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Journal articles on the topic 'Surface plasmon resonance spectroscopy'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Haes, Amanda J., Shengli Zou, Jing Zhao, George C. Schatz, and Richard P. Van Duyne. "Localized Surface Plasmon Resonance Spectroscopy near Molecular Resonances." Journal of the American Chemical Society 128, no. 33 (August 2006): 10905–14. http://dx.doi.org/10.1021/ja063575q.

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2

Ikehata, Akifumi, Tamitake Itoh, and Yukihiro Ozaki. "Surface Plasmon Resonance Near-Infrared Spectroscopy." Analytical Chemistry 76, no. 21 (November 2004): 6461–69. http://dx.doi.org/10.1021/ac049003a.

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3

Tao, N. J., S. Boussaad, W. L. Huang, R. A. Arechabaleta, and J. D’Agnese. "High resolution surface plasmon resonance spectroscopy." Review of Scientific Instruments 70, no. 12 (December 1999): 4656–60. http://dx.doi.org/10.1063/1.1150128.

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4

Ikehata, Akifumi. "Surface Plasmon Resonance near Infrared Spectroscopy." NIR news 16, no. 1 (February 2005): 10–11. http://dx.doi.org/10.1255/nirn.802.

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5

Rheinberger, Timo, Daniel Ohm, Ulmas E. Zhumaev, and Katrin F. Domke. "Extending surface plasmon resonance spectroscopy to platinum surfaces." Electrochimica Acta 314 (August 2019): 96–101. http://dx.doi.org/10.1016/j.electacta.2019.05.063.

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6

LI, Ping, Wei ZHANG, and WeiDong HE. "Surface-enhanced spectroscopy and surface plasmon resonance sensor." Chinese Science Bulletin 56, no. 20 (July 1, 2011): 1585–92. http://dx.doi.org/10.1360/972010-2202.

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7

Willets, Katherine A., and Richard P. Van Duyne. "Localized Surface Plasmon Resonance Spectroscopy and Sensing." Annual Review of Physical Chemistry 58, no. 1 (May 2007): 267–97. http://dx.doi.org/10.1146/annurev.physchem.58.032806.104607.

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8

Chegel, V. I., and Yu M. Shirshov. "SURFACE PLASMON RESONANCE SPECTROSCOPY: POTENTIALITIES AND LIMITATIONS." Sensor Electronics and Microsystem Technologies 1, no. 2 (October 11, 2014): 34–49. http://dx.doi.org/10.18524/1815-7459.2004.2.111890.

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9

Sarkar, Diptabhas, and P. Somasundaran. "Overcoming Contamination in Surface Plasmon Resonance Spectroscopy." Langmuir 18, no. 22 (October 2002): 8271–77. http://dx.doi.org/10.1021/la020130g.

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10

Berezhinsky, L. J., L. S. Maksimenko, I. E. Matyash, S. P. Rudenko, and B. K. Serdega. "Polarization modulation spectroscopy of surface plasmon resonance." Optics and Spectroscopy 105, no. 2 (August 2008): 257–64. http://dx.doi.org/10.1134/s0030400x08080146.

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11

Menegazzo, Nicola, Laurel L. Kegel, Yoon-Chang Kim, Derrick L. Allen, and Karl S. Booksh. "Adaptable infrared surface plasmon resonance spectroscopy accessory." Review of Scientific Instruments 83, no. 9 (September 2012): 095113. http://dx.doi.org/10.1063/1.4752463.

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12

Salamon, Zdzislaw, and Gordon Tollin. "Plasmon resonance spectroscopy: probing molecular interactions at surfaces and interfaces." Spectroscopy 15, no. 3,4 (2001): 161–75. http://dx.doi.org/10.1155/2001/907405.

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Surface plasmon resonance (SPR) spectroscopy can be applied to a wide variety of interfacial systems. It involves resonant excitation by polarized light of electronic oscillations (plasmons) in a thin metal film. These generate a surface‒localized evanescent electromagnetic field that can be used to probe the optical properties perpendicular to the film plane of materials immobilized at the surface. Spectra depend on three parameters: refractive index (n), absorption coefficient (k) and thickness (t). Maxwell's equations provide an analytical relationship between these properties and SPR spectra, allowing their evaluation. An extension of this methodology, called coupled plasmon‒waveguide resonance (CPWR or PWR), is able to characterize film propertiesbothperpendicular and parallel to the surface plane. In a PWR device, the metal film is covered with a dielectric coating that acts as an optical amplifier, provides protection for the metal layer, and possesses a surface that allows various molecular immobilization strategies. The exceptionally narrow line widths of PWR spectra yield enhanced sensitivity and resolution. The application of this technology to several biomembrane systems will be described, demonstrating its ability to observe both binding and structural events occurring during membrane protein function.

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13

Morigaki, Kenichi, and Keiko Tawa. "Vesicle Fusion Studied by Surface Plasmon Resonance and Surface Plasmon Fluorescence Spectroscopy." Biophysical Journal 91, no. 4 (August 2006): 1380–87. http://dx.doi.org/10.1529/biophysj.106.086074.

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14

Liu, Xia, Daqian Song, Qinglin Zhang, Yuan Tian, Lan Ding, and Hanqi Zhang. "Wavelength-modulation surface plasmon resonance sensor." TrAC Trends in Analytical Chemistry 24, no. 10 (November 2005): 887–93. http://dx.doi.org/10.1016/j.trac.2005.05.010.

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15

Sagle, Laura B., Laura K. Ruvuna, Julia A. Ruemmele, and Richard P. Van Duyne. "Advances in localized surface plasmon resonance spectroscopy biosensing." Nanomedicine 6, no. 8 (October 2011): 1447–62. http://dx.doi.org/10.2217/nnm.11.117.

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16

Shimizu, Ken T., Ragip A. Pala, Jason D. Fabbri, Mark L. Brongersma, and Nicholas A. Melosh. "Probing Molecular Junctions Using Surface Plasmon Resonance Spectroscopy." Nano Letters 6, no. 12 (December 2006): 2797–803. http://dx.doi.org/10.1021/nl061893h.

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17

Lahav, Michal, Alexander Vaskevich, and Israel Rubinstein. "Biological Sensing Using Transmission Surface Plasmon Resonance Spectroscopy." Langmuir 20, no. 18 (August 2004): 7365–67. http://dx.doi.org/10.1021/la0489054.

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18

Zhang, Zhe, Leona Nest, Suo Wang, Si-Yi Wang, and Ren-Min Ma. "Lasing-enhanced surface plasmon resonance spectroscopy and sensing." Photonics Research 9, no. 9 (August 11, 2021): 1699. http://dx.doi.org/10.1364/prj.431612.

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19

Tang, Yijun, Xiangqun Zeng, and Jennifer Liang. "Surface Plasmon Resonance: An Introduction to a Surface Spectroscopy Technique." Journal of Chemical Education 87, no. 7 (July 2010): 742–46. http://dx.doi.org/10.1021/ed100186y.

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20

Tawa, Keiko, and Kenichi Morigaki. "Substrate-Supported Phospholipid Membranes Studied by Surface Plasmon Resonance and Surface Plasmon Fluorescence Spectroscopy." Biophysical Journal 89, no. 4 (October 2005): 2750–58. http://dx.doi.org/10.1529/biophysj.105.065482.

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21

Halas, Naomi. "Playing with Plasmons: Tuning the Optical Resonant Properties of Metallic Nanoshells." MRS Bulletin 30, no. 5 (May 2005): 362–67. http://dx.doi.org/10.1557/mrs2005.99.

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AbstractNanoshells, concentric nanoparticles consisting of a dielectric core and a metallic shell, are simple spherical nanostructures with unique, geometrically tunable optical resonances. As with all metallic nanostructures, their optical properties are controlled by the collective electronic resonance, or plasmon resonance, of the constituent metal, typically silver or gold. In striking contrast to the resonant properties of solid metallic nanostructures, which exhibit only a weak tunability with size or aspect ratio, the optical resonance of a nanoshell is extraordinarily sensitive to the inner and outer dimensions of the metallic shell layer. The underlying reason for this lies beyond classical electromagnetic theory, where plasmon-resonant nanoparticles follow a mesoscale analogue of molecular orbital theory, hybridizing in precisely the same manner as the individual atomic wave functions in simple molecules. This plasmon hybridization picture provides an essential “design rule” for metallic nanostructures that can allow us to effectively predict their optical resonant properties. Such a systematic control of the far-field optical resonances of metallic nanostructures is accomplished simultaneously with control of the field at the surface of the nanostructure. The nanoshell geometry is ideal for tuning and optimizing the near-field response as a stand-alone surface-enhanced Raman spectroscopy (SERS) nanosensor substrate and as a surface-plasmon-resonant nanosensor.Tuning the plasmon resonance of nanoshells into the near-infrared region of the spectrum has enabled a variety of biomedical applications that exploit the strong optical contrast available with nanoshells in a spectral region where blood and tissue are optimally transparent.

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22

Kooyman, R. P. H., H. Kolkman, J. Van Gent, and J. Greve. "Surface plasmon resonance immunosensors: sensitivity considerations." Analytica Chimica Acta 213 (1988): 35–45. http://dx.doi.org/10.1016/s0003-2670(00)81337-9.

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23

Wei, Zhongxia, Peng Mao, Lu Cao, and Fengqi Song. "Probing plasmon resonances of individual aluminum nanoparticles." Modern Physics Letters B 32, no. 03 (January 29, 2018): 1850032. http://dx.doi.org/10.1142/s021798491850032x.

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The plasmon resonances of individual aluminum nanoparticles are investigated by electron energy-loss spectroscopy (EELS) in scanning transmission electron microscope (STEM). Surface plasmon mode and bulk plasmon mode of Al nanoparticles are clearly characterized in the EEL spectra. Discrete dipole approximation (DDA) calculations show that as the particle diameter increases from 20 nm to 100 nm, the plasmon resonance shifts to lower energy and higher mode of surface plasmon arises when the diameter reaches 60 nm and larger.

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24

Wang, Jiangcai, Weihua Lin, En Cao, Xuefeng Xu, Wenjie Liang, and Xiaofang Zhang. "Surface Plasmon Resonance Sensors on Raman and Fluorescence Spectroscopy." Sensors 17, no. 12 (November 24, 2017): 2719. http://dx.doi.org/10.3390/s17122719.

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25

Ekgasit, Sanong, Chuchaat Thammacharoen, and Wolfgang Knoll. "Surface Plasmon Resonance Spectroscopy Based on Evanescent Field Treatment." Analytical Chemistry 76, no. 3 (February 2004): 561–68. http://dx.doi.org/10.1021/ac035042v.

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26

Maurat, E., P.-A. Hervieux, and F. Lépine. "Surface plasmon resonance in C60revealed by photoelectron imaging spectroscopy." Journal of Physics B: Atomic, Molecular and Optical Physics 42, no. 16 (July 27, 2009): 165105. http://dx.doi.org/10.1088/0953-4075/42/16/165105.

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27

Serrano, A., O. Rodríguez de la Fuente, V. Collado, J. Rubio-Zuazo, C. Monton, G. R. Castro, and M. A. García. "Simultaneous surface plasmon resonance and x-ray absorption spectroscopy." Review of Scientific Instruments 83, no. 8 (August 2012): 083101. http://dx.doi.org/10.1063/1.4739773.

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28

Sherry, Leif J., Shih-Hui Chang, George C. Schatz, Richard P. Van Duyne, Benjamin J. Wiley, and Younan Xia. "Localized Surface Plasmon Resonance Spectroscopy of Single Silver Nanocubes." Nano Letters 5, no. 10 (October 2005): 2034–38. http://dx.doi.org/10.1021/nl0515753.

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29

Gandubert, Valérie J., and R. Bruce Lennox. "Surface Plasmon Resonance Spectroscopy Study of Electrostatically Adsorbed Layers." Langmuir 22, no. 10 (May 2006): 4589–93. http://dx.doi.org/10.1021/la052751q.

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30

Chan, George H., Jing Zhao, George C. Schatz, and Richard P. Van Duyne. "Localized Surface Plasmon Resonance Spectroscopy of Triangular Aluminum Nanoparticles." Journal of Physical Chemistry C 112, no. 36 (August 15, 2008): 13958–63. http://dx.doi.org/10.1021/jp804088z.

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31

Zhang, Xiaoyu, Chanda Ranjit Yonzon, and Richard P. Van Duyne. "Nanosphere lithography fabricated plasmonic materials and their applications." Journal of Materials Research 21, no. 5 (May 1, 2006): 1083–92. http://dx.doi.org/10.1557/jmr.2006.0136.

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Nanosphere lithography fabricated nanostructures have highly tunable localized surface plasmons, which have been used for important sensing and spectroscopy applications. In this work, the authors focus on biological applications and technologies that utilize two types of related plasmonic phenomena: localized surface plasmon resonance (LSPR) spectroscopy and surface-enhanced Raman spectroscopy (SERS). Two applications of these plasmonic materials are presented: (i) the development of an ultrasensitive nanoscale optical biosensor based on LSPR wavelength-shift spectroscopy and (ii) the SERS detection of an anthrax biomarker.

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32

Reyes Gómez, Faustino, Rafael Rubira, Sabrina Camacho, Cibely Martin, Robson da Silva, Carlos Constantino, Priscila Alessio, Osvaldo Oliveira, and J. Mejía-Salazar. "Surface Plasmon Resonances in Silver Nanostars." Sensors 18, no. 11 (November 8, 2018): 3821. http://dx.doi.org/10.3390/s18113821.

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The recent development of silver nanostars (Ag-NSs) is promising for improved surface-enhanced sensing and spectroscopy, which may be further exploited if the mechanisms behind the excitation of localized surface plasmon resonances (LSPRs) are identified. Here, we show that LSPRs in Ag-NSs can be obtained with finite-difference time-domain (FDTD) calculations by considering the nanostars as combination of crossed nanorods (Ag-NRs). In particular, we demonstrate that an apparent tail at large wavelengths ( λ ≳ 700 nm) observed in the extinction spectra of Ag-NSs is due to a strong dipolar plasmon resonance, with no need to invoke heterogeneity (different number of arms) effects as is normally done in the literature. Our description also indicates a way to tune the strongest LSPR at desired wavelengths, which is useful for sensing applications.

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33

Bouafsoun, Amira, Nicole Jaffrezic-Renault, and Laurence Mora. "Spectroscopy Resonance Plasmon Efficient Tool for Cell Adsorption." Journal of Nano Research 59 (August 2019): 35–45. http://dx.doi.org/10.4028/www.scientific.net/jnanor.59.35.

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It is important to analyze cell monolayer adherence for the development of biomedical devices of anti-thrombogenic vascular grafts. Endothelial cells must be firmly attached to the biomaterials when cells are seeded in order to create a natural lining. Polystyrene (PS) is presented as a reproducible implant model substrate for studying cell – material interactions. Polystyrene was deposited as a thin layer on a thiol functionalized gold electrode. Fibronectin (Fn), a protein promoting the cell monolayer adhesion was adsorbed on PS surface. The different steps of this multilayer assembly were characterized by Surface Plasmon Resonance (SPR) technique. A right shift of the SPR resonance angle θSPR was observed leading an increase from 65.5 deg in the case of gold electrode to 66.8 deg in the case where cell monolayer was cultured onto functionalized gold substrate. A shift in the SPR peak minimum intensity was detected in the SPR response of Au/Thiol/PS/Fn and Au/Thiol/PS/Fn/Cell multilayer assembly structures. This result is explained using Atomic Force Microscopy (AFM) images and according transverse profiles which indicate surface morphological modifications in term of thickness.

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34

Ma, Zhenhe, Yafei Li, Qiongchan Gu, Sheng Hu, Yu Ying, Zhigang Li, Xiaoxiao Jiang, and Jiangtao Lv. "Dynamic Plasmon Resonance Tuning for Surface Enhanced Sensing." Journal of Nanoscience and Nanotechnology 19, no. 6 (June 1, 2019): 3643–46. http://dx.doi.org/10.1166/jnn.2019.16118.

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We report on fabricating plasmonic nanorod crystals using focused ion beam lithography. We first demonstrate manipulating the profiles of nanorods perpendicularly aligned with the substrate. Then we show accurate control of nanorod outlines can be achieved. We also show that it is feasible to manufacture nanorods obliquely aligned with the substrate. Tunable plasmon resonance can be realized with different tilting angles and geometries. Our approach may find important applications in plasmon-assisted sensing and surface enhanced spectroscopy.

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35

Fang, Shiping, Hye Jin Lee, Alastair W. Wark, Hyun Min Kim, and Robert M. Corn. "Determination of Ribonuclease H Surface Enzyme Kinetics by Surface Plasmon Resonance Imaging and Surface Plasmon Fluorescence Spectroscopy." Analytical Chemistry 77, no. 20 (October 2005): 6528–34. http://dx.doi.org/10.1021/ac051283m.

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36

Foerster, Benjamin, Vincent A. Spata, Emily A. Carter, Carsten Sönnichsen, and Stephan Link. "Plasmon damping depends on the chemical nature of the nanoparticle interface." Science Advances 5, no. 3 (March 2019): eaav0704. http://dx.doi.org/10.1126/sciadv.aav0704.

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The chemical nature of surface adsorbates affects the localized surface plasmon resonance of metal nanoparticles. However, classical electromagnetic simulations are blind to this effect, whereas experiments are typically plagued by ensemble averaging that also includes size and shape variations. In this work, we are able to isolate the contribution of surface adsorbates to the plasmon resonance by carefully selecting adsorbate isomers, using single-particle spectroscopy to obtain homogeneous linewidths, and comparing experimental results to high-level quantum mechanical calculations based on embedded correlated wavefunction theory. Our approach allows us to indisputably show that nanoparticle plasmons are influenced by the chemical nature of the adsorbates 1,7-dicarbadodecaborane(12)-1-thiol (M1) and 1,7-dicarbadodecaborane(12)-9-thiol (M9). These surface adsorbates induce inside the metal electric dipoles that act as additional scattering centers for plasmon dephasing. In contrast, charge transfer from the plasmon to adsorbates—the most widely suggested mechanism to date—does not play a role here.

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37

Kashyap, Ritayan, Soumik Chakraborty, Shuwen Zeng, Sikha Swarnakar, Simran Kaur, Robin Doley, and Biplob Mondal. "Enhanced Biosensing Activity of Bimetallic Surface Plasmon Resonance Sensor." Photonics 6, no. 4 (October 21, 2019): 108. http://dx.doi.org/10.3390/photonics6040108.

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Surface plasmon resonance (SPR) sensors present a challenge when high sensitivity and small FWHM (full width at half maximum) are required to be achieved simultaneously. FWHM is defined by the difference between the two extreme values of the independent variable at which the value of the dependent variable is equal to half of its maximum. A smaller value of FWHM indicates better accuracy of SPR measurements. Theoretically, many authors have claimed the possibility of simultaneously achieving high sensitivity and small FWHM, which in most of the cases has been limited by experimental validation. In this report, an experimental study on the improved surface plasmon resonance (SPR) characteristics of gold over silver bimetallic sensor chips of different film thicknesses is presented. A comparative study of antigen–antibody interaction of the bimetallic chip using a custom-made, low-cost, and portable SPR device based on an angular interrogation scheme of Kretschmann configuration is performed. Pulsed direct current (DC) magnetron-sputtered bimetallic films of gold over silver were used in the construction of the SPR chip. The FWHM and sensitivity of the bimetallic sensors were firstly characterized using standard solutions of known refractive index which were later immobilized with monoclonal anti-immunoglobulin G (IgG) in the construction of the SPR biochip. Spectroscopic measurements such as ultraviolet–visible light spectroscopy (UV–Vis) and Fourier-transform infrared spectroscopy (FTIR) were used for the confirmation of the immobilization of the antibody. The performance of the bimetallic SPR biochip was investigated by exposing the sensor to various concentrations of the target protein. The results indicated that the bimetallic sensors of silver/gold had a 3.5-fold reduced FWHM compared to pure gold-based sensors, indicating a higher detection accuracy. In addition, they exhibited a significant shift in resonance angle as high as 8.5 ± 0.2 due to antigen–antibody interaction, which was ~1.42-fold higher than observed for pure silver-based sensors.

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38

Della Gaspera, Enrico, and Alessandro Martucci. "Detecting H2S oscillatory response using surface plasmon spectroscopy." MRS Proceedings 1552 (2013): 77–82. http://dx.doi.org/10.1557/opl.2013.713.

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ABSTRACTThe oscillatory change in the optical absorbance of NiO-TiO2 film containing Au nanoparticles in the presence of H2S gas are investigated. The oscillatory phenomena could be monitored by looking at the variation of the surface plasmon resonance peak of the Au nanoparticles embedded in the TiO2-NiO matrix. Au nanoparticles act as optical probes in the detection of H2S, while the oxide matrix is responsible for the catalytic oxidation of H2S. To the best of our knowledge, it is the first time that oscillatory phenomena are monitored by optical spectroscopy.

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39

Gopinath, Subash C. B., and Penmetcha K. R. Kumar. "Biomolecular discrimination analyses by surface plasmon resonance." Analyst 139, no. 11 (2014): 2678. http://dx.doi.org/10.1039/c3an02052e.

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40

Bousiakou, Leda G., Hrvoje Gebavi, Lara Mikac, Stefanos Karapetis, and Mile Ivanda. "Surface Enhanced Raman Spectroscopy for Molecular Identification- a Review on Surface Plasmon Resonance (SPR) and Localised Surface Plasmon Resonance (LSPR) in Optical Nanobiosensing." Croatica chemica acta 92, no. 4 (2019): 479–94. http://dx.doi.org/10.5562/cca3558.

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Surface plasmon resonance (SPR) allows for real-time, label-free optical detection of many chemical and biological substances. Having emerged in the last two decades, it is a widely used technique due to its non-invasive nature, allowing for the ultra-sensitive detection of a number of analytes. This review article discusses the principles, providing examples and illustrating the utility of SPR within the frame of plasmonic nanobiosensing, while making comparisons with its successor, namely localized surface plasmon resonance (LSPR). In particular LSPR utilizes both metal nanoparticle arrays and single nanoparticles, as compared to a continuous film of gold as used in traditional SPR. LSPR, utilizes metal nanoparticle arrays or single nanoparticles that have smaller sizes than the wavelength of the incident light, measuring small changes in the wavelength of the absorbance position, rather than the angle as in SPR. We introduce LSPR nanobiosensing by describing the initial experiments performed, shift-enhancement methods, exploitation of the short electromagnetic ﬁeld decay length, and single nanoparticle sensors are as pathways to further exploit the strengths of LSPR nanobiosensing. Coupling molecular identiﬁcation to LSPR spectroscopy is also explored and thus examples from surface-enhanced Raman spectroscopy are provided. The unique characteristics of LSPR nanobiosensing are emphasized and the challenges using LSPR nanobiosensors for detection of biomolecules as a biomarker are discussed.

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41

Genç, Aziz, Javier Patarroyo, Jordi Sancho-Parramon, Neus G. Bastús, Victor Puntes, and Jordi Arbiol. "Hollow metal nanostructures for enhanced plasmonics: synthesis, local plasmonic properties and applications." Nanophotonics 6, no. 1 (January 6, 2017): 193–213. http://dx.doi.org/10.1515/nanoph-2016-0124.

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AbstractMetallic nanostructures have received great attention due to their ability to generate surface plasmon resonances, which are collective oscillations of conduction electrons of a material excited by an electromagnetic wave. Plasmonic metal nanostructures are able to localize and manipulate the light at the nanoscale and, therefore, are attractive building blocks for various emerging applications. In particular, hollow nanostructures are promising plasmonic materials as cavities are known to have better plasmonic properties than their solid counterparts thanks to the plasmon hybridization mechanism. The hybridization of the plasmons results in the enhancement of the plasmon fields along with more homogeneous distribution as well as the reduction of localized surface plasmon resonance (LSPR) quenching due to absorption. In this review, we summarize the efforts on the synthesis of hollow metal nanostructures with an emphasis on the galvanic replacement reaction. In the second part of this review, we discuss the advancements on the characterization of plasmonic properties of hollow nanostructures, covering the single nanoparticle experiments, nanoscale characterization via electron energy-loss spectroscopy and modeling and simulation studies. Examples of the applications, i.e. sensing, surface enhanced Raman spectroscopy, photothermal ablation therapy of cancer, drug delivery or catalysis among others, where hollow nanostructures perform better than their solid counterparts, are also evaluated.

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42

Meyer, Stefan A., Eric C. Le Ru, and Pablo G. Etchegoin. "Combining Surface Plasmon Resonance (SPR) Spectroscopy with Surface-Enhanced Raman Scattering (SERS)." Analytical Chemistry 83, no. 6 (March 15, 2011): 2337–44. http://dx.doi.org/10.1021/ac103273r.

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43

Haes, Amanda J., Christy L. Haynes, Adam D. McFarland, George C. Schatz, Richard P. Van Duyne, and Shengli Zou. "Plasmonic Materials for Surface-Enhanced Sensing and Spectroscopy." MRS Bulletin 30, no. 5 (May 2005): 368–75. http://dx.doi.org/10.1557/mrs2005.100.

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AbstractLocalized surface plasmon resonance (LSPR) excitation in silver and gold nanoparticles produces strong extinction and scattering spectra that in recent years have been used for important sensing and spectroscopy applications. This article describes the fabrication, characterization, and computational electrodynamics of plasmonic materials that take advantage of this concept.Two applications of these plasmonic materials are presented: (1) the development of an ultrasensitive nanoscale optical biosensor based on LSPR wavelength-shift spectroscopy and (2) the use of plasmon-sampled and wavelength-scanned surface-enhanced Raman excitation spectroscopy (SERES) to provide new insight into the electromagnetic-field enhancement mechanism.

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44

Wheeler, A. "Poly(dimethylsiloxane) microfluidic flow cells for surface plasmon resonance spectroscopy." Sensors and Actuators B: Chemical 98, no. 2-3 (March 15, 2004): 208–14. http://dx.doi.org/10.1016/j.snb.2003.06.004.

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45

Wang, S., S. Boussaad, S. Wong, and N. J. Tao. "High-Sensitivity Stark Spectroscopy Obtained by Surface Plasmon Resonance Measurement." Analytical Chemistry 72, no. 17 (September 2000): 4003–8. http://dx.doi.org/10.1021/ac000504f.

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46

Akimoto, Takuo, Satoshi Sasaki, Kazunori Ikebukuro, and Isao Karube. "Refractive-index and thickness sensitivity in surface plasmon resonance spectroscopy." Applied Optics 38, no. 19 (July 1, 1999): 4058. http://dx.doi.org/10.1364/ao.38.004058.

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47

Bingham, Julia M., Jeffrey N. Anker, Lauren E. Kreno, and Richard P. Van Duyne. "Gas Sensing with High-Resolution Localized Surface Plasmon Resonance Spectroscopy." Journal of the American Chemical Society 132, no. 49 (December 15, 2010): 17358–59. http://dx.doi.org/10.1021/ja1074272.

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48

Sherry, Leif J., Rongchao Jin, Chad A. Mirkin, George C. Schatz, and Richard P. Van Duyne. "Localized Surface Plasmon Resonance Spectroscopy of Single Silver Triangular Nanoprisms." Nano Letters 6, no. 9 (September 2006): 2060–65. http://dx.doi.org/10.1021/nl061286u.

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49

Salamon, Z., Y. Wang, M. F. Brown, H. A. Macleod, and G. Tollin. "Conformational Changes in Rhodopsin Probed by Surface Plasmon Resonance Spectroscopy." Biochemistry 33, no. 46 (November 1994): 13706–11. http://dx.doi.org/10.1021/bi00250a022.

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Daniyal, Wan Mohd Ebtisyam Mustaqim Mohd, Silvan Saleviter, and Yap Wing Fen. "Development of Surface Plasmon Resonance Spectroscopy for Metal Ion Detection." Sensors and Materials 30, no. 9 (September 13, 2018): 2023. http://dx.doi.org/10.18494/sam.2018.1952.

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