High-temperature all-solid-state batteries with LiBH4 as electrolyte – a case study exploring the performance of TiO2 nanorods, Li4Ti5O12 and graphite as active materials
Marlena Volck, Bernhard Gadermaier, Volker Hennige, H. Martin R. Wilkening, Ilie Hanzu
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引用次数: 0
Abstract
The hexagonal high-temperature form of LiBH4 is known as a fast ion conductor. Here, we investigated its suitability as a solid electrolyte in high-temperature all-solid-state cells when combined with the following active materials: Li metal, graphite, lithium titanium oxide (Li4Ti5O12, LTO), and nanocrystalline rutile (TiO2). First results using lithium anodes and rutile nanorods as cathode material show that a cell constructed by simple cold-pressing operates at reversible discharge capacities in the order of 125 mA h g−1 at a C-rate of C/5 and at temperatures as high as 393 K. Besides TiO2, the compatibility of the LiBH4 with other active materials such as graphite and LTO was tested. We found evidence of possible interface instabilities that manifest through rare, yet still detrimental, self-charge processes that may be relevant for hydrogen storage applications. Moreover, we investigated the long-term cycling behavior of the cells assembled and demonstrate the successful employment of LiBH4 as an easily processable model solid electrolyte in practical test cells.
六方高温型 LiBH4 是众所周知的快速离子导体。在此,我们研究了它与以下活性材料结合后作为高温全固态电池固体电解质的适用性:锂金属、石墨、锂钛氧化物(Li4Ti5O12,LTO)和纳米晶金红石(TiO2)。使用锂阳极和金红石纳米棒作为阴极材料的首批研究结果表明,通过简单的冷压工艺制成的电池在 C/5 的 C 速率和高达 393 K 的温度条件下可达到 125 mA h g-1 的可逆放电容量。我们发现了界面不稳定性的证据,这种不稳定性通过罕见但仍有害的自充电过程表现出来,可能与储氢应用有关。此外,我们还研究了所组装电池的长期循环行为,并证明了 LiBH4 作为一种易于加工的模型固体电解质在实际测试电池中的成功应用。