In this Review, the theory and applications of optical micro-and nano-resonators are presented from the underlying concept of their natural resonances, the so-called quasi-normal modes (QNMs). QNMs are the basic constituents governing the response of resonators. Characterized by complex frequencies, QNMs are initially loaded by a driving field and then decay exponentially in time due to power leakage or absorption. Here, the use of QNM-expansion formalisms to model these basic effects is explored. Such modal expansions that operate at complex frequencies distinguish from the current user habits in electromagnetic modeling, which rely on classical Maxwell's equation solvers operating at real frequencies or in the time domain; they also bring much deeper physical insight into the analysis. An extensive overview of the historical background on QNMs in electromagnetism and a detailed discussion of recent relevant theoretical and numerical advances are therefore presented. Additionally, a concise description of the role of QNMs on a number of examples involving electromagnetic resonant fields and matter, including the interaction between quantum emitters and resonators (Purcell effect, weak and strong coupling, superradiance, . . . ), Fano interferences, the perturbation of resonance modes, and light transport and localization in disordered media is provided. (3 of 38)www.advancedsciencenews.com www.lpr-journal.org Figure 2. Examples of applications whose analysis benefit from QNM-expansion approaches. a) Nonlocal plasmonics. QNMs can be used to predict the nonlocal response of free electron gas on the Purcell factor of an emitter placed in the near-field of a gold nanorod. Predictions from two different nonlocal models-the hydrodynamic Drude model (HDM) and the generalized nonlocal optical response (GNOR) Model-are shown and compared to classical predictions obtained with a Drude model. The inset shows the electric field intensity of the nonlocal GNOR QNM. Adapted with permission. [53] Copyright 2017, Optical Society of America. b) QNM expansion of the scattering matrix. (Upper panel) Absorption cross section of a multi-layered metallic-dielectric sphere in air, demonstrating the good agreement between the results obtained with Mie's scattering theory (dashed black curve) and a QNM-expansion formalism for the scattering matrix (solid red curve) computed with the QNM eigenfrequencies shown in the Lower panel. Reproduced with permission. [40] Copyright 2017, American Physical Society. c) Quantum hybrids. Supperradiant and subradiant decay rates m and energies m of a quantum hybrid formed by 100 molecules that are randomly distributed and oriented around a silver nanorod (diameter 30 nm, length 100 nm), predicted with the QNM formalism. γ 0 denotes the decay rate of every individual molecule in the vacuum. The left inset shows the superradiant state of the hybrid, with a large cooperativity involving more than one half of the molecules. Reproduced with permission. [28] Copyright 2017, American Physical Society. d) Quant...
Elaborating reliable and versatile strategies for efficient light coupling between free space and thin films is of crucial importance for new technologies in energy efficiency. Nanostructured materials have opened unprecedented opportunities for light management, notably in thin-film solar cells. Efficient coherent light trapping has been accomplished through the careful design of plasmonic nanoparticles and gratings, resonant dielectric particles and photonic crystals. Alternative approaches have used randomly textured surfaces as strong light diffusers to benefit from their broadband and wide-angle properties. Here, we propose a new strategy for photon management in thin films that combines both advantages of an efficient trapping due to coherent optical effects and broadband/wide-angle properties due to disorder. Our approach consists of the excitation of electromagnetic modes formed by multiple light scattering and wave interference in two-dimensional random media. We show, by numerical calculations, that the spectral and angular responses of thin films containing disordered photonic patterns are intimately related to the in-plane light transport process and can be tuned through structural correlations. Our findings, which are applicable to all waves, are particularly suited for improving the absorption efficiency of thin-film solar cells and can provide a new approach for high-extraction-efficiency light-emitting diodes.
Light propagation in all-dielectric rod-type metamaterials is studied theoretically. The electric and magnetic dipole moments of the rods are derived analytically in the long-wavelength limit. The effective permittivity and permeability of a square lattice of rods are calculated by homogenizing the corresponding array of dipoles. The role of dipole resonances in the optical properties of the rod array is interpreted. This structure is found to exhibit a true left-handed behavior, confirming previous experiments [L. Peng et al., Phys. Rev. Lett. 98, 157403 (2007)]. A scaling analysis shows that this effect holds at optical frequencies and can be obtained by using rods made, for example, of silicon.
The ability to mold the flow of light at the wavelength scale has been largely investigated in photonic-crystal-based devices, a class of materials in which the propagation of light is driven by interferences between multiply Bragg scattered waves and whose energy dispersion is described by a photonic band diagram [1]. Light propagation in such structures is defined by Bloch modes, which can be engineered by varying the structural parameters of the material [2][3][4]. In disordered media, both the direction and phase of the propagating waves are randomized in a complex manner, making any attempt to control light propagation particularly challenging. Disordered media are currently investigated in several contexts, ranging from the study of collective multiple scattering phenomena [5,6] to cavity quantum electrodynamics and random lasing [7,8], to the possibility to provide efficient solutions in renewable energy [9], imaging [10], and spectroscopy-based applications [11]. Transport in such systems can be described in terms of photonic modes, or quasi-modes, which exhibit characteristic spatial profiles and spectra [12,13]. In diffusive systems, these modes are spatially and spectrally overlapping while in the regime of Anderson localization, they become spatially and spectrally-isolated [14]. Unlike Bloch modes in periodic systems, the precise formation of photonic modes in a single realization of the disorder is unpredictable.Control over light transport can be obtained by shaping the incident wave to excite only a specific part of the modes available in a given system [15][16][17][18]. For fully exploiting the potential of disordered systems, however, a mode control is needed. It was shown 3 theoretically that isolated modes could be selectively tuned and possibly coupled to each other by a local fine modification of the dielectric structure [19,20].In this Article, we demonstrate experimentally the ability to fully control the spectral properties of an individual photonic mode in a two-dimensional disordered photonic structure [21], in a wavelength range that is relevant for photonic research driven applications. A statistical analysis of individual spatially-isolated random photonic modes is performed by multi-dimensional near-field imaging, leading to a detailed determination of intensity fluctuations, decay lengths and mode volumes. We then demonstrate that individual modes can be fine-tuned either by near-field tip perturbation or by local sub-micrometer-scale oxidation of the semiconductor slab [22]. The resonant frequency of a selected mode is gradually shifted until it is in perfect spectral superposition with the frequency of other two modes, located a few micrometers apart and spatially overlapping with the tuned mode. On spectral resonance, we observe frequency crossing and anti-crossing behaviours, respectively, the latter indicating mode interaction. This provides the experimental proof-of- (e) and (f), respectively). The main difference between the two spectra normalized to the average intensity i...
The effect of periodic and disordered photonic structures on the absorption efficiency of amorphous and crystalline Silicon thin-film solar cells is investigated numerically. We show that disordered patterns possessing a short-range correlation in the position of the holes yield comparable, or even superior, absorption enhancements than periodic (photonic crystal) patterns. This work provides clear evidence that non-deterministic photonic structures represent a viable alternative strategy for photon management in thin-film solar cells, thereby opening the route towards more efficient and potentially cheaper photovoltaic technologies.
Hydroxypropyl cellulose (HPC) is a biocompatible cellulose derivative capable of self‐assembling into a lyotropic chiral nematic phase in aqueous solution. This liquid crystalline phase reflects right‐handed circular polarized light of a specific color as a function of the HPC weight fraction. Here, it is demonstrated that, by introducing a crosslinking agent, it is possible to drastically alter the visual appearance of the HPC mesophase in terms of the reflected color, the scattering distribution, and the polarization response, resulting in an exceptional matte appearance in solid‐state films. By exploiting the interplay between order and disorder, a robust and simple methodology toward the preparation of polarization and angular independent color is developed, which constitutes an important step toward the development of real‐world photonic colorants.
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