Ji Cheng, Li Bing, Luo Jie, Zhao Yongsheng, Liu Yuan, Glazyrin Konstantin, Björling Alexander, Marçal Lucas A B, Kahnt Maik, Kalbfleisch Sebastian, Liu Wenjun, Gao Yang, Wang Junyue, Mao Wendy L, Liu Hanyu, Ma Yanming, Ding Yang, Yang Wenge, Mao Ho-Kwang
Center for High Pressure Science and Technology Advanced Research, Beijing, People's Republic of China.
Shanghai Key Laboratory of Material Frontiers Research in Extreme Environments, Shanghai Advanced Research in Physical Sciences, Shanghai, People's Republic of China.
Nature. 2025 May;641(8064):904-909. doi: 10.1038/s41586-025-08936-w. Epub 2025 May 14.
The structural evolution of molecular hydrogen H under multi-megabar compression and its relation to atomic metallic hydrogen is a key unsolved problem in condensed-matter physics. Although dozens of crystal structures have been proposed by theory, only one, the simple hexagonal-close-packed (hcp) structure of only spherical disordered H, has been previously confirmed in experiments. Through advancing nano-focused synchrotron X-ray probes, here we report the observation of the transition from hcp H to a post-hcp structure with a six-fold larger supercell at pressures above 212 GPa, indicating the change of spherical H to various ordered configurations. Theoretical calculations based on our XRD results found a time-averaged structure model in the space group with alternating layers of spherically disordered H and new graphene-like layers consisting of H trimers (H) formed by the association of three H molecules. This supercell has not been reported by any previous theoretical study for the post-hcp phase, but is close to a number of theoretical models with mixed-layer structures. The evidence of a structural transition beyond hcp establishes the trend of H molecular association towards polymerization at extreme pressures, giving clues about the nature of the molecular-to-atomic transition of metallic hydrogen. Considering the spectroscopic behaviours that show strong vibrational and bending peaks of H up to 400 GPa, it would be prudent to speculate the continuation of hydrogen molecular polymerization up to its metallization.
在多兆巴压力下分子氢H的结构演化及其与原子态金属氢的关系是凝聚态物理中一个关键的未解决问题。尽管理论上已经提出了几十种晶体结构,但此前实验中仅证实了一种,即仅由球形无序H构成的简单六方密堆积(hcp)结构。通过改进纳米聚焦同步加速器X射线探针,我们在此报告了在压力高于212 GPa时观察到从hcp H向具有六倍大超胞的后hcp结构的转变,这表明球形H转变为各种有序构型。基于我们的XRD结果进行的理论计算在空间群中发现了一个时间平均结构模型,该模型具有交替排列的球形无序H层和由三个H分子缔合形成的H三聚体(H)组成的新型类石墨烯层。这种超胞在之前关于后hcp相的任何理论研究中均未被报道,但与许多具有混合层结构的理论模型相近。hcp之后结构转变的证据确立了在极端压力下H分子缔合向聚合的趋势,为金属氢的分子到原子转变的性质提供了线索。考虑到在高达400 GPa时显示出H强烈振动和弯曲峰的光谱行为,谨慎推测氢分子聚合直至其金属化的过程会持续下去是合理的。