Electrolysis

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.

This article is about the chemical process. For the cosmetic hair removal procedure, see Electrology.

Illustration of a Hofmann electrolysis apparatus used in a school laboratory

History

The word "electrolysis" was introduced by Michael Faraday in the 19th century, on the suggestion of the Rev. William Whewell, using the Greek words ἤλεκτρον [ɛ̌ːlektron] "amber", which since the 17th century was associated with electrical phenomena, and λύσις [lýsis] meaning "dissolution". Nevertheless, electrolysis, as a tool to study chemical reactions and obtain pure elements, precedes the coinage of the term and formal description by Faraday.

In the early nineteenth century, William Nicholson and Anthony Carlisle sought to further Volta's experiments. They attached two wires to either side of Volta's battery and placed the other ends in a tube filled with water. They noticed when the wires were brought together that each wire produced bubbles. One type was hydrogen, the other was oxygen.[1]

In 1785 a Dutch Scientist named Martinus Van Marum created an electrostatic generator that he used to reduce tin, zinc and antimony from their salts using a process later known as electrolysis. Though he unknowingly produced electrolysis it was not until 1800 when William Nicholson and Anthony Carlisle discovered how electrolysis works.[2]

In 1791 Luigi Galvani experimented with frog legs. He claimed that placing animal muscle between two dissimilar metal sheets resulted in electricity. Responding to these claims, Alessandro Volta conducted his own tests.[3][4] This would give insight to Humphry Davy's ideas on electrolysis. During preliminary experiments, Humphry Davy hypothesized that when two elements combine together to form a compound, electrical energy is released. Humphry Davy would go on to create Decomposition Tables from his preliminary experiments on Electrolysis. The Decomposition Tables would give insight on the energies needed to break apart certain compounds.[5]

In 1817 Johan August Arfwedson determined there was another element, lithium, in some of his samples, however, he could not isolate the component. It was not until 1821 when William Thomas Brande used electrolysis to single it out. Two years later, he streamlined the process using lithium chloride and potassium chloride with electrolysis to produce lithium and lithium hydroxide.[6][7]

During the later years of Humphry Davy's research, Michael Faraday became his assistant. While studying the process of electrolysis under Humphry Davy, Michael Faraday discovered two laws of electrolysis.[4]

During the time of Maxwell and Faraday, concerns came about for electropositive and electronegative activities.[8]

In November 1875, Paul Émile Lecoq de Boisbaudran discovered gallium using electrolysis of gallium hydroxide, producing 3.4 mg of gallium. That following December, he presented his discovery of gallium to the Academie des Science in Paris.[9]

On June 26, 1886, Ferdinand Frederick Henri Moissan finally felt comfortable performing electrolysis on anhydrous hydrogen fluoride to create a gaseous fluorine pure element. Before he used hydrogen fluoride, Henri Moissan used fluoride salts with electrolysis. Thus on June 28, 1886 he performed his experiment in front of the Academie des Science to show his discovery of the new element fluorine.[10] In the cost of trying to find elemental fluorine through electrolysis of fluoride salts, many chemists perished including Pauline Louyet and Jerome Nickels.[11]

In 1886 Charles Martin Hall from America and Paul Héroult from France both filed for American patents, with Héroult submitting his in May and Hall’s in July.[12] Hall was able to get his patent by proving through letters to his brother and family evidence that his method was discovered before the French patent was submitted.[13] This became known as the Hall-Héroult process which benefited many industries because the price of aluminum had dropped from four dollars to thirty cents per pound.[14]

Timeline

Overview

Electrolysis is the passing of a direct electric current through an electrolyte producing chemical reactions at the electrodes and decomposition of the materials.

The main components required to achieve electrolysis are an electrolyte, electrodes, and an external power source. A partition (e.g. an ion-exchange membrane or a salt bridge) is optional to keep the products from diffusing to the vicinity of the opposite electrode.

The electrolyte is a conductive ionic chemical substance which contains free ions and carries electric current (e.g. an ion-conducting polymer, solution, or liquid ionic compound). If the ions are not mobile, as in most solid salts, then electrolysis cannot occur. A liquid electrolyte is produced by:

The electrodes are immersed separated by a distance such that a current flows between them through the electrolyte and are connected to the power source which completes the electrical circuit. A direct current supplied by the power source drives the reaction causing ions in the electrolyte to be attracted toward the respective oppositely charged electrode.

Electrodes of metal, graphite and semiconductor material are widely used. Choice of suitable electrode depends on chemical reactivity between the electrode and electrolyte and manufacturing cost. Historically, when non-reactive anodes were desired for electrolysis, graphite (called plumbago in Faraday's time) or platinum were chosen.[17] They were found to be some of the least reactive materials for anodes. Platinum erodes very slowly compared to other materials, and graphite crumbles and can produce carbon dioxide in aqueous solutions but otherwise does not participate in the reaction. Cathodes may be made of the same material, or they may be made from a more reactive one since anode wear is greater due to oxidation at the anode.

Process of electrolysis

The key process of electrolysis is the interchange of atoms and ions by the removal or addition of electrons due to the applied current. The desired products of electrolysis are often in a different physical state from the electrolyte and can be removed by physical processes (e.g. by collecting gas above an electrode or precipitating a product out of the electrolyte).

The quantity of the products is proportional to the current, and when two or more electrolytic cells are connected in series to the same power source, the products produced in the cells are proportional to their equivalent weight. These are known as Faraday's laws of electrolysis.

Each electrode attracts ions that are of the opposite charge. Positively charged ions (cations) move towards the electron-providing (negative) cathode. Negatively charged ions (anions) move towards the electron-extracting (positive) anode. In this process electrons are effectively introduced at the cathode as a reactant and removed at the anode as a product. In chemistry, the loss of electrons is called oxidation, while electron gain is called reduction.

When neutral atoms or molecules, such as those on the surface of an electrode, gain or lose electrons they become ions and may dissolve in the electrolyte and react with other ions.

When ions gain or lose electrons and become neutral, they may form compounds that separate from the electrolyte. Positive metal ions like Cu2+ deposit onto the cathode in a layer. The terms for this are electroplating, electrowinning, and electrorefining.

When an ion gains or loses electrons without becoming neutral, its electronic charge is altered in the process.

For example, the electrolysis of brine produces hydrogen and chlorine gases which bubble from the electrolyte and are collected. The initial overall reaction is thus:[18]

2 NaCl + 2 H2O → 2 NaOH + H2 + Cl2

The reaction at the anode results in chlorine gas from chlorine ions:

2 Cl− → Cl2 + 2 e−

The reaction at the cathode results in hydrogen gas and hydroxide ions:

2 H2O + 2 e− → H2 + 2 OH−

Without a partition between the electrodes, the OH− ions produced at the cathode are free to diffuse throughout the electrolyte to the anode. As the electrolyte becomes more basic due to the production of OH−, less Cl2 emerges from the solution as it begins to react with the hydroxide producing hypochlorite at the anode:

2 Cl2 + NaOH → NaCl + NaClO + H2O

The more opportunity the Cl2 has to interact with NaOH in the solution, the less Cl2 emerges at the surface of the solution and the faster the production of hypochlorite progresses. This depends on factors such as solution temperature, the amount of time the Cl2 molecule is in contact with the solution, and concentration of NaOH.

Likewise, as hypochlorite increases in concentration, chlorates are produced from them:

3 NaClO → NaClO3 + 2 NaCl

Other reactions occur, such as the self-ionization of water and the decomposition of hypochlorite at the cathode, the rate of the latter depends on factors such as diffusion and the surface area of the cathode in contact with the electrolyte.[19]

Decomposition potential

Decomposition potential or decomposition voltage refers to the minimum voltage (difference in electrode potential) between anode and cathode of an electrolytic cell that is needed for electrolysis to occur.[20]

The voltage at which electrolysis is thermodynamically preferred is the difference of the electrode potentials as calculated using the Nernst equation. Applying additional voltage, referred to as overpotential, can increase the rate of reaction and is often needed above the thermodynamic value. It is especially necessary for electrolysis reactions involving gases, such as oxygen, hydrogen or chlorine.

Oxidation and reduction at the electrodes

Oxidation of ions or neutral molecules occurs at the anode. For example, it is possible to oxidize ferrous ions to ferric ions at the anode:

Fe2+
(aq) → Fe3+
(aq) + e−

Reduction of ions or neutral molecules occurs at the cathode. It is possible to reduce ferricyanide ions to ferrocyanide ions at the cathode:

Fe(CN)3-
6 + e− → Fe(CN)4-
6

Neutral molecules can also react at either of the electrodes. For example: p-Benzoquinone can be reduced to hydroquinone at the cathode:

+ 2 e− + 2 H+ →

In the last example, H+ ions (hydrogen ions) also take part in the reaction and are provided by the acid in the solution, or by the solvent itself (water, methanol, etc.). Electrolysis reactions involving H+ ions are fairly common in acidic solutions. In aqueous alkaline solutions, reactions involving OH− (hydroxide ions) are common.

Sometimes the solvents themselves (usually water) are oxidized or reduced at the electrodes. It is even possible to have electrolysis involving gases, e.g. by using a gas diffusion electrode.

Energy changes during electrolysis

The amount of electrical energy that must be added equals the change in Gibbs free energy of the reaction plus the losses in the system. The losses can (in theory) be arbitrarily close to zero, so the maximum thermodynamic efficiency equals the enthalpy change divided by the free energy change of the reaction. In most cases, the electric input is larger than the enthalpy change of the reaction, so some energy is released in the form of heat. In some cases, for instance, in the electrolysis of steam into hydrogen and oxygen at high temperature, the opposite is true and heat energy is absorbed. This heat is absorbed from the surroundings, and the heating value of the produced hydrogen is higher than the electric input.

Variations

Pulsating current results in products different from DC. For example, pulsing increases the ratio of ozone to oxygen produced at the anode in the electrolysis of an aqueous acidic solution such as dilute sulphuric acid.[21] Electrolysis of ethanol with pulsed current evolves an aldehyde instead of primarily an acid.[22]

The following techniques are related to electrolysis:

  • Electrochemical cells, including the hydrogen fuel cell, use differences in Standard electrode potential to generate an electrical potential that provides useful power. Though related via the interaction of ions and electrodes, electrolysis and the operation of electrochemical cells are quite distinct. However, a chemical cell should not be seen as performing electrolysis in reverse.

Industrial uses
Hall-Heroult process for producing aluminium

Manufacturing processes

In manufacturing, electrolysis can be used for:

  • Electroplating, where a thin film of metal is deposited over a substrate material. Electroplating is used in many industries for either functional or decorative purposes, as in-vehicle bodies and nickel coins.
  • Electrochemical machining (ECM), where an electrolytic cathode is used as a shaped tool for removing material by anodic oxidation from a workpiece. ECM is often used as a technique for deburring or for etching metal surfaces like tools or knives with a permanent mark or logo.

Competing half-reactions in solution electrolysis

Using a cell containing inert platinum electrodes, electrolysis of aqueous solutions of some salts leads to the reduction of the cations (e.g., metal deposition with, e.g., zinc salts) and oxidation of the anions (e.g. evolution of bromine with bromides). However, with salts of some metals (e.g. sodium) hydrogen is evolved at the cathode, and for salts containing some anions (e.g. sulfate SO42−) oxygen is evolved at the anode. In both cases, this is due to water being reduced to form hydrogen or oxidized to form oxygen. In principle, the voltage required to electrolyze a salt solution can be derived from the standard electrode potential for the reactions at the anode and cathode. The standard electrode potential is directly related to the Gibbs free energy, ΔG, for the reactions at each electrode and refers to an electrode with no current flowing. An extract from the table of standard electrode potentials is shown below.

Half-reaction E° (V) Ref.
Na+ + e− ⇌ Na(s) −2.71[23]
Zn2+ + 2e− ⇌ Zn(s) −0.7618[24]
2H+ + 2e− ⇌ H2(g) ≡ 0[24]
Br2(aq) + 2e− ⇌ 2Br− +1.0873[24]
O2(g) + 4H+ + 4e− ⇌ 2H2O +1.23[23]
Cl2(g) + 2e− ⇌ 2Cl− +1.36[23]
S
2O2−
8 + 2e− ⇌ 2SO2−
4		 +2.07[23]

In terms of electrolysis, this table should be interpreted as follows:

  • Moving down the table, E° becomes more positive, and species on the left are more likely to be reduced: for example, zinc ions are more likely to be reduced to zinc metal than sodium ions are to be reduced to sodium metal.
  • Moving up the table, E° becomes more negative, and species on the right are more likely to be oxidized: for example, sodium metal is more likely to be oxidized to sodium ions than zinc metal is to be oxidized to zinc ions.

Using the Nernst equation the electrode potential can be calculated for a specific concentration of ions, temperature and the number of electrons involved. For pure water (pH 7):

  • the electrode potential for the reduction producing hydrogen is −0.41 V
  • the electrode potential for the oxidation producing oxygen is +0.82 V.

Comparable figures calculated in a similar way, for 1M zinc bromide, ZnBr2, are −0.76 V for the reduction to Zn metal and +1.10 V for the oxidation producing bromine. The conclusion from these figures is that hydrogen should be produced at the cathode and oxygen at the anode from the electrolysis of water—which is at variance with the experimental observation that zinc metal is deposited and bromine is produced.[25] The explanation is that these calculated potentials only indicate the thermodynamically preferred reaction. In practice, many other factors have to be taken into account such as the kinetics of some of the reaction steps involved. These factors together mean that a higher potential is required for the reduction and oxidation of water than predicted, and these are termed overpotentials. Experimentally it is known that overpotentials depend on the design of the cell and the nature of the electrodes.

For the electrolysis of a neutral (pH 7) sodium chloride solution, the reduction of sodium ion is thermodynamically very difficult and water is reduced evolving hydrogen leaving hydroxide ions in solution. At the anode the oxidation of chlorine is observed rather than the oxidation of water since the overpotential for the oxidation of chloride to chlorine is lower than the overpotential for the oxidation of water to oxygen. The hydroxide ions and dissolved chlorine gas react further to form hypochlorous acid. The aqueous solutions resulting from this process is called electrolyzed water and is used as a disinfectant and cleaning agent.

Electrolysis of carbon dioxide
Main article: Electrochemical reduction of carbon dioxide

The electrochemical reduction or electrocatalytic conversion of CO2 can produce value-added chemicals such methane, ethylene, ethane, etc.[26][27][28] The electrolysis of carbon dioxide gives formate or carbon monoxide, but sometimes more elaborate organic compounds such as ethylene.[29] This technology is under research as a carbon-neutral route to organic compounds.[30][31]

Electrolysis of acidified water
Main article: Electrolysis of water

Electrolysis of water produces hydrogen and oxygen in a ratio of 2 to 1 respectively.

2 H2O(l) → 2 H2(g) + O2(g); E0 = +1.229 V

The energy efficiency of water electrolysis varies widely. The efficiency of an electrolyzer is a measure of the enthalpy contained in the hydrogen (to undergo combustion with oxygen or some other later reaction), compared with the input electrical energy. Heat/enthalpy values for hydrogen are well published in science and engineering texts, as 144 MJ/kg. Note that fuel cells (not electrolyzers) cannot use this full amount of heat/enthalpy, which has led to some confusion when calculating efficiency values for both types of technology. In the reaction, some energy is lost as heat. Some reports quote efficiencies between 50% and 70% for alkaline electrolyzers; however, much higher practical efficiencies are available with the use of polymer electrolyte membrane electrolysis and catalytic technology, such as 95% efficiency.[32][33]

The National Renewable Energy Laboratory estimated that 1 kg of hydrogen (roughly equivalent to 3 kg, or 4 L, of petroleum in energy terms) could be produced by wind powered electrolysis for between $5.55 in the near term and $2.27 in the long term.[34]

About 4% of hydrogen gas produced worldwide is generated by electrolysis, and normally used onsite. Hydrogen is used for the creation of ammonia for fertilizer via the Haber process, and converting heavy petroleum sources to lighter fractions via hydrocracking. Recently, onsite electrolysis has been utilised to capture hydrogen for hydrogen fuel-cells in hydrogen vehicles.

Carbon/hydrocarbon assisted water electrolysis
Main article: Hydrogen production

Recently, to reduce the energy input, the utilization of carbon (coal), alcohols (hydrocarbon solution), and organic solution (glycerol, formic acid, ethylene glycol, etc.) with co-electrolysis of water has been proposed as a viable option.[35][36] The carbon/hydrocarbon assisted water electrolysis (so-called CAWE) process for hydrogen generation would perform this operation in a single electrochemical reactor. This system energy balance can be required only around 40% electric input with 60% coming from the chemical energy of carbon or hydrocarbon.[37] This process utilizes solid coal/carbon particles or powder as fuels dispersed in acid/alkaline electrolyte in the form of slurry and the carbon contained source co-assist in the electrolysis process as following theoretical overall reactions:[38]

Carbon/Coal slurry (C + 2H2O) -> CO2 + 2H2 E' = 0.21 V (reversible voltage) / E' = 0.46 V (thermo-neutral voltage)

or

Carbon/Coal slurry (C + H2O) -> CO + H2 E' = 0.52 V reversible voltage) / E' = 0.91 V (thermo-neutral voltage)

Thus, this CAWE approach is that the actual cell overpotential can be significantly reduced to below 1 V as compared to 1.5 V for conventional water electrolysis.

Electrocrystallization

A specialized application of electrolysis involves the growth of conductive crystals on one of the electrodes from oxidized or reduced species that are generated in situ. The technique has been used to obtain single crystals of low-dimensional electrical conductors, such as charge-transfer salts and linear chain compounds[39][40]

gollark: Basically by definition, stuff which goes in cannot come out.
gollark: Black holes can't do that.
gollark: You can hardly go around operating on "grapheme clusters" or something all the time. Codepoints are basically good enough.
gollark: That's still heresy. In *cool* languages the `char` type is for an actual Unicode character.
gollark: ' doubles up as an apostrophe, and in some programming languages `'a'` represents a single character a instead of a string `"a"`.

See also

References
  1. Fabbri, Emiliana; Schmidt, Thomas J. (5 October 2018). "Oxygen Evolution Reaction—The Enigma in Water Electrolysis". ACS Catalysis. 8 (10): 9765–9774. doi:10.1021/acscatal.8b02712.
  2. Ashworth, William PhD (20 March 2015). "Martinus van Marum - Scientist of the Day". Linda Hall Library.
  3. Ihde, Aaron J. (1964). The Development of Modern Chemistry. Harper & Row. pp. 125–127.
  4. "The History of Electrochemistry: From Volta to Edison". ECS. Retrieved 11 October 2019.
  5. THORPE, Thomas (1896). Humphry Davy POET AND PHILOSOPHER. New York: MACMILLAN & CO., Limited.
  6. "Lithium - periodicstats.com". www.periodicstats.com.
  7. Helmenstine, Todd (11 January 2018). "Today in Science History - January 12 - Johan August Arfwedson and Lithium". Science Notes and Projects.
  8. Ede, Andrew (2017). A History of Science in Society (third ed.). Toronto, Canada: University of Toronto Press. p. 251. ISBN 978-1-4426-3499-2.
  9. Marshall, James and Virginia. "Rediscovery of the Elements- Gallium" (PDF). University of North Texas.
  10. Wisniak, Jaime. "Henri Moissan- The discoverer of Fluorine". Research Gate.
  11. Marshall, James and Virginia. "Rediscovery of the Elements- Fluorine and Henri Moissan" (PDF). University of North Texas.
  12. Beck, Theodore R. (21 August 2015). "ECS Classics: Hall and Héroult and the Discovery of Aluminum Electrolysis". ECS. Interface.
  13. Hall Process Production and Commercialization of Aluminum - National Historic Chemical Landmark. Oberlin, Ohio: American Chemical Society. 1997.
  14. "Paul Héroult and Charles M. Hall". Science History Institute. 1 June 2016.
  15. The Supplement (1803 edition) to Encyclopædia Britannica 3rd edition (1797), volume 1, page 225, "Mister Van Marum, by means of his great electrical machine, decomposed the calces of tin, zinc, and antimony, and resolved them into their respective metals and oxygen" and gives as a reference Journal de Physiques, 1785.
  16. Lecoq de Boisbaudran P-E (1875). "On certain properties of gallium". The Chemical News and Journal of Industrial Science. 32: 294.
  17. Faraday, Michael (1849). Experimental Researches In Electricity. 1. London: The University of London.
  18. Tilley, R.J.D. (2004). Understanding solids: the science of materials. Understanding Solids: The Science of Materials. John Wiley and Sons. pp. 281–. Bibcode:2004usts.book.....T. ISBN 978-0-470-85276-7. Retrieved 22 October 2011.
  19. Thompson, M. de Kay (1911). Applied Electrochemistry. The MacMillan Company. pp. 84-88.
  20. W. Blum, G. W. Vinal: The Definition of Polarization, Overvoltage and Decomposition Potential. J. Electrochem. Soc. 1934 volume 66, issue 1, 359-367. doi:10.1149/1.3498105
  21. Kremann, R. (1903). "Über den Einfluss der Natur des Elektrolyten und des Elektrodenmaterials auf die Ozonbildung". Zeitschrift für anorganische Chemie. Metzger & Wittig. 36: 403–. doi:10.1002/zaac.19030360152. Retrieved 12 September 2019.
  22. Hale, Arthur J. (1919). The Manufacture of Chemicals by Electrolysis. D. Van Nostrand Co. pp. 16, 73. Retrieved 12 September 2019.
  23. Atkins, Peter (1997). Physical Chemistry, 6th edition (W.H. Freeman and Company, New York).
  24. Vanýsek, Petr (2007). "Electrochemical Series", in Handbook of Chemistry and Physics: 88th Edition (Chemical Rubber Company).
  25. Vogel, A.E. (1951), A textbook of Quantitative Inorganic Analysis, Longmans, Green and Co
  26. Lee, Seunghwa; Ju, Hyungkuk; Machunda, Revocatus; Uhm, Sunghyun; Lee, Jae Kwang; Lee, Hye Jin; Lee, Jaeyoung (2015). "Sustainable production of formic acid by electrolytic reduction of gaseous carbon dioxide". J. Mater. Chem. A. 3 (6): 3029. doi:10.1039/C4TA03893B.
  27. Whipple, Devin T.; Kenis, Paul J.A. (2010). "Prospects of CO2 Utilization via Direct Heterogeneous Electrochemical Reduction". The Journal of Physical Chemistry Letters. 1 (24): 3451. doi:10.1021/jz1012627.
  28. Machunda, Revocatus L.; Ju, Hyungkuk; Lee, Jaeyoung (2011). "Electrocatalytic reduction of CO2 gas at Sn based gas diffusion electrode". Current Applied Physics. 11 (4): 986. Bibcode:2011CAP....11..986M. doi:10.1016/j.cap.2011.01.003.
  29. Hori, Y. "Electrochemical CO2 Reduction on Metal Electrodes" (2008) pp. 141–153 in Modern Aspects of Electrochemistry, ed. C.G. Vayeanas, R. White and M.E. Gamboa-Aldeco, Springer, New York, no. 42. doi:10.1007/978-0-387-49489-0_3 ISBN 978-0-387-49489-0.
  30. Appel, Aaron M.; Bercaw, John E.; Bocarsly, Andrew B.; Dobbek, Holger; Dubois, Daniel L.; Dupuis, Michel; Ferry, James G.; Fujita, Etsuko; Hille, Russ; Kenis, Paul J.A.; Kerfeld, Cheryl A.; Morris, Robert H.; Peden, Charles H.F.; Portis, Archie R.; Ragsdale, Stephen W.; Rauchfuss, Thomas B.; Reek, Joost N.H.; Seefeldt, Lance C.; Thauer, Rudolf K.; Waldrop, Grover L. (2013). "Frontiers, Opportunities, and Challenges in Biochemical and Chemical Catalysis of CO2 Fixation". Chemical Reviews. 113 (8): 6621–6658. doi:10.1021/cr300463y. PMC 3895110. PMID 23767781.
  31. Qiao, Jinli; Liu, Yuyu; Hong, Feng; Zhang, Jiujun (2014). "A review of catalysts for the electroreduction of carbon dioxide to produce low-carbon fuels". Chem. Soc. Rev. 43 (2): 631–675. doi:10.1039/C3CS60323G. PMID 24186433.
  32. Carmo, M; Fritz D; Mergel J; Stolten D (2013). "A comprehensive review on PEM water electrolysis". Journal of Hydrogen Energy. 38 (12): 4901. doi:10.1016/j.ijhydene.2013.01.151.
  33. Zittel, Werner; Wurster, Reinhold (8 July 1996). "Chapter 3: Production of Hydrogen. Part 4: Production from electricity by means of electrolysis". HyWeb: Knowledge – Hydrogen in the Energy Sector. Ludwig-Bölkow-Systemtechnik GmbH. Archived from the original on 7 February 2007.
  34. Levene, J.; Kroposki, B.; Sverdrup, G. (March 2006). "Wind Energy and Production of Hydrogen and Electricity – Opportunities for Renewable Hydrogen – Preprint" (PDF). National Renewable Energy Laboratory. Retrieved 20 October 2008.
  35. Ju, Hyungkuk; Badwal, Sukhvinder; Giddey, Sarbjit (2018). "A comprehensive review of carbon and hydrocarbon assisted water electrolysis for hydrogen production". Applied Energy. 231: 502–533. doi:10.1016/j.apenergy.2018.09.125.
  36. Ju, Hyungkuk; Giddey, Sarbjit; Badwal, Sukhvinder P.S.; Mulder, Roger J. (2016). "Electro-catalytic conversion of ethanol in solid electrolyte cells for distributed hydrogen generation". Electrochimica Acta. 212: 744–757. doi:10.1016/j.electacta.2016.07.062.
  37. Giddey, S.; Kulkarni, A.; Badwal, S.P.S. (2015). "Low emission hydrogen generation through carbon assisted electrolysis". International Journal of Hydrogen Energy. 40: 70–74. doi:10.1016/j.ijhydene.2014.11.033.
  38. Ju, Hyungkuk; Giddey, Sarbjit; Badwal, Sukhvinder P.S. (2018). "Role of iron species as mediator in a PEM based carbon-water co-electrolysis for cost-effective hydrogen production". International Journal of Hydrogen Energy. 43 (19): 9144–9152. doi:10.1016/j.ijhydene.2018.03.195.
  39. Bechgaard, K.; Carneiro, K.; Rasmussen, F. B.; Olsen, M.; Rindorf, G.; Jacobsen, C.S.; Pedersen, H.J.; Scott, J.C. (1981). "Superconductivity in an organic solid. Synthesis, structure, and conductivity of bis(tetramethyltetraselenafulvalenium) perchlorate, (TMTSF)2ClO4". Journal of the American Chemical Society. 103 (9): 2440. doi:10.1021/ja00399a065.
  40. Williams, Jack M (2007). "Highly Conducting and Superconducting Synthetic Metals". Inorganic Syntheses. Inorganic Syntheses. 26. pp. 386–394. doi:10.1002/9780470132579.ch70. ISBN 978-0-470-13257-9.
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