An electrochemical cell is a device capable of either generating electrical energy from chemical reactions or using electrical energy to cause chemical reactions. The electrochemical cells which generate an electric current are called voltaic cells or galvanic cells and those that generate chemical reactions, via electrolysis for example, are called electrolytic cells. A common example of a galvanic cell is a standard 1.5 volt cell meant for consumer use. A battery consists of one or more cells, connected either in parallel, series or series-and-parallel pattern. A cell is a device which can convert chemical energy into electrical energy. A simple cell does this by using a combination of two metals (electrodes) and an electrolyte solution (which could be acid/alkali/salt solution). Metals can conduct electricity due to metallic bonding. Metallic bonds are the electrostatic force of attraction between negatively charged delocalised electrons and the positively charged metal ions. Metal atoms are surrounded by a “sea” of delocalised electrons. This means they are free to move within the structure- this gives metals its conducting abilities as an electric current can flow through it. A reaction between metals where electrons are gained is a reduction, while a reaction where electrons are lost is an oxidation. A reaction where both reduction and oxidation occur is a redox reaction. A redox reaction occurs when electrons are transferred from a substance that is oxidized to one that is being reduced.
An electrolytic cell is an electrochemical cell that drives a non-spontaneous redox reaction through the application of electrical energy. They are often used to decompose chemical compounds, in a process called electrolysis—the Greek word lysis means to break up.
Important examples of electrolysis are the decomposition of water into hydrogen and oxygen, and bauxite into aluminium and other chemicals. Electroplating (e.g. of copper, silver, nickel or chromium) is done using an electrolytic cell. Electrolysis is a technique that uses a direct electric current (DC).
An electrolytic cell has three component parts: an electrolyte and two electrodes (a cathode and an anode). The electrolyte is usually a solution of water or other solvents in which ions are dissolved. Molten salts such as sodium chloride are also electrolytes. When driven by an external voltage applied to the electrodes, the ions in the electrolyte are attracted to an electrode with the opposite charge, where charge-transferring (also called faradaic or redox) reactions can take place. Only with an external electrical potential (i.e. voltage) of correct polarity and sufficient magnitude can an electrolytic cell decompose a normally stable, or inert chemical compound in the solution. The electrical energy provided can produce a chemical reaction which would not occur spontaneously otherwise.
Galvanic cell or Voltaic cellEdit
A galvanic cell, or voltaic cell, named after Luigi Galvani, or Alessandro Volta respectively, is an electrochemical cell that derives electrical energy from spontaneous redox reactions taking place within the cell. It generally consists of two different metals connected by a salt bridge, or individual half-cells separated by a porous membrane.
Volta was the inventor of the voltaic pile, the first electrical battery. In common usage, the word "battery" has come to include a single galvanic cell, but a battery properly consists of multiple cells.
A primary cell is a Galvanic battery that is designed to be used once and discarded, and not recharged with electricity and reused like a secondary cell (rechargeable battery). 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 and is useless. 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.
Primary batteries make up about 90% of the $50 billion battery market, but secondary batteries have been gaining market share. About 15 billion primary batteries are thrown away worldwide every year, virtually all ending up in landfills. Due to the toxic heavy metals and strong acids or alkalis they contain, batteries are hazardous waste. Most municipalities classify them as such and require separate disposal. The energy needed to manufacture a battery is about 50 times greater than the energy it contains. Due to their high pollutant content compared to their small energy content, the primary battery is considered a wasteful, environmentally unfriendly technology. Due mainly to increasing sales of wireless devices and cordless tools which cannot be economically powered by primary batteries and come with integral rechargeable batteries, the secondary battery industry has high growth and has slowly been replacing the primary battery in high end products.
A secondary cell, commonly referred to as a rechargeable battery is an electrochemical cell that can be run as both a galvanic cell or as an electrolytic cell. This is used as a convenient way to store electricity, when current flows one way the levels of one or more chemicals build up (charging), while it is discharging they reduce and the resulting electromotive force can do work.
A fuel cell is an electrochemical cell that converts the chemical energy from a fuel into electricity through an electrochemical reaction of hydrogen fuel with oxygen or another oxidizing agent. Fuel cells are different from batteries in requiring a continuous source of fuel and oxygen (usually from air) to sustain the chemical reaction, whereas in a battery the chemical energy comes from chemicals already present in the battery. Fuel cells can produce electricity continuously for as long as fuel and oxygen are supplied.
The first fuel cells were invented in 1838. The first commercial use of fuel cells came more than a century later in NASA space programmes to generate power for satellites and space capsules. Since then, fuel cells have been used in many other applications. Fuel cells are used for primary and backup power for commercial, industrial and residential buildings and in remote or inaccessible areas. They are also used to power fuel cell vehicles, including forklifts, automobiles, buses, boats, motorcycles and submarines.
There are many types of fuel cells, but they all consist of an anode, a cathode, and an electrolyte that allows positively charged hydrogen ions (protons) to move between the two sides of the fuel cell. At the anode a catalyst causes the fuel to undergo oxidation reactions that generate protons (positively charged hydrogen ions) and electrons. The protons flow from the anode to the cathode through the electrolyte after the reaction. At the same time, electrons are drawn from the anode to the cathode through an external circuit, producing direct current electricity. At the cathode, another catalyst causes hydrogen ions, electrons, and oxygen to react, forming water. Fuel cells are classified by the type of electrolyte they use and by the difference in startup time ranging from 1 second for proton exchange membrane fuel cells (PEM fuel cells, or PEMFC) to 10 minutes for solid oxide fuel cells (SOFC). A related technology is flow batteries, in which the fuel can be regenerated by recharging. Individual fuel cells produce relatively small electrical potentials, about 0.7 volts, so cells are "stacked", or placed in series, to create sufficient voltage to meet an application's requirements. In addition to electricity, fuel cells produce water, heat and, depending on the fuel source, very small amounts of nitrogen dioxide and other emissions. The energy efficiency of a fuel cell is generally between 40–60%; however, if waste heat is captured in a cogeneration scheme, efficiencies up to 85% can be obtained.
The fuel cell market is growing, and in 2013 Pike Research estimated that the stationary fuel cell market will reach 50 GW by 2020.
An electrochemical cell consists of two half-cells. Each half-cell consists of an electrode and an electrolyte. The two half-cells may use the same electrolyte, or they may use different electrolytes. The chemical reactions in the cell may involve the electrolyte, the electrodes, or an external substance (as in fuel cells that may use hydrogen gas as a reactant). In a full electrochemical cell, species from one half-cell lose electrons (oxidation) to their electrode while species from the other half-cell gain electrons (reduction) from their electrode.
A salt bridge (e.g., filter paper soaked in KNO3, NaCl, or some other electrolyte) is often employed to provide ionic contact between two half-cells with different electrolytes, yet prevent the solutions from mixing and causing unwanted side reactions. An alternative to a salt bridge is to allow direct contact (and mixing) between the two half-cells, for example in simple electrolysis of water.
As electrons flow from one half-cell to the other through an external circuit, a difference in charge is established. If no ionic contact were provided, this charge difference would quickly prevent the further flow of electrons. A salt bridge allows the flow of negative or positive ions to maintain a steady-state charge distribution between the oxidation and reduction vessels, while keeping the contents otherwise separate. Other devices for achieving separation of solutions are porous pots and gelled solutions. A porous pot is used in the Bunsen cell (right).
Each half-cell has a characteristic voltage. Various choices of substances for each half-cell give different potential differences. Each reaction is undergoing an equilibrium reaction between different oxidation states of the ions: When equilibrium is reached, the cell cannot provide further voltage. In the half-cell that is undergoing oxidation, the closer the equilibrium lies to the ion/atom with the more positive oxidation state the more potential this reaction will provide. Likewise, in the reduction reaction, the closer the equilibrium lies to the ion/atom with the more negative oxidation state the higher the potential.
The cell potential can be predicted through the use of electrode potentials (the voltages of each half-cell). These half-cell potentials are defined relative to the assignment of 0 volts to the standard hydrogen electrode (SHE). (See table of standard electrode potentials). The difference in voltage between electrode potentials gives a prediction for the potential measured. When calculating the difference in voltage, one must first rewrite the half-cell reaction equations to obtain a balanced oxidation-reduction equation.
- Reverse the reduction reaction with the smallest potential ( to create an oxidation reaction/ overall positive cell potential)
- Half-reactions must be multiplied by integers to achieve electron balance.
Cell potentials have a possible range of roughly zero to 6 volts. Cells using water-based electrolytes are usually limited to cell potentials less than about 2.5 volts due to high reactivity of the powerful oxidizing and reducing agents with water that is needed to produce a higher voltage. Higher cell potentials are possible with cells using other solvents instead of water. For instance, lithium cells with a voltage of 3 volts are commonly available.
The cell potential depends on the concentration of the reactants, as well as their type. As the cell is discharged, the concentration of the reactants decreases and the cell potential also decreases.
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Electrochemical cells which generate an electric current are called voltaic cells or galvanic cells, and common batteries consist of one or more such cells. In other electrochemical cells an externally supplied electric current is used to drive a chemical reaction which would not occur spontaneously. Such cells are called electrolytic cells.
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