Sol-gel synthesis, structural refinement, and electrochemical properties of potassium manganese phosphate for supercapacitors
Using sol-gel thermolysis method, potassium manganese phosphate (a mixture of KMnPO 4 ⋅H 2 O and KMnPO 4 phases) was synthesized for supercapacitor applications. XRD analysis revealed phase composition and crystal structure of the prepared material. The dittmarite-type structure of KMnPO 4 ⋅H 2 O as...
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Veröffentlicht in: | Ionics 2018-07, Vol.24 (7), p.2073-2082 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Using sol-gel thermolysis method, potassium manganese phosphate (a mixture of KMnPO
4
⋅H
2
O and KMnPO
4
phases) was synthesized for supercapacitor applications. XRD analysis revealed phase composition and crystal structure of the prepared material. The dittmarite-type structure of KMnPO
4
⋅H
2
O as the primary phase was identified through full profile Rietveld refinement technique. The possible four normal modes of vibrations ν
1
(A1), ν
2
(E), ν
3
(F2), and ν
4
(F2) were analyzed through FTIR spectrum. Submicron-sized particles are identified using FE-SEM and TEM images. The layered structure of potassium manganese phosphate was corroborated through SAED pattern. Electrochemical performances of the mixed potassium manganese phosphate are investigated using cyclic voltammetry (CV) to identify the suitable aqueous electrolytes (1 M KOH, 1 M LiOH, and 1 M NaOH). It provides the maximum specific capacitance of 516 F g
−1
at 2 mV s
−1
in 1 M KOH aqueous electrolyte. The Trasatti plot revealed that the observed high specific capacitance mainly arises from the inner surface charge contribution. The electrode shows the better specific capacity of 329 F g
−1
at a current density of 0.6 mA cm
−2
in galvanostatic charge-discharge measurements. The electrochemical impedance spectral analysis (EIS) further corroborates that the charge-transfer resistance (
R
ct
) is low in 1 M KOH (2.25 Ω) electrolyte than in 1 M LiOH (9.2 Ω) and 1 M NaOH (50.7 Ω) electrolytes. |
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ISSN: | 0947-7047 1862-0760 |
DOI: | 10.1007/s11581-018-2449-y |