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用于增强表面增强拉曼光谱的镀金超薄阳极多孔氧化铝基底的制备

Fabrication of Gold-Coated Ultra-Thin Anodic Porous Alumina Substrates for Augmented SERS.

作者信息

Toccafondi Chiara, Proietti Zaccaria Remo, Dante Silvia, Salerno Marco

机构信息

Nanophysics Department, Istituto Italiano di Tecnologia, Genova 16163, Italy.

Laboratoire de Physique des Interfaces et des Couches Minces (LPICM), Centre National de la Recherche Scientifique (CNRS), Ecole Polytechnique, Université Paris Saclay, Palaiseau 91128, France.

出版信息

Materials (Basel). 2016 May 24;9(6):403. doi: 10.3390/ma9060403.

Abstract

Anodic porous alumina (APA) is a nanostructured material used as a template in several nanotechnological applications. We propose the use of APA in ultra-thin form (<100 nm) for augmented surface-enhanced Raman scattering (SERS). Here, the effect of in-depth thinning of the APA nanostructures for possible maximization of SERS was addressed. Anodization was carried out on ultra-thin films of aluminum on glass and/or silicon, followed by pore-opening. Gold (Au) was overcoated and micro‑Raman/SERS measurements were carried out on test target analytes. Finite integration technique simulations of the APA-Au substrate were used both for the experimental design and simulations. It was observed that, under optimized conditions of APA and Au thickness, the SERS enhancement is higher than on standard APA-Au substrates based on thin (~100 nm) APA by up to a factor of ~20 for test molecules of mercaptobenzoic acid. The agreement between model and experimental results confirms the current understanding of SERS as being mainly due to the physical origin of plasmon resonances. The reported results represent one step towards micro-technological, integrated, disposable, high-sensitivity SERS chemical sensors and biosensors based on similar substrates.

摘要

阳极多孔氧化铝(APA)是一种纳米结构材料,在多种纳米技术应用中用作模板。我们提议使用超薄形式(<100 nm)的APA来增强表面增强拉曼散射(SERS)。在此,研究了APA纳米结构深度减薄对实现SERS最大化的影响。在玻璃和/或硅上的铝超薄膜上进行阳极氧化,随后进行开孔。在其上覆盖金(Au),并对测试目标分析物进行显微拉曼/SERS测量。APA-Au基底的有限积分技术模拟用于实验设计和模拟。观察到,在APA和Au厚度的优化条件下,对于巯基苯甲酸测试分子,SERS增强比基于约100 nm厚的APA的标准APA-Au基底高出约20倍。模型与实验结果之间的一致性证实了目前对SERS主要源于等离子体共振物理起源的理解。所报道的结果代表了朝着基于类似基底的微型技术、集成、一次性、高灵敏度SERS化学传感器和生物传感器迈出的一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff93/5456800/af5879e18e3d/materials-09-00403-g001.jpg

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