4.8 Article

Effect of Particle Size and Anion Vacancy on Electrochemical Potassium Ion Insertion into Potassium Manganese Hexacyanoferrates

期刊

CHEMSUSCHEM
卷 14, 期 4, 页码 1166-1175

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202002628

关键词

batteries; insertion materials; ionic diffusion; potassium; Prussian blue analogues

资金

  1. MEXT program ESICB [JPMXP0112101003]
  2. JST through the A-STEP program [JPMJTS1611]
  3. JSPS KAKENHI [JP16K14103, JP16H04225, JP18K14327, JP20J13077]
  4. JSPS

向作者/读者索取更多资源

Potassium manganese hexacyanoferrate (KMnHCF) can be used as a positive electrode for potassium-ion batteries due to its high energy density. The performance of KMnHCF in terms of capacity and rate capability is influenced by particle size and anion vacancies. Anion vacancies contribute to the enhancement of K+ ion diffusion and ultimately improve the electrochemical performance of KMnHCF.
Potassium manganese hexacyanoferrate (KMnHCF) can be used as a positive electrode for potassium-ion batteries because of its high energy density. The effect of particle size and [Fe(CN)(6)](n-) vacancies on the electrochemical potassium insertion of KMnHCFs was examined through experimental data and theoretical calculations. When nearly stoichiometric KMnHCF was synthesized and tested, smaller particle sizes were found to be important for achieving superior electrochemical performance in terms of capacity and rate capability. However, even in the case of larger particles, introducing a suitable number of anion vacancies enabled KMnHCF to exhibit comparable electrode performance. Electrochemical tests and density functional theory calculations indicated that anion vacancies contribute to the enhancement of K+ ion diffusion, which realizes good electrochemical performance. Structural design, including crystal vacancies and particle size, is the key to their high performance as a positive electrode.

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