生物还原法制备金纳米颗粒的光学非线性

A. Balbuena Ortega, M. L. Arroyo Carrasco, V. L. Gayou, A. Orduña Díaz, R. Delgado Macuil, M. Rojas López
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引用次数: 0

摘要

纳米金属粒子的非线性光学和电子特性由于其强烈的和尺寸相关的等离子体共振吸收而引起了人们的广泛关注。在金属纳米粒子体系中,如分散在透明基质中的金,由于表面等离子体共振,通常在可见光谱区观察到一个吸收峰。金属纳米颗粒由于其相对较大的三阶非线性(χ3)和超快的响应时间而成为光学开关和计算的非线性材料。本研究的目的是分析生物合成金纳米颗粒的非线性光学性质。以酵母提取物为还原剂,采用生物合成法制备了纳米颗粒,并采用功率为20 mW、波长为514 nm的单束z扫描技术研究了纳米颗粒的非线性光学性质。利用金纳米粒子在不同pH(3 ~ 6)水溶液中的紫外可见光谱监测金属离子与酵母提取物的反应。随着pH值变化4 ~ 6,表面等离激元的峰位从528 nm移动到573 nm。采用Fernig法根据吸收峰位置计算平均粒径,范围为42 ~ 103 nm。z扫描曲线显示出负的非局部非线性折射率,其大小与纳米颗粒的大小有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The optical nonlinearity of gold nanoparticles prepared by bioreduction method
Nonlinear optical and electronic properties of nanosized metal particles have drawn considerable attention because of their strong and size-dependent plasmon resonance absorption. In a metal nanoparticle system such as gold dispersed in a transparent matrix, an absorption peak due to surface plasmon resonance is usually observed in the visible spectral region. Metal nanoparticles are of special interest as nonlinear materials for optical switching and computing because of their relatively large third-order nonlinearity (χ3) and ultrafast response time. The purpose of this study was to analyze the nonlinear optical properties of biosynthesized gold nanoparticles. The samples were prepared by biosynthesis method using yeast extract as reducing agent and the nonlinear optical properties of the nanoparticles were investigated using a single beam Z-scan technique with a beam power of 20 mW and operated at wavelength of 514 nm. The reaction between metal ions and yeast extracts were monitored by UV–visible spectra of Au nanoparticles in aqueous solution with different pH (3-6). The surface plasmon peak position was shifted from 528 nm to 573 nm, according to of pH variation 4 to 6. The average particle size was calculated by the absorption peak position using the Fernig method, from 42 to 103 nm. The z-scan curves showed a negative nonlocal nonlinear refractive index with a magnitude dependent on the nanoparticle size.
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