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首页> 外文期刊>Electrochimica Acta >Investigation of iron hexacyanoferrate as a high rate cathode for aqueous batteries: Sodium-ion batteries and lithium-ion batteries
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Investigation of iron hexacyanoferrate as a high rate cathode for aqueous batteries: Sodium-ion batteries and lithium-ion batteries

机译:用于含水电池高速速率阴极铁六氰基甲醛的研究:钠离子电池和锂离子电池

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In this study, highly crystalline FeFe(CN)(6) with metal-organic framework is synthesized and measured in NaNO3 and LiNO3. Electrochemical kinetics, physical and chemical changes about the insertion and extraction processes of sodium ions and lithium ions in FeFe(CN)(6) are compared and discussed. Intriguingly, it exhibits a good electrochemical performance in sodium aqueous batteries, with a capacity of 118 mAh g(-1) at 400 mA g(-1), but a poor electrochemical behavior in lithium aqueous batteries. This study sheds light on the different insertion processes between sodium ions and lithium ions in FeFe(CN)(6), that the outer petaloid-like structure forms on the surface of FeFe(CN)(6) after Li ions insertion with little volume expansion, while FeFe(CN)(6) after Na ions insertion could still maintain the cubic-like structure with lattice change. Different insertion mechanisms of sodium ions and lithium ions are proposed that hydrated Na ions could insert at interstitial sites, while hydrated Li ions are more likely to occupy large open sites due to the larger radius of hydrated Li ions than hydrated Na ions. Besides, insertion/extraction performance and capacitive preformance dominate in NaNO3 and LiNO3, respectively. These differences may lead to the different electrochemical behaviors between sodium-ion and lithium-ion aqueous batteries. (c) 2018 Elsevier Ltd. All rights reserved.
机译:在该研究中,在纳米3和LinO3中合成并测量具有金属有机骨架的高结晶FeFE(CN)(6)。对电化学动力学,对FEFE(CN)(6)中的钠离子和锂离子的插入和提取过程的物理和化学变化进行了讨论。有趣的是,它在钠含水电池中表现出良好的电化学性能,其容量为118mAg(-1),在400mA g(-1),但锂含水电池中的电化学行为差。本研究揭示了FeFe(CN)(6)中的钠离子和锂离子之间的不同插入过程,即在Li离子插入少量的FeFe(CN)(6)的表面上形成外壳状结构膨胀,而FEFE(CN)(6)在Na离子插入后仍然可以保持立方体状结构,晶格变化。提出了不同的插入机制和锂离子的插入机制,即水合Na离子可以在间质部位插入,而水合的Li离子更可能由于水合Li离子的较大半径而不是水合的Na离子而占据大的开放位点。此外,分别插入/提取性能和电容性预成形分别在纳米3和LINO3中占主导地位。这些差异可能导致钠离子和锂离子含水电池之间的不同电化学行为。 (c)2018年elestvier有限公司保留所有权利。

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