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通过层层组装制备功能性核/壳纳米颗粒。控制颗粒聚集及增强分散稳定性的实验参数研究。

Functional core/shell nanoparticles via layer-by-layer assembly. investigation of the experimental parameters for controlling particle aggregation and for enhancing dispersion stability.

作者信息

Schneider Grégory, Decher Gero

机构信息

Institut Charles Sadron, CNRS UPR022, 6 rue Boussingault, F-67083 Strasbourg Cedex, France.

出版信息

Langmuir. 2008 Mar 4;24(5):1778-89. doi: 10.1021/la7021837. Epub 2008 Jan 29.

Abstract

Gold nanoparticles (AuNPs) with a size of 13.5 nm were synthesized using well-established methods as described earlier by Turkevich (Turkevich, J.; Stevenson, P. C.; Hillier, J. Discuss. Faraday Soc. 1961, 11, 55-75) and Frens (Frens, G. Nature (London), Phys. Sci. 1973, 241, 20-22) using citrate as the reducing agent. It has already been reported that such AuNPs can easily be coated with polymeric shells using electrostatic layer-by-layer assembly of certain polyelectrolytes. Here, we show which parameters, namely, the polyelectrolyte concentration, the contour length of the polyelectrolyte chain, and the ionic strength, are preventing bridging flocculation during polyelectrolyte adsorption and enhancing the stability of the colloidal dispersion. For the preparation of individually coated particles with high yield, we identified optimal conditions such as the degree of polymerization of the polyelectrolytes used, the polyelectrolyte concentration, the nanoparticle concentration, and the concentration of added NaCl during multilayer buildup. Surprisingly, such functional nanoparticles are obtained with highest yield at a moderate excess of polyions. In contrast to expectations, a larger excess of polyions leads again to slight destabilization of the dispersion. The present findings raise our confidence to establish layer-by-layer deposition as a general method for functionalizing even different nanoparticles using a single method.

摘要

采用如Turkevich(Turkevich, J.; Stevenson, P. C.; Hillier, J. Discuss. Faraday Soc. 1961, 11, 55 - 75)和Frens(Frens, G. Nature (London), Phys. Sci. 1973, 241, 20 - 22)之前所描述的成熟方法,以柠檬酸盐作为还原剂,合成了尺寸为13.5纳米的金纳米颗粒(AuNPs)。已有报道称,通过某些聚电解质的静电逐层组装,此类AuNPs能够轻松地被聚合物壳层包覆。在此,我们展示了哪些参数,即聚电解质浓度、聚电解质链的轮廓长度以及离子强度,在聚电解质吸附过程中能够防止桥连絮凝并增强胶体分散体的稳定性。为了以高产率制备单独包覆的颗粒,我们确定了最佳条件,例如所用聚电解质的聚合度、聚电解质浓度、纳米颗粒浓度以及多层组装过程中添加的NaCl浓度。令人惊讶的是,在适度过量的聚离子条件下能够以最高产率获得此类功能化纳米颗粒。与预期相反,更大过量的聚离子再次导致分散体轻微失稳。目前的研究结果增强了我们的信心,即可以将逐层沉积确立为一种使用单一方法对甚至不同纳米颗粒进行功能化的通用方法。

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