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This work reports the color-tunable mixed photoluminescence (PL) emission from an Alq3 organic layer in an Au-Alq3-Au plasmonic structure through the combination of organic fluorescence emission and another form of emission that is enabled by the surface plasmons in the plasmonic structure.
We investigate the enhancement of the resonance energy transfer rate between donor and acceptor associated by the surface plasmons of the Ag nanorods on a SiO2 substrate.
Absorption of light by the surface plasmons of small metallic particles accounts for the colorful appearance of suspensions of those particles.
In summary, we have investigated the enhancement of the RET rate between donor and acceptor associated by the surface plasmons of the Ag nanorods on a SiO2 substrate.
This increase is attributed to the fact that since the energy of the surface plasmon mode is lower than e Vbias, the electron transitions in the molecule in the energy range lower than e Vbias are enhanced by the surface plasmons.
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We know that the THz absorption in the Au/PS nanosphere array is mainly induced by the surface plasmon resonance and the absorption frequency is determined mainly by the surface plasmon frequency.
This enhancement is attributed to photon scattering and trapping by the surface plasmon generated in the metallic nanoparticles.
The enhancement of Raman signal was mainly attributed to the electromagnetic enhancement on the metal surface which was induced by the surface plasmon resonance (SPR).
The non-linear properties of nanocomposite glasses equipped with such particles are induced by the surface plasmon resonance at the interface between particles and glass matrix.
The spectra were dominated by the surface plasmon modes of the Au nanoarrays superimposed on the effects of interference through the films.
It is believed that absorption of light by metal nanoparticles is dominated by the surface plasmon (SP) resonance changing both the static and dynamic optical properties.
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