New metallic ice phase under high pressure†

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL Physical Chemistry Chemical Physics Pub Date : 2024-10-22 DOI:10.1039/D4CP02543A
Yingying Huang, Liuyuan Zhu, Hanlin Li, Haiping Fang, Ruoyang Chen and Shiqi Sheng
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Abstract

Crystal materials can exhibit novel properties under high pressure, which are completely different from properties under ambient conditions. Water ice has an exceptionally rich phase diagram with at least 20 known crystalline ice phases from experiments, where the high-pressure ice X and ice XVIII behave as an ionic state and a superionic state, respectively. Thus, the ice structures stabilized under high pressure are very likely to possess other novel properties. Herein, we constructed a sequence of hypothetical high-pressure ices whose structures were generated according to the topological frameworks of common metal oxides. Based on density functional theory calculations, the pressure-induced phase transition sequence is in order that the known Ag2O-Pnm structure (ice X) transformed into a previously undiscovered TiO2_brookite-Pbca structure at a pressure of 300 GPa, followed by a transition to a new NaO2-Pa3 structure at a pressure of 2120 GPa. Hitherto unreported NaO2-Pa3 ice with a cubic structure is in the ionic state, where the oxygen atoms in NaO2-Pa3 have a face-centered cubic (fcc) sublattice, and the coordination number of H atoms increases to 3. These two structures are dynamically stable according to phonon spectrum analysis and remain stable at temperature of 100 K based on ab initio molecular dynamics (AIMD) simulations. More importantly, the NaO2-Pa3 ice exhibits novel metallic properties with a closing band gap above a pressure of 2600 GPa, owing to the electron orbital coupling of oxygen atoms in close proximity induced by pressure.

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高压下的新型金属冰相
晶体材料在高压下会表现出与环境条件下完全不同的新特性。水冰的相图异常丰富,实验中已知的结晶冰相至少有 20 种,其中高压冰 X 和冰 XVIII 表现为离子态和超离子态。因此,在高压下稳定的冰结构很可能具有其他新特性。在此,我们根据常见金属氧化物的拓扑框架构建了一系列假定的高压冰结构。根据密度泛函理论计算,压力诱导的相变序列依次为:已知的 Ag2O-Pn3-m 结构(冰 X)在压力为 3000 千巴时转变为之前未被发现的 TiO2_brookite-Pbca 结构,随后在压力为 22000 千巴时转变为新的 NaO2-Pa3 结构。更重要的是,它表现出了新颖的金属特性,在 26000 千巴压力以上,带隙逐渐缩小,这是由于压力引起的氧原子近距离电子轨道耦合所致。
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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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