Coexistence of Zero-Dimensional Electride State and Superconductivity in AlH<sub>2</sub> Monolayer
Qiuping 秋萍 Yang 杨, Xue 雪 Jiang 蒋, Jijun 纪军 Zhao 赵
Abstract
Electrides, which confine “excess anionic electrons” in subnanometer-sized cavities of a lattice, are exotic ionic crystals. We propose a non-stoichiometric strategy to realize intrinsic two-dimensional (2D) superconducting electride. AlH 2 monolayer, which is structurally identical to 1H-MoS 2 , possesses zero-dimensionally confined anionic electrons in the interstitial sites of Al triangles, corresponding to a chemical formula of [AlH 2 ] + e − . The interaction between interstitial anionic electrons (IAEs) and host cation lattice mainly accounts for stabilization of 1H-AlH 2 electride. Impressively, 1H-AlH 2 monolayer is an intrinsic Bardeen–Cooper–Schrieffer superconductor with T c = 38 K, which is the direct consequence of strong coupling of the H-dominated high electronic states with Al acoustic branch vibrations and mid-frequency H-derived phonon softening modes caused by Kohn anomalies. Under tensile strain, IAEs transform into itinerant electrons, favoring the formation of stable Cooper pairs. Therefore, T c reaches up to 53 K at a biaxial fracture strain of 5%. Our findings provide valuable insights into the correlation between non-stoichiometric electrides and superconducting microscopic mechanisms at the 2D limit.