School of Chemistry and Biochemistry, Thapar University, Patiala, 147 004 Punjab, India.
J Colloid Interface Sci. 2012 Feb 15;368(1):250-6. doi: 10.1016/j.jcis.2011.11.022. Epub 2011 Nov 25.
The CdS nanostructure undergoes photochemical dissolution, and hence, the photocatalytic activity deteriorates with light irradiation time. A thin layer of silica coating over CdS surface may prevent the photocorrosion and coalescence of quantum size CdS particles. Hence, we synthesized SiO(2)@CdS nanocomposites of different shapes and characterized them by XRD, HRTEM, EDX, SAED, BET surface area measurement and absorption and emission study. The dispersion of spherical CdS (Cd-2.62 at% and S-2.33 at%) nanoparticles of cubic crystal structure into thick amorphous SiO(2) (43.79 at%) matrix is demonstrated here. The fabrication of core (CdS)-shell (SiO(2)) structure (SiO(2)@CdS) consisting of CdS nanorod (Cd-19.79 at% and S-22.90 at%) core (length ~126 nm and width ~6 nm) having characteristic lattice fringes of hexagonal crystals and thin SiO(2) (12.81 at%) shell (thickness=1-1.4 nm) is successfully achieved for the first time. The surface area (21.2m(2)/g) of CdS nanorod (aspect ratio=21) is found to increase (42.3m(2)/g) after SiO(2) coating. The photoluminescence of CdS nanosphere (485 nm) and nanorod (501 nm) is highly quenched after SiO(2) layer formation. The superior photocatalytic activity of SiO(2)@CdS composites for the benzaldehyde oxidation under UV irradiation has been displayed.
CdS 纳米结构经历光化学溶解,因此,光催化活性随着光照时间的增加而恶化。CdS 表面的一层薄二氧化硅涂层可以防止光腐蚀和量子尺寸 CdS 颗粒的聚结。因此,我们合成了不同形状的 SiO(2)@CdS 纳米复合材料,并通过 XRD、HRTEM、EDX、SAED、BET 表面积测量和吸收和发射研究对其进行了表征。这里展示了立方晶体结构的球形 CdS(Cd-2.62 at%和 S-2.33 at%)纳米粒子分散在厚无定形 SiO(2)(43.79 at%)基质中。首次成功制备了由 CdS 纳米棒(Cd-19.79 at%和 S-22.90 at%)核(长度126nm,宽度6nm,具有六边形晶体的特征晶格条纹)和薄 SiO(2)(12.81 at%)壳(厚度=1-1.4nm)组成的核壳(SiO(2)@CdS)结构。CdS 纳米棒(纵横比=21)的表面积(21.2m(2)/g)在涂覆 SiO(2)后发现增加(42.3m(2)/g)。CdS 纳米球(485nm)和纳米棒(501nm)的光致发光在形成 SiO(2)层后高度猝灭。SiO(2)@CdS 复合材料在紫外光照射下对苯甲醛氧化具有优异的光催化活性。