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      From tunable core-shell nanoparticles to plasmonic drawbridges: Active control of nanoparticle optical properties

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          Abstract

          Redox electrochemistry was used to reversibly tune the optical properties of plasmonic core-shell nanoparticles and dimers.

          Abstract

          The optical properties of metallic nanoparticles are highly sensitive to interparticle distance, giving rise to dramatic but frequently irreversible color changes. By electrochemical modification of individual nanoparticles and nanoparticle pairs, we induced equally dramatic, yet reversible, changes in their optical properties. We achieved plasmon tuning by oxidation-reduction chemistry of Ag-AgCl shells on the surfaces of both individual and strongly coupled Au nanoparticle pairs, resulting in extreme but reversible changes in scattering line shape. We demonstrated reversible formation of the charge transfer plasmon mode by switching between capacitive and conductive electronic coupling mechanisms. Dynamic single-particle spectroelectrochemistry also gave an insight into the reaction kinetics and evolution of the charge transfer plasmon mode in an electrochemically tunable structure. Our study represents a highly useful approach to the precise tuning of the morphology of narrow interparticle gaps and will be of value for controlling and activating a range of properties such as extreme plasmon modulation, nanoscopic plasmon switching, and subnanometer tunable gap applications.

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          Most cited references33

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          Probing the ultimate limits of plasmonic enhancement.

          Metals support surface plasmons at optical wavelengths and have the ability to localize light to subwavelength regions. The field enhancements that occur in these regions set the ultimate limitations on a wide range of nonlinear and quantum optical phenomena. We found that the dominant limiting factor is not the resistive loss of the metal, but rather the intrinsic nonlocality of its dielectric response. A semiclassical model of the electronic response of a metal places strict bounds on the ultimate field enhancement. To demonstrate the accuracy of this model, we studied optical scattering from gold nanoparticles spaced a few angstroms from a gold film. The bounds derived from the models and experiments impose limitations on all nanophotonic systems.
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            Revealing the quantum regime in tunnelling plasmonics.

            When two metal nanostructures are placed nanometres apart, their optically driven free electrons couple electrically across the gap. The resulting plasmons have enhanced optical fields of a specific colour tightly confined inside the gap. Many emerging nanophotonic technologies depend on the careful control of this plasmonic coupling, including optical nanoantennas for high-sensitivity chemical and biological sensors, nanoscale control of active devices, and improved photovoltaic devices. But for subnanometre gaps, coherent quantum tunnelling becomes possible and the system enters a regime of extreme non-locality in which previous classical treatments fail. Electron correlations across the gap that are driven by quantum tunnelling require a new description of non-local transport, which is crucial in nanoscale optoelectronics and single-molecule electronics. Here, by simultaneously measuring both the electrical and optical properties of two gold nanostructures with controllable subnanometre separation, we reveal the quantum regime of tunnelling plasmonics in unprecedented detail. All observed phenomena are in good agreement with recent quantum-based models of plasmonic systems, which eliminate the singularities predicted by classical theories. These findings imply that tunnelling establishes a quantum limit for plasmonic field confinement of about 10(-8)λ(3) for visible light (of wavelength λ). Our work thus prompts new theoretical and experimental investigations into quantum-domain plasmonic systems, and will affect the future of nanoplasmonic device engineering and nanoscale photochemistry.
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              Nanogap-engineerable Raman-active nanodumbbells for single-molecule detection.

              Surface-enhanced Raman scattering (SERS)-based signal amplification and detection methods using plasmonic nanostructures have been widely investigated for imaging and sensing applications. However, SERS-based molecule detection strategies have not been practically useful because there is no straightforward method to synthesize and characterize highly sensitive SERS-active nanostructures with sufficiently high yield and efficiency, which results in an extremely low cross-section area in Raman sensing. Here, we report a high-yield synthetic method for SERS-active gold-silver core-shell nanodumbbells, where the gap between two nanoparticles and the Raman-dye position and environment can be engineered on the nanoscale. Atomic-force-microscope-correlated nano-Raman measurements of individual dumbbell structures demonstrate that Raman signals can be repeatedly detected from single-DNA-tethered nanodumbbells. These programmed nanostructure fabrication and single-DNA detection strategies open avenues for the high-yield synthesis of optically active smart nanoparticles and structurally reproducible nanostructure-based single-molecule detection and bioassays.
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                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                December 2015
                04 December 2015
                : 1
                : 11
                : e1500988
                Affiliations
                [1 ]Smalley-Curl Institute Applied Physics Program, Rice University, Houston, TX 77005, USA.
                [2 ]Department of Chemistry, Rice University, Houston, TX 77005, USA.
                [3 ]Department of Physics and Astronomy, Rice University, Houston, TX 77005, USA.
                [4 ]School of Chemistry and Bio21 Institute, University of Melbourne, Parkville, Victoria 3010, Australia.
                [5 ]Materials Science and Nanoengineering, Rice University, Houston, TX 77005, USA.
                [6 ]Department of Electrical and Computer Engineering, Rice University, Houston, TX 77005, USA.
                Author notes
                [* ]Corresponding author. E-mail: cflandes@ 123456rice.edu
                Author information
                http://orcid.org/0000-0003-0274-4815
                http://orcid.org/0000-0002-1633-2937
                Article
                1500988
                10.1126/sciadv.1500988
                4672758
                26665175
                eb4cba3d-a9df-476e-8267-c00c93f566e1
                Copyright © 2015, The Authors

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 24 July 2015
                : 28 October 2015
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000928, Welch Foundation (US);
                Award ID: ID0EOVAK3885
                Award ID: C-1787
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation (US);
                Award ID: ID0ES1AK3886
                Award ID: CHE-1151647
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100006770, American Chemical Society Petroleum Research Fund (US);
                Award ID: ID0EW6AK3887
                Award ID: 54684-NDS
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000928, Welch Foundation (US);
                Award ID: ID0E1EBK3888
                Award ID: C-1664
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation (US);
                Award ID: ID0EWJBK3889
                Award ID: CHE-0955286
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100006831, U.S. Air Force (US);
                Award ID: ID0ESOBK3890
                Award ID: MURI FA9550-15-1-0022
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation (US);
                Award ID: ID0EOTBK3891
                Award ID: 0940902
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation (US);
                Award ID: ID0EIXBK3892
                Award ID: 0940902
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation (US);
                Award ID: ID0EY3BK3893
                Award ID: 0940902
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000928, Welch Foundation (US);
                Award ID: ID0EBBCK3894
                Award ID: C-1222
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000928, Welch Foundation (US);
                Award ID: ID0ESGCK3895
                Award ID: 1220
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100006831, U.S. Air Force (US);
                Award ID: ID0ENLCK3896
                Award ID: MURI FA9550-15-1-0022
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100006831, U.S. Air Force (US);
                Award ID: ID0E5QCK3897
                Award ID: MURI FA9550-15-1-0022
                Award Recipient :
                Funded by: Smalley-Curl Institute;
                Award ID: ID0EZVCK3898
                Award Recipient :
                Categories
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                Nanomaterials
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                Meann Ramirez

                materials science,nanoparticles,optical properties,interparticle gaps,charge transfer plasmon,active plasmonics

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