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

机译:环保的微波辅助绿色技术,快速合成稳定的金和核壳银金纳米粒子

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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 wellstabilized 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. (c) 2015 Elsevier Ltd. All rights reserved.
机译:在这里,我们提出了一种新的合成金纳米颗粒(AuNPs)的新方法,并作为双金属核壳纳米颗粒(AgNPs-AuNPs)合成。通过使用柯德兰(CRD)生物聚合物来执行还原剂和封端剂的双重作用,以及微波辅助技术,除了受前体浓度影响的那些纳米粒子以外,还可以改变浓度来影响所述纳米粒子,从而使该方法的新颖性最大化。因此,为了制备AuNPs,将姜黄素溶于碱溶液中,然后添加四氯金酸(HAuCl4)。然后将含有HAuCl4的柯德兰溶液进行微波辐射长达10分钟。通过用等量的硝酸银(AgNO3)代替一定量的HAuCl4,可以使用合成AuNPs所获得的最佳条件来制备核-壳银-金纳米颗粒。首先加入AgNO 3的一部分,并通过在微波辐射下的凝胶多糖的双重作用使其减少。然后加入相应的HAuCl4部分,使其完全反应。使用紫外可见光谱,TEM,FTIR,XRD,ζ电位和AFM分析对AuNPs和AgNPs-AuNPs核-壳进行表征。因此,胶体颗粒的强峰在最大波长540 nm处显示出表面等离子体共振(SPR),证明形成了稳定的金纳米颗粒。 TEM研究表明,在不同Au(+3)浓度下形成的AuNPs的主要尺寸在20 nm以下,且尺寸分布较窄。同时,AgNPs-AuNPs核壳的SPR带不同于从原始AgNPs(420 nm)和AuNPs(540 nm)获得的SPR带。由于沉积在AgNPs核上的Au纳米壳的SPR引起的这种位移受到所施加的双金属比率变化的显着影响。 TEM显微照片显示深银芯和浅金壳之间的对比度变化。银离子比例的增加导致所形成的双金属核-壳的ζ电势显着降低。 FT-IR揭示了CRD与金属纳米颗粒之间的相互作用,这可能是还原和稳定金属和双金属纳米颗粒的问题。由于Ag和Au的晶格常数接近,XRD图案假设AuNPs和AgNPs-AuNPs核-壳样品的差异不足。在AFM的基础上,AuNPs和AgNPs-AuNPs核壳表现出良好的单分散性,在所研究的样品中具有大小不同的球形颗粒。发现金属和双金属核-壳的平均尺寸分​​别为52和45nm。 (c)2015 Elsevier Ltd.保留所有权利。

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