Sakamoto Ryo, Yamashita Maho, Nakamoto Kosuke, Zhou Yongquan, Yoshimoto Nobuko, Fujii Kenta, Yamaguchi Toshio, Kitajou Ayuko, Okada Shigeto
Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga-koen, Kasuga 816-8580, Japan.
Phys Chem Chem Phys. 2020 Nov 25;22(45):26452-26458. doi: 10.1039/d0cp04376a.
Aqueous Na-ion batteries with highly concentrated NaClO4 aq. electrolytes are drawing attention as candidates for large-scale rechargeable batteries with a high safety level. However, the detailed mechanism by which the potential window in 17 m NaClO4 aq. electrolyte was expanded remains unclear. Therefore, we investigated the local structure around a Na+ ion or a ClO4- ion using X-ray diffraction combined with empirical potential structure refinement (EPSR) modelling and Raman spectroscopy. The results showed that in 17 m NaClO4 aq. electrolyte, most of the water molecules were coordinated to Na+ ions and few free water molecules were present. The 17 m NaClO4 aq. electrolyte could be interpreted as widening the potential window because almost all water molecules participated in hydration of the Na+ ions.
具有高浓度高氯酸钠水溶液电解质的水系钠离子电池作为具有高安全水平的大规模可充电电池候选者正受到关注。然而,在17m高氯酸钠水溶液电解质中电位窗口扩大的详细机制仍不清楚。因此,我们结合经验势能结构精修(EPSR)建模和拉曼光谱,利用X射线衍射研究了Na+离子或ClO4-离子周围的局部结构。结果表明,在17m高氯酸钠水溶液电解质中,大多数水分子与Na+离子配位,几乎没有游离水分子存在。17m高氯酸钠水溶液电解质可以解释为拓宽了电位窗口,因为几乎所有水分子都参与了Na+离子的水合作用。