Ion transport number

Short description: Fraction of total electric current carried in an electrolyte by an ionic species

In chemistry, ion transport number, also called the transference number, is the fraction of the total electric current carried in an electrolyte by a given ionic species i:[1][2]

ti=IiItot

Differences in transport number arise from differences in electrical mobility. For example, in an aqueous solution of sodium chloride, less than half of the current is carried by the positively charged sodium ions (cations) and more than half is carried by the negatively charged chloride ions (anions) because the chloride ions are able to move faster, i.e., chloride ions have higher mobility than sodium ions. The sum of the transport numbers for all of the ions in solution always equals unity:

∑iti=1

The concept and measurement of transport number were introduced by Johann Wilhelm Hittorf in the year 1853.[3] Liquid junction potential can arise from ions in a solution having different ion transport numbers.

At zero concentration, the limiting ion transport numbers may be expressed in terms of the limiting molar conductivities of the cation (λ0+), anion (λ0−), and electrolyte (Λ0):

t+=ν+⋅λ0+Λ0

and

t−=ν−⋅λ0−Λ0,

where ν+ and ν− are the numbers of cations and anions respectively per formula unit of electrolyte.[1] In practice the molar ionic conductivities are calculated from the measured ion transport numbers and the total molar conductivity. For the cation λ0+=t+⋅Λ0ν+, and similarly for the anion. In solutions, where ionic complexation or associaltion are important, two different transport/transference numbers can be defined.[4]

The practical importance of high (i.e. close to 1) transference numbers of the charge-shuttling ion (i.e. Li+ in lithium-ion batteries) is related to the fact, that in single-ion devices (such as lithium-ion batteries) electrolytes with the transfer number of the ion near 1, concentration gradients do not develop. A constant electrolyte concentration is maintained during charge-discharge cycles. In case of porous electrodes a more complete utilization of solid electroactive materials at high current densities is possible, even if the ionic conductivity of the electrolyte is reduced.[5][4]

## Contents

* 1 Experimental measurement
* 1.1 Hittorf method
* 1.2 Moving boundary method
* 1.3 Concentration cells
* 1.4 Electrophoretic magnetic resonance imaging method
* 2 See also
* 3 Notes
* 4 External links

## Experimental measurement

There are several experimental techniques for the determination of transport numbers.[4] The Hittorf method is based on measurements of ion concentration changes near the electrodes. The moving boundary method involves measuring the speed of displacement of the boundary between two solutions due to an electric current.[6]

### Hittorf method

This method was developed by German physicist Johann Wilhelm Hittorf in 1853,[6] and is based on observations of the changes in concentration of an electrolyte solution in the vicinity of the electrodes. In the Hittorf method, electrolysis is carried out in a cell with three compartments: anode, central, and cathode. Measurement of the concentration changes in the anode and cathode compartments determines the transport numbers.[7] The exact relationship depends on the nature of the reactions at the two electrodes. For the electrolysis of aqueous copper(II) sulfate (CuSO
4) as an example, with Cu2+(aq) and SO2−
4(aq) ions, the cathode reaction is the reduction Cu2+(aq) + 2 e−
→ Cu(s) and the anode reaction is the corresponding oxidation of Cu to Cu2+. At the cathode, the passage of Q coulombs of electricity leads to the reduction of Q/2F moles of Cu2+, where F is the Faraday constant. Since the Cu2+ ions carry a fraction t+ of the current, the quantity of Cu2+ flowing into the cathode compartment is t+(Q/2F) moles, so there is a net decrease of Cu2+ in the cathode compartment equal to (1−t+)(Q/2F)=t−(Q/2F).[8] This decrease may be measured by chemical analysis in order to evaluate the transport numbers. Analysis of the anode compartment gives a second pair of values as a check, while there should be no change of concentrations in the central compartment unless diffusion of solutes has led to significant mixing during the time of the experiment and invalidated the results.[8]

### Moving boundary method

This method was developed by British physicists Oliver Lodge in 1886 and William Cecil Dampier in 1893.[6] It depends on the movement of the boundary between two adjacent electrolytes under the influence of an electric field. If a colored solution is used and the interface stays reasonably sharp, the speed of the moving boundary can be measured and used to determine the ion transference numbers.

The cation of the indicator electrolyte should not move faster than the cation whose transport number is to be determined, and it should have same anion as the principle electrolyte. Besides the principal electrolyte (e.g., HCl) is kept light so that it floats on indicator electrolyte. CdCl
2 serves best because Cd2+ is less mobile than H+
and Cl−
is common to both CdCl
2 and the principal electrolyte HCl.

For example, the transport numbers of hydrochloric acid (HCl(aq)) may be determined by electrolysis between a cadmium anode and an Ag-AgCl cathode. The anode reaction is Cd → Cd2+ \+ 2 e−
so that a cadmium chloride (CdCl
2) solution is formed near the anode and moves toward the cathode during the experiment. An acid-base indicator such as bromophenol blue is added to make visible the boundary between the acidic HCl solution and the near-neutral CdCl
2 solution.[9] The boundary tends to remain sharp since the leading solution HCl has a higher conductivity than the indicator solution CdCl
2, and therefore a lower electric field to carry the same current. If a more mobile H+
ion diffuses into the CdCl
2 solution, it will rapidly be accelerated back to the boundary by the higher electric field; if a less mobile Cd2+ ion diffuses into the HCl solution it will decelerate in the lower electric field and return to the CdCl
2 solution. Also the apparatus is constructed with the anode below the cathode, so that the denser CdCl
2 solution forms at the bottom.[1]

The cation transport number of the leading solution is then calculated as

t+=z+cLAFIΔt

where z+ is the cation charge, c the concentration, L the distance moved by the boundary in time Δt, A the cross-sectional area, F the Faraday constant, and I the electric current.[1]

### Concentration cells

This quantity can be calculated from the slope of the function ET=f(E) of two concentration cells, without or with ionic transport.

The EMF of transport concentration cell involves both the transport number of the cation and its activity coefficient:

ET=−zRTF∫IIIt+dln⁡a+/−

where a2 and a1 are activities of HCl solutions of right and left hand electrodes, respectively, and tM is the transport number of Cl−

### Electrophoretic magnetic resonance imaging method

This method is based on magnetic resonance imaging of the distribution of ions comprising NMR-active nuclei (usually 1H, 19F, 7Li) in an electrochemical cells upon application of electric current. [10]

## See also

* Activity coefficient
* Born equation
* Debye length
* Einstein relation (kinetic theory)
* Electrochemical kinetics
* Ion selective electrode
* ITIES
* Law of dilution
* Liquid junction potential
* Solvated electron
* Solvation shell
* Supporting electrolyte
* Thermogalvanic cell
* van't Hoff factor

## Notes

1. ↑ 1.0 1.1 1.2 1.3 Peter Atkins and Julio de Paula, Physical Chemistry (8th ed. Oxford University Press, 2006) p.768-9 ISBN 0-7167-8759-8
2. ↑ Bruce, Peter G. (1991). "Ion association in polymer electrolytes: transport and materials optimization". Synthetic Metals 45 (45): 267-278.
3. ↑ Pathways to Modern Chemical Physics by Salvatore Califano (Springer 2012) p.61 ISBN 9783642281808
4. ↑ 4.0 4.1 4.2 Lacey, Matt (2023-07-02). "Transport and transference in battery electrolytes" (in en-US). Matt Lacey. http://lacey.se/science/transference/.
5. ↑ M. Doyle, T. F. Fuller and J. Newman, "The importance of the lithium ion transference number in lithium/polymer cells." Electrochim Acta, 39, 2073 (1994) 10.1016/0013-4686(94)85091-7
6. ↑ 6.0 6.1 6.2 Laidler K.J. and Meiser J.H., Physical Chemistry (Benjamin/Cummings 1982) p.276-280 ISBN 0-8053-5682-7
7. ↑ Electrochemistry Dictionary - H Corrosion Doctors.
8. ↑ 8.0 8.1 Principles and Applications of Electrochemistry D.R.Crow (4th ed., CRC Press 1994) p.165-169 ISBN 0748743782
9. ↑ Transport numbers and ionic mobilities by the moving boundary method, G. A. Lonergan and D. C. Pepper, J. Chem. Educ., 1965, 42 (2), p. 82. doi:10.1021/ed042p82
10. ↑ Klett, Matilda; Giesecke, Marianne; Nyman, Andreas; Hallberg, Fredrik; Lindström, Rakel Wreland; Lindbergh, Göran; Furó, István (2012). "Quantifying Mass Transport during Polarization in a Li Ion Battery Electrolyte by in Situ 7Li NMR Imaging". Journal of the American Chemical Society 134 (36): 14654–14657. doi:10.1021/ja305461j. PMID 22900791. Bibcode: 2012JAChS.13414654K. https://pubs.acs.org/doi/10.1021/ja305461j.

## External links

* Aqueous Solutions of Simple Electrolytes. Boston, MA: Springer US. 1973. doi:10.1007/978-1-4684-2955-8. ISBN 978-1-4684-2957-2. https://link.springer.com/book/10.1007/978-1-4684-2955-8.

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