Institut de Chimie et des Matériaux Paris Est (ICMPE), GESMAT, UMR 7182 CNRS-Université Paris Est Créteil, 2 rue Henri Dunant, 94320, Thiais, France.
School of Engineering, National Laboratory Astana, Nazarbayev University, 53 Kabanbay Batyr Avenue, Astana, 010000, Kazakhstan.
ChemSusChem. 2019 Dec 6;12(23):5192-5198. doi: 10.1002/cssc.201902093. Epub 2019 Oct 30.
A bilayered potassium vanadate K V O (KVO) is synthesized by a fast and facile synthesis route and evaluated as a positive electrode material for Na-ion batteries. Half the potassium ions can be topotactically extracted from KVO through the first charge, allowing 1.14 Na ions to be reversibly inserted. A good rate capability is also highlighted, with 160 mAh g at C/10, 94 mAh g at C/2, 73 mAh g at 2C and excellent cycling stability with 152 mAh g still available after 50 cycles at C/10. Ex situ X-ray diffraction reveals weak and reversible structural changes resulting in soft breathing of the KVO host lattice upon Na extraction-insertion cycles (ΔV/V≈3 %). A high structure stability upon cycling is also achieved, at both the long-range order and atomic scale probed by Raman spectroscopy. This remarkable behavior is ascribed to the large interlayer spacing of KVO (≈9.5 Å) stabilized by pillar K ions, which is able to accommodate Na ions without any critical change to the structure. Kinetics measurements reveal a good Na diffusivity that is hardly affected upon discharge. This study opens an avenue for further exploration of potassium vanadates and other bronzes in the field of Na-ion batteries.
通过一种快速简便的合成方法合成了双层钒酸钾 KV O(KVO),并将其评估为钠离子电池的正极材料。通过首次充电,KVO 中的一半钾离子可以进行拓扑提取,从而允许可逆插入 1.14 个钠离子。还突出了良好的倍率性能,在 C/10 时为 160 mAh g-1,在 C/2 时为 94 mAh g-1,在 2C 时为 73 mAh g-1,在 C/10 时经过 50 次循环后仍具有 152 mAh g-1 的出色循环稳定性。原位 X 射线衍射揭示了较弱且可逆的结构变化,导致在 Na 提取-插入循环过程中 KVO 主体晶格的软呼吸(ΔV/V≈3%)。通过拉曼光谱在长程有序和原子尺度上也实现了循环过程中的高结构稳定性。这种显著的行为归因于 KVO 较大的层间距(≈9.5 Å)由支柱 K 离子稳定,其能够容纳 Na 离子而不会对结构产生任何关键变化。动力学测量表明 Na 扩散率良好,在放电过程中几乎不受影响。这项研究为在钠离子电池领域进一步探索钾钒酸盐和其他青铜开辟了道路。