations in capacity are due to manufacturing variances, assembly variances (e.g., cells from one production run mixed with others), cell aging, impurities, or environmental exposure (e.g., some cells may be subject to additional heat from nearby sources like motors, electronics, etc.), and can be exacerbated by the cumulative effect of parasitic loads, such as the cell monitoring circuitry often found in a battery management system (BMS).

Balancing a multi-cell pack helps to maximize capacity and service life of the pack by working to maintain equivalent state-of-charge of every cell, to the degree possible given their different capacities, over the widest possible range. Balancing is only necessary for packs that contain more than one cell in series. Parallel cells will naturally balance since they are directly connected to each other, but groups of parallel wired cells, wired in series ( parallel-series wiring ) must be balanced between cell groups.

To prevent undesirable, and often unsafe conditions, the battery management system must monitor the condition of individual cells for operational characteristics such as temperature, voltage, and sometimes current drawn – although the latter is often only measured per-pack rather than per-cell, perhaps with one-shot protection at the cell level against abnormally high current (such as in a short, or other failure condition.)

Under normal operation, discharging must stop when any cell first runs out of charge even though other cells may still hold significant charge. Likewise, charging must stop when any cell reaches its maximum safe charging voltage. Failure to do either may cause permanent damage to the cells, or in extreme cases, may drive cells into reverse polarity, cause internal gassing, thermal runaway, or other catastrophic failures. If the cells are not balanced, such that the high and low cutoff are at least aligned with the state of the lowest capacity cell, the energy that can be taken from and returned to the battery will be limited.

There are two major approaches to balancing: Passive balancing, and active balancing.

Passive balancing equalizes the state of charge at some fixed point – usually either "top balanced", with all cells reaching 100% SOC at the same time; or "bottom balanced", with all cells reaching minimum SOC at the same time. This can be accomplished by bleeding energy from the cells with higher state of charge (e.g., a controlled short through a resistor or transistor), or shunting energy through a path in parallel with a cell during the charge cycle so that less of the (typically regulated constant) current is consumed by the cell. Passive balancing is inherently wasteful, with some of the pack's energy spent as heat for the sake of equalizing the state of charge between cells. The build-up of waste heat may also limit the rate at which balancing can occur.

In contrast, active balancing attempts to redistribute energy from cells at full charge to those with a lower state of charge. Energy can be bled from a cell at higher SOC by switching a reservoir capacitor in-circuit with the cell, then disconnecting the capacitor and reconnecting it to a cell with lower SOC, or through a DC-to-DC converter connected across the entire pack. Due to inefficiencies, some energy is still wasted as heat, but not to the same degree. Despite the obvious advantages, the additional cost and complexity of an active balancing topology can be substantial, and doesn't always make sense depending on the application.

A full BMS might include active balancing as well as temperature monitoring, charging, and other features to maximize the life of a battery pack.[3]

Lithium ion rechargeable battery cells are rather more sensitive to overcharging, overheating, improper charge levels during storage, and other forms of mistreatment, than most commonly used battery chemistries. The reason is that the various lithium battery chemistries are susceptible to chemical damage (e.g., cathode fouling, molecular breakdown, etc.) by only very slight overvoltages (i.e., millivolts) during charging, or more charging current than the internal chemistry can tolerate at this point in its charge/discharge cycle, and so on. Heat accelerates these unwanted, but so far inescapable, chemical reactions and overheating during charging amplifies those effects. Because lithium chemistries often permit flexible membrane structures, lithium cells can be deployed in flexible though sealed bags, which permits higher packing densities within a battery pack. Some of the breakdown products (usually of electrolyte chemicals or additives) outgas when mistreated; such cells will become 'puffy' and are very much on the way to failure. In sealed lithium ion cylinders, the same outgassing has caused rather large pressures (800+ psi has been reported[citation needed]); such cells can explode if not provided with a pressure relief mechanism. Compounding the danger is that many lithium cell chemistries include hydrocarbon chemicals[citation needed] (the exact nature of which is typically proprietary) which are flammable. Not only is explosion a possibility with mistreated lithium cells, but even a non-explosive leak can cause a fire.

Most battery chemistries have less dramatic, and less dangerous, failure modes. The chemicals in most batteries are often toxic to some degree, but are rarely explosive or flammable[citation needed]; many are corrosive, which accounts for advice to avoid leaving batteries inside equipment for long periods as the batteries may leak and damage the equipment. Lead acid batteries are an exception, for charging them generates hydrogen gas, which can explode if exposed to an ignition source (e.g., a lit cigarette ) and such an explosion will spray sulfuric acid in all directions. Since this is corrosive and potentially blinding, this is a particular danger.

TechnologyEdit

 
Different states of charge in a battery pack. Cell 5 has lower capacity. Cell 5 has high self-discharge rate

Balancing can be active or passive.[4] The term battery regulator typically refers only to devices that perform passive balancing.

In passive balancing, energy is drawn from the most charged cell and dissipated as heat, usually through resistors.

In active balancing, energy is drawn from the most charged cell and transferred to the least charged cells, usually through capacitor-based, inductor-based or DC-DC converters.[5]

Battery balancing can be performed by DC-DC converters, in one of 3 topologies:

  • Cell-to-battery
  • Battery-to-cell
  • Bidirectional

Typically, the power handled by each DC-DC converter is a few orders of magnitude lower than the power handled by the battery pack as a whole.

See alsoEdit

ReferencesEdit

  1. ^ http://ww1.microchip.com/downloads/en/AppNotes/00231a.pdf
  2. ^ Voltage controlled bypass regulator with digital interface. Manzanitamicro.com (2006-02-22). Retrieved on 2013-04-27.
  3. ^ Battery Management and Monitoring Systems BMS. Mpoweruk.com. Retrieved on 2013-04-27.
  4. ^ Wen, Sihua (September 2009). "Cell balancing buys extra run time and battery life" (PDF). Analog Applications Journal: 14.
  5. ^ Diao, Weiping; et al. (July 2017). "Active battery cell equalization based on residual available energy maximization". Applied Energy: 9. doi:10.1016/j.apenergy.2017.07.137.

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