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研究生: 蔡振庭
Tsai, Chen-Ting
論文名稱: 波長相關拉曼增強在奈米結構平板
Wavelength-dependent Raman Enhancement on Nanostructure Plate
指導教授: 崔祥辰
Chui, Hsiang-Chen
學位類別: 碩士
Master
系所名稱: 理學院 - 光電科學與工程學系
Department of Photonics
論文出版年: 2019
畢業學年度: 107
語文別: 中文
論文頁數: 61
中文關鍵詞: 金奈米結構表面增強式拉曼波長相關
外文關鍵詞: Nanostructure, Surface-Enhanced Raman Scattering, Wavelength-dependent
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  • 近十年來,全球在奈米材料之研究與應用大幅成長,展望21世紀,諸多的科學和技術的發展將根植於奈米技術及材料,也就是將材料應用設計推至原子級 (Atomic Level)和奈米級(Nano Level),預期奈米新材料和量子理論,可望突破目前大部分科技的極限。奈米材料和技術在聲、光、電、磁、熱等領域中,均具有重大的潛在應用前景及產生眾多的未來明星產業。於本論文,我們以金作為材料,研究三種奈米柱樣品(R40、R100、R120)在不同波長的雷射下的表面增強式拉曼,藉此了解樣品的光學性質。
    首先,我們模擬結構在不同介質中的反射率,發現在R40、R100兩樣品的綠光波段反射率較好,而R120在可見光波段反射率表現不佳。接著,我們使用R6G溶液做為表面增強式拉曼的待測物,將結構浸泡於溶液。我們測量R6G的拉曼訊號,分析所有峰值的組成並進行擬合。在相同波長的光源下,我們發現結構R100有最好的表面增強式拉曼效果,結構R120的效果最差。進而比較不同波長的效果,將紅光與綠光功率皆固定在6 mW,在所有條件設定一致下,比較兩組光譜的峰值強度,得知綠光效果較好。我們又使用藍光進行量測,發現藍光下的拉曼光譜較不理想,受到結構本身影響。

    Over the past decade, the researches and applications of nanomaterials has grown up significantly around the world. The scientific and technological developments were rooted in nanotechnology and materials, which is designed to push material were applied to the atomic level and nanoscale. Nano materials and technologies in the fields of sound, light and other applications fields, have significant potential application prospects and produce a large number of future star industries. In this thesis, we use gold as material to study the Surface-Enhanced Raman Scattering (SERS) of three kinds of nano-column samples (R40, R100, R120) under different wavelengths, so as the optical properties of samples.
    First, we simulated the reflectivity of samples in different media. It was found that the reflectance of R40 and R100 these two samples was best in the green band, while the reflectance of R120 in the visible band was not good. We used the Rhodamine 6G (R6G) solution as a surface enhanced Raman medium. We took these structures to soak in the solution. We measured the Raman signals of R6G. Then we analyzed the composition of all the peaks and fitting them. At the same wavelength, the sample R100 had the best Raman enhancement effect, and R120 had the worst effect. The effects of different wavelengths were compared. The red and green power were fixed at 6 mW. We analyzed the Raman spectrum of red laser and green laser. We also found the blue laser is not the ideal wavelength, because the Raman spectrum affected by the structure itself.

    中文摘要 III Abstract IV Extended Absract V 致謝 XIII 目錄 XIV 表目錄 XVI 圖目錄 XVII 第1章 緒論 1 1-1 前言 1 1-2 動機 2 1-3 論文架構 2 第2章 原理與背景 3 2-1微拉曼光譜 3 2-2拉曼散射的物理機制 4 2-3表面增強式拉曼光譜(SERS) 6 2-3-1表面增強式拉曼的歷史與演化 6 2-3-2電磁增強機制 7 2-3-3表面電漿共振 (LSPR) 7 2-3-4化學增強機制 10 2-3-5熱點效應 11 2-3光致螢光(PL) 11 2-4 電子束光刻簡介 12 第3章 實驗儀器與架設 14 3-1 微拉曼系統 14 3-2 樣品與配置 17 3-2-1 奈米陣列樣品 17 3-2-2 羅丹明6G溶液 19 第4章 實驗結果與分析 21 4-1 結構在不同環境下的模擬 21 4-2 光致螢光光譜 22 4-3 樣品的表面增強式拉曼 25 第5章 結論 40 5-1 結論 40 5-2 未來工作 41 Reference 42

    [1] C. Han, S. Liu, Z.-R. Tang, and Y.-J. J. C. O. C. Xu, "One-dimensional Nanostructures for Photocatalytic Organic Synthesis," vol. 19, no. 6, pp. 484-497, 2015.
    [2] Y. Xia et al., "One‐dimensional nanostructures: synthesis, characterization, and applications," vol. 15, no. 5, pp. 353-389, 2003.
    [3] C. V. Raman and K. S. J. N. Krishnan, "A new type of secondary radiation," vol. 121, no. 3048, p. 501, 1928.
    [4] A. Zumbusch, G. R. Holtom, and X. S. J. P. r. l. Xie, "Three-dimensional vibrational imaging by coherent anti-Stokes Raman scattering," vol. 82, no. 20, p. 4142, 1999.
    [5] E. S. a. G. Dent, "Modern Raman Spectroscopy – A Practical Approach," pp. p. 1-4, 2005.
    [6] H. J. P. R. Foley, "The pressure broadening of spectral lines," vol. 69, no. 11-12, p. 616, 1946.
    [7] N. Agarwal et al., "Structure and chain polarization of long polyynes investigated with infrared and Raman spectroscopy," vol. 44, no. 10, pp. 1398-1410, 2013.
    [8] M. Fleischmann, P. J. Hendra, and A. J. J. C. P. L. McQuillan, "Raman spectra of pyridine adsorbed at a silver electrode," vol. 26, no. 2, pp. 163-166, 1974.
    [9] A. Campion and P. J. C. s. r. Kambhampati, "Surface-enhanced Raman scattering," vol. 27, no. 4, pp. 241-250, 1998.
    [10] R. Perez, A. Ruperez, and J. J. A. c. a. Laserna, "Evaluation of silver substrates for surface-enhanced Raman detection of drugs banned in sport practices," vol. 376, no. 2, pp. 255-263, 1998.
    [11] I. Srnová-Šloufová, B. Vlčková, T. L. Snoeck, D. J. Stufkens, and P. J. I. c. Matějka, "Surface-Enhanced Raman Scattering and Surface-Enhanced Resonance Raman Scattering Excitation Profiles of Ag-2, 2 ‘-Bipyridine Surface Complexes and of [Ru (bpy) 3] 2+ on Ag Colloidal Surfaces: Manifestations of the Charge-Transfer Resonance Contributions to the Overall Surface Enhancement of Raman Scattering," vol. 39, no. 16, pp. 3551-3559, 2000.
    [12] P. L. Stiles, J. A. Dieringer, N. C. Shah, and R. P. J. A. R. A. C. Van Duyne, "Surface-enhanced Raman spectroscopy," vol. 1, pp. 601-626, 2008.
    [13] R. A. J. T. j. o. p. c. l. Alvarez-Puebla, "Effects of the Excitation Wavelength on the SERS Spectrum," vol. 3, no. 7, pp. 857-866, 2012.
    [14] W. Cai et al., "Investigation of surface-enhanced Raman scattering from platinum electrodes using a confocal Raman microscope: dependence of surface roughening pretreatment," vol. 406, no. 1-3, pp. 9-22, 1998.
    [15] M. Kuisma et al., "Localized surface plasmon resonance in silver nanoparticles: Atomistic first-principles time-dependent density-functional theory calculations," vol. 91, no. 11, p. 115431, 2015.
    [16] R. Klinkla, U. Pinsook, and S. J. P. Boonchui, "Role of symmetry in coupled localized surface plasmon resonance of a nanosphere pair," vol. 10, no. 3, pp. 643-653, 2015.
    [17] J. A. Sánchez-Gil, J. V. García-Ramos, and E. R. J. O. E. Méndez, "Electromagnetic mechanism in surface-enhanced Raman scattering from Gaussian-correlated randomly rough metal substrates," vol. 10, no. 17, pp. 879-886, 2002.
    [18] K. A. Willets and R. P. J. A. R. P. C. Van Duyne, "Localized surface plasmon resonance spectroscopy and sensing," vol. 58, pp. 267-297, 2007.
    [19] A. M. Michaels, M. Nirmal, and L. J. J. o. t. A. C. S. Brus, "Surface enhanced Raman spectroscopy of individual rhodamine 6G molecules on large Ag nanocrystals," vol. 121, no. 43, pp. 9932-9939, 1999.
    [20] S. Siddhanta, C. J. N. Narayana, and Nanotechnology, "Surface enhanced Raman spectroscopy of proteins: Implications in drug designing," vol. 2, no. Godište 2012, pp. 2-1, 2012.
    [21] J. R. Lombardi, R. L. Birke, T. Lu, and J. J. T. J. o. c. p. Xu, "Charge‐transfer theory of surface enhanced Raman spectroscopy: Herzberg–Teller contributions," vol. 84, no. 8, pp. 4174-4180, 1986.
    [22] Richard W. Taylor, Rubén Esteban, Sumeet Mahajan, Javier Aizpurua, and Jeremy J. Baumberg," Optimizing SERS From Gold Nanoparticle Clusters: Addressing The Near-field By An Embedded Chain Plasmon Model"
    [23] K. Vanheusden, W. L. Warren, C. H. Seager, D. R. Tallant, J. A. Voigt, and B. E. Gnade, "Mechanisms behind green photoluminescence in ZnO phosphor powders," Journal of Applied Physics, vol. 79, no. 10, pp. 7983-7990, 1996.
    [24]https://web.phys.ntu.edu.tw/asc/FunPhysExp/ModernPhys/exp/Microsoft%20Word%20-%20semiconductor%20photoluminescence.pdf 2019/07/08
    [25] K. Li, L. Clime, B. Cui, and T. J. N. Veres, "Surface enhanced Raman scattering on long-range ordered noble-metal nanocrescent arrays," vol. 19, no. 14, p. 145305, 2008.

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