Silver chloride electrode

A silver chloride electrode is a type of reference electrode, commonly used in electrochemical measurements. For environmental reasons it has widely replaced the saturated calomel electrode. For example, it is usually the internal reference electrode in pH meters and it is often used as reference in reduction potential measurements. As an example of the latter, the silver chloride electrode is the most commonly used reference electrode for testing cathodic protection corrosion control systems in sea water environments.

Ag-AgCl reference electrode

The electrode functions as a redox electrode and the equilibrium is between the silver metal (Ag) and its salt—silver chloride (AgCl, also called silver(I) chloride).

The corresponding half-reactions can be presented as follows:

{\ce {Ag+ + e^- <=> Ag(s)}}

{\ce {AgCl(s) + e^- <=> Ag(s) + Cl-}}

or can be written together:

{\ce {AgCl(s) + Ag(s) + e^- <=> Ag(s) + e^- + Cl^- + Ag+}}

which can be simplified:

{\ce {AgCl(s) <=> Ag+ + Cl^-}}

This reaction is characterized by fast electrode kinetics, meaning that a sufficiently high current can be passed through the electrode with 100% efficiency of the redox reaction (dissolution of the metal or cathodic deposition of the silver-ions). The reaction has been proven to obey these equations in solutions of pH values between 0 and 13.5.

The Nernst equation below shows the dependence of the potential of the silver-silver(I) chloride electrode on the activity or effective concentration of chloride-ions:

E=E^{0}-{\frac {RT}{F}}\ln a_{{\ce {Cl-}}}

The standard electrode potential E⁰ against standard hydrogen electrode (SHE) is 0.230 V ± 10 mV. The potential is however very sensitive to traces of bromide ions which make it more negative. (The more exact standard potential given by an IUPAC review paper is +0.22249 V, with a standard deviation of 0.13 mV at 25 °C.[1])

Applications

Commercial reference electrodes consist of a plastic tube electrode body. The electrode is a silver wire that is coated with a thin layer of silver chloride, either physically by dipping the wire in molten silver chloride, chemically by electroplating the wire in concentrated hydrochloric acid[2] or electrochemically by oxidising the silver in a chloride solution.

A porous plug on one end allows contact between the field environment with the silver chloride electrolyte. An insulated lead wire connects the silver rod with measuring instruments. A voltmeter negative lead is connected to the test wire.

The electrode body contains potassium chloride to stabilize the silver chloride concentration. When working in seawater, this body can be removed and the chloride concentration is fixed by the stable salinity of the water. The potential of a silver:silver chloride reference electrode with respect to standard hydrogen electrode depends on the electrolyte composition.

**Reference Electrode Potentials**
Electrode	Potential E⁰+E_lj	Temperature Coef.
	(V) at 25 °C	(mV/°C) at around 25 °C
SHE	0.000	0.000 [3]
Ag/AgCl/Sat. KCl	+0.197	-1.01
Ag/AgCl/3.5 mol/kg KCl[4]	+0.205	-0.73
Ag/AgCl/3.0 mol/kg KCl	+0.210	?
Ag/AgCl/1.0 mol/kg KCl	+0.235	+0.25
Ag/AgCl/0.6 mol/kg KCl	+0.25
Ag/AgCl (Seawater)	+0.266

Notes to the Table: (1) The table data source is,[5] except where a separate reference is given. (2) E_lj is the potential of the liquid junction between the given electrolyte and the electrolyte with the activity of chloride of 1 mol/kg.

The electrode has many features making it suitable for use in the field:

Simple construction
Inexpensive to manufacture
Stable potential
Non-toxic components

They are usually manufactured with saturated potassium chloride electrolyte, but can be used with lower concentrations such as 1 mol/kg potassium chloride. As noted above, changing the electrolyte concentration changes the electrode potential. Silver chloride is slightly soluble in strong potassium chloride solutions, so it is sometimes recommended the potassium chloride be saturated with silver chloride to avoid stripping the silver chloride off the silver wire.

Biological electrode systems

Tab electrode using silver/silver chloride sensing for electrocardiography (ECG)[6]

Silver chloride electrodes are also used by many applications of biological electrode systems such as biomonitoring sensors as part of electrocardiography (ECG) and electroencephalography (EEG), and in transcutaneous electrical nerve stimulation (TENS) to deliver current. Historically, the electrodes were fabricated from solid materials such as silver, brass coated with silver, tin and nickel. In today's applications, most biomonitoring electrodes are silver/silver chloride sensors which are fabricated by coating a thin layer of silver on plastic substrates and the outer layer of silver is converted to silver chloride.[7]

The principle of silver/silver chloride sensors operation is the conversion of ion current at the surface of human tissues to electron current to be delivered through the lead wire to the instrument to read. An important part of the operation is electrolyte gel which is applied between the electrode and tissues. The gel contains free chloride ions such that the charge can be carried through the electrolyte, therefore the electrolyte can be considered as conductive for ion current as the human tissues. When the ion current exists, the silver atoms in the electrode oxidize and discharge cations to the electrolyte and the electrons carry charge through the lead wire. At the same time, the chloride ions which are anions in the electrolyte travel toward the electrode and they are reduced as they bond with silver of the electrode resulting in silver chloride and free electrons to deliver to the lead wire. The reaction allows current to pass from electrolyte to electrode and the electron current passes through the lead wire for the instrument to read.[8][9]

When there is an uneven distribution of cations and anions, there will be a small voltage called half-cell potential associated with the current. In the DC system that is used by the ECG and EEG instruments, the difference between the half-cell potential and the zero potential is shown as DC offset which is an undesirable characteristic. Silver/silver chloride is a popular choice of biological electrodes due to its low half-cell potential of approximately 220 mV and low impedance.[8]

Elevated temperature application

When appropriately constructed, the silver chloride electrode can be used up to 300 °C. The standard potential (i.e., the potential when the chloride activity is 1 mol/kg) of the silver chloride electrode is a function of temperature as follows:[10]

**Temperature Dependence of the Standard Potential of the Silver/Silver Chloride Electrode**
Temperature	Potential E⁰
°C	V versus SHE at the same temperature
25	0.22233
60	0.1968
125	0.1330
150	0.1032
175	0.0708
200	0.0348
225	-0.0051
250	-0.054
275	-0.090

Bard et al.[11] give the following correlations for the standard potential of the silver chloride electrode between 0 and 95°C as a function of temperature (where t is temperature in °C):

E^{0}(V)=0.23695-\left(4.8564\times 10^{-4}\right)t-\left(3.4205\times 10^{-6}\right)t^{2}-\left(5.869\times 10^{-9}\right)t^{3}

The same source also gives the fit to the high-temperature potential between 25 and 275°C, which reproduces the data in the table above:

E^{0}(V)=0.23735-\left(5.3783\times 10^{-4}\right)t-\left(2.3728\times 10^{-6}\right)t^{2}

The extrapolation to 300°C gives $E^{0}(V)=-0.138\ \mathrm {V}$ .

Farmer[12] gives the following correction for the potential of the silver chloride electrode with 0.1 mol/kg KCl solution between 25 and 275°C, accounting for the activity of Cl⁻ at the elevated temperature:

E^{0.1\ {\ce {mol/kg\ KCl}}}(V)=0.23735-\left(5.3783\times 10^{-4}\right)t-\left(2.3728\times 10^{-6}\right)t^{2}+\left(2.2671\times 10^{-4}\right)(t+273)

gollark: Anyway, inoteaur-nim™ is only 2.4MB, versus about 80MB for minoteaur-rs™ (both debug builds).

gollark: To really shrink your C binary try osmarkslibc™, coming soon.

gollark: Large binaries probably yes. Rust also does that. Nim doesn't somehow. I don't know why or particularly care.

gollark: But both seem to have pretty large dependency trees.

gollark: Might be a difference in dependency culture I guess.

References

R.G. Bates and J.B. MacAskill, "Standard Potential of the Silver-Silver Chloride Electrode", Pure & Applied Chem., Vol. 50, pp. 1701–1706, http://www.iupac.org/publications/pac/1978/pdf/5011x1701.pdf
Detail of Making and Setting up a Microelectrode, University of Denver, http://carbon.cudenver.edu/~bstith/detailelectrode.doc%5B%5D (link is obsolete)
Bratsch, Steven G. (1989), "Standard Electrode Potentials and Temperature Coefficients in Water at 298.15 K" (PDF), J. Phys. Chem. Ref. Data, 18 (1): 1–21, Bibcode:1989JPCRD..18....1B, doi:10.1063/1.555839
D.T. Sawyer, A. Sobkowiak, J.L. Roberts, "Electrochemistry for Chemists", 2nd edition, J. Wiley and Sons Inc., 1995.
"NACE International CP Specialist Course Manual"
"CARDEX Electrodes". CARDEX. Retrieved 21 August 2014.
Emma, Salvatore Jr. (8 August 2011). "A Brief Look at ECG Sensor Technology". Medical Design Technology Magazine. Retrieved 20 August 2014.
Lee, Stephen; Kruse, John. "Biopotential Electrode Sensors in ECG/EEG/EMG Systems" (PDF). Analog Devices, Inc. Retrieved 21 August 2014. Cite journal requires |journal= (help)
Dickter, Cheryl L; Kieffaber, Paul D (20 December 2013). EEG Methods for the Psychological Sciences. SAGE. pp. 14–15. ISBN 9781446296745. Retrieved 21 August 2014.
R.S. Greeley, J. Phys. Chemistry, 64, 652, 1960.
A.J. Bard, R. Parson, J. Jordan, "Standard Potentials in Aqueous Solution", Marcel Dekker, Inc., 1985.
Joseph Farmer, "Waste Package Degradation Expert Elicitation Panel: Input on the Corrosion of CRM Alloy C-22", Lawrence Livermore National Laboratory, report UCRL-ID-130064 "Information Bridge: DOE Scientific and Technical Information" – Sponsored by OSTI (pdf)

External links

NACE International Website for Corrosion Professionals

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[1] R.G. Bates and J.B. MacAskill, "Standard Potential of the Silver-Silver Chloride Electrode", Pure & Applied Chem., Vol. 50, pp. 1701–1706, http://www.iupac.org/publications/pac/1978/pdf/5011x1701.pdf

[2] Detail of Making and Setting up a Microelectrode, University of Denver, http://carbon.cudenver.edu/~bstith/detailelectrode.doc%5B%5D (link is obsolete)

[3] Bratsch, Steven G. (1989), "Standard Electrode Potentials and Temperature Coefficients in Water at 298.15 K" (PDF), J. Phys. Chem. Ref. Data, 18 (1): 1–21, Bibcode:1989JPCRD..18....1B, doi:10.1063/1.555839

[4] D.T. Sawyer, A. Sobkowiak, J.L. Roberts, "Electrochemistry for Chemists", 2nd edition, J. Wiley and Sons Inc., 1995.

[5] "NACE International CP Specialist Course Manual"

[6] "CARDEX Electrodes". CARDEX. Retrieved 21 August 2014.

[7] Emma, Salvatore Jr. (8 August 2011). "A Brief Look at ECG Sensor Technology". Medical Design Technology Magazine. Retrieved 20 August 2014.

[Lee-8] Lee, Stephen; Kruse, John. "Biopotential Electrode Sensors in ECG/EEG/EMG Systems" (PDF). Analog Devices, Inc. Retrieved 21 August 2014. Cite journal requires |journal= (help)

[Dickter-9] Dickter, Cheryl L; Kieffaber, Paul D (20 December 2013). EEG Methods for the Psychological Sciences. SAGE. pp. 14–15. ISBN 9781446296745. Retrieved 21 August 2014.

[10] R.S. Greeley, J. Phys. Chemistry, 64, 652, 1960.

[11] A.J. Bard, R. Parson, J. Jordan, "Standard Potentials in Aqueous Solution", Marcel Dekker, Inc., 1985.

[12] Joseph Farmer, "Waste Package Degradation Expert Elicitation Panel: Input on the Corrosion of CRM Alloy C-22", Lawrence Livermore National Laboratory, report UCRL-ID-130064 "Information Bridge: DOE Scientific and Technical Information" – Sponsored by OSTI (pdf)