Fast Microwave-Assisted Hydrothermal Synthesis of Pure Layered δ-MnO₂ for Multivalent Ion Intercalation
This work reports on the synthesis of layered manganese oxides (δ-MnO₂) and their possible application as cathode intercalation materials in Al-ion and Zn-ion batteries. By using a one-pot microwave-assisted synthesis route in 1.6 M KOH (Mn :Mn = 0.33), a pure layered δ-MnO₂ phase without any traces...
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Veröffentlicht in: | Materials 2018-11, Vol.11 (12), p.2399 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This work reports on the synthesis of layered manganese oxides (δ-MnO₂) and their possible application as cathode intercalation materials in Al-ion and Zn-ion batteries. By using a one-pot microwave-assisted synthesis route in 1.6 M KOH (Mn
:Mn
= 0.33), a pure layered δ-MnO₂
phase without any
traces was obtained after only a 14 h reaction time period at 110 °C. Attempts to enhance crystallinity level of as-prepared
through increasing of reaction time up to 96 h in 1.6 M KOH failed and led to decreases in crystallinity and the emergence of an additional
phase. The influence of Mn
:OH
ratio (1:2 to 1:10) on phase crystallinity and
phase formation for 96 h reaction time was investigated as well. By increasing alkalinity of the reaction mixture up to 2.5 M KOH, a slight increase in crystallinity of
phase was achieved, but
formation couldn't be inhibited as hoped. The as-prepared layered δ-MnO₂ powder material was spray-coated on a carbon paper and tested in laboratory cells with Al or Zn as active materials. The Al-ion tests were carried out in EMIMCl/AlCl₃ while the Zn-Ion experiments were performed in water containing choline acetate (ChAcO) or a ZnSO₄ solution. Best performance in terms of capacity was yielded in the Zn-ion cell (200 mWh g
for 20 cycles) compared to about 3 mAh g
for the Al-ion cell. The poor activity of the latter system was attributed to low dissociation rate of tetrachloroaluminate ions (AlCl₄
) in the EMIMCl/AlCl₃ mixture into positive Al complexes which are needed for charge compensation of the oxide-based cathode during the discharge step. |
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ISSN: | 1996-1944 1996-1944 |
DOI: | 10.3390/ma11122399 |