Ahmed M, Guleria A, Rath M C, Singh A K, Adhikari S, Sarkar S K
J Nanosci Nanotechnol. 2014 Aug;14(8):5730-42. doi: 10.1166/jnn.2014.8857.
Herein, we have demonstrated a facile and green approach for the synthesis of Cadmium selenide (CdSe) quantum dots (QDs). The process was mediated by bovine serum albumin (BSA) and it was found that BSA plays the dual role of reducing agent as well as a stabilizing agent. The QDs exhibited sharp excitonic absorption features at ~500 nm and subsequently showed reasonably good photoluminescence (PL) at room temperature. The PL is seen to be strongly dependent on the concentration of the precursors and hence, the luminescence of these QDs could be conveniently tuned across the visible spectrum simply by varying molar ratio of the precursors. It can be envisaged from the fact that a red-shift of about 100 nm in the PL peak position was observed when the molar ratio of the precursors ([Cd2+]:[Se2-], in mM) was varied from 10:5 to 10:40. Subsequently, the charge carrier relaxation dynamics associated with the different molar ratio of precursors has been investigated and very interesting information regarding the energy level structures of these QDs were revealed. Most importantly, in conjunction with the optical tuning, the nanomorphology of these nanoparticles was found to vary with the change in molar ratios of Se and Cd precursors. This aspect can provide a new direction of controlling the shape of CdSe nanoparticles. The possible mechanism of the formation as well as for the shape variation of these nanoparticles with the molar ratios of precursors has been proposed, taking into account the role of amino acid residues (present in BSA). Moreover, the QDs were water soluble and possessed fairly good colloidal stability therefore, can have potential applications in catalysis and bio-labeling. On the whole, the present methodology of protein assisted synthesis is relatively new especially for semiconducting nanomaterials and may provide some unique and interesting aspects to control and fine tune the morphology vis-à-vis, their optical properties.
在此,我们展示了一种简便且绿色的合成硒化镉(CdSe)量子点(QDs)的方法。该过程由牛血清白蛋白(BSA)介导,并且发现BSA起到了还原剂和稳定剂的双重作用。量子点在约500 nm处表现出尖锐的激子吸收特征,随后在室温下显示出相当良好的光致发光(PL)。可以看出PL强烈依赖于前驱体的浓度,因此,仅通过改变前驱体的摩尔比,就可以方便地在可见光谱范围内调节这些量子点的发光。从以下事实可以设想,当前驱体的摩尔比([Cd2 +]:[Se2-],单位为mM)从10:5变为10:40时,PL峰位置观察到约100 nm的红移。随后,研究了与不同摩尔比前驱体相关的电荷载流子弛豫动力学,并揭示了有关这些量子点能级结构的非常有趣的信息。最重要的是,结合光学调谐,发现这些纳米颗粒的纳米形态随Se和Cd前驱体摩尔比的变化而变化。这方面可以为控制CdSe纳米颗粒的形状提供一个新方向。考虑到氨基酸残基(存在于BSA中)的作用,已经提出了这些纳米颗粒的形成以及形状随前驱体摩尔比变化的可能机制。此外,量子点是水溶性的并且具有相当好的胶体稳定性,因此,在催化和生物标记方面可能具有潜在应用。总体而言,目前这种蛋白质辅助合成方法对于半导体纳米材料来说相对较新,并且可能在控制和微调其形态及其光学性质方面提供一些独特而有趣的方面。