International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology (ICL-2D MOST), Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University , Shenzhen 518060, China.
Department of Chemistry, Centre for Advanced 2D Materials (CA2DM) and Graphene Research Centre, National University of Singapore , 3 Science Drive 3, Singapore 117543, Singapore.
ACS Appl Mater Interfaces. 2018 Jan 10;10(1):642-650. doi: 10.1021/acsami.7b15407. Epub 2017 Dec 28.
Potassium ion batteries (KIBs), because of their low price, may exhibit advantages over lithium ion batteries as potential candidates for large-scale energy storage systems. However, owing to the large ionic radii of K-ions, it is challenging to find a suitable intercalation host for KIBs and thus the rechargeable KIB electrode materials are still largely unexplored. In this work, a reticular VO·0.6HO xerogel was synthesized via a hydrothermal process as a cathode material for rechargeable KIBs. Compared with the orthorhombic crystalline VO, the hydrated vanadium pentoxide (VO·0.6HO) exhibits the ability of accommodating larger alkali metal ions of K because of the enlarged layer space by hosting structural HO molecules in the interlayer. By intercalation of HO into the VO layers, its potassium electrochemical activity is significantly improved. It exhibits an initial discharge capacity of ∼224.4 mA h g and a discharge capacity of ∼103.5 mA h g even after 500 discharge/charge cycles at a current density of 50 mA g, which is much higher than that of the VO electrode without structural water. Meanwhile, X-ray diffraction and X-ray photoelectron spectroscopy combined with energy dispersive spectroscopy techniques are carried out to investigate the potassiation/depotassiation process of the VO·0.6HO electrodes, which confirmed the potassium intercalation storage mechanisms of this hydrated material. The results demonstrate that the interlayer-spacing-enlarged VO·0.6HO is a promising cathode candidate for KIBs.
钾离子电池(KIBs)由于其价格低廉,可能优于锂离子电池,成为大规模储能系统的潜在候选者。然而,由于 K 离子的离子半径较大,寻找合适的 KIB 嵌入宿主具有挑战性,因此可充电 KIB 电极材料仍在很大程度上未被探索。在这项工作中,通过水热法合成了一种网状 VO·0.6HO 水凝胶,作为可充电 KIB 的阴极材料。与正交晶相 VO 相比,水合五氧化二钒(VO·0.6HO)由于在层间容纳结构 HO 分子而扩大了层间距,因此具有容纳更大碱金属离子 K 的能力。通过将 HO 嵌入 VO 层中,可以显著提高其钾电化学活性。在 50 mA g 的电流密度下,经过 500 次充放电循环后,其初始放电容量约为 224.4 mA h g,放电容量约为 103.5 mA h g,远高于没有结构水的 VO 电极。同时,采用 X 射线衍射和 X 射线光电子能谱结合能谱技术研究了 VO·0.6HO 电极的钾化/脱钾过程,证实了这种水合材料的钾嵌入存储机制。结果表明,层间距扩大的 VO·0.6HO 是一种很有前途的 KIB 阴极候选材料。