层状KTi Nb O5因具有离子可交换、层间结构均一可控等优点而引起了广泛的关注。采用高温固相法制备的KTi Nb O5为前驱体,经H+交换、剥离改性制备出HTi Nb O5纳米片并以其作为基体材料与Fe2O3纳米粒子复合制备出e-HTi Nb O5@Fe2O3纳米复合材料。采用XRD、Raman、BET、HRTEM、TG-DSC和UV-vis DRS对样品的结构和光响应特征进行表征。结果表明,e-HTi Nb O5@Fe2O3保留了主体纳米片聚集体的孔隙结构特征,客体材料分散于主体材料表面,并与主体纳米片上的活性官能团之间发生相互作用,导致主体纳米片的热稳定性增加。另外,e-HTi Nb O5@Fe2O3的BET表面积明显增加的同时,其在可见光区有明显的吸收,禁带宽度为2.08 e V,该纳米复合材料在自然光辐射下可将乙硫醇光催化氧化为磺酸盐。
A three-dimensional （3D） coordination polymer {[Co（bdc）（dpb）]·H2O}n （1） was prepared by solvothermal reaction of 1,3-dipyridyl benzene （dpb） with deprotonated 1,3-benzene- dicarboxylate （H2bdc）, and was characterized by elemental analysis, IR spectroscopy, and X-ray single-crystal diffraction. It crystallizes in the monoclinic system, space group C2/c with α = 15.478（6）, b = 12.865（5）, c = 24.091（10） ？, β = 95.599（5）°, V = 4774（3） ？3, C24H18CoN2O5, Mr = 473.34, Dc = 1.267 g/cm3, F（000） = 1864.0, μ = 0.748 mm-1 and Z = 8. Each Co（II） ion links three bdc2- anions to form an infinitely 1D ladder-shaped chain containing binuclear [（COO）Co]2 cluster, and dpb links adjacent 1D chains to form a 3D pcu framework. In addition, the UV-vis of 1 was also studied.
