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Synthesis of Silver Nano- and Microstructures for Surface-enhanced Raman Spectroscopy and Applications in Chemo- and Biosensing.

机译:用于表面增强拉曼光谱的银纳米结构和微结构的合成及其在化学和生物传感中的应用。

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摘要

This thesis consists of two parts. Part I covers Chapters 1 to 4, and focuses on the electrochemical synthesis of well-defined Ag nano- and microstructures and their application as substrates in single particle SERS. Part II includes Chapters 5 to 7, and is devoted to the applications of Ag nanoparticle-nanocavity dual-structured network film in SERS-based biosensing.;In Part I, after a concise overview of the relevant work done by others in Chapter 1, Chapters 2 to 4 describe several electrochemical methods for the synthesis of homogeneous Ag structures. Chapter 2 presents a cyclic voltammetric method for the synthesis of homogenous Ag fractal, nest, cube, cubic cage, flower and rod by tuning the concentration of precursor without employing any seeds and surface capping agent (concentration-tuning method). Chapter 3 demonstrates an amperometric method for the synthesis of Ag cube, cubic cage, truncated cube, nest, flower and fractal by changing deposition time only without using any seeds and capping agent (time-tuning method). Chapter 4 reports the electrochemical methods for the synthesis of 2-dimensional Ag fractal matrices on template arrays, with variable size and density. To the best of our knowledge, this is the first report for the synthesis of 2-dimensional noble metal fractal arrays.;The surfaces of the Ag structures synthesized in Chapters 2 to 4 are clean, allowing the chemical modification by desired molecules. The as-prepared Ag structures were employed as the substrates to demonstrate real time, far-field single particle SERS in the study of molecules without (4-mercaptobenzoic acid or 4-MBA) and with electronic resonance (Rhodamine 6G), and with biological relevance (cytochrome-c). The as-prepared Ag structures can be easily visible and tracked under conventional optical microscope, making it very convenient to conduct single particle SERS. Regular Ag structures display high SERS activity attributable to their edges and vertexes. The surface enhancement factor of several types Ag structures reaches as high as ∼108. The as-synthesized Ag fractals display very high activity in SERS with estimated enhancement factors higher than 109.;In Part II, following an introduction of the relevant work done by others in Chapter 5, Chapters 6 and 7 report nonelectrochemically fabricated nanostructured Ag network films, originally developed in our lab, for the detection of single strand DNA (ssDNA) and microRNA (miRNA) in Chapter 6, and a SERS-based aptameric biosensor for ATP detection in Chapter 7. The concentration of the target ssDNA and miRNA at 1 nmol can be easily detected. This platform can differentiate three mismatched bases in the middle of a 26-mer miRNA. On the SERS-based aptameric biosensor, 0.5 µm of ATP can be easily and selectivity detected in the presence of GTP, cAMP and cGMP. These two examples demonstrated that 2-dimensional nanoparticle-nanocavity dual-structured network films can be employed as a good SERS-active substrate for applications in SERS-based biosensing.;At the end, a brief summary and future perspective are given on the basis of the studies carried out in this thesis.
机译:本文分为两部分。第一部分涵盖了第1至第4章,重点介绍了明确定义的Ag纳米和微观结构的电化学合成及其在单颗粒SERS中作为底物的应用。第二部分包括第5至第7章,专门介绍Ag纳米颗粒-纳米度双结构网络膜在基于SERS的生物传感中的应用。第一部分,在简要概述了其他人在第1章中所做的相关工作之后,第2章至第4章介绍了几种用于合成均相Ag结构的电化学方法。第2章介绍了一种循环伏安法,该方法通过不使用任何种子和表面封端剂的情况下调节前体的浓度来合成均质的Ag分形,巢状,立方体状,立方笼状,花状和杆状(浓度调节方法)。第3章演示了仅通过改变沉积时间而无需使用任何种子和加帽剂来合成Ag立方体,立方笼,截头立方体,巢,花和分形的电流法(时间调整方法)。第4章介绍了在尺寸可变和密度可变的模板阵列上合成二维Ag分形矩阵的电化学方法。据我们所知,这是二维贵金属分形阵列合成的第一份报告。在第2章至第4章中合成的Ag结构的表面是干净的,可以通过所需的分子进行化学修饰。所制备的Ag结构被用作底物,以在没有(4-巯基苯甲酸或4-MBA)和电子共振(Rhodamine 6G)且具有生物活性的分子的研究中展示实时,远场单粒子SERS。相关性(cytochrome-c)。所制备的Ag结构可以在常规光学显微镜下轻松看到和追踪,从而非常方便地进行单颗粒SERS。规则的Ag结构显示出高的SERS活性,这归因于其边缘和顶点。几种类型的Ag结构的表面增强因子高达〜108。合成后的Ag分形在SERS中显示出很高的活性,估计的增强因子高于109。第二部分,在第5章,第6章和第7章介绍了其他人所做的相关工作之后,报告了非电化学制备的纳米Ag网络膜,最初是在我们的实验室中开发的,在第6章中用于检测单链DNA(ssDNA)和microRNA(miRNA),在第7章中是用于ATP检测的基于SERS的适体生物传感器。目标ssDNA和miRNA的浓度为1 nmol易于检测。该平台可以区分26-mer miRNA中间的三个错配碱基。在基于SERS的适体生物传感器上,可以轻松检测到0.5 µm的ATP,并在存在GTP,cAMP和cGMP的情况下检测出选择性。这两个例子表明二维纳米颗粒-纳米双结构网络薄膜可以作为良好的SERS活性基质用于基于SERS的生物传感中。最后,在此基础上进行了简要的总结和展望。本文进行的研究。

著录项

  • 作者

    Hu, Jian-Bing.;

  • 作者单位

    Hong Kong University of Science and Technology (Hong Kong).;

  • 授予单位 Hong Kong University of Science and Technology (Hong Kong).;
  • 学科 Chemistry General.;Chemistry Analytical.;Chemistry Physical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 328 p.
  • 总页数 328
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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