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首页> 外文期刊>Journal of Solid State Chemistry >5Pb2Sn3S13 and Ba6PbSn3Se13]]>
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5Pb2Sn3S13 and Ba6PbSn3Se13]]>

机译:<![CDATA [CDATA [含两种含铅金属硫芥菜的合成与表征:BA 5 PB 2 SN 3 S 13 和BA PBSN 3 SE 13 ]]>

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摘要

Abstract Two new metal chalcogenides, Ba5Pb2Sn3S13 (BPSS) and Ba6PbSn3Se13 (BPSSe), were successfully synthesized in vacuum–sealed silica tubes for the first time. Both of them are isostructural and crystallize in the Pnma space group of orthorhombic system. Their three-dimensional (3D) framework structures are composed of 2D layers formed by the interconnection of [(Pb/Ba)Q n ] (n = 6 and 7) polyhedra and isolated SnQ4 tetrahedra and charge–balanced Ba atoms filled into the interlayers. Note that the Q8 atoms are only surrounded by two Pb/Ba and four Ba atoms to form the distorted octahedra without the covalent Sn-Q bonds in their structures. Measured results of diffuse reflection and Raman spectra show that title compounds possess the wide transmission ranges from 0.5 to 20μm. Electronic structures and linear optical properties were also systematically investigated by the first–principle calculation, and calculated results indicate that title compounds possess the large birefringences about 0.123 and 0.135 for BPSS and BPSSe at 1μm, respectively, which indicate that they may be expected as potential IR birefringent materials. 展开▼
机译:<![cdata [ 抽象 两种新的金属Chalogenere,BA 5 PB 2 SN 3 S 13 (BPS)和BA 6 PBSN 3 SE 13 < / CE:INF>(BPSSE)首次在真空密封的二氧化硅管中成功合成。它们中的两者都是在 pnma 透析系统的空间组中的isostrontuctuctuctoral和结晶。它们的三维(3D)框架结构由由[(pb / ba)q n ]( n = 6和7)Polyhedra和孤立的SNQ 4 四面体和电荷平衡的BA原子填充到中间层。注意,Q8原子仅被两个Pb / BA和四个BA原子包围,以形成扭曲的八面体,而无需在其结构中的共价Sn-Q键。漫反射和拉曼光谱的测量结果表明,标题化合物具有0.5至20 μm的宽传动范围。通过第一原理计算还系统地研究了电子结构和线性光学性质,并且计算结果表明标题化合物具有大约0.123和0.135的大型双射归,并且在1 μm分别表明它们可以预期它们是潜在的IR双折射材料。

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