| 1. |
- Ogier, Robin, 1987, et al.
(författare)
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Macroscopic Layers of Chiral Plasmonic Nanoparticle Oligomers from Colloidal Lithography
- 2014
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Ingår i: ACS Photonics. - : American Chemical Society (ACS). - 2330-4022. ; 1:10, s. 1074-1081
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Tidskriftsartikel (refereegranskat)abstract
- Optical near-field coupling between closely spaced plasmonic metal nanoparticles is important to a range of nanophotonic applications of high contemporary interest, including surface-enhanced molecular spectroscopy, nanooptical sensing, and various novel light-harvesting concepts. Here we report on monolayers of chiral heterotrimers and heterotetramers composed of closely spaced silver and/or gold nanodisks of different heights fabricated through facile hole-mask colloidal lithography. These quasi-three-dimensional oligomers are interesting for applications because they exhibit "hot" gaps and crevices of nanometric dimensions, a pronounced circular dichroism, and optical chirality in the visible to near-infrared wavelength range, and they can be produced in large ensembles (>109) of identical orientation. We analyze the optical properties of the samples based on simulation results and find that the circular dichroism is due to strong near-field coupling and intricate phase retardation effects originating in the three-dimensional character of the individual oligomers.
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| 2. |
- Svedendahl, Mikael, et al.
(författare)
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Complete light annihilation in an ultrathin layer of gold nanoparticles.
- 2013
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Ingår i: Nano letters (Print). - : American Chemical Society (ACS). - 1530-6984 .- 1530-6992. ; 13:7, s. 3053-3058
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Tidskriftsartikel (refereegranskat)abstract
- We experimentally demonstrate that an incident light beam can be completely annihilated in a single layer of randomly distributed, widely spaced gold nanoparticle antennas. Under certain conditions, each antenna dissipates more than 10 times the number of photons that enter its geometric cross-sectional area. The underlying physics can be understood in terms of a critical coupling to localized plasmons in the nanoparticles or, equivalently, in terms of destructive optical Fano interference and so-called coherent absorption.
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| 3. |
- Wersäll, Martin, 1985, et al.
(författare)
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Directional Nanoplasmonic Antennas for Self-Referenced Refractometric Molecular Analysis
- 2014
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Ingår i: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 118:36, s. 21075-21080
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Tidskriftsartikel (refereegranskat)abstract
- Localized surface-plasmon resonance (LSPR) sensors are typically based on tracing resonance peak shifts that precisely follow changes in the local refractive index. Such measurements usually require a spectrometer, a stable light source, and an accurate LSPR position tracing technique. As a simple but efficient alternative, we investigated a self-referenced single-wavelength sensing scheme based on angle-dependent and highly directional radiation patterns originating from a monolayer of asymmetric gold nanodimers. We found that one could easily trace a model biotinneutravidin recognition reaction as well as minute bulk refractive index changes, by measuring the intensity ratio between the light scattered in two different directions with respect to the dimers. The refractometric resolution of the methodology was estimated to be on the order of Delta n approximate to 10(-5) RIU. These results may be particularly useful for label-free biosensing applications that require a combination of simple and cost-effective optical readout with a reasonable sensitivity.
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| 4. |
- Zengin, Gülis, 1982, et al.
(författare)
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Approaching the strong coupling limit in single plasmonic nanorods interacting with J-aggregates
- 2013
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Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322 .- 2045-2322. ; 3
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Tidskriftsartikel (refereegranskat)abstract
- We studied scattering and extinction of individual silver nanorods coupled to the J-aggregate form of the cyanine dye TDBC as a function of plasmon - exciton detuning. The measured single particle spectra exhibited a strongly suppressed scattering and extinction rate at wavelengths corresponding to the J-aggregate absorption band, signaling strong interaction between the localized surface plasmon of the metal core and the exciton of the surrounding molecular shell. In the context of strong coupling theory, the observed "transparency dips" correspond to an average vacuum Rabi splitting of the order of 100 meV, which approaches the plasmon dephasing rate and, thereby, the strong coupling limit for the smallest investigated particles. These findings could pave the way towards ultra-strong light-matter interaction on the nanoscale and active plasmonic devices operating at room temperature.
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| 5. |
- Aissaoui, Nesrine, 1983, et al.
(författare)
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FRET enhancement close to gold nanoparticles positioned in DNA origami constructs
- 2017
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Ingår i: Nanoscale. - Cambridge, United Kingdom : Royal Society of Chemistry (RSC). - 2040-3372 .- 2040-3364. ; 9:2, s. 673-683
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Tidskriftsartikel (refereegranskat)abstract
- Here we investigate the energy transfer rates of a Förster resonance energy transfer (FRET) pair positioned in close proximity to a 5 nm gold nanoparticle (AuNP) on a DNA origami construct. We study the distance dependence of the FRET rate by varying the location of the donor molecule, D, relative to the AuNP while maintaining a fixed location of the acceptor molecule, A. The presence of the AuNP induces an alteration in the spontaneous emission of the donor (including radiative and non-radiative rates) which is strongly dependent on the distance between the donor and AuNP surface. Simultaneously, the energy transfer rates are enhanced at shorter D-A (and D-AuNP) distances. Overall, in addition to the direct influence of the acceptor and AuNP on the donor decay there is also a significant increase in decay rate not explained by the sum of the two interactions. This leads to enhanced energy transfer between donor and acceptor in the presence of a 5 nm AuNP. We also demonstrate that the transfer rate in the three "particle" geometry (D + A + AuNP) depends approximately linearly on the transfer rate in the donor-AuNP system, suggesting the possibility to control FRET process with electric field induced by 5 nm AuNPs close to the donor fluorophore. It is concluded that DNA origami is a very versatile platform for studying interactions between molecules and plasmonic nanoparticles in general and FRET enhancement in particular.
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| 6. |
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| 7. |
- Alegret, Joan, 1977, et al.
(författare)
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Green's tensor calculations of plasmon resonances of single holes and hole pairs in thin gold films
- 2008
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Ingår i: New Journal of Physics. - Bristol, UK : IOP Publishing. - 1367-2630. ; 10, s. 13-
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Tidskriftsartikel (refereegranskat)abstract
- We present numerical calculations of the plasmon properties of single-hole and hole-pair structures in optically thin gold films obtained with the Green's tensor formalism for stratified media. The method can be used to obtain the optical properties of a given hole system, without problems associated with the truncation of the infinite metal film. The calculations are compared with previously published experimental data and an excellent agreement is found. In particular, the calculations are shown to reproduce the evolution of the hole plasmon resonance spectrum as a function of hole diameter, film thickness and hole separation.
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| 8. |
- Alegret, Joan, et al.
(författare)
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Top-down extended meshing algorithm and its applications to Green's tensor nano-optics calculations
- 2007
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Ingår i: Physical Review E. Statistical, Nonlinear, and Soft Matter Physics. - : The American Physical Society. - 1063-651X .- 1095-3787. ; 75:4
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Tidskriftsartikel (refereegranskat)abstract
- We present a computational algorithm which speeds up Green's tensor nano-optics calculations by means of optimizing the mesh that represents the system we want to investigate. The algorithm automates the process of creating a variable-size mesh that describes an arbitrary nanostructure. The total number of elements of this mesh is smaller than that of a regular mesh representing the same structure, and thus the Green's tensor calculations can be performed faster. Precision, however, is kept at a similar level than for the regular mesh. Typically, the algorithm yields a mesh that speeds up Green's tensor calculations by a factor of 4, while giving a maximum error in the field magnitude of about 5%. The speed-up factor makes it very suitable for otherwise lengthy calculations, and the error should be acceptable for most applications.
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| 9. |
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| 10. |
- Andrén, Daniel, 1991, et al.
(författare)
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Probing Photothermal Effects on Optically Trapped Gold Nanorods by Simultaneous Plasmon Spectroscopy and Brownian Dynamics Analysis
- 2017
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Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 11:10, s. 10053-10061
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Tidskriftsartikel (refereegranskat)abstract
- Plasmonic gold nanorods are prime candidates for a variety of biomedical, spectroscopy, data storage, and sensing applications. It was recently shown that gold nanorods optically trapped by a focused circularly polarized laser beam can function as extremely efficient nanoscopic rotary motors. The system holds promise for-applications ranging from nanofluidic flow control and nanorobotics to biomolecular actuation and analysis. However, to fully exploit this potential, one needs to be able to control and understand heating effects associated with laser trapping. We investigated photothermal heating of individual rotating gold nanorods by simultaneously probing their localized surface plasmon resonance spectrum and rotational Brownian dynamics over extended periods of time. The data reveal an extremely slow nanoparticle reshaping process, involving migration of the order of a few hundred atoms per minute, for moderate laser powers and a trapping wavelength close to plasmon resonance. The plasmon spectroscopy and Brownian analysis allows for separate temperature estimates based on the refractive index and the viscosity of the water surrounding a trapped nanorod. We show that both measurements yield similar effective temperatures, which correspond to the actual temperature at a distance of the order 10-15 nm from the particle surface. Our results shed light on photothermal processes on the nanoscale and will be useful in evaluating the applicability and performance of nanorod motors and optically heated nanoparticles for a variety of applications.
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