Anode

Diagram of a zinc anode in a galvanic cell. Note how electrons move out of the cell, and the conventional current moves into it in the opposite direction.

An anode is an electrode through which conventional current flows into a polarized electrical device. A common mnemonic is ACID for "anode current into device".^[1] The direction of (positive) electric current is opposite to the direction of electron flow: (negatively charged) electrons flow out the anode to the outside circuit.

The polarity of voltage on an anode with respect to an associated cathode varies depending on the device type and on its operating mode. In the following examples, the anode is negative in a device that provides power, and positive in a device that consumes power:

In a discharging battery or galvanic cell (diagram at right), the anode is the negative terminal because it is where current flows into "the device" (i.e. the battery cell). This inward current is carried externally by electrons moving outwards, negative charge flowing in one direction being electrically equivalent to positive charge flowing in the opposite direction.
In a recharging battery, or an electrolytic cell, the anode is the positive terminal, which receives current from an external generator. The current through a recharging battery is opposite to the direction of current during discharge; in other words, the electrode which was the cathode during battery discharge becomes the anode while the battery is recharging.
In a diode, the anode is the positive terminal at the tail of the arrow symbol (flat side of the triangle), where current flows into the device. Note electrode naming for diodes is always based on the direction of the forward current (that of the arrow, in which the current flows "most easily"), even for types such as Zener diodes or solar cells where the current of interest is the reverse current.
In a cathode ray tube, the anode is the positive terminal where electrons flow out of the device, i.e., where positive electric current flows in.

Etymology

The word was coined in 1834 from the Greek ἄνοδος (anodos), 'ascent', by William Whewell, who had been consulted^[2] by Michael Faraday over some new names needed to complete a paper on the recently discovered process of electrolysis. In that paper Faraday explained that when an electrolytic cell is oriented so that electric current traverses the "decomposing body" (electrolyte) in a direction "from East to West, or, which will strengthen this help to the memory, that in which the sun appears to move", the anode is where the current enters the electrolyte, on the East side: "ano upwards, odos a way ; the way which the sun rises" (,^[3] reprinted in ^[4]).

The use of 'East' to mean the 'in' direction (actually 'in' → 'East' → 'sunrise' → 'up') may appear contrived. Previously, as related in the first reference cited above, Faraday had used the more straightforward term "eisode" (the doorway where the current enters). His motivation for changing it to something meaning 'the East electrode' (other candidates had been "eastode", "oriode" and "anatolode") was to make it immune to a possible later change in the direction convention for current, whose exact nature was not known at the time. The reference he used to this effect was the Earth's magnetic field direction, which at that time was believed to be invariant. He fundamentally defined his arbitrary orientation for the cell as being that in which the internal current would run parallel to and in the same direction as a hypothetical magnetizing current loop around the local line of latitude which would induce a magnetic dipole field oriented like the Earth's. This made the internal current East to West as previously mentioned, but in the event of a later convention change it would have become West to East, so that the East electrode would not have been the 'way in' any more. Therefore, "eisode" would have become inappropriate, whereas "anode" meaning 'East electrode' would have remained correct with respect to the unchanged direction of the actual phenomenon underlying the current, then unknown but, he thought, unambiguously defined by the magnetic reference. In retrospect the name change was unfortunate, not only because the Greek roots alone do not reveal the anode's function any more, but more importantly because as we now know, the Earth's magnetic field direction on which the "anode" term is based is subject to reversals whereas the current direction convention on which the "eisode" term was based has no reason to change in the future.

Since the later discovery of the electron, an easier to remember and more durably correct technically although historically false, etymology has been suggested: anode, from the Greek anodos, 'way up', 'the way (up) out of the cell (or other device) for electrons'.

Flow of electrons

The flow of electrons is always from anode to cathode outside of the cell or device, regardless of the cell or device type and operating mode, with the exception of diodes, where electrode naming always assumes current in the forward direction (that of the arrow symbol), i.e., electrons flow in the opposite direction, even when the diode reverse-conducts either by accident (breakdown of a normal diode) or by design (breakdown of a Zener diode, photo-current of a photodiode).

Electrolytic anode

In electrochemistry, the anode is where oxidation occurs and is the positive polarity contact in an electrolytic cell.^[5] At the anode, anions (negative ions) are forced by the electrical potential to react chemically and give off electrons (oxidation) which then flow up and into the driving circuit. Mnemonics: LEO Red Cat (Loss of Electrons is Oxidation, Reduction occurs at the Cathode), or AnOx Red Cat (Anode Oxidation, Reduction Cathode), or OIL RIG (Oxidation is Loss, Reduction is Gain of electrons), or Roman Catholic and Orthodox (Reduction – Cathode, anode – Oxidation), or LEO the lion says GER (Losing electrons is Oxidation, Gaining electrons is Reduction).

This process is widely used in metals refining. For example, in copper refining, copper anodes, an intermediate product from the furnaces, are electrolysed in an appropriate solution (such as sulfuric acid) to yield high purity (99.99%) cathodes. Copper cathodes produced using this method are also described as electrolytic copper.

Battery or galvanic cell anode

Galvanic cell

In a battery or galvanic cell, the anode is the negative electrode from which electrons flow out towards the external part of the circuit. Internally the positively charged cations are flowing away from the anode (even though it is negative and therefore would be expected to attract them, this is due to electrode potential relative to the electrolyte solution being different for the anode and cathode metal/electrolyte systems); but, external to the cell in the circuit, electrons are being pushed out through the negative contact and thus through the circuit by the voltage potential as would be expected. Note: in a galvanic cell, contrary to what occurs in an electrolytic cell, no anions flow to the anode, the internal current being entirely accounted for by the cations flowing away from it (cf drawing).

In the United States, many battery manufacturers regard the positive electrode as the anode, particularly in their technical literature. Though technically incorrect, it does resolve the problem of which electrode is the anode in a secondary (or rechargeable) cell. Using the traditional definition, the anode switches ends between charge and discharge cycles.

Vacuum tube anode

Cutaway diagram of a triode vacuum tube, showing the plate (anode)

In electronic vacuum devices such as a cathode ray tube, the anode is the positively charged electron collector. In a tube, the anode is a charged positive plate that collects the electrons emitted by the cathode through electric attraction. It also accelerates the flow of these electrons.

Diode anode

In a semiconductor diode, the anode is the P-doped layer which initially supplies holes to the junction. In the junction region, the holes supplied by the anode combine with electrons supplied from the N-doped region, creating a depleted zone. As the P-doped layer supplies holes to the depleted region, negative dopant ions are left behind in the P-doped layer ('P' for positive charge-carrier ions). This creates a base negative charge on the anode. When a positive voltage is applied to anode of the diode from the circuit, more holes are able to be transferred to the depleted region, and this causes the diode to become conductive, allowing current to flow through the circuit. The terms anode and cathode should not be applied to a Zener diode, since it allows flow in either direction, depending on the polarity of the applied potential (i.e. voltage).

Sacrificial anode

Sacrificial anodes mounted "on the fly" for corrosion protection of a metal structure

In cathodic protection, a metal anode that is more reactive to the corrosive environment of the system to be protected is electrically linked to the protected system, and partially corrodes or dissolves, which protects the metal of the system it is connected to. As an example, an iron or steel ship's hull may be protected by a zinc sacrificial anode, which will dissolve into the seawater and prevent the hull from being corroded. Sacrificial anodes are particularly needed for systems where a static charge is generated by the action of flowing liquids, such as pipelines and watercraft. Sacrificial anodes are also generally used in tank-type water heaters.

In 1824 to reduce the impact of this destructive electrolytic action on ships hulls, their fastenings and underwater equipment, the scientist-engineer Sir Humphry Davy, developed the first and still most widely used marine electrolysis protection system. Davy installed sacrificial anodes made from a more electrically reactive (less noble) metal attached to the vessel hull and electrically connected to form a cathodic protection circuit.

A less obvious example of this type of protection is the process of galvanising iron. This process coats iron structures (such as fencing) with a coating of zinc metal. As long as the zinc remains intact, the iron is protected from the effects of corrosion. Inevitably, the zinc coating becomes breached, either by cracking or physical damage. Once this occurs, corrosive elements act as an electrolyte and the zinc/iron combination as electrodes. The resultant current ensures that the zinc coating is sacrificed but that the base iron does not corrode. Such a coating can protect an iron structure for a few decades, but once the protecting coating is consumed, the iron rapidly corrodes.

If, conversely, tin is used to coat steel, when a breach of the coating occurs it actually accelerates oxidation of the iron.

Related antonym

The opposite of an anode is a cathode. When the current through the device is reversed, the electrodes switch functions, so anode becomes cathode, while cathode becomes anode, as long as the reversed current is applied, with the exception of diodes where electrode naming is always based on the forward current direction.

References

↑ http://www.av8n.com/physics/anode-cathode.htm#sec-def
↑ Ross, S (1961). "Faraday Consults the Scholars: The Origins of the Terms of Electrochemistry". Notes and Records of the Royal Society of London (1938–1996) 16 (2): 187–220. doi:10.1098/rsnr.1961.0038.
↑ Faraday, Michael (January 1834). "Experimental Researches in Electricity. Seventh Series". Philosophical Transactions of the Royal Society 124 (1): 77. doi:10.1098/rstl.1834.0008. (in which Faraday introduces the words electrode, anode, cathode, anion, cation, electrolyte, electrolyze)
↑ Faraday, Michael (1849). "Experimental Researches in Electricity" 1.
↑ http://goldbook.iupac.org/A00370.html

External links

Galvanic cells

Types	Voltaic pile Battery Flow battery Trough battery Concentration cell Fuel cell Thermogalvanic cell

Primary cell (non-rechargable)	Alkaline Aluminium–air Bunsen Chromic acid Clark Daniell Dry Edison-Lalande Grove Leclanché Lithium Mercury Nickel oxyhydroxide Silicon–air Silver oxide Weston Zamboni Zinc–air Zinc–carbon

Secondary cell (rechargeable)	Automotive Lead–acid gel / VRLA Lithium–air Lithium–ion Lithium polymer Lithium iron phosphate Lithium titanate Lithium–sulfur Dual carbon battery Molten salt Nanopore Nanowire Nickel–cadmium Nickel–hydrogen Nickel–iron Nickel–lithium Nickel–metal hydride Nickel–zinc Polysulfide bromide Potassium-ion Rechargeable alkaline Sodium-ion Sodium–sulfur Vanadium redox Zinc–bromine Zinc–cerium

Cell parts	Anode Binder Catalyst Cathode Electrode Electrolyte Half-cell Ions Salt bridge Semipermeable membrane

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