Color selectivity of surface-plasmon holograms illuminated with white light

2013 ◽  
Vol 52 (27) ◽  
pp. 6788 ◽  
Author(s):  
Miyu Ozaki ◽  
Jun-ichi Kato ◽  
Satoshi Kawata
1987 ◽  
Vol 57 (3) ◽  
pp. 712-739 ◽  
Author(s):  
B. M. Dow ◽  
R. G. Vautin

The present study examines the chromatic organization of foveal striate cortex in the awake monkey by means of a series of microelectrode penetrations made as perpendicular as possible to the layers. The study includes 79 penetrations and 261 cells, of which 218 were tested systematically for color selectivity. Detailed analyses are conducted on a subset of 41 penetrations, which included 164 color-tested cells, an average of four cells per penetration. The penetrations were divided into two major categories on the basis of orientation selectivity testing. One group of penetrations contained at least one nonoriented cell in the first 600 microns of microelectrode trajectory (upper layers), whereas the other group of penetrations contained only oriented cells in the first 600 microns of microelectrode trajectory. The two groups were called N (nonoriented) and O (oriented), respectively. Analysis of the color properties of cells in N and O penetrations revealed that middle layer cells in N penetrations showed poor responses to white light, and color preferences for endspectral wavelengths, i.e., red or blue. Middle layer cells in O penetrations, by contrast, responded well to white light and to midspectral wavelengths. There were two subgroups of N penetrations, characterized by predominantly red (NR) or blue (NB) sensitivity in the middle layers. O penetrations could likewise be divided up into three subgroups (OG, OY, OW), characterized, respectively, by predominant sensitivity to greenish wavelengths (490-540 nm), yellowish wavelengths (550–600 nm), or white (i.e., all colors). Despite the identification of five subgroups, similarities between NR and OY, between NB and OG, and between OY and OW subgroups might be consistent with a continuum. The middle layers of N penetrations contained a unique class of cells with excitatory responses restricted to the two spectral ends, endspectral double-peak cells. A model is proposed for the color organization of layer 4 in foveal striate cortex, with red and blue zones in register with alternate cytochrome oxidase “blobs” of layers 2 and 3, white zones in register with interblob centers, and yellow and green zones in between.


Nanomaterials ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 1052
Author(s):  
Fu Deng ◽  
Hongfeng Liu ◽  
Yuanyuan Peng ◽  
Mingcheng Panmai ◽  
Sheng Lan

We investigate experimentally and numerically the scattering properties of liquid gallium nanoparticles coupled to a thin gold or silver film. The gallium nanoparticles are excited either directly by using inclined white light or indirectly by surface plasmon polaritons generated on the surface of the gold/silver film. In the former case, the scattering spectrum is always dominated by a scattering peak at ∼540 nm with a long-wavelength shoulder which is redshifted with increasing diameter of the gallium nanoparticle. Under the excitation of the surface plasmon polaritons, optical resonances with much narrower linewidths, which are dependent on the incidence angle of the white light, appear in the scattering spectra. In this case, the scattering spectrum depends weakly on the diameter of the gallium nanoparticle but the radiation pattern exhibits a strong dependence. In addition, a significant enhancement of electric field is expected in the gap region between the gallium nanoparticles and the gold film based on numerical simulation. As compared with the gallium nanoparticle coupled to the gold film which exhibit mainly yellow and orange colors, vivid scattering light spanning the visible light spectrum can be achieved in the gallium nanoparticles coupled to the silver film by simply varying the incidence angle. Gallium nanoparticles coupled to thin metal films may find potential applications in light–matter interaction and color display.


2011 ◽  
Vol 57 (1) ◽  
pp. 90-92 ◽  
Author(s):  
S. Chandramohan ◽  
Beo Deul Ryu ◽  
P. Uthirakumar ◽  
Ji Hye Kang ◽  
Hyun Kyu Kim ◽  
...  

Nanophotonics ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Pilar Gomez-Rodriguez ◽  
Esther Soria ◽  
Yu Jin ◽  
Andrés Caño ◽  
Irene Llorente ◽  
...  

Abstract We study the light emission of plasmonic-luminescent hybrid nanostructures consisting of Ag nanoparticles (NPs) embedded in europium oxide (EuOX). The Ag NPs present a bidimensional organization in the nanostructures and they optically behave as oblate spheroids. The photoluminescence (PL) spectral response of the nanostructures evolves from a narrow red emission characteristic of Eu3+ ions in absence of Ag NPs to a broad blue-green emission band associated with Eu2+ ions when the layer of Ag NPs is present. This behavior is not related to a change in the Eu2+/Eu3+ ratio, which is verified by compositional analysis. Instead, a detailed investigation of the PL emission of the nanostructures suggests that the coupling of the Ag NPs to the Eu2+ ions present in the EuOX layer, which manifests itself in an efficient sensitization of these ions, enhances their broad visible emission. In particular, the longitudinal mode of the Ag NPs surface plasmon is considered to be responsible for the efficient energy transfer for the non-normal incidence excitation PL configuration used. Finally, the use of a capping amorphous Al2O3 layer allows improving the robustness of hybrid nanostructures and further enhances their PL emission. These findings provide a new path to actively control the selective excitation of Eu2+ and Eu3+ ions via a controlled coupling with the surface plasmon resonance modes of the Ag NPs and points to these nanostructures as promising building blocks for the development of integrable white light sources.


2008 ◽  
Vol 131 (1) ◽  
pp. 241-246 ◽  
Author(s):  
Jong Seol Yuk ◽  
Jae-Wan Jung ◽  
Jinho Hyun ◽  
Young-Myeong Kim ◽  
Kwon-Soo Ha

Science ◽  
2011 ◽  
Vol 332 (6026) ◽  
pp. 218-220 ◽  
Author(s):  
M. Ozaki ◽  
J.-i. Kato ◽  
S. Kawata

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