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二氧化碳在高压下的电子结构及分子到非分子转变的研究。

Electronic structure of carbon dioxide under pressure and insights into the molecular-to-nonmolecular transition.

机构信息

Departments of Earth Sciences, and Physics and Astronomy, University of Western Ontario, London, ON, Canada N6A 5B7.

出版信息

Proc Natl Acad Sci U S A. 2013 Nov 12;110(46):18402-6. doi: 10.1073/pnas.1305116110. Epub 2013 Oct 28.

DOI:10.1073/pnas.1305116110
PMID:24167283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3832016/
Abstract

Knowledge of the high-pressure behavior of carbon dioxide (CO2), an important planetary material found in Venus, Earth, and Mars, is vital to the study of the evolution and dynamics of the planetary interiors as well as to the fundamental understanding of the C-O bonding and interaction between the molecules. Recent studies have revealed a number of crystalline polymorphs (CO2-I to -VII) and an amorphous phase under high pressure-temperature conditions. Nevertheless, the reported phase stability field and transition pressures at room temperature are poorly defined, especially for the amorphous phase. Here we shed light on the successive pressure-induced local structural changes and the molecular-to-nonmolecular transition of CO2 at room temperature by performing an in situ study of the local electronic structure using X-ray Raman scattering, aided by first-principle exciton calculations. We show that the transition from CO2-I to CO2-III was initiated at around 7.4 GPa, and completed at about 17 GPa. The present study also shows that at ~37 GPa, molecular CO2 starts to polymerize to an extended structure with fourfold coordinated carbon and minor CO3 and CO-like species. The observed pressure is more than 10 GPa below previously reported. The disappearance of the minority species at 63(± 3) GPa suggests that a previously unknown phase transition within the nonmolecular phase of CO2 has occurred.

摘要

二氧化碳(CO2)是金星、地球和火星上的一种重要行星物质,其高压行为的知识对于研究行星内部的演化和动力学以及对于 C-O 键合和分子间相互作用的基本理解至关重要。最近的研究揭示了在高压-高温条件下存在多种晶相多形体(CO2-I 到 -VII)和非晶相。然而,报道的室温相稳定性场和相变压力定义较差,特别是对于非晶相。在这里,我们通过使用 X 射线拉曼散射原位研究局部电子结构,并辅以第一性原理激子计算,揭示了 CO2 在室温下的连续压力诱导的局部结构变化和分子到非分子转变。我们表明,从 CO2-I 到 CO2-III 的转变始于约 7.4 GPa,并在约 17 GPa 完成。本研究还表明,在约 37 GPa 时,分子 CO2 开始聚合为具有四配位碳和少量 CO3 和 CO 类似物的扩展结构。观察到的压力比以前报道的低 10 GPa 以上。在 63(±3)GPa 时少数物种的消失表明 CO2 的非分子相内发生了以前未知的相变。

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