Epifani Mauro, Pellicer Eva, Arbiol Jordi, Sergent Nicolas, Pagnier Thierry, Morante Joan R
Consiglio Nazionale delle Ricerche - Istituto per la Microelettronica ed i Microsistemi (C.N.R.-I.M.M.), via Monteroni, I-73100 Lecce, Italy.
Langmuir. 2008 Oct 7;24(19):11182-8. doi: 10.1021/la801859z. Epub 2008 Aug 27.
Amorphous CdSe nanoparticles were prepared by a base-catalyzed room-temperature reaction between cadmium nitrate and selenourea, with dodecanethiol as a capping ligand. The nanoparticle size could be controlled from 1.9 to 3.6 nm by increasing the water concentration in the reaction. When the nanoparticles were heated in a pyridine suspension, excitonic peaks appeared in the initially featureless optical absorption spectra. By changing the suspension solvent and the capping ligand and its concentration, it was shown that the dynamic surface exchange between the ligand and pyridine controls the crystallization process. This phenomenon was interpreted as a surface rigidity effect imposed by the ligand, whose importance was separately evidenced on the dried nanoparticles by the evolution of X-ray diffraction patterns and Raman spectra. In particular, both techniques showed that a threshold temperature is needed before crystallization occurs, and such a threshold was related to ligand desorption. The surface effect was directly visualized by high-resolution transmission electron microscopy observations of the amorphous particles, where crystallization under the electron beam was observed to start by the formation of a crystalline nucleus in the nanoparticle interior and then to extend to the whole structure.
通过硝酸镉与硒脲在碱催化的室温反应中制备了非晶态CdSe纳米颗粒,使用十二烷硫醇作为封端配体。通过增加反应中的水浓度,纳米颗粒的尺寸可以控制在1.9至3.6纳米之间。当纳米颗粒在吡啶悬浮液中加热时,在最初无特征的光吸收光谱中出现了激子峰。通过改变悬浮溶剂、封端配体及其浓度,结果表明配体与吡啶之间的动态表面交换控制了结晶过程。这种现象被解释为配体施加的表面刚性效应,通过X射线衍射图谱和拉曼光谱的演变,在干燥的纳米颗粒上分别证明了其重要性。特别是,这两种技术都表明在结晶发生之前需要一个阈值温度,并且这样的阈值与配体解吸有关。通过对非晶颗粒的高分辨率透射电子显微镜观察直接可视化了表面效应,在该观察中,观察到在电子束下结晶通过在纳米颗粒内部形成晶核开始,然后扩展到整个结构。