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环保型微波辅助绿色快速合成稳定的金和核壳型金银纳米粒子。

Eco-friendly microwave-assisted green and rapid synthesis of well-stabilized gold and core-shell silver-gold nanoparticles.

机构信息

National Research Centre, Textile Research Division, Dokki, Cairo, Egypt.

National Research Centre, Textile Research Division, Dokki, Cairo, Egypt.

出版信息

Carbohydr Polym. 2016 Jan 20;136:1128-36. doi: 10.1016/j.carbpol.2015.10.003. Epub 2015 Oct 9.


DOI:10.1016/j.carbpol.2015.10.003
PMID:26572455
Abstract

Herein, we present a new approach for the synthesis of gold nanoparticles (AuNPs) individually and as bimetallic core-shell nanoparticles (AgNPs-AuNPs). The novelty of the approach is further maximized by using curdlan (CRD) biopolymer to perform the dual role of reducing and capping agents and microwave-aided technology for affecting the said nanoparticles with varying concentrations in addition to those affected by precursor concentrations. Thus, for preparation of AuNPs, curdlan was solubilized in alkali solution followed by an addition of tetrachloroauric acid (HAuCl4). The curdlan solution containing HAuCl4 was then subjected to microwave radiation for up to 10 min. The optimum conditions obtained with the synthesis of AuNPs were employed for preparation of core-shell silver-gold nanoparticles by replacing definite portion of HAuCl4 with an equivalent portion of silver nitrate (AgNO3). The portion of AgNO3 was added initially and allowed to be reduced by virtue of the dual role of curdlan under microwave radiation. The corresponding portion of HAuCl4 was then added and allowed to complete the reaction. Characterization of AuNPs and AgNPs-AuNPs core-shell were made using UV-vis spectra, TEM, FTIR, XRD, zeta potential, and AFM analysis. Accordingly, strong peaks of the colloidal particles show surface plasmon resonance (SPR) at maximum wavelength of 540 nm, proving the formation of well-stabilized gold nanoparticles. TEM investigations reveal that the major size of AuNPs formed at different Au(+3)concentration lie below 20 nm with narrow size distribution. Whilst, the SPR bands of AgNPs-AuNPs core-shell differ than those obtained from original AgNPs (420 nm) and AuNPs (540 nm). Such shifting due to SPR of Au nanoshell deposited onto AgNPs core was significantly affected by the variation of bimetallic ratios applied. TEM micrographs show variation in contrast between dark silver core and the lighter gold shell. Increasing the ratio of silver ions leads to significant decrease in zeta potential of the formed bimetallic core-shell. FT-IR discloses the interaction between CRD and metal nanoparticles, which could be the question of reducing and stabilizing metal and bimetallic nanoparticles. XRD patterns assume insufficient difference for the AuNPs and AgNPs-AuNPs core-shell samples due to close lattice constants of Ag and Au. Based on AFM, AuNPs and AgNPs-AuNPs core-shell exhibited good monodispersity with spherical particles possessing different sizes in the studied samples. The average sizes of both metal and bimetallic core-shell were found to be 52 and 45 nm, respectively.

摘要

在此,我们提出了一种新的方法来合成金纳米粒子(AuNPs)和双金属核壳纳米粒子(AgNPs-AuNPs)。该方法的新颖之处在于,使用了卡拉胶(CRD)生物聚合物来同时发挥还原和包覆剂的双重作用,并采用微波辅助技术,在不同浓度的前体浓度影响之外,还对所述纳米粒子产生影响。因此,为了制备 AuNPs,将卡拉胶溶解在碱溶液中,然后加入四氯金酸(HAuCl4)。含有 HAuCl4 的卡拉胶溶液随后在微波辐射下进行 10 分钟。用所获得的最佳条件通过用等摩尔的硝酸银(AgNO3)替代部分 HAuCl4 来制备核壳银金纳米粒子。最初加入 AgNO3 部分,并通过在微波辐射下卡拉胶的双重作用使其还原。然后加入相应部分的 HAuCl4,使其完成反应。使用 UV-vis 光谱、TEM、FTIR、XRD、Zeta 电位和 AFM 分析对 AuNPs 和 AgNPs-AuNPs 核壳进行了表征。相应地,胶体粒子的强峰在 540nm 处显示出表面等离子体共振(SPR),证明了稳定的金纳米粒子的形成。TEM 研究表明,在不同的 Au(+3)浓度下形成的 AuNPs 的主要尺寸小于 20nm,且尺寸分布较窄。而 AgNPs-AuNPs 核壳的 SPR 带与原始 AgNPs(420nm)和 AuNPs(540nm)获得的 SPR 带不同。由于沉积在 AgNPs 核上的 Au 纳米壳的 SPR,这种由于 SPR 引起的变化对所施加的双金属比有显著影响。TEM 显微照片显示了暗银核和较轻的金壳之间对比度的变化。增加银离子的比例会导致形成的双金属核壳的 Zeta 电位显著降低。FT-IR 揭示了 CRD 与金属纳米粒子之间的相互作用,这可能是还原和稳定金属和双金属纳米粒子的问题。XRD 图谱由于 Ag 和 Au 的晶格常数相近,对于 AuNPs 和 AgNPs-AuNPs 核壳样品,其差异不明显。基于 AFM,AuNPs 和 AgNPs-AuNPs 核壳表现出良好的单分散性,具有不同尺寸的球形粒子。两种金属和双金属核壳的平均尺寸分别为 52nm 和 45nm。

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