Studies concerning charged nickel hydroxide electrodes IV. Reversible potentials in LiOH,NaOH, RbOH and CsOH |
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Authors: | R. Barnard C. F. Randell F. L. Tye |
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Affiliation: | (1) Group Technical Centre, Berec Group Limited, St. Ann's Road, London, UK |
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Abstract: | The variation of reversible potential Er with log amoh and has been studied for several nickel hydroxide/oxyhydroxide couples in various alkali hydroxides. Both activated and deactivated -phase couples show only a small dependence ofEr with logmoh (or where known) in LiOH, NaOH, RbOH and CsOH electrolytes. The change in MOH content on oxidation/reduction is found to be about 0.1 mol MOH per two-electron transfer and is the same as found previously in KOH. These results confirm that the bulk oxidized -phase lattice is devoid of alkali cation although a small quantity may be adsorbed by the surface. On the other hand both activated and deactivated /-phase couples show a marked dependence of 0.45 mol MOH per two-electron transfer in LiOH, NaOH and RbOH (at concentrations > 0.5 m), also in good agreement with earlier data for KOH. On the basis of these results a general stoichiometry can be inferred for the -phase, namely M0.32NiO2 · 0.7H2O where M=Li+, Na+, K+ or Rb+. Measurements imply that the Cs+ ion or the Rb+ ion at low concentration (<0.5 m) do not enter the interlayer structure of the -phase. This behaviour is thought to be related to the low Rb-O and Cs-O bond strengths afforded by the -phase structure. |
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