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Luminescent gold-poly(thiophene) nanoaggregates prepared by one-step oxidative polymerization

机译:通过一步氧化聚合制备的发光金-聚(噻吩)纳米聚集体

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摘要

We report the facile synthesis, formation mechanism, and photoluminescent (PL) properties of gold-poly(thiophene) (Au-PTh) nanoaggregates. They were prepared by one-step oxidative polymerization, in which Au~(3+) ion was utilized as an oxidizing agent for the polymerization of thiophene. Transmission electron microscopy (TEM) and high-resolution TEM (HR-TEM) analyses demonstrated that the 'raspberry-like' Au-PTh nanoaggregates consist of individual Au NPs covered by PTh and stabilized by Tween 80. For Au-PTh nanoaggregates, a clear red shift in the SP peak was observed in the UV absorption spectra as compared with pristine Au nanoparticles (NPs). This red shift of the SP band is a consequence of the location of π-conjugated PTh on the surface of Au NPs, resulted from a strong binding between sulfur atoms of PTh and the Au NPs (sulfur-gold interaction). The strong interaction between the gold and sulfur atoms of PTh in the Au-PTh nanoaggregates was observed by X-ray photoelectron spectroscopy (XPS) analysis. The SP effect contributes to the PL intensity enhancement of the Au-PTh nanoaggregates and was confirmed by confocal laser scanning microscopy (CLSM).
机译:我们报告了金-聚(噻吩)(Au-PTh)纳米聚集体的简便合成,形成机理和光致发光(PL)特性。它们是通过一步氧化聚合制备的,其中Au〜(3+)离子被用作噻吩聚合的氧化剂。透射电子显微镜(TEM)和高分辨率TEM(HR-TEM)分析表明,“树莓状” Au-PTh纳米聚集体由被PTh覆盖并由Tween 80稳定的单个Au NP组成。对于Au-PTh纳米聚集体,与原始金纳米颗粒(NPs)相比,在UV吸收光谱中观察到SP峰出现明显的红移。 SP谱带的这种红移是π共轭PTh在Au NPs表面上定位的结果,这是由于PTh的硫原子与Au NPs之间的牢固结合(硫金相互作用)所致。通过X射线光电子能谱(XPS)分析观察到Au-PTh纳米聚集体中PTh的金和硫原子之间的强相互作用。 SP效应有助于增强Au-PTh纳米聚集体的PL强度,并已通过共聚焦激光扫描显微镜(CLSM)证实。

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