Yang Jian, Elim Hendry Izaac, Zhang QingBo, Lee Jim Yang, Ji Wei
Molecular Engineering of Biological and Chemical Systems, Singapore-MIT Alliance, E4-04-10, 4 Engineering Drive 3, Singapore 117576.
J Am Chem Soc. 2006 Sep 13;128(36):11921-6. doi: 10.1021/ja062494r.
High-quality, monodisperse PbS-Au(1), PbS-Au(4), and PbS-Au(n) nanostructures have been synthesized via a facile and convenient solution chemistry approach. HRTEM images of these nanostructures showed good selectivity of gold deposition on the semiconductor in several spatially correlated directions. The formation of these regular nanostructures can be explained by the difference in polarity of crystal facets that led to the selective growth of metal on the semiconductor surface. Owing to their narrow size distribution and intrinsic high-symmetry, the resulting PbS-Au(4) and PbS-Au(n) heterogeneous nanostructures could spontaneously self-assemble into ordered arrays with different symmetries. From the results of the pump-probe measurements, the presence of Au in PbS-Au(4) nanostructures has substantially altered the nonlinear optical response of PbS nanocrystals.
通过一种简便的溶液化学方法合成了高质量、单分散的PbS-Au(1)、PbS-Au(4)和PbS-Au(n)纳米结构。这些纳米结构的高分辨透射电子显微镜(HRTEM)图像显示,金在半导体上沿几个空间相关方向的沉积具有良好的选择性。这些规则纳米结构的形成可以用晶面极性差异来解释,这种差异导致金属在半导体表面选择性生长。由于其窄尺寸分布和固有的高对称性,所得的PbS-Au(4)和PbS-Au(n)异质纳米结构能够自发地自组装成具有不同对称性的有序阵列。从泵浦-探测测量结果来看,PbS-Au(4)纳米结构中Au的存在显著改变了PbS纳米晶体的非线性光学响应。