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Reference electrode

 
Sci-Tech Dictionary: reference electrode
(′ref·rəns i′lek′trōd)

(physical chemistry) A nonpolarizable electrode that generates highly reproducible potentials; used for pH measurements and polarographic analyses; examples are the calomel electrode, silver-silver chloride electrode, and mercury pool.


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Sci-Tech Encyclopedia: Reference electrode
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An electrode with an invariant potential. In electrochemical methods, where it is necessary to observe, measure, or control the potential of another electrode (denoted indicator, test, or working electrode), it is necessary to use a reference electrode, which maintains a potential that remains practically unchanged during the course of an electrochemical measurement. Potentials of indicator or working electrodes are measured or expressed relative to reference electrodes.

One such electrode, the normal hydrogen electrode, has been chosen as a reference standard, relative to which potentials of other electrodes and those of oxidation-reduction couples are often expressed. By maintaining a constant pressure of hydrogen gas the potential of a hydrogen electrode can be used for determination of the activity of hydrogen ions in the tested solution. However, in practice the determination of the hydrogen-ion activity (pH) is performed by using a glass electrode. The hydrogen electrode itself is used only in fundamental studies and some nonaqueous solutions. The hydrogen electrode, however, remains important for providing a reference standard. See also Activity (thermodynamics); pH.

In practice, potentials are measured against reference electrodes that are easier to work with than the normal hydrogen electrode. Such electrodes are known as secondary reference electrodes; the most common are the calomel and silver–silver chloride electrodes. See also Electrode; Solvent.


Wikipedia: Reference electrode
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A Reference electrode is an electrode which has a stable and well-known electrode potential. The high stability of the electrode potential is usually reached by employing a redox system with constant (buffered or saturated) concentrations of each participants of the redox reaction.[1]

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.

Contents

Aqueous Reference Electrodes

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

Nonaqueous Reference Electrodes

While it is convenient to compare between solvents to qualitativley compare systems it 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 acetonitirile 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.[2] 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.[3]

A Quasi-Reference Electrode (QRE) avoids the issues mentioned above. A QRE with Ferrocene or similar internal standard (Cobaltocene) 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. In 1984 IUPAC recommend ferrocene (II/III) as a standard redox couple.[4] The preparation of the QRE electrode is simple allowing a fresh reference to be prepared with each set of experiments. Since QREs are made fresh there is also no concern of improper storage or maintenance of the electrode. QREs are also more affordable than other reference electrodes.

  • Making a quasi-reference electrode (QRE).
  1. Inserting a piece of Silver wire into concentrated HCl then allow the wire to dry on a chem-wipe. This forms an insoluble layer of AgCl on the surface of the electrode and gives you a 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 (II/III) couple should lie around 400 mV versus this Ag/AgCl QRE in an acetonitrile solution. This potential will varying up to 200 mV with the specific undefined conditions. Thus adding an internal standard such as ferrocene at some point during the experiment is always necessary.

Pseudo-reference electrodes

A pseudo-reference electrode is a term that is not well defined and boarders on having multiple meanings since pseudo and quasi are often used interchangeably. There 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 electrode 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 studying 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 electrode can be employed as a reference with notable applications at elevated temperatures.[5]

See also

Further reading

  • Ives, David J. G.; George J. Janz (1961). Reference Electrodes, Theory and Practice (1st ed.). Academic Press. 
  • Zanello, P. (2003-10-01). Inorganic Electrochemistry: Theory, Practice, and Application (1 ed.). Royal Society of Chemistry. ISBN 0854046615. 
  • Bard, Allen J.; Larry R. Faulkner (2000-12-18). Electrochemical Methods: Fundamentals and Applications (2 ed.). Wiley. ISBN 0471043729. 

References

  1. ^ Bard, Allen J.; Faulkner, Larry R. (2000-12-18). Electrochemical Methods: Fundamentals and Applications (2 ed.). Wiley. ISBN 0471043729. 
  2. ^ Pavlishchuk, Vitaly V.; Anthony W. Addison (2000-01). "Conversion constants for redox potentials measured versus different reference electrodes in acetonitrile solutions at 25°C". Inorganica Chimica Acta 298 (1): 97-102. doi:10.1016/S0020-1693(99)00407-7. http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TG5-3YDGGKF-J&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=949c49796859c129c5fdfdfa8dc96704. Retrieved 2009-04-17. 
  3. ^ Geiger, William E. (2007-11-01). "Organometallic Electrochemistry: Origins, Development, and Future". Organometallics 26 (24): 5738-5765. doi:10.1021/om700558k. http://dx.doi.org/10.1021/om700558k. Retrieved 2009-04-16. 
  4. ^ Gritzner, G.; J. Kuta (1984). "Recommendations on reporting electrode potentials in nonaqueous solvents". Pure Appl. Chem. 56 (4): 461-466. doi:10.1351/pac198456040461. http://iupac.org/publications/pac/56/4/0461/. Retrieved 2009-04-17. 
  5. ^ R.W. Bosch, D.Feron, and J.P. Celis, "Electrochemistry in Light Water Reactors", CRC Press, 2007.

 
 

 

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