We directly observe the states of topological photonic crystals at telecom wavelengths. Using the states’ intrinsic radiation, we measure dispersion, loss, pseudospin, and spin-spin scattering. We image spin-selective unidirectional propagation around sharp corners and junctions.

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We demonstrate that the scattering matrix of nanophotonic systems is completely determined by their quasinormal modes and present a first-principle expansion technique which is directly applicable to an arbitrary number of modes and input-output channels.

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We develop a theoretical formalism which explains asymmetric transmission (AT) in chiral resonators from their eigenmodes. We derive a fundamental limit for AT and propose the design of a chiral photonic crystal offering 84% AT.

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It is well known that the quasinormal modes (or resonant states) of photonic structures can be associated with the poles of the scattering matrix of the system in the complex-frequency plane. In this work, the inverse problem, i.e., the reconstruction of the scattering matrix from the knowledge of the quasinormal modes, is addressed. We develop a general and scalable quasinormal-mode expansion of the scattering matrix, requiring only the complex eigenfrequencies and the far-field properties of the eigenmodes. The theory is validated by applying it to illustrative nanophotonic systems with multiple overlapping electromagnetic modes. The examples demonstrate that our theory provides an accurate first-principles prediction of the scattering properties, without the need for postulating ad hoc nonresonant channels.@en

We observe that the asymmetric transmission (AT) through photonic systems with a resonant chiral response is strongly related to the far-field properties of eigenmodes of the system. This understanding can be used to predict the AT for any resonant system from its complex eigenmodes. We find that the resonant chiral phenomenon of AT is related to, and is bounded by, the nonresonant scattering properties of the system. Using the principle of reciprocity, we determine a fundamental limit to the maximum AT possible for a single mode in any chiral resonator. We propose and follow a design route for a highly chiral dielectric photonic crystal structure that reaches this fundamental limit for AT.

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The scattering matrix is a fundamental tool to quantitatively describe the properties of resonant systems. In particular, it enables the understanding of many photonic devices of current interest, such as photonic metasurfaces and nanostructured optical scatterers. In this contribution, we show that the scattering matrix of a photonic system is completely determined by its quasinormal modes, i.e., the self-sustaining electromagnetic excitations at a complex frequency. On the basis of temporal coupled-mode theory, we derive an expression for the expansion of the scattering matrix on quasinormal modes, which is directly applicable to an arbitrary number of modes and input/output channels. Our theory does not require any ad-hoc assumptions, such as the fitting of an additional nonresonant background. We validate and discuss the theoretical formalism with some illustrative examples. This demonstrates that the theory represents a powerful and predictive tool for calculating the highly structured spectra of resonant nanophotonic systems, and, at the same time, a key for unravelling the physical mechanisms at the heart of such intricate spectral structures.

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