Reversible hydrogen electrode

A reversible hydrogen electrode (RHE) is a reference electrode, more specifically a subtype of the standard hydrogen electrodes, for electrochemical processes. Unlike the standard hydrogen electrode, its measured potential does not change with the pH, so it can be directly used in the electrolyte.^[1]^[2]^[3]

The name refers to the fact that the electrode is in the actual electrolyte solution and not separated by a salt bridge. The hydrogen ion concentration is therefore not 1, but corresponds to that of the electrolyte solution; in this way we can achieve a stable potential with a changing pH value. The potential of the RHE correlates to the pH value:

E_{0}=0.000-0.059\times \mathrm {pH}

In general, for hydrogen electrodes in which the reaction:

{\ce {{2H3O+}+{2e^{-}}<=>{H2}+{2H2O}}}

expires, the following dependence of the equilibrium potential $E$ , hydrogen pressure $p{\ce {[H2]}}$ and the activity $a{\ce {[H3O+]}}$ of the hydronium ions:

E=E_{00}+{\frac {R\;T}{F}}\left(\ln \left(a[{\ce {H3O+}}]\right)-{\tfrac {1}{2}}\ln \left(\;p[{\ce {H2}}]\right)\right)

Here $E_{{00}}$ is the standard reduction potential (this is by definition equal to zero), R is the universal gas constant, T the absolute temperature and F is the Faraday constant.

Surges occur in the electrolysis of water which means that the required cell voltage due to kinetic inhibition is higher than the equilibrium potential. The voltage increases with increasing current density at the electrodes. The measurement of equilibrium potentials is therefore possible without power.

Principle

The reversible hydrogen electrode is a fairly practical and reproducible electrode "standard." The term refers to a hydrogen electrode immersed in the electrolyte solution actually used.

The benefit of that electrode is that no salt bridge is needed:

no contamination of the electrolyte by Cl⁻ or SO₄²⁻
no diffusion potentials at the electrolyte bridge (liquid junction potential). This is important at temperature different to 25 °C.
long time measurements possible (no electrolyte bridge means no maintenance of the bridge)

References

↑ Cai, Yu; Anderson, Alfred B. (2004). "The reversible hydrogen electrode: potential-dependent activation energies over platinum from quantum theory". The Journal of Physical Chemistry B. 108 (28): 9829. doi:10.1021/jp037126d.
↑ Staehler, M.; Wipperman, K. & Stolten, D. "Instabilities of the reversible hydrogen reference electrode in direct methanol fuel cells" (PDF). 2004 Joint International Meeting of the Electrochemical Society, abstract 1863.
↑ MacInnes, Duncan A. & Adler, Leon (1919). "Hydrogen overvoltage". Proceedings of the National Academy of Sciences of the United States of America. 5 (5): 160–3. doi:10.1073/pnas.5.5.160. JSTOR 84265. PMC 1091559. PMID 16576366.

This article is issued from Wikipedia - version of the 7/26/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.

Reversible hydrogen electrode

Principle

See also

References