Effects of the variation of metal substitution and electrolyte on the electrochemical reaction of metal hexacyanoferratesElectronic supplementary information (ESI) available: Information of specific surface area analysis, photographs of CuHCF and CdHCF films coated using spin coating and an applicator, and parameters of the Gaussian function for IR spectra fitting. See DOI: 10.1039/c8ra08091g

• Main Authors: Asai, Miyuki, Takahashi, Akira, Tajima, Kazuki, Tanaka, Hisashi, Ishizaki, Manabu, Kurihara, Masato, Kawamoto, Tohru
• Format: Journal Article
• Published: 06.11.2018
• ISSN: 2046-2069
• DOI: 10.1039/c8ra08091g

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 = 0.98 D 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 H 2 O was presumed in the reduced state. The redox potential of metal hexacyanoferrates (MHCFs), also called Prussian blue analogs, is qualitatively understood with the hydration energy of the cations in the supporting electrolyte.