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用于多价离子插层的纯层状δ-MnO₂的快速微波辅助水热合成

Fast Microwave-Assisted Hydrothermal Synthesis of Pure Layered δ-MnO₂ for Multivalent Ion Intercalation.

作者信息

Eckert Martin, Peters Willi, Drillet Jean-Francois

机构信息

DECHEMA Forschungsinstitut, Theodor-Heuss-Allee 25, 60486 Frankfurt am Main, Germany.

出版信息

Materials (Basel). 2018 Nov 28;11(12):2399. doi: 10.3390/ma11122399.

Abstract

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.

摘要

这项工作报道了层状氧化锰(δ-MnO₂)的合成及其作为铝离子和锌离子电池阴极插层材料的潜在应用。通过在1.6 M KOH(锰:锰 = 0.33)中采用一锅法微波辅助合成路线,在110°C下仅反应14小时后,就获得了不含任何杂质的纯层状δ-MnO₂相。试图通过在1.6 M KOH中将反应时间延长至96小时来提高所制备产物的结晶度,但未成功,反而导致结晶度降低并出现了一个额外的相。还研究了锰:氢氧根比例(1:2至1:10)对反应96小时后的相结晶度和相形成的影响。通过将反应混合物的碱度提高到2.5 M KOH,δ-MnO₂相的结晶度略有增加,但未能如愿抑制其他相的形成。将所制备的层状δ-MnO₂粉末材料喷涂在碳纸上,并在以铝或锌作为活性材料的实验室电池中进行测试。铝离子测试在EMIMCl/AlCl₃中进行,而锌离子实验在含有醋酸胆碱(ChAcO)的水溶液或硫酸锌溶液中进行。与铝离子电池约3 mAh/g的容量相比,锌离子电池在容量方面表现出最佳性能(20个循环中为200 mWh/g)。后一种体系活性较差的原因是,在EMIMCl/AlCl₃混合物中四氯铝酸根离子(AlCl₄)分解为正铝配合物的速率较低,而这些正铝配合物是放电步骤中基于氧化物的阴极进行电荷补偿所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3564/6317168/eb0c26cdab9a/materials-11-02399-g0A1.jpg

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