Yu Kui, Zaman Badruz, Ripmeester John A
Steacie Institute for Molecular Sciences, National Research Council of Canada, Ottawa, Ontario KIA OR6, Canada.
J Nanosci Nanotechnol. 2005 Apr;5(4):669-81. doi: 10.1166/jnn.2005.123.
Colloidal CdSe nanocrystals were synthesized in reaction media consisting of tri-n-octylphosphine (TOP) without addition of other species; the single-step approach used cadmium oxide (CdO) and TOPSe as Cd and Se sources, respectively. The temporal evolution of the optical properties of the growing TOP-capped CdSe nanocrystals was monitored for a couple of hours, showing that there are two distinguishable stages of growth: an early stage (less than 5 minutes) and a later stage; the growth kinetics of the two stages is a function of the Cd-to-Se precursor molar ratios. A rational choice of 2-6Cd-to-1Se molar ratio was found, based on the temporal evolution of the photoluminescent (PL) efficiency (studied as PL intensity and sensitivity to the media of dispersion, and non-resonant Stokes shifts). For a 2Cd-to-1Se synthesis, the growth in size was slow in the early stages and became fast in the later stages; this fast-later-stage feature could be suppressed by going to a synthesis with a 4-6Cd-to-1Se mole ratio: the nanocrystals between 0.5-60 min growth time exhibit very much similar optical properties, with less than 19 nm redshift of bandgap absorption and emission occurring. Thus, the synthetic route developed here, with a rational 4-6Cd-to-1Se molar ratio, enables us to produce high-quality CdSe nanocrystals on a large-scale with a high degree of synthetic reproducibility. The insights gained facilitate a deeper understanding of the concept of what constitutes high-quality nano-crystals: high PL efficiency resulting from a low growth rate, which can be thoroughly and readily investigated by the red-shift rate of the band-gap peak positions; in addition, the insights gained help us to define a proper synthetic approach for large-scale production with high-quality product.
在由三正辛基膦(TOP)组成的反应介质中,不添加其他物质合成了胶体CdSe纳米晶体;单步方法分别使用氧化镉(CdO)和TOPSe作为Cd和Se源。对生长中的TOP包覆的CdSe纳米晶体的光学性质随时间的演变进行了数小时的监测,结果表明存在两个可区分的生长阶段:早期阶段(少于5分钟)和后期阶段;两个阶段的生长动力学是Cd与Se前驱体摩尔比的函数。基于光致发光(PL)效率的时间演变(以PL强度、对分散介质的敏感性和非共振斯托克斯位移来研究),发现了2 - 6Cd与1Se摩尔比的合理选择。对于2Cd与1Se的合成,早期尺寸增长缓慢,后期变得快速;通过采用4 - 6Cd与1Se摩尔比的合成可以抑制这种后期快速生长的特征:生长时间在0.5 - 60分钟之间的纳米晶体表现出非常相似的光学性质,带隙吸收和发射的红移小于19 nm。因此,这里开发的具有合理4 - 6Cd与1Se摩尔比的合成路线,使我们能够大规模生产高质量的CdSe纳米晶体,且具有高度的合成可重复性。所获得的见解有助于更深入地理解构成高质量纳米晶体的概念:低生长速率导致高PL效率,这可以通过带隙峰值位置的红移速率进行全面且容易的研究;此外,所获得的见解帮助我们定义一种适当的合成方法,以实现高质量产品的大规模生产。