Abstract
The nucleation rate plays a critical role in the synthesis of Prussian blue analogs. Rapid precipitation may lead to a large number of vacancies and a large amount of interstitial water in the material, resulting in poor electrochemical performance in batteries. Hence, sodium citrate is used to compete with [Fe(CN)6]4- to slow down the coordination rates of Ni2+ and Mn2+ ions with ferrous cyanide ions. The feasibility of the experiment is also confirmed by theoretical analysis. Benefiting from stable crystal structure and the removal of interstitial water, the as-prepared Na2NixMnyFe(CN)6 sample exhibits a high reversible capacity of 150 mA h g-1. In addition, a high rate performance of 77 mA h g-1 is achieved at a current density of 1600 mA g-1. Most noteworthy, the Coulombic efficiency and specific capacity gradually increase in the first few cycles, which can be ascribed to the formation of a passivation layer on the surface of the electrode. Continuous testing in an electrolyte solution of 1 M NaPF6 dissolved in sulfone reveals that the presence of a passivation film is very important for the stability of the electrode.
| Original language | English |
|---|---|
| Pages (from-to) | 31669-31676 |
| Number of pages | 8 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 8 |
| Issue number | 46 |
| DOIs | |
| Publication status | Published - 23 Nov 2016 |
Keywords
- Prussian blue analogues
- cathode materials
- electrolyte
- kinetic activation
- nucleation rate
- sodium ion batteries
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