化学
锌相
结晶学
四方晶系
单独一对
晶体结构
金刚烷
电子能带结构
带隙
密度泛函理论
空间组
相(物质)
原子轨道
八面体
X射线晶体学
衍射
电子
计算化学
分子
凝聚态物理
物理
有机化学
量子力学
光学
作者
Xiao‐Cun Liu,Na Lin,Jian Wang,Mingyan Pan,Xian Zhao,Xutang Tao,Sheng‐Qing Xia
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2013-09-30
卷期号:52 (20): 11836-11842
被引量:12
摘要
A new quaternary arsenide Zintl phase, Ba13Si6Sn8As22, has been synthesized from the Sn-flux reactions, and the structure was determined by the single-crystal X-ray diffraction methods. The compound crystallizes in the tetragonal non-centrosymmetric space group I42m (No. 121) with unit cell parameters of a = b = 14.4857(3) Å, c = 13.5506(7) Å, V = 2843.40(17) Å(3). Its polyanion structure can be viewed as composed of [Si4As10] adamantane-like clusters and SiAs4 tetrahedra, which are linked via the [Sn2As4] groups built through two edge-sharing SnAs3 triangular pyramids. Differential thermal analysis and thermogravimetry measurements indicate that Ba13Si6Sn8As22 has good thermal stability, and does not melt or decompose below 1045 K under Ar atmosphere. Density functional calculations were performed on Ba13Si6Sn8As22 and the results suggest a band gap of around 1.0 eV for Ba13Si6Sn8As22, confirmed by the diffuse reflectance spectrum measurement. In addition, the extensively existing lone pairs of electrons on the p-orbitals of As and Sn may also hint interesting nonlinear optical properties considering the noncentrosymmetric structure.
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