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Water-mediated cation intercalation of open-framework indium hexacyanoferrate with highvoltage and fast kinetics

机译:高架空骨架六氰合铁酸铟的水介导阳离子嵌入电压和快速动力学

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摘要

Rechargeable aqueous metal-ion batteries made from non-flammable and low-cost materials offer promising opportunities in large-scale utility grid applications, yet low voltage and energy output, as well as limited cycle life remain critical drawbacks in their electrochemical operation. Here we develop a series of high-voltage aqueous metal-ion batteries based on ‘M+/N+-dual shuttles' to overcome these drawbacks. They utilize open-framework indium hexacyanoferrates as cathode materials, and TiP2O7 and NaTi2(PO4)3 as anode materials, respectively. All of them possess strong rate capability as ultra-capacitors. Through multiple characterization techniques combined with ab initio calculations, water-mediated cation intercalation of indium hexacyanoferrate is unveiled. Water is supposed to be co-inserted with Li+ or Na+, which evidently raises the intercalation voltage and reduces diffusion kinetics. As for K+, water is not involved in the intercalation because of the channel space limitation.
机译:由不易燃且低成本的材料制成的可充电水性金属离子电池在大规模公用电网应用中提供了可喜的机遇,但是低电压和能量输出以及有限的循环寿命仍然是其电化学操作的关键缺点。在这里,我们基于“ M + / N + 双梭子”开发了一系列高压水性金属离子电池,以克服这些缺点。他们分别使用开放框架的六氰合铁酸铟作为阴极材料,并将TiP2O7和NaTi2(PO4)3用作阳极材料。它们都具有作为超级电容器的强大速率能力。通过多种表征技术与从头算相结合,揭示了六氰合铁酸铟的水介导阳离子嵌入。水应该与Li + 或Na + 共同插入,这显然会增加嵌入电压并降低扩散动力学。至于K + ,由于通道空间的限制,水不参与插层。

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