In recent years, there have been rapid advances in the parallel fields of electronic and photonic topological crystals. Topological photonic crystals in particular show promise for coherent transport of light and quantum information at macroscopic scales. In this work, we apply for the first time the recently developed theory of “topological quantum chemistry” to the study of band structures in photonic crystals. This method allows us to design and diagnose topological photonic band structures using only group theory and linear algebra. As an example, we focus on a family of crystals formed by elliptical rods in a triangular lattice. We show that the symmetry of Bloch states in the Brillouin zone can determine the position of the localized photonic wave packets describing groups of bands. By modifying the crystal structure and inverting bands, we show how the centers of these wave packets can be moved between different positions in the unit cell. Finally, we show that for shapes of dielectric rods, there exist isolated topological bands which do not admit a well-localized description, representing the first physical instance of “fragile” topology in a truly noninteracting system. Our work demonstrates how photonic crystals are the natural platform for the future experimental investigation of fragile topological bands.

We analyze the robustness of corner modes in topological photonic crystals, taking a $C_6$-symmetric breathing honeycomb photonic crystal as an example. First, we employ topological quantum chemistry and Wilson loop calculations to demonstrate that the topological properties of the bulk crystal stem from an obstructed atomic limit phase. We then characterize the topological corner modes emerging within the gapped edge modes employing a semianalytical model, determining the appropriate real-space topological invariants. We provide a detailed account of the effect of long-range interactions on the topological modes in photonic crystals, and we quantify their robustness to perturbations. We conclude that, while photonic long-range interactions inevitably break chiral symmetry, the system is reducible to a chirally symmetric limit and the corner modes are protected by this together with lattice symmetries.

The inherently weak nature of chiral light–matter interactions can be enhanced by orders of magnitude utilizing artificially-engineered nanophotonic structures. These structures enable high spatial concentration of electromagnetic fields with controlled helicity and chirality. However, the effective design and optimization of nanostructures requires defining physical observables which quantify the degree of electromagnetic helicity and chirality. In this perspective, we discuss optical helicity, optical chirality, and their related conservation laws, describing situations in which each provides the most meaningful physical information in free space and in the context of chiral light–matter interactions. First, an instructive comparison is drawn to the concepts of momentum, force, and energy in classical mechanics. In free space, optical helicity closely parallels momentum, whereas optical chirality parallels force. In the presence of macroscopic matter, the optical helicity finds its optimal physical application in the case of lossless, dual-symmetric media, while, in contrast, the optical chirality provides physically observable information in the presence of lossy, dispersive media. Finally, based on numerical simulations of a gold and silicon nanosphere, we discuss how metallic and dielectric nanostructures can generate chiral electromagnetic fields upon interaction with chiral light, offering guidelines for the rational design of nanostructure-enhanced electromagnetic chirality.

The directionality and polarization of light show peculiar properties when the scattering by a dielectric sphere can be described exclusively by electric and magnetic dipolar modes. Particularly, when these modes oscillate in phase with equal amplitude, at the so-called first Kerker condition, the zero optical backscattering condition emerges for nondissipating spheres. However, the role of absorption and optical gain in the first Kerker condition remains unexplored. In this work, we demonstrate that either absorption or optical gain precludes the first Kerker condition and, hence, the absence of backscattered radiation light, regardless of the particle’s size, incident wavelength, and incoming polarization. Finally, we derive the necessary prerequisites of the second Kerker condition of the zero forward light scattering, finding that optical gain is a compulsory requirement.