A lemon battery is a simple battery often made for the purpose of education. Typically, a piece of zinc metal (such as a galvanized nail) and a piece of copper (such as a penny) are inserted into a lemon and connected by wires. Power generated by reaction of the metals is used to power a small device such as a light-emitting diode (LED).
The lemon battery is similar to the first electrical battery invented in 1800 by Alessandro Volta, who used brine (salt water) instead of lemon juice. [1] The lemon battery illustrates the type of chemical reaction (oxidation-reduction) that occurs in batteries. [2] [3] [4] The zinc and copper are called the electrodes, and the juice inside the lemon is called the electrolyte. There are many variations of the lemon cell that use different fruits (or liquids) as electrolytes and metals other than zinc and copper as electrodes.
There are numerous sets of instructions for making lemon batteries and for obtaining components such as light-emitting diodes, (LEDs), electrical meters (multimeters), and zinc-coated (galvanized) nails and screws. [5] [6] Commercial "potato clock" science kits include electrodes and a low-voltage digital clock. After one cell is assembled, a multimeter can be used to measure the voltage or the electric current from the voltaic cell; a typical voltage is 0.9 V with lemons. Currents are more variable, but range up to about 1 mA (the larger the electrode surfaces, the bigger the current). For a more visible effect, lemon cells can be connected in series to power an LED (see illustration) or other devices. The series connection increases the voltage available to devices. Swartling and Morgan have published a list of low-voltage devices along with the corresponding number of lemon cells that were needed to power them; they included LEDs, piezoelectric buzzers, and small digital clocks. With the zinc/copper electrodes, at least two lemon cells were needed for any of these devices. [7] Substituting a magnesium electrode for the zinc electrode makes a cell with a larger voltage (1.5−1.6 V), and a single magnesium/copper cell will power some devices. [7] Note that incandescent light bulbs from flashlights are not used because the lemon battery is not designed to produce enough electric current to light them. Such a battery typically produces 0.001 A (1 mA) of current at a potential difference of 0.7 V; these values are multiplied together to determine the overall power of 0.0007 W (0.7 mW).
Many fruits and liquids can be used for the acidic electrolyte. Fruit is convenient, because it provides both the electrolyte and a simple way to support the electrodes. The acid involved in citrus fruits (lemons, oranges, grapefruits, etc.) is citric acid. The acidity, which is indicated by the measured pH, varies substantially.
Potatoes have phosphoric acid and work well; they are the basis for commercial "potato clock" kits. [8] [9] Potato batteries with LED lighting have been proposed for use in poor countries or by off-grid populations. International research begun in 2010 showed that boiling potatoes for eight minutes improves their electrical output, as does placing slices of potatoes between multiple copper and zinc plates. Boiled and chopped plantain pith (stem) is also suitable, according to Sri Lankan researchers. [10]
Instead of fruit, liquids in various containers can be used. Household vinegar (acetic acid) works well. [11] Sauerkraut (lactic acid) was featured in one episode of the US television program Head Rush (an offshoot of the MythBusters program). The sauerkraut had been canned, and became the electrolyte while the can itself was one of the electrodes. [12]
Zinc and copper electrodes are reasonably safe and easy to obtain. Other metals such as lead, iron, magnesium, etc., can be studied as well; they yield different voltages than the zinc/copper pair. In particular, magnesium/copper electrodes can generate voltages as large as 1.6 V in lemon cells. This voltage is larger than obtainable using zinc/copper cells. It is comparable to that of standard household batteries (1.5 V), which is useful in powering devices with a single cell instead of using cells in series. [7]
For the youngest pupils, about ages 5–9, the educational goal is utilitarian: [13] batteries are devices that can power other devices, as long as they are connected by a conductive material. Batteries are components in electrical circuits; hooking a single wire between a battery and a light bulb will not power the bulb.
For children in the age range 10−13, batteries are used to illustrate the connection between chemistry and electricity as well as to deepen the circuit concept for electricity. The fact that different chemical elements such as copper and zinc are used can be placed in the larger context that the elements do not disappear or break down when they undergo chemical reactions.
For older pupils and for college students, batteries serve to illustrate the principles of oxidation-reduction reactions. [13] [14] Students can discover that two identical electrodes yield no voltage and that different pairs of metals (beyond copper and zinc) yield different voltages. The voltages and currents from series and parallel combinations of the batteries can be examined. [15]
The current that is output by the battery through a meter will depend on the size of the electrodes, how far the electrodes are inserted into the fruit, and how close to each other the electrodes are placed; the voltage is fairly independent of these details of the electrodes. [16]
Most textbooks present the following model for the chemical reactions of a lemon battery. [1] [3] [17] When the cell is providing an electric current through an external circuit, the metallic zinc at the surface of the zinc electrode is dissolving into the solution. Zinc atoms dissolve into the liquid electrolyte as electrically charged ions (Zn2+), leaving 2 negatively charged electrons (e−) behind in the metal:
This reaction is called oxidation. While zinc is entering the electrolyte, two positively charged hydrogen ions (H+) from the electrolyte combine with two electrons at the copper electrode's surface and form an uncharged hydrogen molecule (H2):
This reaction is called reduction. The electrons used in the copper to form the molecules of hydrogen are transferred from the zinc through an external wire connecting between the copper and the zinc. The hydrogen molecules formed on the surface of the copper by the reduction reaction ultimately bubble away as hydrogen gas.
This model of the chemical reactions makes several predictions that were examined in experiments published by Jerry Goodisman in 2001. Goodisman notes that numerous recent authors propose chemical reactions for the lemon battery that involve dissolution of the copper electrode into the electrolyte. Goodisman excludes this reaction as being inconsistent with the experiments, and notes that the correct chemistry, which involves the evolution of hydrogen at the copper electrode but also can use silver instead of copper, has been known for many years. [4] Most of the detailed predictions of the model apply to the battery's voltage that is measured directly by a meter at open circuit (nothing else is connected to the battery). When the electrolyte was modified by adding zinc sulfate (ZnSO4), the voltage from the cell was reduced as predicted using the Nernst equation for the model. The Nernst equation essentially says how much the voltage drops as more zinc sulfate is added. The addition of copper sulfate (CuSO4) did not affect the voltage. This result is consistent with the fact that copper atoms from the electrode are not involved in the chemical reaction model for the cell.
When the battery is hooked up to an external circuit and a significant electric current is flowing, the zinc electrode loses mass, as predicted by the zinc oxidation reaction above. Similarly, hydrogen gas evolves as bubbles from the copper electrode. Finally, the voltage from the cell depended upon the acidity of the electrolyte, as measured by its pH; decreasing acidity (and increasing pH) causes the voltage to fall. This effect is also predicted by the Nernst equation; the particular acid that was used (citric, hydrochloric, sulfuric, etc.) does not affect the voltage except through the pH value.
The Nernst equation prediction failed for strongly acid electrolytes (pH < 3.4), when the zinc electrode dissolves into the electrolyte even when the battery is not providing any current to a circuit. The two oxidation-reduction reactions listed above only occur when electrical charge can be transported through the external circuit. The additional, open-circuit reaction can be observed by the formation of bubbles at the zinc electrode under open-circuit. This effect ultimately limited the voltage of the cells to 1.0 V near room temperature at the highest levels of acidity.
The energy comes from the chemical change in the zinc when it dissolves into the acid. The energy does not come from the lemon or potato. The zinc is oxidized inside the lemon, exchanging some of its electrons with the acid in order to reach a lower energy state, and the energy released provides the power. [4]
In current practice, zinc is produced by electrowinning of zinc sulfate or pyrometallurgical reduction of zinc with carbon, which requires an energy input. The energy produced in the lemon battery comes from reversing this reaction, recovering some of the energy input during the zinc production.
From 1840 to the late 19th century, large, voltaic cells using a zinc electrode and a sulfuric acid electrolyte were widely used in the printing industry. While copper electrodes like those in lemon batteries were sometimes used, in 1840 Alfred Smee invented a refined version of this cell that used silver with a rough platinum coating instead of a copper electrode. [18] [19] Hydrogen gas clinging to the surface of a silver or copper electrode reduces the electric current that can be drawn from a cell; the phenomenon is called "polarization". [17] [20] The roughened, "platinized" surface speeds up the bubbling of the hydrogen gas, and increases the current from the cell. Unlike the zinc electrode, the copper or platinized silver electrodes are not consumed by using the battery, and the details of this electrode do not affect the cell's voltage. The Smee cell was convenient for electrotyping, which produced copper plates for letterpress printing of newspapers and books, and also statues and other metallic objects. [19] [21] [22] [23] [24]
The Smee cell used amalgamated zinc instead of pure zinc; the surface of amalgamated zinc has been treated with mercury. [23] Apparently amalgamated zinc was less prone to degradation by an acidic solution than is pure zinc. [25] Amalgamated zinc and plain zinc electrodes give essentially the same voltage when the zinc is pure. [26] With the imperfectly refined zinc in 19th century laboratories they typically gave different voltages. [25]
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An anode is an electrode of a polarized electrical device through which conventional current enters the device. This contrasts with a cathode, an electrode of the device through which conventional current leaves the device. A common mnemonic is ACID, for "anode current into device". The direction of conventional current in a circuit is opposite to the direction of electron flow, so electrons flow from the anode of a galvanic cell, into an outside or external circuit connected to the cell. For example, the end of a household battery marked with a "+" is the cathode.
A cathode is the electrode from which a conventional current leaves a polarized electrical device. This definition can be recalled by using the mnemonic CCD for Cathode Current Departs. A conventional current describes the direction in which positive charges move. Electrons have a negative electrical charge, so the movement of electrons is opposite to that of the conventional current flow. Consequently, the mnemonic cathode current departs also means that electrons flow into the device's cathode from the external circuit. For example, the end of a household battery marked with a + (plus) is the cathode.
Electrochemistry is the branch of physical chemistry concerned with the relationship between electrical potential difference and identifiable chemical change. These reactions involve electrons moving via an electronically-conducting phase between electrodes separated by an ionically conducting and electronically insulating electrolyte.
An electrochemical cell is a device that generates electrical energy from chemical reactions. Electrical energy can also be applied to these cells to cause chemical reactions to occur. Electrochemical cells that generate an electric current are called voltaic or galvanic cells and those that generate chemical reactions, via electrolysis for example, are called electrolytic cells.
The voltaic pile was the first electrical battery that could continuously provide an electric current to a circuit. It was invented by Italian chemist Alessandro Volta, who published his experiments in 1799. Its invention can be traced back to an argument between Volta and Luigi Galvani, Volta's fellow Italian scientist who had conducted experiments on frogs' legs. The voltaic pile then enabled a rapid series of other discoveries including the electrical decomposition (electrolysis) of water into oxygen and hydrogen by William Nicholson and Anthony Carlisle (1800) and the discovery or isolation of the chemical elements sodium (1807), potassium (1807), calcium (1808), boron (1808), barium (1808), strontium (1808), and magnesium (1808) by Humphry Davy.
In chemistry and manufacturing, electrolysis is a technique that uses direct electric current (DC) to drive an otherwise non-spontaneous chemical reaction. Electrolysis is commercially important as a stage in the separation of elements from naturally occurring sources such as ores using an electrolytic cell. The voltage that is needed for electrolysis to occur is called the decomposition potential. The word "lysis" means to separate or break, so in terms, electrolysis would mean "breakdown via electricity".
In electromagnetism and electronics, electromotive force is an energy transfer to an electric circuit per unit of electric charge, measured in volts. Devices called electrical transducers provide an emf by converting other forms of energy into electrical energy. Other electrical equipment also produce an emf, such as batteries, which convert chemical energy, and generators, which convert mechanical energy. This energy conversion is achieved by physical forces applying physical work on electric charges. However, electromotive force itself is not a physical force, and ISO/IEC standards have deprecated the term in favor of source voltage or source tension instead.
A galvanic cell or voltaic cell, named after the scientists Luigi Galvani and Alessandro Volta, respectively, is an electrochemical cell in which an electric current is generated from spontaneous oxidation–reduction reactions. A common apparatus generally consists of two different metals, each immersed in separate beakers containing their respective metal ions in solution that are connected by a salt bridge or separated by a porous membrane.
An electrolytic cell is an electrochemical cell that utilizes an external source of electrical energy to force a chemical reaction that would otherwise not occur. The external energy source is a voltage applied between the cell's two electrodes; an anode and a cathode, which are immersed in an electrolyte solution. This is in contrast to a galvanic cell, which itself is a source of electrical energy and the foundation of a battery. The net reaction taking place in a galvanic cell is a spontaneous reaction, i.e., the Gibbs free energy remains -ve, while the net reaction taking place in an electrolytic cell is the reverse of this spontaneous reaction, i.e., the Gibbs free energy is +ve.
An alkaline battery is a type of primary battery where the electrolyte has a pH value above 7. Typically these batteries derive energy from the reaction between zinc metal and manganese dioxide.
A primary battery or primary cell is a battery that is designed to be used once and discarded, and not recharged with electricity and reused like a secondary cell. In general, the electrochemical reaction occurring in the cell is not reversible, rendering the cell unrechargeable. As a primary cell is used, chemical reactions in the battery use up the chemicals that generate the power; when they are gone, the battery stops producing electricity. In contrast, in a secondary cell, the reaction can be reversed by running a current into the cell with a battery charger to recharge it, regenerating the chemical reactants. Primary cells are made in a range of standard sizes to power small household appliances such as flashlights and portable radios.
The Daniell cell is a type of electrochemical cell invented in 1836 by John Frederic Daniell, a British chemist and meteorologist, and consists of a copper pot filled with a copper (II) sulfate solution, in which is immersed an unglazed earthenware container filled with sulfuric acid and a zinc electrode. He was searching for a way to eliminate the hydrogen bubble problem found in the voltaic pile, and his solution was to use a second electrolyte to consume the hydrogen produced by the first. Zinc sulfate may be substituted for the sulfuric acid. The Daniell cell was a great improvement over the existing technology used in the early days of battery development. A later variant of the Daniell cell called the gravity cell or crowfoot cell was invented in the 1860s by a Frenchman named Callaud and became a popular choice for electrical telegraphy.
A zinc–carbon battery (or carbon zinc battery in U.S. English) is a dry cell primary battery that provides direct electric current from the electrochemical reaction between zinc (Zn) and manganese dioxide (MnO2) in the presence of an ammonium chloride (NH4Cl) electrolyte. It produces a voltage of about 1.5 volts between the zinc anode, which is typically constructed as a cylindrical container for the battery cell, and a carbon rod surrounded by a compound with a higher Standard electrode potential (positive polarity), known as the cathode, that collects the current from the manganese dioxide electrode. The name "zinc-carbon" is slightly misleading as it implies that carbon is acting as the oxidizing agent rather than the manganese dioxide.
Electrochemistry, a branch of chemistry, went through several changes during its evolution from early principles related to magnets in the early 16th and 17th centuries, to complex theories involving conductivity, electric charge and mathematical methods. The term electrochemistry was used to describe electrical phenomena in the late 19th and 20th centuries. In recent decades, electrochemistry has become an area of current research, including research in batteries and fuel cells, preventing corrosion of metals, the use of electrochemical cells to remove refractory organics and similar contaminants in wastewater electrocoagulation and improving techniques in refining chemicals with electrolysis and electrophoresis.
Batteries provided the primary source of electricity before the development of electric generators and electrical grids around the end of the 19th century. Successive improvements in battery technology facilitated major electrical advances, from early scientific studies to the rise of telegraphs and telephones, eventually leading to portable computers, mobile phones, electric cars, and many other electrical devices.
An electric battery is a source of electric power consisting of one or more electrochemical cells with external connections for powering electrical devices. When a battery is supplying power, its positive terminal is the cathode and its negative terminal is the anode. The terminal marked negative is the source of electrons that will flow through an external electric circuit to the positive terminal. When a battery is connected to an external electric load, a redox reaction converts high-energy reactants to lower-energy products, and the free-energy difference is delivered to the external circuit as electrical energy. Historically the term "battery" specifically referred to a device composed of multiple cells; however, the usage has evolved to include devices composed of a single cell.
The Glossary of fuel cell terms lists the definitions of many terms used within the fuel cell industry. The terms in this fuel cell glossary may be used by fuel cell industry associations, in education material and fuel cell codes and standards to name but a few.
The penny battery is a voltaic pile which uses various coinage as the metal disks (pennies) of a traditional voltaic pile. The coins are stacked with pieces of electrolyte soaked paper in between. The penny battery experiment is common during electrochemistry units in an educational setting.
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This article provides information on the following six methods of producing electric power.
Formerly, a galvanic battery was a stupendous, and an expensive, machine occupying a large space and costing a considerable sum to keep it in its short-lived action. Now, a far more powerful instrument may be made in a snuff box and carried in the pocket. These remarks are forced upon us by the astonishing platinum batteries of Mr. Grove, and the chemico-mechanical batteries invented by Mr. Smee ...
The first real improvement over the plain zinc-copper in acid cell was due to Dr. Alfred Smee, who noticed that the hydrogen gas liberated at the negative plate was evolved from it much more readily, hence polarization took place much less rapidly if the surface of this plate were roughened instead of being quite smooth; and the means he found most efficient was that of coating the silver sheet or sheets with finely divided platinum ...
Of the application of this cell a very important modification can be arranged, by converting it into an ACID battery, analogous to the platinized silver of Mr. Smee. Those who are acquainted with the ingenious device of that gentleman, are aware that the characteristic of his arrangement is, that the negative plate, where hydrogen is released, shall part with this hydrogen very readily. Under ordinary circumstances, the hydrogen adheres very much to the plates of an acid battery, and throws a considerable portion of the plates out of the action, by its presence on their surfaces. To remedy this, he has, as he terms it, "platinized" the surfaces.
In 1840 Smee invented a battery which made electrotyping possible commercially. ... Perhaps one of the greatest forward steps in connection with electrotyping was made when the plating dynamo was invented. The first adoption of a dynamo, in place of the Smee type of battery, was by Leslie, of New York, in 1872.Primer for apprentices in the printing industry. Good short introduction to the history of electrotyping.
The Smee cell is the cell most commonly employed because of its extreme simplicity of construction and management.A detailed discussion of the construction and maintenance of Smee cells, c. 1874.
Some extremely important commissions were made in electrotypes, such as the "bronzes" that adorn the Opera, Paris, and the 320 cm high statue of Prince Albert and four accompanying figures, erected behind the Albert Hall in London as a memorial to the Great Exhibition of 1851.
The singular property possessed by amalgamated zinc of not being attacked by sulphuric acid diluted with water is due to the adhesion of hydrogen on the plate in the acid solution