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| Hauptverfasser: | , , , |
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| Format: | Preprint |
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2026
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| Online-Zugang: | https://arxiv.org/abs/2601.16797 |
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| _version_ | 1866912843758043136 |
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| author | Santos, Paulo S. S. dos Mendes, João P. de Almeida, José M. M M. Coelho, Luís C. C. |
| author_facet | Santos, Paulo S. S. dos Mendes, João P. de Almeida, José M. M M. Coelho, Luís C. C. |
| contents | Accurate and fast calculations of localized surface plasmon resonances (LSPR) in metallic nanoparticles is essential for applications in sensing, nano-optics, and energy harvesting. Although full-wave numerical techniques such as the boundary element method (BEM) or the discrete dipole approximation (DDA) provide high accuracy, their computational cost often hinders rapid parametric studies. Here it is presented an ultrafast method that avoids solving large eigenproblems. Instead, only the dipolar component of the induced surface charge density \((σ_{dipolar})\) is retained through a expansion into Cartesion dipole basis, yielding a compact $3\times3$ geometric formulation that avoids full boundary-integral solves. The spectral response is obtained in a similar way, by projecting the Neumann--Poincaré surface operator onto the dipole subspace and evaluating a Rayleigh quotient, giving geometry-only eigenvalues again without an $N\times N$ eigenproblem. A major advantage of this method is that all geometry-dependent quantities are computed once per nanoparticle, while material dispersion and environmental changes enter only through simple algebraic expressions for the polarizability, enabling rapid evaluation across wavelengths. Retardation effects are incorporated through the modified long-wavelength approximation (MLWA), extending accuracy into the weakly retarded regime. The resulting framework provides a valuable tool for fast modelling and optimization of plasmonic nanoparticles at a significant lesser computational cost than BEM, DDA, and other standard tools. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2601_16797 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Ultrafast Dipolar Electrostatic Modeling of Plasmonic Nanoparticles with Arbitrary Geometry Santos, Paulo S. S. dos Mendes, João P. de Almeida, José M. M M. Coelho, Luís C. C. Optics Mathematical Physics Computational Physics Accurate and fast calculations of localized surface plasmon resonances (LSPR) in metallic nanoparticles is essential for applications in sensing, nano-optics, and energy harvesting. Although full-wave numerical techniques such as the boundary element method (BEM) or the discrete dipole approximation (DDA) provide high accuracy, their computational cost often hinders rapid parametric studies. Here it is presented an ultrafast method that avoids solving large eigenproblems. Instead, only the dipolar component of the induced surface charge density \((σ_{dipolar})\) is retained through a expansion into Cartesion dipole basis, yielding a compact $3\times3$ geometric formulation that avoids full boundary-integral solves. The spectral response is obtained in a similar way, by projecting the Neumann--Poincaré surface operator onto the dipole subspace and evaluating a Rayleigh quotient, giving geometry-only eigenvalues again without an $N\times N$ eigenproblem. A major advantage of this method is that all geometry-dependent quantities are computed once per nanoparticle, while material dispersion and environmental changes enter only through simple algebraic expressions for the polarizability, enabling rapid evaluation across wavelengths. Retardation effects are incorporated through the modified long-wavelength approximation (MLWA), extending accuracy into the weakly retarded regime. The resulting framework provides a valuable tool for fast modelling and optimization of plasmonic nanoparticles at a significant lesser computational cost than BEM, DDA, and other standard tools. |
| title | Ultrafast Dipolar Electrostatic Modeling of Plasmonic Nanoparticles with Arbitrary Geometry |
| topic | Optics Mathematical Physics Computational Physics |
| url | https://arxiv.org/abs/2601.16797 |