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Electrolysis of water
From Wikipedia, the free encyclopedia

Electrolysis of water is the decomposition of water (H2O) into oxygen (O2) and hydrogen gas (H2) due to an electric current being passed through the water.

Contents
1 2 3 4 5 6 Principle History Equations Thermodynamics of the process Electrolyte selection Techniques 6.1 Fundamental demonstration 6.2 Hofmann voltameter 6.3 Industrial electrolysis 6.4 High pressure electrolysis 6.5 High-temperature electrolysis

7 Applications 8 Efficiency 9 See also 10 References 11 External links

Principle
An electrical power source is connected to two electrodes, or two plates (typically made from some inert metal such as platinum or stainless steel) which are placed in the water. Hydrogen will appear at the cathode (the negatively charged electrode, where electrons enter the water), and oxygen will appear at the anode (the positively charged electrode). Assuming ideal faradaic efficiency, the amount of hydrogen generated is twice the number of moles of oxygen, and both are proportional to the total electrical charge conducted by the solution. However, in many cells competing side reactions dominate, resulting in different products and less than ideal faradaic efficiency. Electrolysis of pure water requires excess energy in the form of overpotential to overcome various activation barriers. Without the excess energy the electrolysis of pure water occurs very slowly or not at all. This is in part due to the limited self-ionization of water. Pure water has an electrical conductivity about one millionth that of seawater. Many electrolytic cells may also lack the requisite electrocatalysts.

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The efficacy of electrolysis is increased through the addition of an electrolyte (such as a salt, an acid or a base) and the use of electrocatalysts. Currently the electrolytic process is rarely used in industrial applications since hydrogen can currently be produced more affordably from fossil fuels.

History
Jan Rudolph Deiman and Adriaan Paets van Troostwijk used in 1789 an electrostatic machine to produce electricity which was discharged on gold electrodes in a Leyden [1] In 1800 Alessandro Volta invented the voltaic pile, a few weeks jar with water. later William Nicholson and Anthony Carlisle used it for the electrolysis of water. When Znobe Gramme invented the Gramme machine in 1869 electrolysis of water became a cheap method for the production of hydrogen. A method of industrial synthesis of hydrogen and oxygen through electrolysis was developed by Dmitry [2] Lachinov in 1888.

Equations
In the pure water at the negatively charged cathode, a reduction reaction takes place, with electrons (e ) from the cathode being given to hydrogen cations to form hydrogen gas (the half reaction balanced with acid):
+ Reduction at cathode: 2 H (aq) + 2e H2(g)

At the positively charged anode, an oxidation reaction occurs, generating oxygen gas and giving electrons to the anode to complete the circuit:
+ Anode (oxidation): 2 H2O(l) O2(g) + 4 H (aq) + 4e

The same half reactions can also be balanced with base as listed below. Not all half reactions must be balanced with acid or base. Many do like the oxidation or reduction of water listed here. To add half reactions they must both be balanced with either acid or base.
Cathode (reduction): 2 H2O(l) + 2e H2(g) + 2 OH (aq) Anode (oxidation): 4 OH (aq) O2(g) + 2 H2O(l) + 4 e

Combining either half reaction pair yields the same overall decomposition of water into oxygen and hydrogen: Overall reaction: 2 H2O(l) 2 H2(g) + O2(g) The number of hydrogen molecules produced is thus twice the number of oxygen molecules. Assuming equal temperature and pressure for both gases, the produced hydrogen gas has therefore twice the volume of the produced oxygen gas. The
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number of electrons pushed through the water is twice the number of generated hydrogen molecules and four times the number of generated oxygen molecules.

Thermodynamics of the process

Eox = -1.23 V (Ered =

Ered = 0.00 V

Thus, the standard potential of the water electrolysis cell is -1.23 V at 25 C at pH 0 + + 7 M) based on the (H = 1.0 M). It is also -1.23 V at 25 C at pH 7 (H = 1.0 10 Nernst Equation. The negative voltage indicates the Gibbs free energy for electrolysis of water is greater than zero for these reactions. This can be found using the G = -nFE equation from chemical kinetics, where n is the moles of electrons and F is the Faraday constant. The reaction cannot occur without adding necessary energy, usually supplied by an external electrical power source.

Electrolyte selection
If the above described processes occur in pure water, + H cations will accumulate at the anode and OH anions will accumulate at the cathode. This can be verified by adding a pH indicator to the water: the water near the anode is acidic while the water near the cathode is basic. The negative hydroxyl ions that approach the anode mostly combine with the positive hydronium ions + (H3O ) to form water. The positive hydronium ions that approach the negative cathode mostly combine with negative hydroxyl ions to form water. Relatively few hydronium (hydroxyl) ions reach the cathode (anode). This can cause a concentration overpotential at both electrodes.

Hoffman voltameter connected to a direct current power supply.

Pure water is a fairly good insulator since it has a low autoionization, Kw = 1.0 x 14 at room temperature and thus pure water conducts current poorly, 0.055 10 1 Scm . Unless a very large potential is applied to cause an increase in the autoionization of water the electrolysis of pure water proceeds very slowly limited by the overall conductivity. If a water-soluble electrolyte is added, the conductivity of the water rises

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considerably. The electrolyte disassociates into cations and anions; the anions rush + towards the anode and neutralize the buildup of positively charged H there; similarly, the cations rush towards the cathode and neutralize the buildup of [4] negatively charged OH there. This allows the continued flow of electricity. Care must be taken in choosing an electrolyte, since an anion from the electrolyte is in competition with the hydroxide ions to give up an electron. An electrolyte anion with less standard electrode potential than hydroxide will be oxidized instead of the hydroxide, and no oxygen gas will be produced. A cation with a greater standard electrode potential than a hydrogen ion will be reduced in its stead, and no hydrogen gas will be produced.
+ The following cations have lower electrode potential than H and are therefore + + + + 2+ 2+ 2+ + suitable for use as electrolyte cations: Li , Rb , K , Cs , Ba , Sr , Ca , Na , and 2+ Mg . Sodium and lithium are frequently used, as they form inexpensive, soluble salts. + If an acid is used as the electrolyte, the cation is H , and there is no competitor for + the H created by disassociating water. The most commonly used anion is sulfate

(SO4 ), as it is very dicult to oxidize, with the standard potential for oxidation of this ion to the peroxodisulfate ion being 2.05 volts. Strong acids such as sulfuric acid (H2SO4), and strong bases such as potassium hydroxide (KOH), and sodium hydroxide (NaOH) are frequently used as electrolytes. A solid polymer electrolyte can also be used such as NAFION and when applied with a special catalyst on each side of the membrane can efficiently split the water molecule with as little as 1.8 Volts.

Techniques
Fundamental demonstration
Two leads, running from the terminals of a battery, are placed in a cup of water with a quantity of electrolyte to establish conductivity in the solution. Using NaCl as an electrolyte results in chlorine gas rather than oxygen due to a competing half-reaction. With the correct electrodes and correct electrolyte hydrogen and oxygen gases will stream from the oppositely charged electrodes. Oxygen will collect at the anode and hydrogen will collect at the cathode.

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Hofmann voltameter
Main article: Hofmann voltameter The Hofmann voltameter is often used as a small-scale electrolytic cell. It consists of three joined upright cylinders. The inner cylinder is open at the top to allow the addition of Match test used to water and the electrolyte. A platinum electrode is placed at detect the presence the bottom of each of the two side cylinders, connected to the of hydrogen gas. positive and negative terminals of a source of electricity. When current is run through the Hofmann voltameter, gaseous oxygen forms at the anode(negative) and gaseous hydrogen at the cathode(positive). Each gas displaces water and collects at the top of the two outer tubes, where it can be drawn off with a stopcock.

Industrial electrolysis
Many industrial electrolysis cells are very similar to Hofmann voltameters, with complex platinum plates or honeycombs as electrodes. Generally the only time hydrogen is intentionally produced from electrolysis is for specific point of use application such as is the case with oxyhydrogen torches or when extremely high hydrogen purity or oxygen is desired. The vast majority of hydrogen is produced from hydrocarbons and as a result contains trace amounts of carbon monoxide among other impurities. The carbon monoxide impurity can be detrimental to various systems including many fuel cells.

High pressure electrolysis

High-temperature electrolysis
Main article: High-temperature electrolysis High-temperature electrolysis (also HTE or steam electrolysis) is a method currently being investigated for water electrolysis with a heat engine. High temperature electrolysis is more efficient than traditional room-temperature electrolysis because some of the energy is supplied as heat, which is cheaper than electricity, and [7][8] because the electrolysis reaction is more efficient at higher temperatures.

Applications
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About four percent of hydrogen gas produced worldwide is created by electrolysis. The majority of this hydrogen produced through electrolysis is a side product in the production of chlorine. This is a prime example of a competing side reaction. 2 NaCl + 2 H2O Cl2 + H2 + 2 NaOH The electrolysis of brine (saltwater), a water sodium chloride mixture, is only half the electrolysis of water since the chloride ions are oxidized to chlorine rather than water being oxidized to oxygen. The hydrogen produced from this process is either burned (converting it back to water), used for the production of specialty chemicals, or various other small scale applications.

Efficiency
Water electrolysis does not convert 100% of the electrical energy into the chemical energy of hydrogen. The process requires more extreme potentials than what would be expected based on the cell's total reversible reduction potentials. This excess potential accounts for various forms of overpotential by which the extra energy is eventually lost as heat. For a well designed cell the largest overpotential is the reaction overpotential for the four electron oxidation of water to oxygen at the anode. An effective electrocatalyst to facilitate this reaction has not been developed. Platinum alloys are the default state of the art for this oxidation. Developing a cheap [9] effective electrocatalyst for this reaction would be a great advance (see also ). In 2008, a group led by Daniel Nocera announced the development of an [10] Other electrocatalyst composed of the abundant metal cobalt and phosphate. [11] researchers are pursuing carbon-based catalysts. The simpler two-electron reaction to produce hydrogen at the cathode can be electrocatalyzed with almost no reaction overpotential by platinum or in theory a hydrogenase enzyme. If other, less effective, materials are used for the cathode then another large overpotential must be paid. The energy eciency of water electrolysis varies widely with the numbers cited [12][13][14] These values refer only below on the optimistic side. Some report 5080%. to the eciency of converting electrical energy into hydrogen's chemical energy. The energy lost in generating the electricity is not included. For instance, when considering a power plant that converts the heat of nuclear reactions into hydrogen [15] although the via electrolysis, the total eciency may be closer to 3045%, inefficiencies of powerplants in turning heat into electrical energy is not usually included in efficiency, so the former measure of 50-80% efficient is probably a more realistic efficiency.

See also
Electrochemistry Electrolysis Hydrogen production Noryl Gas cracker

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