Tsuruoka Takaaki, Takahashi Rena, Akamatsu Kensuke, Nawafune Hidemi
Graduate School of Science, Konan University, 8-9-1 Okamoto, Higashinada, Kobe, 658-8501, Japan.
Phys Chem Chem Phys. 2008 Apr 28;10(16):2221-6. doi: 10.1039/b717770d. Epub 2008 Feb 27.
Changes in the optical properties of CdTe nanocrystals through selective surface exchange reaction with thiolate molecules in the organic phase are studied with an aim to investigate the mechanism and the role of organic ligands. The reaction was mediated by dissociation of Te anions via oxidation in air from CdTe nanocrystals, followed by attachment of thiolate molecules in a 1:1 stoichiometric manner. This results in a gradual shell formation and a corresponding decrease in the size of the fluorescent CdTe cores, which induces a blue shift of both the absorption edge and emission wavelength in the visible region. A systematic study including the addition of ligands at different concentrations revealed that Te dissociation is the rate-determining step for the process and the degree of blue shift is significantly dependent on the amount of organic ligands present. The process could also be kinetically controlled through the addition of an excess amount of thiolate ligands, allowing systematic tuning of the emission properties of nanocrystals under ambient conditions.
通过与有机相中的硫醇盐分子进行选择性表面交换反应,研究了CdTe纳米晶体光学性质的变化,旨在探究有机配体的作用机制。该反应通过空气中的氧化作用使CdTe纳米晶体中的Te阴离子解离来介导,随后硫醇盐分子以1:1的化学计量比附着。这导致逐渐形成壳层,荧光CdTe核的尺寸相应减小,从而在可见光区域引起吸收边缘和发射波长的蓝移。一项包括添加不同浓度配体的系统研究表明,Te解离是该过程的速率决定步骤,蓝移程度显著取决于存在的有机配体的量。通过添加过量的硫醇盐配体,该过程也可以在动力学上得到控制,从而在环境条件下对纳米晶体的发射性质进行系统调节。