Institut für Chemie and IRIS Adlershof , Humboldt-Universität zu Berlin , Brook-Taylor-Str. 2 , D-12489 Berlin , Germany.
ACS Appl Mater Interfaces. 2019 Sep 11;11(36):33132-33139. doi: 10.1021/acsami.9b10659. Epub 2019 Aug 30.
The search for new cathode materials is primordial for alkali-ion battery systems, which are facing a constantly growing demand for high energy density storage devices. In quest of more performing active compounds on the positive side, anhydrous iron(III) fluoride demonstrated to be a good compromise in terms of high capacity, operating voltage, and low cost. However, its reaction toward lithium leads to complicated insertion/conversion reactions, which hinder its performances in Li-ion cells. Cycling this material against larger ions such as sodium and potassium is hard or simply impossible due to the size of the channels of the FeF framework impeding ions diffusion. Herein, we propose a strategy based on the use of cubic perovskite AFeF (A = K, NH) as starting materials, allowing the straightforward insertion (after a first disinsertion of the alkali and/or NH ion) of lithium within the structure and enabling the cycling toward larger alkali ions such as sodium and potassium. For example, a cubic KFeF perovskite, produced by a facile synthesis method, shows superior rate capability toward lithium retaining a capacity of up to 132 mA·h·g at 5 C or of 120 mA·h·g at 5 C toward sodium and enabling cycling toward potassium. Moreover, cubic NHFeF perovskite is discussed for the first time as the suitable cathode material for alkali-ion batteries.
对于碱离子电池系统而言,寻找新型阴极材料至关重要,因为这些系统面临着对高能量密度存储设备的需求不断增长。为了寻求在正极方面具有更高性能的活性化合物,无水三氟化铁 (FeF3) 在高容量、工作电压和低成本方面表现出了良好的折衷。然而,其与锂的反应导致了复杂的插入/转化反应,这阻碍了其在锂离子电池中的性能。由于 FeF 骨架的通道尺寸阻碍了离子扩散,因此很难甚至不可能使这种材料与钠离子和钾离子等较大的离子循环。在此,我们提出了一种基于使用立方钙钛矿 AFeF(A = K、NH)作为起始材料的策略,允许锂在结构内直接插入(在首先脱插碱和/或 NH 离子之后),并使循环朝向较大的碱离子(如钠和钾)。例如,通过简便的合成方法制备的立方 KFeF 钙钛矿在 5 C 时具有高达 132 mA·h·g 的优异倍率性能,在 5 C 时对钠的容量保持率为 120 mA·h·g,并能够循环至钾。此外,首次讨论了立方 NHFeF 钙钛矿作为碱离子电池的合适阴极材料。