Shraer Semyon D, Luchinin Nikita D, Trussov Ivan A, Aksyonov Dmitry A, Morozov Anatoly V, Ryazantsev Sergey V, Iarchuk Anna R, Morozova Polina A, Nikitina Victoria A, Stevenson Keith J, Antipov Evgeny V, Abakumov Artem M, Fedotov Stanislav S
Skoltech Center for Energy Science and Technology, Skolkovo Institute of Science and Technology, 121205, Moscow, Russian Federation.
Department of Chemistry, Lomonosov Moscow State University, 119991, Moscow, Russian Federation.
Nat Commun. 2022 Jul 14;13(1):4097. doi: 10.1038/s41467-022-31768-5.
Polyanion compounds offer a playground for designing prospective electrode active materials for sodium-ion storage due to their structural diversity and chemical variety. Here, by combining a NaVPOF composition and KTiOPO-type framework via a low-temperature (e.g., 190 °C) ion-exchange synthesis approach, we develop a high-capacity and high-voltage positive electrode active material. When tested in a coin cell configuration in combination with a Na metal negative electrode and a NaPF-based non-aqueous electrolyte solution, this cathode active material enables a discharge capacity of 136 mAh g at 14.3 mA g with an average cell discharge voltage of about 4.0 V. Furthermore, a specific discharge capacity of 123 mAh g at 5.7 A g is also reported for the same cell configuration. Through ex situ and operando structural characterizations, we also demonstrate that the reversible Na-ion storage at the positive electrode occurs mostly via a solid-solution de/insertion mechanism.
聚阴离子化合物由于其结构多样性和化学多样性,为设计用于钠离子存储的潜在电极活性材料提供了一个平台。在此,通过低温(例如190°C)离子交换合成方法将NaVPOF组成与KTiOPO型框架相结合,我们开发了一种高容量、高电压的正极活性材料。当与Na金属负极和基于NaPF的非水电解质溶液结合在硬币电池配置中进行测试时,这种正极活性材料在14.3 mA g下能够实现136 mAh g的放电容量,平均电池放电电压约为4.0 V。此外,对于相同的电池配置,还报道了在5.7 A g下123 mAh g的比放电容量。通过非原位和原位结构表征,我们还证明了正极处可逆的Na离子存储主要通过固溶体脱/嵌入机制发生。