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Metallic Icosahedron Phase of Sodium at Terapascal Pressures

机译:兆帕斯卡压力下钠的金属二十面体相

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Alkali metals exhibit unexpected structures and electronic behavior at high pressures. Compression of metallic sodium (Na) to 200 GPa leads to the stability of a wide-band-gap insulator with the double hexagonal hP4 structure. Post-hP4 structures remain unexplored, but they are important for addressing the question of the pressure at which Na reverts to a metal. Here, we report the reentrant metallicity of Na at the very high pressure of 15.5 terapascal (TPa), predicted using first-principles structure searching simulations. Na is therefore insulating over the large pressure range of 0.2-15.5 TPa. Unusually, Na adopts an oP8 structure at pressures of 117-125 GPa and the same oP8 structure at 1.75-15.5 TPa. The metallization of Na occurs on the formation of a stable and striking body-centered cubic cI24 electride structure consisting of Na_(12) icosahedra, each housing at its center about one electron that is not associated with any Na ions.
机译:碱金属在高压下表现出出乎意料的结构和电子行为。将金属钠(Na)压缩到200 GPa会导致具有双六边形hP4结构的宽带隙绝缘子的稳定性。 hP4后的结构仍待探索,但对于解决Na还原成金属的压力问题很重要。在这里,我们报道了使用第一性原理结构搜索模拟预测的,在15.5兆帕斯卡(TPa)的极高压力下Na的折返金属性。因此,Na在0.2-15.5 TPa的较大压力范围内是绝缘的。通常,Na在117-125 GPa的压力下采用oP8结构,而在1.75-15.5 TPa的压力下采用相同的oP8结构。 Na的金属化发生在形成稳定且引人注目的体心立方cI24氮化物结构上,该结构由Na_(12)二十面体组成,每个结构的中心都围绕着一个不与任何Na离子缔合的电子。

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