Goncharenko Igor, Loubeyre Paul
Laboratoire Léon Brillouin CEA-CNRS, CEA Saclay, 91191 Gif-sur-Yvette, France.
Nature. 2005 Jun 30;435(7046):1206-9. doi: 10.1038/nature03699.
The solid hydrogen compounds D2, HD and H2 remain quantum molecular solids up to pressures in the 100 GPa range. A remarkable macroscopic consequence is the existence of a pressure-induced broken symmetry phase transition, in which the molecules go from a spherical rotational state to an anisotropic rotational state. Theoretical understanding of the broken symmetry phase structure remains controversial, despite numerous studies. Some open questions concern the existence of long- or short-range orientational order; whether a strong isotopic shift on the transition pressure should be assigned to the nuclear zero-point motion or to quantum localization; and whether the structures are cubic, hexagonal or orthorhombic. Here we present experimental data on the structure of the broken symmetry phase in solid D2, obtained by a combination of neutron and X-ray diffraction up to 60 GPa. Our data are incompatible with orthorhombic structures predicted by recent theoretical works. We find that the broken symmetry phase structure is incommensurate with local orientational order, being similar to that found in metastable cubic para-D2.
固态氢化合物D₂、HD和H₂在高达100 GPa的压力范围内仍为量子分子固体。一个显著的宏观结果是存在压力诱导的对称性破缺相变,其中分子从球形旋转状态转变为各向异性旋转状态。尽管有大量研究,但对对称性破缺相结构的理论理解仍存在争议。一些悬而未决的问题涉及长程或短程取向有序的存在;跃迁压力上的强同位素位移应归因于核零点运动还是量子局域化;以及结构是立方、六方还是正交晶系。在此,我们展示了通过中子和X射线衍射相结合获得的、高达60 GPa的固态D₂中对称性破缺相结构的实验数据。我们的数据与近期理论工作预测的正交晶系结构不相符。我们发现,对称性破缺相结构与局部取向有序不相称,类似于在亚稳立方对D₂中发现的结构。