5d轨道对应性控制了BaOO的高压多态
Sophie Kogan1, Anastassia N Alexandrova1, Harry W T Morgan1,2
1University of California, Los Angeles, Department of Chemistry and Biochemistry, 607 Charles E Young Drive East, Los Angeles, CA, 90095, USA.
Chemistry (Weinheim an der Bergstrasse, Germany)
|June 30, 2025
概括
金属d轨道显著影响土金属氧化物中的高压结构. 合性,特别是在氧化 (BaO) 中,驱动在氧化 (CaO) 或氧化 (SrO) 中未见的独特结构转变.
科学领域:
- 固态化学 固态化学
- 计算材料科学科学 计算材料科学
- 量子化学 是一个量子化学.
背景情况:
- 土金属氧化物 (CaO,SrO,BaO) 在高压下表现出复杂的结构行为.
- 了解这些转变对于材料科学和地球化学至关重要.
- 金属d轨道在这些转换中的作用尚未完全阐明.
研究的目的:
- 研究金属d轨道对CaO,SrO和BaO的高压结构的影响.
- 分析这些氧化物在压力下的化学结合和结构稳定性.
- 扩大对d轨道参与II组化学的理解.
主要方法:
- 密度函数理论 (DFT) 的计算.
- 化学结合分析. 化学结合分析.
- 高压结构阶段过渡研究.
主要成果:
- 从B1 (岩盐) 转变为B2 (化) 的结构.
- 宝氧呈现出一个独特的过渡序列:B1-B8 (NiAs结构) 和B8-dB2 (扭曲的B2).
- DFT计算显示,金属-氧共价性由金属d轨道介导,稳定了BaO中的B8和dB2相.
结论:
- 金属d轨道在土金属氧化物,特别是BaO中稳定高压相方面发挥着至关重要的作用.
- 在BaO中,的大5d轨道增强了共价性,导致独特的B8和扭曲的B2结构.
- 这项研究强调了d轨道在压力下II组化学中的扩大作用.
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