Geophysical Laboratory, Carnegie Institution of Washington, 5251 Broad Branch Road NW, Washington, DC 20015, USA.
J Chem Phys. 2010 Oct 28;133(16):164512. doi: 10.1063/1.3505299.
Optical microscopy, spectroscopic and x-ray diffraction studies at high-pressure are used to investigate intermolecular interactions in binary mixtures of germane (GeH(4)) + hydrogen (H(2)). The measurements reveal the formation of a new molecular compound, with the approximate stoichiometry GeH(4)(H(2))(2), when the constituents are compressed above 7.5 GPa. Raman and infrared spectroscopic measurements show multiple H(2) vibrons substantially softened from bulk solid hydrogen. With increasing pressure, the frequencies of several Raman and infrared H(2) vibrons decrease, indicating anomalous attractive interaction for closed-shell, nonpolar molecules. Synchrotron powder x-ray diffraction measurements show that the compound has a structure based on face-centered cubic (fcc) with GeH(4) molecules occupying fcc sites and H(2) molecules likely distributed between O(h) and T(d) sites. Above ca. 17 GPa, GeH(4) molecules in the compound become unstable with respect to decomposition products (Ge + H(2)), however, the compound can be preserved metastably to ca. 27 GPa for time-scales of the order of several hours.
采用光学显微镜、高压光谱和 X 射线衍射研究了锗烷(GeH4)+氢气(H2)二元混合物中的分子间相互作用。测量结果表明,当反应物在 7.5GPa 以上被压缩时,会形成一种新的分子化合物,其近似化学计量比为 GeH4(H2)2。拉曼和红外光谱测量表明,多个 H2振动子明显软化,与体相固态氢相比。随着压力的增加,几个拉曼和红外 H2振动子的频率降低,表明对于闭壳、非极性分子存在异常的吸引力。同步辐射粉末 X 射线衍射测量表明,该化合物具有面心立方(fcc)结构,GeH4分子占据 fcc 位,H2分子可能分布在 O(h)和 T(d)位之间。在 ca.17GPa 以上,化合物中的 GeH4分子相对于分解产物(Ge+H2)变得不稳定,然而,该化合物可以在 ca.27GPa 下亚稳存在几个小时的时间尺度。