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Snippet from Wikipedia: Nickel–metal hydride battery

A nickel metal hydride battery, abbreviated NiMH or Ni–MH, is a type of rechargeable battery. The chemical reaction at the positive electrode is similar to that of the nickel–cadmium cell (NiCd), with both using nickel oxide hydroxide (NiOOH). However, the negative electrodes use a hydrogen-absorbing alloy instead of cadmium. A NiMH battery can have two to three times the capacity of an equivalent size NiCd, and its energy density can approach that of a lithium-ion battery.



A nickel–metal hydride battery, abbreviated NiMH or Ni–MH, is a type of rechargeable battery. Its chemical reactions are somewhat similar to the largely obsolete nickel–cadmium cell (NiCd). NiMH use positive electrodes of nickel oxyhydroxide (NiOOH), like the NiCd, but the negative electrodes use a hydrogen-absorbing alloy instead of cadmium, being in essence a practical application of nickel–hydrogen battery chemistry. A NiMH battery can have two to three times the capacity of an equivalent size NiCd, and their energy density approaches that of a lithium-ion cell.

The typical specific energy for small NiMH cells is about 100 W·h/kg, and for larger NiMH cells about 75 W·h/kg (270 kJ/kg). This is significantly better than the typical 40–60 W·h/kg for NiCd, and similar to the 100–160 W·h/kg for lithium-ion batteries. NiMH has a volumetric energy density of about 300 W·h/L (1,080 MJ/m3), significantly better than NiCd at 50–150 W·h/L, and about the same as lithium-ion at 250–360 W·h/L.

NiMH batteries have replaced NiCd for many roles, notably small rechargeable batteries. NiMH batteries are very common for AA (penlight-size) batteries, which have nominal charge capacities (C) of 1.1–2.8&nbsp;A·h at 1.2&nbsp;V, measured at the rate that discharges the cell in five hours. Useful discharge capacity is a decreasing function of the discharge rate, but up to a rate of around 1×C (full discharge in one hour), it does not differ significantly from the nominal capacity.<ref>See graph, p.8 of

</ref> NiMH batteries normally operate at 1.2&nbsp;V per cell, somewhat lower than conventional 1.5&nbsp;V cells, but will operate most devices designed for that voltage.

About 22% of portable rechargeable batteries sold in Japan in 2010 were NiMH.<ref name=“bajstat”>

</ref> In Switzerland in 2009, the equivalent statistic was approximately 60%.<ref>

</ref> This percentage has fallen over time due to the increase in manufacture of lithium-ion batteries: in 2000, almost half of all portable rechargeable batteries sold in Japan were NiMH. By 2011, NiMH only represented about 22% of secondary batteries.<ref name=“bajstat”/>

The significant disadvantage of NiMH batteries is the high rate of self-discharge; NiMH batteries typically lose 4% of their charge per day of storage. In 2005, a low self-discharge (LSD) variant was developed. LSD NiMH batteries significantly lower self-discharge, but at the cost of lowering capacity by about 20%.


File:Nimh disassembled.jpg|thumb|Disassembled NiMH AA cell: {{ordered list | Positive terminal | Outer metal casing (also negative terminal) | Positive electrode | Negative electrode with current collector (metal grid, connected to metal casing) | Separator (between electrodes) }}

The first consumer grade NiMH cells became commercially available in 1989.<ref>In search of the perfect battery, The Economist, 6 March 2008</ref>

The earliest work on NiMH batteries based on sintered Ti2Ni+TiNi+x alloys and NiOOH-electrodes

was conducted at the Battelle-Geneva Research Center starting after its invention in 1967. The development work was sponsored over nearly two decades by Daimler-Benz in Stuttgart, Germany, and by Volkswagen AG within the framework of Deutsche Automobilgesellschaft, now a subsidiary of Daimler AG. The batteries showed specific energy up to 50&nbsp;W·h/kg (180&nbsp;kJ/kg), power density up to 1000 W/kg and a life of 500 charge cycles (at 100% depth of discharge). Patent applications were filed in European countries (priority: Switzerland), the United States, and Japan, and the patents transferred to Daimler-Benz.<ref>The US patent is

. For the performance data, see the “Examples” section.</ref>

Interest grew in the 1970s with the commercialisation of the nickel–hydrogen battery for satellite applications. Hydride technology promised an alternative much less bulky way to store the hydrogen. Research carried out by Philips Laboratories and France's CNRS developed new high-energy hybrid alloys incorporating rare earth metals for the negative electrode. However, these suffered from the instability of the alloys in alkaline electrolyte and consequently insufficient cycle life. In 1987, Willems and Buschow demonstrated a successful battery based on this approach (using a mixture of La0.8Nd0.2Ni2.5Co2.4Si0.1) which kept 84% of its charge capacity after 4000&nbsp;charge–discharge cycles. More economically viable alloys using mischmetal instead of lanthanum were soon developed and modern NiMH cells are based on this design.<ref name=rdjapan>


Ovonic Battery Co. in Michigan altered and improved the Ti–Ni alloy structure and composition according to their patent<ref>

</ref> and licensed NiMH batteries to over 50 companies worldwide. Ovonic's NiMH variation consisted of special alloys with disordered alloy structure and specific multicomponent alloy compositions. Unfortunately, linked to their composition, the calendar and cycle life of such alloys always remains very low, and all NiMH batteries manufactured at the present time consist of AB5-type rare earth metal alloys.

A high-energy pasted electrode

developed by Dr. Masahiko Oshitani from GS Yuasa Company led to the NiMH cell.

In 2008, more than 2 million hybrid cars worldwide were manufactured with NiMH batteries.<ref>Avicenne Conf., Nice 2008, M.A. Fetcenko/ECD</ref>

In the EU and due to the Battery Directive, Nickel–metal hydride batteries have replaced Ni–Cd batteries for portable use by consumers.


The negative electrode reaction occurring in a NiMH cell is:

: H2O + M + e


The charge reaction is read left-to-right and the discharge reaction is read right-to-left.

On the positive electrode, nickel oxyhydroxide, NiO(OH), is formed:

: Ni(OH)2 + OH

NiO(OH) + H2O + e

The “metal” M in the negative electrode of a NiMH cell is actually an intermetallic compound. Many different compounds have been developed for this application, but those in current use fall into two classes. The most common is AB5, where A is a rare earth mixture of lanthanum, cerium, neodymium, praseodymium and B is nickel, cobalt, manganese, and/or aluminium. Very few cells use higher-capacity negative electrode materials based on AB2 compounds, where A is titanium and/or vanadium and B is zirconium or nickel, modified with chromium, cobalt, iron, and/or manganese, due to the reduced life performances.<ref>

</ref> Any of these compounds serve the same role, reversibly forming a mixture of metal hydride compounds.

When overcharged at low rates, oxygen produced at the positive electrode passes through the separator and recombines at the surface of the negative. Hydrogen evolution is suppressed and the charging energy is converted to heat. This process allows NiMH cells to remain sealed in normal operation and to be maintenance-free.

NiMH cells have an alkaline electrolyte, usually potassium hydroxide. For separation hydrophilic polyolefin nonwovens are used.<ref>Japanese Nonwoven Battery Applications</ref>


The charging voltage is in the range of 1.4–1.6 V/cell. In general, a constant-voltage charging method cannot be used for automatic charging. When fast-charging, it is advisable to charge the NiMH cells with a smart battery charger to avoid overcharging, which can damage cells and even be dangerous.<ref name=“PanasonicChargeMethods”>

</ref> A NiCd charger should not be used as a substitute for an automatic NiMH charger.

Trickle charging

The simplest way to safely charge a NiMH cell is with a fixed low current, with or without a timer. Most manufacturers claim that overcharging is safe at very low currents, below 0.1&nbsp;C (C/10) (where C is the current equivalent to the capacity of the battery divided by one hour).<ref name=“duracell_charge”>

</ref> The Panasonic NiMH charging manual warns that overcharging for long enough can damage a battery and suggests limiting the total charging time to 10 to 20 hours.<ref name=PanasonicChargeMethods/>

Duracell further suggests that, for applications where the battery must be kept in a fully charged state, a trickle charge at C/300 can be used.<ref name=duracell_charge/> Some chargers do this after the charge cycle, to offset the natural self-discharge rate of the battery. A similar approach is suggested by Energizer<ref name=“Energizer”>

</ref> which indicates that the self catalysis can recombine gas formed at the anode for charge rates up to C/10, but as this leads to cell heating, recommends C/30 or C/40 for indefinite applications where long life is important. This is the approach taken in maintained emergency light fittings (which in Europe must remain on for 4 hours in the event of a power cut) where the design remains essentially the same as that used in older NiCd units, but for an increase in the trickle charging resistor value. In comparison, NiCd cells can ordinarily be charged indefinitely at C/10 without damage.

Panasonic's handbook, however, recommends that NiMH batteries on standby are kept charged by a lower duty cycle approach, where a pulse of a higher current is used whenever the battery's voltage drops below

This can extend battery life and use less energy.<ref name=PanasonicChargeMethods/>

Δ''V'' charging method

File:Charge NiMH.svg

In order to charge a NiMH battery more quickly than the trickle method suggested above, a charger must stop charging before the battery is damaged. One method is to monitor the change of voltage across the battery with time. As can be seen in the charge curve diagram, when the battery is fully charged the voltage across its terminals drops slightly. The charger can detect this and stop charging. This method is often used with nickel–cadmium cells which have a large drop in voltage at full charge. However, the voltage drop is much less pronounced for NiMH and can be non-existent at low charge rates, which can make the approach unreliable.

Another option is to monitor the change of voltage with respect to time and stop when this becomes zero, but this runs the risk of premature cutoffs.<ref name=duracell_charge/> With this method, a much higher charging rate can be used than with a trickle charge, up to 1&nbsp;C. At this charge rate, looking for a voltage drop, ΔV is approximately 5–10&nbsp;mV per cell.<ref name=PanasonicChargeMethods/> Since this method measures the voltage across the battery, a constant current (rather than a constant voltage) charging circuit must be used. This is unlike a lead–acid cell for example, which can, in theory, be more easily charged at a suitably chosen constant voltage.

Δ''T'' temperature charging method

The ΔT temperature change method is similar in principle to the ΔV method. Because the charging voltage is nearly constant, constant-current charging delivers energy at a near-constant rate. When the cell is not fully charged, most of this energy is converted to chemical energy. However, when the cell reaches full charge, most of the charging energy is converted to heat. This increases the rate of change of battery temperature, which can be detected by a sensor such as a thermistor. Both Panasonic and Duracell suggest a maximum rate of temperature increase of

per minute. Using a temperature sensor also allows an absolute temperature cutoff, which Duracell suggests at

<ref name=duracell_charge/>

With both the ΔT and the ΔV charging methods, both manufacturers recommend a further period of trickle charging to follow the initial rapid charge.

Charging at high and low temperatures

Charging temperature limits for NiMH are stricter than operational limits. Nickel-based batteries are most forgiving in accepting charge at low temperatures, however, when charging below

, the ability to recombine oxygen and hydrogen diminishes. If NiCd and NiMH are charged too rapidly, pressure builds up in the cell that will lead to venting. Not only do escaping gases deplete the electrolyte, the hydrogen released is highly flammable. The charge current of all nickel-based batteries should be reduced to 0.1C below freezing down to


To enable fast-charging at all temperatures, some industrial batteries include a thermal blanket that heats the battery to an acceptable temperature; other chargers adjust the charge rate to prevailing temperatures. Consumer chargers do not have these provisions and users should make all attempts to only charge batteries at room temperatures.<ref name=“batteryuniversity”>



A good safety feature of a custom-built charger is to use a resettable fuse in series with the cell, particularly of the bimetallic strip type. This fuse will open if either the current or the temperature goes too high.<ref name=duracell_charge/>

Modern NiMH cells contain catalysts to immediately deal with gases developed as a result of over-charging without being harmed (2 H2&nbsp;+ O2 — catalyst → 2 H2O). However, this only works with overcharging currents of up to 0.1&nbsp;C (nominal capacity divided by ten hours). As a result of this reaction, the batteries will heat up considerably, marking the end of the charging process.<ref name=duracell_charge/> Some quick chargers have a fan to keep the batteries cool.

A method for very rapid charging called in-cell charge control involves an internal pressure switch in the cell, which disconnects the charging current in the event of overpressure.

There is an inherent risk with NiMH chemistry that overcharging will cause a buildup of hydrogen, causing the cell to rupture. Therefore, cells have a vent. Hydrogen will be emitted from the vent in the event of serious overcharging.<ref>Mukund R. Patel (2005), “Spacecraft Power Systems” CRC Press ISBN 978-0-8493-2786-5 p. 209</ref>


A fully charged cell supplies an average 1.25 V/cell during discharge, down to about 1.0–1.1 V/cell (further discharge may cause permanent damage in the case of multi-cell packs, due to polarity reversal). Under a light load (0.5 ampere), the starting voltage of a freshly charged AA NiMH cell in good condition is about 1.4 volts.<ref>Energizer NH15-2300mAh datasheet</ref>


A complete discharge of a battery can result in one or more cells going into polarity reversal, which can cause permanent damage to those cells. This situation can occur in the common arrangement of four AA cells in series in a digital camera, where one will be completely discharged before the others due to small differences in capacity among the cells. When this happens, the good cells will start to drive the discharged cell in reverse, which can cause permanent damage to that cell. Some cameras, GPS receivers and PDAs detect the safe end-of-discharge voltage of the series cells and auto-shutdown, but devices like flashlights and some toys do not. A single cell driving a load or a cell connected in parallel to other cells can't suffer from polarity reversal, because there are no other cells to reverse-charge it when it becomes discharged. (Cells parallel-connected to a discharged cell will tend to forward-charge it.)

Irreversible damage from polarity reversal is a particular danger in systems, even when a low voltage threshold cutout is employed, where cells in the battery are of different temperatures. This is because the capacity of NiMH cells significantly declines as the cells are cooled. This results in a lower voltage under load of the colder cells.<ref>Sandeep Dhameja (2002), Electric Vehicle Battery Systems, Newnes, ISBN 0-7506-9916-7, pp. 118, 123</ref>


NiMH cells historically had a somewhat higher self-discharge rate (equivalent to internal leakage) than NiCd cells. The self-discharge rate varies greatly with temperature, where lower storage temperature leads to slower discharge rate and longer battery life. The self-discharge is

on the first day and stabilizes around

per day at room temperature.<ref>

than at

. Age also affects self-discharge. Older battery packs self-discharge faster than new ones. }}</ref><ref>




</ref> But at

it is approximately

as high.<ref name=duracell_charge/><!–seems unsupported by source, but perhaps the page 10 figure 5.8.1 is the claim–> This is not a problem in the short term but makes them unsuitable for many light-duty uses, such as clocks, remote controls, or safety devices, where the battery would normally be expected to last many months or years. The highest capacity cells on the market

are reported to have the highest self-discharge rates.

Low self-discharge cells

The low self-discharge nickel–metal hydride battery(LSD NiMH) was introduced in 2005. It has a significantly lower rate of self-discharge, so holds its charge longer if left charged but unused. By using an improved electrode separator and improved positive electrode, manufacturers claim the cells retain 70% to 85% of their capacity after one year when stored at

, compared to about half for normal NiMH batteries. They are otherwise similar to other NiMH batteries, and can be charged in the same chargers. These cells are marketed as “hybrid”, “ready-to-use” or “pre-charged” rechargeables. Retention of charge depends a lot on the battery's impedance or internal resistance (the lower the better), and on the physical size of the battery as well as the charge capacity.

Low self-discharge cells have lower capacity than many standard NiMH cells due to the larger area of the separator. The highest-capacity low-self-discharge AA cells have 2000–2500&nbsp;mA·h capacity, and AAA 1000&nbsp;mA·h, compared to 2800&nbsp;mA·h and 1300&nbsp;mA·h for high-capacity AA and AAA NiMH cells.<ref> Product information for Sanyo Eneloop XX</ref>

Separators keep the two electrodes apart to slow electrical discharge while also allowing the transport of ionic charge carriers that are needed to close the circuit during the passage of current.<ref>Flaim, Tony, Yubao Wang, and Ramil Mercado. “High Refractive Index Polymer Coatings.” SPIE Proceedings of Optical Systems Design. Web</ref> High quality separators are very important for battery performance.

Thick separators provide a simple way to reduce self discharge, but take up space and reduce capacity; thin separators tend to raise the self-discharge rate. Some batteries may have overcome this tradeoff using thin separators with more precise manufacturing techniques, and by using a more advanced sulfonated polyolefin separator.

Batteries with low internal resistance waste less energy on self-heating during rapid discharge and recharge. Low self-discharge NiMH batteries typically have significantly lower internal resistance than other NiMH batteries.

LSD NiMH batteries were introduced in November 2005 by Sanyo,<ref>://

</ref> marketing them under the brand “eneloop”.

There are many brand names for LSD NiMH batteries. Most manufacturers produce only size AAA and AA batteries, and most low self-discharge batteries are sold in these sizes. Larger size C and D cells are available, though some are actually AA cells inside a C/D-sized case. Maha offers an LSD “D”-cell called the “Imedion” self-rated at 9500&nbsp;mA·h, Accupower offers the “Acculoop” self-rated at 8500&nbsp;mA·h, and Tenergy offers the “Centura” self-rated at 8000&nbsp;mA·h.

Tenergy also offers 9V cells.

Varta (USA: Rayovac) and Ansmann increased their LSD NiMH batteries' capacity to roughly 2300&nbsp;mA·h. Sanyo introduced a new version of its Eneloop batteries with increased capacity and life expectancy. The “Eneloop plus” incorporates a PTC thermistor that disconnects the power if the battery overheats, in order to make it safe for use in toys for small children.

Environmental impact

Improper disposal of NiMH batteries poses less environmental hazard than that of NiCd because of the absence of toxic cadmium. However, mining and processing the various alternate metals that form the negative electrode may pose other types of environmental impact, depending on the metal, mining method, and environmental practices of the mine.

Most industrial nickel is recycled, due to the relatively easy retrieval of the magnetic element from scrap using electromagnets, and due to its high value.

Comparison with other battery types

NiMH cells and chargers are readily available in retail stores in the common sizes AAA and AA. Adapter sleeves are available to use the more common AA size in C and D applications. The sizes C and D cells are somewhat available, but are often just an AA core hidden in an outer shell, with a rating of about 2500&nbsp;mA·h, much less than ordinary alkaline C and D batteries.

Real NiMH C and D batteries are expensive (and the chargers are uncommon); they should be rated at least 5000&nbsp;mA·h for C and 10,000&nbsp;mA·h for D sizes. However, 12,000&nbsp;mA·h D size batteries and 15,000&nbsp;mA·h. F size batteries also exist.

PP3 (nine volt) NiMH batteries are available; these usually have an output voltage of 8.4&nbsp;V (1.2 × 7) and a capacity of roughly 200&nbsp;mA·h.<ref>Energizer type HR-22 data sheet: Actually says 175&nbsp;mA·h, but that's “roughly 200&nbsp;mA·h”</ref> Also available are eight-cell nine volt batteries with a nominal output voltage of 9.6&nbsp;V (1.2 × 8).

NiMH cells are often used in digital cameras and other high drain devices, where over the duration of single charge use they outperform primary (such as alkaline) batteries.

NiMH cells are particularly advantageous for high current drain applications, due in large part to their low internal resistance. Alkaline batteries, which might have approximately 3000&nbsp;mA·h capacity at low current demand (200&nbsp;mA), will have about 700&nbsp;mA·h capacity with a 1000&nbsp;mA load.<ref>Alkaline Drain Chart

at</ref> Digital cameras with LCDs and flashlights can draw over 1000&nbsp;mA, quickly depleting alkaline batteries. NiMH cells can deliver these current levels without similar loss of capacity.

Certain devices that were designed to operate using primary alkaline chemistry (or zinc–carbon/chloride) cells will not function when one uses NiMH cells as substitutes. However, this is rare, as most devices compensate for the voltage drop of an alkaline as it discharges down to about 1 volt. Low internal resistance allows NiMH cells to deliver a near-constant voltage until they are almost completely discharged. This will cause a battery level indicator to overstate the remaining charge if it was designed to read only the voltage curve of alkaline cells. The voltage of alkaline cells decreases steadily during most of the discharge cycle.

Lithium-ion batteries have a higher specific energy than nickel–metal hydride batteries,<ref>

</ref> but they are significantly more expensive to produce.<ref name=“ECD”>

</ref> In October 2009, ECD Ovonics announced that their next-generation NiMH batteries will provide specific energy and power that are comparable to those of lithium ion batteries at a cost that is significantly lower than the cost of lithium ion batteries.<ref name=“ECD” />


, Japan]]

, Museum Autovision, Altlussheim, Germany]]

Applications of NiMH electric vehicle batteries include all-electric plug-in vehicles such as the General Motors EV1, Honda EV Plus, Ford Ranger EV and Vectrix scooter. Hybrid vehicles such as the Toyota Prius, Honda Insight, Ford Escape Hybrid, Chevrolet Malibu Hybrid, and Honda Civic Hybrid also use them. NiMH technology is used extensively in rechargeable batteries for consumer electronics like robotic vacuum cleaners of Neato Robotics, and it will also be used on the Alstom Citadis low floor tram ordered for Nice, France; as well as the humanoid prototype robot ASIMO designed by Honda. NiMH batteries are also commonly used in remote control cars.

Electric vehicles

Stanford R. Ovshinsky invented and patented (a popular improvement of) the NiMH battery and founded Ovonic Battery Company in 1982. General Motors purchased the patent from Ovonics in 1994. By the late 1990s, NiMH batteries were being used successfully in many fully electric vehicles, such as the General Motors EV1 and Dodge Caravan EPIC minivan. In October 2000, the patent was sold to Texaco and a week later Texaco was acquired by Chevron. Chevron's Cobasys subsidiary will only provide these batteries to large OEM orders. General Motors shut down production of the EV1 citing lack of battery availability as one of their chief obstacles. The Cobasys control of NiMH batteries has created a patent encumbrance of large automotive NiMH batteries.<ref>New Hybrid Reviews, News & Hybrid Mileage (MPG) Info | Hybrid Cars<!-- Bot generated title --></ref><ref name=“Boschert06”>

</ref><ref name=“TheCarThatCould”>

</ref><ref name=“ocweekly20030515”>

</ref><ref name=“ovshinsky20081014”>



In recent years, NiMH batteries have been deployed to provide reliable backup power to load equipment located in a network environment of a typical telecommunications service provider.

The NiMH batteries are recommended

for use in the Central Office (CO), Outside Plant (OSP), and at locations such as Controlled Environmental Vaults (CEVs), Electronic Equipment Enclosures (EEEs), huts, and in uncontrolled structures such as cabinets.

To ensure conformance and product safety, the telecommunications industry has accepted a three-level compliance system, which is described in GR-3168, ''Generic Requirements for Nickel Metal Hydride (NiMH) Battery Systems for Telecommunications Use''. The compliance system provides a common framework for evaluating and qualifying various NiMH battery technologies. The framework intends to alleviate the complexities associated with product introduction and qualification.

The service life of NiMH batteries is extremely important in a telecommunications environment. The main failure modes of lead–acid batteries are very temperature sensitive. Grid corrosion and water loss are sped up as the battery temperature increases. The service life is halved with each

rise in temperature. Thus, a battery designed to operate for


would last approximately only


, and would last only



Nickel–cadmium (NiCd) batteries fail in a different manner. NiCd batteries are susceptible to failures caused by short circuiting due to dissolution/crystallization reactions occurring at the negative electrode, which can result in dendrite growth of Cd creating a short to the positive plate.

NiMH batteries do not fail in the same way as NiCd or lead–acid batteries. NiMH batteries fail in two predominant modes that are somewhat interrelated. The metal hydride material used for the negative electrode undergoes gradual corrosion in a strong alkaline environment. This corrosion results in less negative active material for hydrogen storage and also consumes water from the electrolyte.

This results in a gradual loss of power as water is consumed, increasing the cell resistance and a gradual loss in capacity as active material is converted to corrosion products. By optimization of the alloy composition, this corrosion process can be controlled at very low rates. The rate of corrosion will be impacted by various factors including temperature, State of Charge (SoC), and control of overcharge and oxygen recombination. Studies under controlled overcharge conditions predict that the service life is halved for each approximately

rise in temperature. Thus, a battery designed to operate for


would last



Extrapolation beyond

is not linear since other failure modes, caused by decreasing charge acceptance resulting in positive electrode swelling and thermal instability, could control the battery life.

See also


nickel_metal_hydride_battery.txt · Last modified: 2020/03/12 18:36 (external edit)