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Journal articles on the topic 'Surface-enhanced Raman spectroscopy'

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Published: 4 June 2021
Last updated: 18 May 2024

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1

NISHINO, Tomoaki. "Surface-enhanced Raman Spectroscopy." Analytical Sciences 34, no. 9 (September 10, 2018): 1061–62. http://dx.doi.org/10.2116/analsci.highlights1809.

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2

Stiles, Paul L., Jon A. Dieringer, Nilam C. Shah, and Richard P. Van Duyne. "Surface-Enhanced Raman Spectroscopy." Annual Review of Analytical Chemistry 1, no. 1 (July 2008): 601–26. http://dx.doi.org/10.1146/annurev.anchem.1.031207.112814.

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3

Haynes, Christy L., Adam D. McFarland, and Richard P. Van Duyne. "Surface-Enhanced Raman Spectroscopy." Analytical Chemistry 77, no. 17 (September 2005): 338 A—346 A. http://dx.doi.org/10.1021/ac053456d.

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4

Garrell, Robin L. "Surface-enhanced Raman spectroscopy." Analytical Chemistry 61, no. 6 (March 15, 1989): 401A—411A. http://dx.doi.org/10.1021/ac00181a001.

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5

Sur, Ujjal Kumar. "Surface-enhanced Raman spectroscopy." Resonance 15, no. 2 (February 2010): 154–64. http://dx.doi.org/10.1007/s12045-010-0016-6.

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6

Popp, Jürgen, and Thomas Mayerhöfer. "Surface-enhanced Raman spectroscopy." Analytical and Bioanalytical Chemistry 394, no. 7 (June 10, 2009): 1717–18. http://dx.doi.org/10.1007/s00216-009-2864-z.

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7

Bell, Steven E. J., and Narayana M. S. Sirimuthu. "Quantitative surface-enhanced Raman spectroscopy." Chemical Society Reviews 37, no. 5 (2008): 1012. http://dx.doi.org/10.1039/b705965p.

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8

Nie, Shuming, Leigh Ann Lipscomb, and Nai-Teng Yu. "Surface-Enhanced Hyper-Raman Spectroscopy." Applied Spectroscopy Reviews 26, no. 3 (September 1991): 203–76. http://dx.doi.org/10.1080/05704929108050881.

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9

Keller, Emily L., Nathaniel C. Brandt, Alyssa A. Cassabaum, and Renee R. Frontiera. "Ultrafast surface-enhanced Raman spectroscopy." Analyst 140, no. 15 (2015): 4922–31. http://dx.doi.org/10.1039/c5an00869g.

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10

Kudelski, Andrzej. "Nanomaterials for Surface Enhanced Raman Spectroscopy." Nanomaterials 13, no. 3 (January 18, 2023): 402. http://dx.doi.org/10.3390/nano13030402.

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11

Shupeng Liu, Shupeng Liu, Lianxin Li Lianxin Li, Zhenyi Chen Zhenyi Chen, Na Chen Na Chen, Zhangmin Dai Zhangmin Dai, Jing Huang Jing Huang, and Bo Lu Bo Lu. "Surface-enhanced Raman spectroscopy measurement of cancerous cells with optical fiber sensor." Chinese Optics Letters 12, s1 (2014): S13001–313003. http://dx.doi.org/10.3788/col201412.s13001.

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12

Qiu, Yuxuan, Cuifang Kuang, Xu Liu, and Longhua Tang. "Single-Molecule Surface-Enhanced Raman Spectroscopy." Sensors 22, no. 13 (June 29, 2022): 4889. http://dx.doi.org/10.3390/s22134889.

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Single-molecule surface-enhanced Raman spectroscopy (SM-SERS) has the potential to detect single molecules in a non-invasive, label-free manner with high-throughput. SM-SERS can detect chemical information of single molecules without statistical averaging and has wide application in chemical analysis, nanoelectronics, biochemical sensing, etc. Recently, a series of unprecedented advances have been realized in science and application by SM-SERS, which has attracted the interest of various fields. In this review, we first elucidate the key concepts of SM-SERS, including enhancement factor (EF), spectral fluctuation, and experimental evidence of single-molecule events. Next, we systematically discuss advanced implementations of SM-SERS, including substrates with ultra-high EF and reproducibility, strategies to improve the probability of molecules being localized in hotspots, and nonmetallic and hybrid substrates. Then, several examples for the application of SM-SERS are proposed, including catalysis, nanoelectronics, and sensing. Finally, we summarize the challenges and future of SM-SERS. We hope this literature review will inspire the interest of researchers in more fields.
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13

Le Ru, Eric C., and Pablo G. Etchegoin. "Single-Molecule Surface-Enhanced Raman Spectroscopy." Annual Review of Physical Chemistry 63, no. 1 (May 5, 2012): 65–87. http://dx.doi.org/10.1146/annurev-physchem-032511-143757.

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14

Frontiera, Renee R., Anne-Isabelle Henry, Natalie L. Gruenke, and Richard P. Van Duyne. "Surface-Enhanced Femtosecond Stimulated Raman Spectroscopy." Journal of Physical Chemistry Letters 2, no. 10 (April 29, 2011): 1199–203. http://dx.doi.org/10.1021/jz200498z.

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15

Barhoumi, Aoune, Dongmao Zhang, Felicia Tam, and Naomi J. Halas. "Surface-Enhanced Raman Spectroscopy of DNA." Journal of the American Chemical Society 130, no. 16 (April 2008): 5523–29. http://dx.doi.org/10.1021/ja800023j.

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16

Tian, Z. Q., W. H. Li, B. W. Mao, S. Z. Zou, and J. S. Gao. "Potential-Averaged Surface-Enhanced Raman Spectroscopy." Applied Spectroscopy 50, no. 12 (December 1996): 1569–77. http://dx.doi.org/10.1366/0003702963904575.

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This paper describes a novel technique called potential-averaged surface-enhanced Raman spectroscopy (PASERS) which has several advantages over SERS. A PASERS spectrum is acquired when the electrode is rapidly modulated between two potentials by applying a square-wave voltage. The potential-averaged SERS spectrum contains all the information on the surface species at the two modulated potentials, and each individual SERS spectrum can then be extracted by deconvolution. By properly choosing the two modulating potentials, one can obtain SERS spectra of surface species at electrode potentials where SERS-active sites are normally unstable. PASERS also leads to a unique way of studying complex interfacial kinetic processes by controlling the voltage pulse height, frequency, and shape. Moreover, the measurement of time-resolved spectra in the very low vibrational frequency region can be achieved by PASERS with the use of a conventional scanning spectrometer with a single-channel detector. In this paper, the main advantages of PASERS are illustrated by studying two typical SERS systems, i.e., thiocyanate ion and thiourea adsorbed at silver electrodes, respectively. It is shown that the potential-averaging method can be applied as a common method to many other existing spectroelectrochemical techniques.
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17

Schedin, Fred, Elefterios Lidorikis, Antonio Lombardo, Vasyl G. Kravets, Andre K. Geim, Alexander N. Grigorenko, Kostya S. Novoselov, and Andrea C. Ferrari. "Surface-Enhanced Raman Spectroscopy of Graphene." ACS Nano 4, no. 10 (September 21, 2010): 5617–26. http://dx.doi.org/10.1021/nn1010842.

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18

Xiong, Min, and Jian Ye. "Reproducibility in surface-enhanced Raman spectroscopy." Journal of Shanghai Jiaotong University (Science) 19, no. 6 (November 30, 2014): 681–90. http://dx.doi.org/10.1007/s12204-014-1566-7.

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19

Abu-Hatab, Nahla A., Joshy F. John, Jenny M. Oran, and Michael J. Sepaniak. "Multiplexed Microfluidic Surface-Enhanced Raman Spectroscopy." Applied Spectroscopy 61, no. 10 (October 2007): 1116–22. http://dx.doi.org/10.1366/000370207782217842.

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Over the past few decades, surface-enhanced Raman spectroscopy (SERS) has garnered respect as an analytical technique with significant chemical and biological applications. SERS is important for the life sciences because it can provide trace level detection, a high level of structural information, and enhanced chemical detection. However, creating and successfully implementing a sensitive, reproducible, and robust SERS active substrate continues to be a challenging task. Herein, we report a novel method for SERS that is based upon using multiplexed microfluidics (MMFs) in a polydimethylsiloxane platform to perform parallel, high throughput, and sensitive detection/identification of single or various analytes under easily manipulated conditions. A facile passive pumping method is used to deliver Ag colloids and analytes into the channels where SERS measurements are done under nondestructive flowing conditions. With this approach, SERS signal reproducibility is found to be better than 7%. Utilizing a very high numerical aperture microscope objective with a confocal-based Raman spectrometer, high sensitivity is achieved. Moreover, the long working distance of this objective coupled with an appreciable channel depth obviates normal alignment issues expected with translational multiplexing. Rapid evaluation of the effects of anion activators and the type of colloid employed on SERS performance are used to demonstrate the efficiency and applicability of the MMF approach. SERS spectra of various pesticides were also obtained. Calibration curves of crystal violet (non-resonant enhanced) and Mitoxantrone (resonant enhanced) were generated, and the major SERS bands of these analytes were observable down to concentrations in the low nM and sub-pM ranges, respectively. While conventional random morphology colloids were used in most of these studies, unique cubic nanoparticles of silver were synthesized with different sizes and studied using visible wavelength optical extinction spectrometry, scanning electron microscopy, and the MMF-SERS approach.
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20

Toscano, G., S. Raza, S. Xiao, M. Wubs, A. P. Jauho, S. I. Bozhevolnyi, and N. A. Mortensen. "Surface-enhanced Raman spectroscopy: nonlocal limitations." Optics Letters 37, no. 13 (June 21, 2012): 2538. http://dx.doi.org/10.1364/ol.37.002538.

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21

Rohr, Thomas E., Therese Cotton, Ni Fan, and Peter J. Tarcha. "Immunoassay employing surface-enhanced Raman spectroscopy." Analytical Biochemistry 182, no. 2 (November 1989): 388–98. http://dx.doi.org/10.1016/0003-2697(89)90613-1.

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22

Hu, Jun, Rong Sheng Sheng, Zhi San Xu, and Yun'e Zeng. "Surface enhanced Raman spectroscopy of lysozyme." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 51, no. 6 (June 1995): 1087–96. http://dx.doi.org/10.1016/0584-8539(94)00225-z.

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23

Zhang, Lu, Chao Meng, Hao Yang, and Wending Zhang. "Azimuthal vector beam illuminating plasmonic tips circular cluster for surface-enhanced Raman spectroscopy." Chinese Optics Letters 21, no. 3 (2023): 033603. http://dx.doi.org/10.3788/col202321.033603.

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24

D’Acunto, Mario. "Surface Enhanced Raman Spectroscopy and Intracellular Components." Proceedings 27, no. 1 (September 20, 2019): 14. http://dx.doi.org/10.3390/proceedings2019027014.

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In the last decade, surface-enhanced Raman spectroscopy (SERS) met increasing interest in the detection of chemical and biological agents due to its rapid performance and ultra-sensitive features. SERS is a combination of Raman spectroscopy and nanotechnology; it includes the advantages of Raman spectroscopy, providing rapid spectra collection, small sample sizes, and characteristic spectral fingerprints for specific analytes. In this paper, we detected label-free SERS signals for arbitrarily configurations of dimers, trimers, etc., composed of gold nanoshells (AuNSs) and applied to the mapping of osteosarcoma intracellular components.
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25

PETTINGER, Bruno, Gennaro PICARDI, Rolf SCHUSTER, and Gerhard ERTL. "Surface Enhanced Raman Spectroscopy: Towards Single Molecule Spectroscopy." Electrochemistry 68, no. 12 (December 5, 2000): 942–49. http://dx.doi.org/10.5796/electrochemistry.68.942.

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26

Sinha, Rajeev K. "An Inexpensive Raman, Spectroscopy Setup for Raman, Polarized Raman, and Surface Enhanced Raman, Spectroscopy." Instruments and Experimental Techniques 64, no. 6 (November 2021): 840–47. http://dx.doi.org/10.1134/s002044122106018x.

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27

Vo-Dinh, T., and D. L. Stokes. "Surface-Enhanced Raman Vapor Dosimeter." Applied Spectroscopy 47, no. 10 (October 1993): 1728–32. http://dx.doi.org/10.1366/0003702934334679.

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This paper describes a new direct-reading personal dosimeter designed to detect vapors of organic chemicals. The device employs the surface-enhanced Raman scattering (SERS) technique for direct measurement of the amount of analyte collected on the dosimeter, requiring no sample desorption or wet-chemical extraction procedure. The time-weighted average exposure to the chemical vapors can be determined on the dosimeter substrate. The results with benzoic acid used as the model compound illustrate the usefulness of this SERS-based dosimeter.
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28

Panneerselvam, Rajapandiyan, Guo-Kun Liu, Yao-Hui Wang, Jun-Yang Liu, Song-Yuan Ding, Jian-Feng Li, De-Yin Wu, and Zhong-Qun Tian. "Surface-enhanced Raman spectroscopy: bottlenecks and future directions." Chemical Communications 54, no. 1 (2018): 10–25. http://dx.doi.org/10.1039/c7cc05979e.

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This feature article discusses developmental bottleneck issues in surface Raman spectroscopy in its early stages and surface-enhanced Raman spectroscopy (SERS) in the past four decades and future perspectives.
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29

Sánchez-Cortés, S., M. Vasina, O. Francioso, and J. V. Garcı́a-Ramos. "Raman and surface-enhanced Raman spectroscopy of dithiocarbamate fungicides." Vibrational Spectroscopy 17, no. 2 (September 1998): 133–44. http://dx.doi.org/10.1016/s0924-2031(98)00025-3.

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30

Leopold, N., J. R. Baena, M. Bolboacǎ, O. Cozar, W. Kiefer, and B. Lendl. "Raman, IR, and surface-enhanced Raman spectroscopy of papaverine." Vibrational Spectroscopy 36, no. 1 (October 2004): 47–55. http://dx.doi.org/10.1016/j.vibspec.2004.02.008.

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31

Matsukovich, A. S., E. V. Shabunya-Klyachkovskaya, M. Sawczak, K. Grochowska, D. Maskowicz, and G. Śliwiński. "Gold Nanoparticles for Surface-Enhanced Raman Spectroscopy." International Journal of Nanoscience 18, no. 03n04 (June 2019): 1940069. http://dx.doi.org/10.1142/s0219581x19400696.

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This work shows comparative analysis of surface-enhanced Raman scattering (SERS) activity of gold nanoparticles fabricated by chemical synthesis and laser ablation methods. The gold nanoparticles prepared by laser ablation (Au-LA) are more effective for SERS than those prepared chemically (Au-citr). The “analyte on Au film” configuration allows obtaining enhancement of Raman scattering up to 104 in case of Au-LA nanoparticles and up to 102 in case of Au-citr. Also the “sandwich” configuration for Au-LA gives additional enhancement of SERS up to two times, and for Au-citr up to one order, that is consistent with theoretical calculations.
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32

Gruenke, Natalie L., M. Fernanda Cardinal, Michael O. McAnally, Renee R. Frontiera, George C. Schatz, and Richard P. Van Duyne. "Ultrafast and nonlinear surface-enhanced Raman spectroscopy." Chemical Society Reviews 45, no. 8 (2016): 2263–90. http://dx.doi.org/10.1039/c5cs00763a.

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33

Feng Shangyuan, 冯尚源, 陈荣 Chen Rong, 李永增 Li Yongzeng, 陈冠楠 Chen Guannan, 林居强 Lin Juqiang, 林文硕 Lin Wenshuo, 陈伟炜 Chen Weiwei, 陈杰斯 Chen Jiesi, and 俞允 Yu Yun. "Surface-Enhanced Raman Spectroscopy of Dangshen Decoction." Chinese Journal of Lasers 37, no. 1 (2010): 121–24. http://dx.doi.org/10.3788/cjl20103701.0121.

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34

Meheretu, Getnet Melese, Dana Cialla, and J. Popp. "Surface Enhanced Raman Spectroscopy on Silver Nanoparticles." International Journal of Biochemistry and Biophysics 2, no. 4 (October 2014): 63–67. http://dx.doi.org/10.13189/ijbb.2014.020403.

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35

Zhang Ming, 张. 明., 朱绍玲 Zhu Shaoling, 高. 飞. Gao Fei, and 罗. 果. Luo Guo. "Breast cancer oxyhemoglobin surface enhanced Raman spectroscopy." Infrared and Laser Engineering 46, no. 4 (2017): 433001. http://dx.doi.org/10.3788/irla201746.0433001.

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36

Wu, De-Yin, Jian-Feng Li, Bin Ren, and Zhong-Qun Tian. "Electrochemical surface-enhanced Raman spectroscopy of nanostructures." Chemical Society Reviews 37, no. 5 (2008): 1025. http://dx.doi.org/10.1039/b707872m.

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37

Ding, Song-Yuan, En-Ming You, Zhong-Qun Tian, and Martin Moskovits. "Electromagnetic theories of surface-enhanced Raman spectroscopy." Chemical Society Reviews 46, no. 13 (2017): 4042–76. http://dx.doi.org/10.1039/c7cs00238f.

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38

Alvarez-Puebla, Ramo´n A., Xing Yi Ling, Patrizio Candeloro, and Marc Lamy de la Chapelle. "Special issue on surface-enhanced Raman spectroscopy." Journal of Optics 17, no. 11 (October 23, 2015): 110201. http://dx.doi.org/10.1088/2040-8978/17/11/110201.

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39

Ran An, 安冉, 欧全宏 Quanhong Ou, 刘刚 Gang Liu, 杨卫梅 Weimei Yang, 符致秋 Zhiqiu Fu, 李建美 Jianmei Li, and 时有明 Youming Shi. "Surface-Enhanced Raman Spectroscopy of Mushroom Spores." Laser & Optoelectronics Progress 56, no. 15 (2019): 153001. http://dx.doi.org/10.3788/lop56.153001.

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40

McFarland, Adam D., Matthew A. Young, Jon A. Dieringer, and Richard P. Van Duyne. "Wavelength-Scanned Surface-Enhanced Raman Excitation Spectroscopy." Journal of Physical Chemistry B 109, no. 22 (June 2005): 11279–85. http://dx.doi.org/10.1021/jp050508u.

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41

Nagai, Yusuke, Tatsuya Yamaguchi, and Kotaro Kajikawa. "Angular-Resolved Polarized Surface Enhanced Raman Spectroscopy." Journal of Physical Chemistry C 116, no. 17 (April 23, 2012): 9716–23. http://dx.doi.org/10.1021/jp211234p.

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42

Lorén, A., J. Engelbrektsson, C. Eliasson, M. Josefson, J. Abrahamsson, M. Johansson, and K. Abrahamsson. "Internal Standard in Surface-Enhanced Raman Spectroscopy." Analytical Chemistry 76, no. 24 (December 2004): 7391–95. http://dx.doi.org/10.1021/ac0491298.

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43

Perevedentseva, E., A. Karmenyan, P. H. Chung, Y. T. He, and C. L. Cheng. "Surface enhanced Raman spectroscopy of carbon nanostructures." Surface Science 600, no. 18 (September 2006): 3723–28. http://dx.doi.org/10.1016/j.susc.2006.01.074.

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44

Milekhin, A. G., L. L. Sveshnikova, T. A. Duda, N. A. Yeryukov, E. E. Rodyakina, A. K. Gutakovskii, S. A. Batsanov, A. V. Latyshev, and D. R. T. Zahn. "Surface-enhanced Raman spectroscopy of semiconductor nanostructures." Physica E: Low-dimensional Systems and Nanostructures 75 (January 2016): 210–22. http://dx.doi.org/10.1016/j.physe.2015.09.013.

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45

Chauvet, Romain, Fabienne Lagarde, Thomas Charrier, Ali Assaf, Gerald Thouand, and Philippe Daniel. "Microbiological identification by surface-enhanced Raman spectroscopy." Applied Spectroscopy Reviews 52, no. 2 (July 7, 2016): 123–44. http://dx.doi.org/10.1080/05704928.2016.1209760.

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46

Haynes, Christy L., and Richard P. Van Duyne. "Plasmon-Sampled Surface-Enhanced Raman Excitation Spectroscopy†." Journal of Physical Chemistry B 107, no. 30 (July 2003): 7426–33. http://dx.doi.org/10.1021/jp027749b.

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47

Lemma, Tibebe, Jin Wang, Kai Arstila, Vesa P. Hytönen, and J. Jussi Toppari. "Identifying yeasts using surface enhanced Raman spectroscopy." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 218 (July 2019): 299–307. http://dx.doi.org/10.1016/j.saa.2019.04.010.

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48

Durucan, Onur, Tomas Rindzevicius, Michael Stenbæk Schmidt, Marco Matteucci, and Anja Boisen. "Nanopillar Filters for Surface-Enhanced Raman Spectroscopy." ACS Sensors 2, no. 10 (September 29, 2017): 1400–1404. http://dx.doi.org/10.1021/acssensors.7b00499.

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49

Lin, Xiu-Mei, Yan Cui, Yan-Hui Xu, Bin Ren, and Zhong-Qun Tian. "Surface-enhanced Raman spectroscopy: substrate-related issues." Analytical and Bioanalytical Chemistry 394, no. 7 (April 19, 2009): 1729–45. http://dx.doi.org/10.1007/s00216-009-2761-5.

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50

Vongsvivut, Jitraporn, Evan G. Robertson, and Don McNaughton. "Surface-Enhanced Raman Scattering Spectroscopy of Resveratrol." Australian Journal of Chemistry 61, no. 12 (2008): 921. http://dx.doi.org/10.1071/ch08204.

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We report here, for the first time, the surface-enhanced Raman scattering (SERS) spectra of resveratrol using KNO3-aggregated citrate-reduced silver (Ag) colloids. The technique provided a substantial spectral enhancement and therefore good quality spectra of resveratrol at parts per million (ppm) concentrations. The detection limit was found to be <1 μM, equivalent to <0.2 ppm. The SERS profile additionally closely resembled its normal solid-state Raman spectrum with some changes in relative intensity. These intensity changes, together with a precise band assignment aided by density functional theory calculations at the B3LYP/6–31G(d) level, allowed the determination of the structural orientation of the adsorbed resveratrol on the surface of the metal nanoparticles. In particular, the SERS spectra obtained at different resveratrol concentrations exhibited concentration-dependent features, suggesting an influence of surface coverage on the orientation of the adsorbed molecules. At a high concentration, an adoption of close-to-upright orientation of resveratrol adsorbed on the metal surface through the p-OH phenyl ring is favoured. The binding structure is, however, altered at lower surface coverage when the concentration decreases to a tilted orientation with the trans-olefin C=C bond aligning closer to parallel to the surface of the Ag nanoparticles.
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