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Lithium batteries
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Fundamental knowledge: Definitions | Types | Components | History
Lithium batteries | Alkaline batteries | Ni-MH batteries | Lithium ion batteries |
Lead acid batteries | Ni-Cd batteries | Chargers(adaptors)
 
  • Definitions of batteries

A battery is a device which can store chemical energy and, on demand, convert it into electrical energy to drive an external circuit.

The electrical energy results from a spontaneous chemical energy change(i.e. redox reaction with a negative free energy) within the battery. The redox reagents must not react directly but are consumed at different sites in the battery, at the anode and the cathode, and it is this which causes electrons to flow throuugh the externalcircuit betweenthe battery terminals.

  • Types of batteries
  • Components of batteries

1. Container

The battery case must be resistant to corrosion from both inside and outside, and hence it must be stable to chemical attack by the electrolyte, active mertials and the envirement at the operating temperature.

In addition it must have the required mechanical strength, be cheap and light, and there must be a simple method od sealing. This required case is named the container of batteries.

2. Separator

The separator must be chemically stable to the electrolyte and to the active materials at the temperature of operation. It is also necessary for the membrane to have the correct qualities of wettability, selectivity, resistivity and flexibility for the particular battery system.

3. Current collector

In order for the battery to have an acceptable capacity, the active material is almost always a thick layer of porous, particulate paste, and the electronic conductivity of this material is seldom very high. Hence it is necessary to have a current collector, which is usually a metal grid or sheet, to provide a conducting path through the paste and thereby minimize the resistance of the battery. The current collector also acts as a physical support for the active mass which otherwise would be a very brittle structure.

Clearly, the current collector must be stable to chemical attack by both electrolyte and active material, and this limits the choice of material.

4. Electrolyte

The selection of electrolyte is determined by the electrode reactions and its concentration is also important. This will control the plate potentials, the electrolyte resistance and viscosity and, by its effect on the rate of diffusion, the differences in concentrations of species between the inside and the outside of the pores of the active paste.

Temperature has a large effect on electrolyte properties and both viscosity and resistance increase by more an order of magnitude as the temperature drops from abient to -30°C. This largely accounts for the poorer performance of the battery at lower remperature.

The weight of the electrolye is a major contribution to that of the complete battery and hence must be minimized. In any case the electrode spacings should be small to minimize battery resistance.

5. Active materials

For a battery with a reasonable discharge rate and capacity, the electroactive species must be readily available at the sites of electron transfer and be present in large quantities. In most batteries these necessities are provided by using solid reactants, and at least in secondary batteries the product of the electrode process is also solid; the anion of electrolyte and sometimes the proton are also participants in the chemical change during the charge or discharge process. Hence if the change is to be accomplished at a reasonable rate, intimate contact and a high-area surface between the solid reactants and electrolyte are essential. This is accomplished by using the electroactive materials in the form of a paste on the current collector.

The sizes of the particles and the pores, i.e. the porosity of the paste, are important in determining the performance of the battery. In practice, porosity should be about 50%. Below this value, the unilization of the active material suffers due to pore blocking, and above it the mechanical stability becomes a problem. Hence there is a trade-off between capacity and cycle life.

The loading of the paste, the thickness of the porous layer, also affects performance. Thin plates improve capacity particularly at high discharge rates and also give a higjer power density.

 
  • History of batteries
Ages Main Inventer Items
1600 Gilbert (England) Establishment electrochemistry study
1791 Galvani (Italy)  Discovery of 'animal electricity'
1800  Volta (Italy) Invention of the voltaic cell
1802 Cruickshank (England) First electric battery capable of mass production
1820 Ampère (France) Electricity through magnetism
1833 Faraday (England) Announcement of Faraday's Law
1836 Daniell (England) Invention of the Daniell cell
1859 Planté (France) Invention of the Lead acid battery
1868 Leclanché (France) Invention of the Leclanché cell
1888 Gassner (USA) Completion of the dry cell
1899 Jungner (Sweden) Invention of the Nickel-Cadmium battery
1901 Edison (USA) Invention of the Nickel-iron battery
1932 Shlecht&Ackermann (Germany) Invention of the sintered pole plate
1947 Neumann (France) Successfully sealing the Nickel-Cadmium battery
Mid 1960 Union Carbide (USA) Development of primary alkaline battery
Mid 1970   Development of valve regulated Lead acid battery
1990    Commercialization Nickel-metal hydride battery
1992 Kordesch (Canada) Commercialization reusable alkaline battery
1999   Commercialization Lithium-ion polymer
2001    Anticipated volume production of proton exchange membrane fuel cell
 
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