Reference articles on history, science, culture and more
Encyclopedia

Reference electrode

Electrode with a stable and accurate electrode potential

Image credit is listed at the end of this article.

A reference electrode is an electrode that has a stable and well-known electrode potential. The overall chemical reaction taking place in a cell is made up of two independent half-reactions, which describe chemical changes at the two electrodes. To focus on the reaction at the working electrode, the reference electrode is standardized with constant (buffered or saturated) concentrations of each participant of the redox reaction.

There are many ways reference electrodes are used. The simplest is when the reference electrode is used as a half-cell to build an electrochemical cell. This allows the potential of the other half cell to be determined. An accurate and practical method to measure an electrode's potential in isolation (absolute electrode potential) has yet to be developed.

01Aqueous reference electrodes

Common reference electrodes and potential with respect to the standard hydrogen electrode (SHE):

Cu-Cu(II) reference electrode
Cu-Cu(II) reference electrode

02Nonaqueous reference electrodes

While it is convenient to compare between solvents to qualitatively compare systems, this is not quantitatively meaningful. Much as pKa are related between solvents, but not the same, so is the case with E°. While the SHE might seem to be a reasonable reference for nonaqueous work as it turns out the platinum is rapidly poisoned by many solvents including acetonitrile causing uncontrolled drifts in potential. Both the SCE and saturated Ag/AgCl are aqueous electrodes based around saturated aqueous solution. While for short periods it may be possible to use such aqueous electrodes as references with nonaqueous solutions the long-term results are not trustworthy. Using aqueous electrodes introduces undefined, variable, and unmeasurable junction potentials to the cell in the form of a liquid-liquid junction as well as different ionic composition between the reference compartment and the rest of the cell. The best argument against using aqueous reference electrodes with nonaqueous systems, as mentioned earlier, is that potentials measured in different solvents are not directly comparable. For instance, the potential for the Fc0/+ couple is sensitive to solvent.

Solvent Formula E1/2 (V)
(FeCp20/+ vs SCE,
0.1 M NBu4PF6 at 298 K)
Acetonitrile CH3CN 0.40, 0.382
Dichloromethane CH2Cl2 0.46, 0.475
Tetrahydrofuran THF 0.56, 0.547
Dimethylformamide DMF 0.45, 0.470
Acetone (CH3)2C=O 0.48
Dimethylsulfoxide DMSO 0.435
Dimethoxyethane DME 0.51, 0.580

A quasi-reference electrode (QRE) avoids the issues mentioned above. A QRE with ferrocene or another internal standard, such as cobaltocene or decamethylferrocene, referenced back to ferrocene is ideal for nonaqueous work. Since the early 1960s ferrocene has been gaining acceptance as the standard reference for nonaqueous work for a number of reasons, and in 1984, IUPAC recommended ferrocene (0/1+) as a standard redox couple. The preparation of the QRE electrode is simple, allowing for a fresh reference to be prepared with each set of experiments. Since QREs are made fresh, there is also no concern with improper storage or maintenance of the electrode. QREs are also more affordable than other reference electrodes.

To make a quasi-reference electrode (QRE):

  1. Insert a piece of silver wire into concentrated HCl then allow the wire to dry on a lint-free cleaning cloth. This forms an insoluble layer of AgCl on the surface of the electrode and gives you an Ag/AgCl wire. Repeat dipping every few months or if the QRE starts to drift.
  2. Obtain a Vycor glass frit (4 mm diameter) and glass tubing of similar diameter. Attach Vycor glass frit to the glass tubing with heat shrink Teflon tubing.
  3. Rinse then fill the clean glass tube with supporting electrolyte solution and insert Ag/AgCl wire.
  4. The ferrocene (0/1+) couple should lie around 400 mV versus this Ag/AgCl QRE in an acetonitrile solution. This potential will vary up to 200 mV with specific undefined conditions, thus adding an internal standard such as ferrocene at some point during the experiment is always necessary.

03Pseudo reference electrodes

A pseudo reference electrode is a term that is not well defined and borders on having multiple meanings since pseudo and quasi are often used interchangeably. They are a class of electrodes named pseudo-reference electrodes because they do not maintain a constant potential but vary predictably with conditions. If the conditions are known, the potential can be calculated and the electrode can be used as a reference. Most electrodes work over a limited range of conditions, such as pH or temperature, outside of this range the electrodes behavior becomes unpredictable. The advantage of a pseudo-reference electrode is that the resulting variation is factored into the system allowing researchers to accurately study systems over a wide range of conditions.

Yttria-stabilized zirconia (YSZ) membrane electrodes were developed with a variety of redox couples, e.g., Ni/NiO. Their potential depends on pH. When the pH value is known, these electrodes can be employed as a reference with notable applications at elevated temperatures.

Watch videos about Reference electrodeExplainers and documentaries on YouTube (opens in a new tab)

Sources and credits

This article is adapted from the Wikipedia article Reference electrode, written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.

Images, from Wikimedia Commons:

Fathomly is not affiliated with or endorsed by the Wikimedia Foundation. Spotted a problem? Tell us.

Continue exploring

Related topics

Auxiliary electrode

In electrochemistry, the auxiliary electrode, often also called the counter electrode, is an electrode used in a three-electrode electrochemical cell for voltammetric analysis or other reactions in which an electric current is expected to flow. The auxiliary electrode is distinct from the reference electrode, which establishes the electrical potential against which other potentials may be measured, and the working electrode, at which the cell reaction takes place.

Cyclic voltammetry

In electrochemistry, cyclic voltammetry is a type of voltammetric measurement where the potential of the working electrode is ramped linearly versus time. Unlike in linear sweep voltammetry, after the set potential is reached in a CV experiment, the working electrode's potential is ramped in the opposite direction to return to the initial potential.

Standard electrode potential (data page)

The data below tabulates standard electrode potentials, in volts relative to the standard hydrogen electrode (SHE), at: Temperature 298.15 K (25.00 °C; 77.00 °F); Effective concentration (activity) 1 mol/dm3 for each aqueous or amalgamated (mercury-alloyed) species; Unit activity for each solvent and pure solid or liquid species; and Absolute partial pressure 101.325 kPa (1.00000 atm; 1.01325 bar) for each gaseous reagent, the convention in most literature data but not the current standard state (100 kPa (0.99 atm; 1.0 bar)). Variations from these ideal conditions affect measured voltage via the Nernst equation.