How Does Ion Exchange Construct Binary Hexacyanoferrate? A Case Study

Abstract

In this work, using electrochemical active Fe as an ion-exchange element (attack side) and the Na x MnFe(CN) 6 slurry with a high solid content (MnHCF) as a template (defensive side), a series of binary hexacyanoferrates are prepared via a simple Mn/Fe ion-exchange process, in which Na x FeFe(CN) 6 (FeHCF) and solid solution Na x (FeMn)Fe(CN) 6 are concentrated on the shell and the core, respectively. The proportions of the two structures are mainly controlled by the competition between the ion-exchange rate in the bulk material and dissolution-reprecipitation rate. Slowing down the attacking rate, such as the use of a chelating agent complexed with the attacker Fe, is advantageous to form a thermodynamically metastable state with homogeneous distribution of elements since the diffusion of Fe 2+ in the solid MnHCF is relatively fast. The shell FeHCF could be adjusted by the dissolution-reprecipitation rate, which is driven by the solubility difference. Adding the chelating agent in the defensive side will promote the dissolution of MnHCF and reprecipitation of FeHCF on the surface. Meanwhile, with the increase of Fe sources, the thickness of the shell FeHCF increases, and correspondingly the content of solid solution decreased due to FeHCF is more stable than solid solutions in thermodynamics. Finally, such a design principle in this case study could also be generalized to other ion-exchange processes. Considering the difference of two components in solubility, the larger difference can make the core/shell structure more clear due to the enhancement of dissolution–reprecipitation route.