超导电性
笼状水合物
材料科学
范德瓦尔斯力
氢
化学物理
金属氢
电子结构
价电子
硼
分子
金属
结晶学
凝聚态物理
电子
物理
化学
水合物
冶金
核物理学
有机化学
量子力学
作者
Akinwumi Akinpelu,Mangladeep Bhullar,Timothy A. Strobel,Yansun Yao
标识
DOI:10.1088/1674-1056/ada757
摘要
Abstract The recent discovery of type-VII boron–carbon clathrates with calculated superconducting transition temperatures approaching ∼100 K has sparked interest in exploring new conventional superconductors that may be stabilized at ambient pressure. The electronic structure of the clathrate is highly tunable based on the ability to substitute different metal atoms within the cages, which may also be large enough to host small molecules. Here we introduce molecular hydrogen (H 2 ) within the clathrate cages and investigate its impact on electron–phonon coupling interactions and the superconducting transition temperature ( T c ). Our approach involves combining molecular hydrogen with the new diamond-like covalent framework, resulting in a hydrogen-encapsulated clathrate, (H 2 )B 3 C 3 . A notable characteristic of (H 2 )B 3 C 3 is the dynamic behavior of the H 2 molecules, which exhibit nearly free rotations within the B–C cages, resulting in a dynamic structure that remains cubic on average. The static structure of (H 2 )B 3 C 3 (a snapshot in its dynamic trajectory) is calculated to be dynamically stable at ambient and low pressures. Topological analysis of the electron density reveals weak van der Waals interactions between molecular hydrogen and the B–C cages, marginally influencing the electronic structure of the material. The electron count and electronic structure calculations indicate that (H 2 )B 3 C 3 is a hole conductor, in which H 2 molecules donate a portion of their valence electron density to the metallic cage framework. Electron–phonon coupling calculation using the Migdal–Eliashberg theory predicts that (H 2 )B 3 C 3 possesses a T c of 46 K under ambient pressure. These results indicate potential for additional light-element substitutions within the type-VII clathrate framework and suggest the possibility of molecular hydrogen as a new approach to optimizing the electronic structures of this new class of superconducting materials.
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