Chen Yuanzheng, Qin Haifei, Zhou Jun, Yang Tong, Sun Bai, Ni Yuxiang, Wang Hongyan, Redfern Simon A T, Miao Maosheng, Lin Hai-Qing, Feng Yuan Ping
Beijing Computational Science Research Center, Haidian District, Beijing 100193, China.
School of Physical Science and Technology, Southwest Jiaotong University, Chengdu 610031, China.
J Phys Chem Lett. 2022 Aug 18;13(32):7439-7447. doi: 10.1021/acs.jpclett.2c01888. Epub 2022 Aug 5.
Two-dimensional (2D) electrides, characterized by excess interstitial anionic electron (IAE) in a crystalline 2D material, offer promising opportunities for the development of electrode materials, in particular in rechargeable metal-ion batteries applications. Although a few such potential electride materials have been reported, they generally show low metal-ion storage capacity, and the effect of IAE on the ion storage performance remains elusive so far. Here we report a novel 2D electride, [ScSi]·1e, with fascinating IAE-driven high alkali metal-ion storage capacity. In particular, its K-ion specific capacity can reach up to 1497 mA h g, higher than any previously reported 2D materials-based anodes in K-ion batteries (PIBs). The IAE in the [ScSi]·1e crystal accounts for such high capacity behavior, which can drift away and balance the charge on the metal-cation, playing a crucial role in stabilizing the metal-ion adsorption and enhancing multilayer-ions adsorption. This proposed IAE-driven storage mechanism provides an unprecedented avenue for the future design of high storage capacity electrode materials.
二维(2D)电子化合物,其特征是在晶体二维材料中存在过量的间隙阴离子电子(IAE),为电极材料的开发提供了广阔前景,特别是在可充电金属离子电池应用方面。尽管已经报道了一些这类潜在的电子化合物材料,但它们通常表现出较低的金属离子存储容量,并且到目前为止,IAE对离子存储性能的影响仍不明确。在此,我们报道了一种新型二维电子化合物[ScSi]·1e,它具有由IAE驱动的出色的高碱金属离子存储容量。特别是,其钾离子比容量可达1497 mA h g,高于此前报道的钾离子电池(PIB)中任何基于二维材料的负极。[ScSi]·1e晶体中的IAE导致了这种高容量行为,它可以漂移并平衡金属阳离子上的电荷,在稳定金属离子吸附和增强多层离子吸附方面起着关键作用。这种提出的由IAE驱动的存储机制为未来高存储容量电极材料的设计提供了一条前所未有的途径。