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在太帕斯卡压力下氧分子的持续存在和最终消失。

Persistence and eventual demise of oxygen molecules at terapascal pressures.

机构信息

Lehrstuhl für Theoretische Chemie, Ruhr-Universität Bochum, 44780 Bochum, Germany.

出版信息

Phys Rev Lett. 2012 Jan 27;108(4):045503. doi: 10.1103/PhysRevLett.108.045503.

Abstract

Computational searches for structures of solid oxygen under high pressures in the multi-TPa range are carried out using density-functional-theory methods. We find that molecular oxygen persists to about 1.9 TPa at which it transforms into a semiconducting square-spiral-like polymeric structure (I4(1)/acd) with a band gap of ~3.0 eV. Solid oxygen forms a metallic zigzag chainlike structure (Cmcm) at about 3.0 TPa, but the chains in each layer gradually merge as the pressure is increased and a structure of Fmmm symmetry forms at about 9.3 TPa in which each atom has four nearest neighbors. The superconducting properties of molecular oxygen do not vary much with compression, although the structure becomes more symmetric. The electronic properties of oxygen have a complex evolution with pressure, swapping between insulating, semiconducting, and metallic.

摘要

使用密度泛函理论方法对高压多太帕范围内的固态氧结构进行了计算搜索。我们发现,分子氧在约 1.9 太帕的压力下保持稳定,随后转变为具有约 3.0 eV 带隙的半导体四方螺旋状聚合结构(I4(1)/acd)。固态氧在约 3.0 太帕时形成金属锯齿链状结构(Cmcm),但随着压力的增加,各层中的链逐渐合并,在约 9.3 太帕时形成 Fmmm 对称结构,其中每个原子有四个最近邻。尽管结构变得更加对称,但分子氧的超导性质随压缩变化不大。氧的电子性质随压力经历了复杂的演变,在绝缘、半导体和金属之间转换。

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