Effects of the variation of metal substitution and electrolyte on the electrochemical reaction of metal hexacyanoferrates

Abstract

Metal hexacyanoferrates (MHCFs), also called Prussian blue analogs, are known as electrochemical electrodes and are ion-adsorbent. To investigate the effect of the ionic radius of the adsorbate (cations adsorbed upon reduction) and the pore size of the adsorbent (porous electrode that stores cations upon reduction), we investigated the electrochemical reactions with various alkali cations and by changing the metal sites of the MHCFs. First, we succeeded in controlling the pore sizes of the MHCFs, where the lattice constant a could be estimated as a = 0.98D_sum + 7.21, where D_sum represented the sum of the ionic diameters of the metal M and Fe. Concerning the electrochemical reaction, the redox potential increased when the hydration energy of the adsorbate decreased, implying that the hydration energy of the adsorbate affected the stability of the reduced state. With cadmium hexacyanoferrate, which has a large pore size, the variation of the redox potential was suppressed in comparison to that with copper hexacyanoferrate, which has a small pore size. With Fourier transform-infrared (FT-IR) analysis before and after the redox reactions, Na⁺ insertion accompanied by H₂O was presumed in the reduced state.