Lin Hua, Chen Hong, Liu Peng-Fei, Yu Ju-Song, Zheng Yu-Jun, Ali Khan Muhammad, Chen Ling, Wu Li-Ming
Key Laboratory of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, People's Republic of China.
Dalton Trans. 2016 Apr 7;45(13):5775-82. doi: 10.1039/c6dt00193a. Epub 2016 Mar 3.
Five new quaternary rare-earth selenides, Cs[RE9Cd4Se18] (RE = Tb-Tm), which are the first examples with closed cavities in the quaternary A/RE/Cd/Q (A = alkali metal; RE = rare earth metal; Q = chalcogenide) system, have been synthesized by high-temperature solid state reactions with a modified reactive CsCl flux. Single crystal X-ray diffraction analyses show that these isostructural materials adopted a known BaV13O18-structure type in the trigonal space group R3[combining macron] (no. 148) with cell parameters of a = 17.773(2)-17.489(6) Å, c = 9.918(2)-9.765(5) Å and Z = 3. The structure is composed of MSe6 (centered by disordered RE and Cd) and RESe6 octahedra that share edges to form a 3D framework, inside which the cuboctahedral Se12 closed cavities accommodate Cs cations. It is interesting to note that these compounds exhibit atomic distributions different from the recently reported Mn-compounds Cs[RE9Mn4Se18]. In Cd-compounds, Cd and RE atoms are statistically mixed only at one of the 18f sites; the rest of the RE atoms are fully occupied at the two framework sites: 18f and 3a. Moreover, the theoretical studies have greatly aided the understanding of the site-preference about a Cd atom in the 3D framework. The synthesis, structural characterization, electronic band structure as well as physical properties of the title compounds are also discussed.
通过高温固态反应和改进的活性CsCl助熔剂合成了五种新型的四元稀土硒化物Cs[RE9Cd4Se18](RE = Tb - Tm),它们是四元A/RE/Cd/Q(A = 碱金属;RE = 稀土金属;Q = 硫族元素)体系中首个具有封闭空腔的例子。单晶X射线衍射分析表明,这些同构材料采用了已知的BaV13O18结构类型,属于三方空间群R3[combining macron](编号148),晶胞参数为a = 17.773(2) - 17.489(6) Å,c = 9.918(2) - 9.765(5) Å,Z = 3。该结构由MSe6(以无序的RE和Cd为中心)和RESe6八面体组成,它们共享棱边形成三维框架,在其内部立方八面体的Se12封闭空腔容纳Cs阳离子。值得注意的是,这些化合物表现出与最近报道的Mn化合物Cs[RE9Mn4Se18]不同的原子分布。在Cd化合物中,Cd和RE原子仅在18f位点之一上统计混合;其余的RE原子完全占据两个框架位点:18f和3a。此外,理论研究极大地有助于理解三维框架中Cd原子的位点偏好。还讨论了标题化合物的合成、结构表征、电子能带结构以及物理性质。