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Enhancement for phonon-mediated superconductivity up to 37 K in few-hydrogen metal-bonded layered magnesium hydride under atmospheric pressure.

作者信息

He Yong, Du Juan, Liu Shi-Ming, Tian Chong, Zhang Min, Zhu Yao-Hui, Zhong Hongxia, Wang Xinqiang, Shi Jun-Jie

机构信息

State Key Laboratory for Artificial Microstructures and Mesoscopic Physics, School of Physics, Peking University Yangtze Delta Institute of Optoelectronics, Peking University, Beijing 100871, China.

Department of Physics and Optoelectronic Engineering Faculty of Science, Beijing University of Technology, Beijing 100124, China.

出版信息

Phys Chem Chem Phys. 2023 Aug 9;25(31):21037-21044. doi: 10.1039/d3cp02620e.

Abstract

The discovery of superconductivity in layered MgB has renewed interest in the search for high-temperature conventional superconductors, leading to the synthesis of numerous hydrogen-dominated materials with high critical temperatures () under high pressures. However, achieving a high- superconductor under ambient pressure remains a challenging goal. In this study, we propose a novel approach to realize a high-temperature superconductor under ambient pressure by introducing a hexagonal H monolayer into the hexagonal close-packed magnesium lattice, resulting in a new and stable few-hydrogen metal-bonded layered magnesium hydride (Mg)H. This compound exhibits superior ductility compared to multi-hydrogen, cuprate, and iron-based superconductors due to its metallic bonding. Our unconventional strategy diverges from the conventional design principles used in hydrogen-dominated covalent high-temperature superconductors. Using anisotropic Migdal-Eliashberg equations, we demonstrate that the stable (Mg)H compound is a typical phonon-mediated superconductor, characterized by strong electron-phonon coupling and an excellent of 37 K under ambient conditions, comparable to that of MgB. Our findings not only present a new pathway for exploring high-temperature superconductors but also provide valuable insights for future experimental synthesis endeavors.

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