Botan-Neto Benedito Donizeti, Santamaria-Perez David, Bayarjargal Lkhamsuren, Bykova Elena, Gonzalez-Platas Javier, Otero-de-la-Roza Alberto
Departamento de Física Aplicada-ICMUV, MALTA Consolider Team, Universitat de València, Valencia 46100, Spain.
Institute of Geosciences, Goethe University Frankfurt, Frankfurt 60438, Germany.
Inorg Chem. 2024 Aug 26;63(34):15762-15771. doi: 10.1021/acs.inorgchem.4c01699. Epub 2024 Aug 12.
The study of the structural stability of carbonates under different pressure and temperature conditions is important for modeling the carbon budget in the Earth's interior and the stability of carbonation products of carbon capture and storage (CCS) solutions. In this work, we confirm the existence of the two dense polymorphs of the hydrated magnesium carbonate MgCO·3HO nesquehonite mineral previously reported, and we characterize their structures using synchrotron single-crystal X-ray diffraction at 3.1 and 11.6 GPa. Phase transitions entail the distortion and atomic rearrangement of the Mg-centered polyhedra and the tilting of the [CO] carbonate units. In particular, the Mg coordination number increases from 6 in nesquehonite to 7 in the second high-pressure phase, while maintaining a topology based on complex MgCO(HO) chains. We also studied their vibrational behavior upon compression using Raman spectroscopy and complemented the experimental results with density-functional theory (DFT) calculations. The role played by hydrogen bonds in the compressibility and the polymorphism of this hydrated carbonate is also discussed.
研究不同压力和温度条件下碳酸盐的结构稳定性,对于模拟地球内部的碳收支以及碳捕获与封存(CCS)解决方案的碳酸化产物稳定性而言至关重要。在这项工作中,我们证实了先前报道的水合碳酸镁MgCO₃·3H₂O镍菱镁矿矿物的两种致密多晶型物的存在,并使用同步加速器单晶X射线衍射在3.1吉帕和11.6吉帕下对其结构进行了表征。相变导致以Mg为中心的多面体发生畸变和原子重排,以及[CO₃]碳酸根单元发生倾斜。特别是,Mg的配位数从镍菱镁矿中的6增加到第二个高压相中的7,同时保持基于复杂MgCO₃(H₂O)链的拓扑结构。我们还使用拉曼光谱研究了它们在压缩时的振动行为,并用密度泛函理论(DFT)计算对实验结果进行了补充。还讨论了氢键在这种水合碳酸盐的可压缩性和多晶型性中所起的作用。