Discrete Dipole Approximation (DDA) is a computational technique to simulate the optical properties of nanostructures of different shapes, sizes, and compositions. The influence of the target size on the optical response of 5 nm-diameter nanoparticles arranged in a monolayer hexagonal array is investigated by using DDA at various incident angles of the incident light on the target considered for silver (Ag), gold (Au) and copper (Cu) nanoparticles. In our study, the target size is controlled by the number of the spherical nanoparticles used to generate the two dimensional arrays. The interparticle distance is kept constant in all the simulations. The anisotropic response of noble-metal nanoparticles is generally characterized by the excitation of the high-energy (transverse) surface plasmon (SP) mode and the low-energy (longitudinal) SP mode. Results of the simulations for the three chosen metals show an exponential dependency of the absorption efficiency of the SP modes with respect to the target size. As the target size is increased, the energy of Ag-longitudinal SP mode is red-shifted and it displays an exponential decay while the band position of the transverse mode is blue-shifted. They however overlap when the smallest target size is considered. Although, the optical response of Au and Cu nanoparticle arrays shows the same dependency on the target size as observed in the case of Ag, the positions of their respective longitudinal and transverse modes are very close, making these almost indistinguishable. The dependency of the absorption efficiency of SP modes on the incident angle is fitted linearly for Cu, Au and longitudinal-Ag modes to the target size, while the transverse-Ag mode shows an exponential fitting. No change in the Ag-SP band position is observed when the incident angle is changed, but the SP bands for both Au and Cu exhibit exponential variation behavior.
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Tohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, JapanTohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Huang, Chi-Hsien
Wang, Xuan-Yu
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Tohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, JapanTohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Wang, Xuan-Yu
Igarashi, Makoto
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Tohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, JapanTohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Igarashi, Makoto
Murayama, Akihiro
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Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, Japan
Hokkaido Univ, Grad Sch Informat Sci & Technol, Kita Ku, Sapporo, Hokkaido 0600814, JapanTohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Murayama, Akihiro
Okada, Yoshitaka
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Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, Japan
Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, JapanTohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Okada, Yoshitaka
Yamashita, Ichiro
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Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, Japan
Panasonic Co Ltd, Adv Technol Res Labs, Kyoto 6190237, JapanTohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Yamashita, Ichiro
Samukawa, Seiji
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Tohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, JapanTohoku Univ, Inst Fluid Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
机构:
Chinese Univ Hong Kong, Dept Elect Engn, Shatin, Hong Kong, Peoples R China
Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Elect Engn, Shatin, Hong Kong, Peoples R China
Li, J.
Xu, J. B.
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Chinese Univ Hong Kong, Dept Elect Engn, Shatin, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Elect Engn, Shatin, Hong Kong, Peoples R China
Xu, J. B.
Ong, H. C.
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Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Dept Elect Engn, Shatin, Hong Kong, Peoples R China