Search for: All records

Recent advances in fundamental performance limits for power quantities based on Lagrange duality are proving to be a powerful theoretical tool for understanding electromagnetic wave phenomena. To date, however, in any approach seeking to enforce a high degree of physical reality, the linearity of the wave equation plays a critical role. In this manuscript, we generalize the current quadratically constrained quadratic program framework for evaluating linear photonics limits to incorporate nonlinear processes under the undepleted pump approximation. Via the exemplary objective of enhancing second harmonic generation in a (free-form) wavelength-scale structure, we illustrate a model constraint scheme that can be used in conjunction with standard convex relaxations to bound performance in the presence of nonlinear dynamics. Representative bounds are found to anticipate features observed in optimized structures discovered via computational inverse design. The formulation can be straightforwardly modified to treat other frequency-conversion processes, including Raman scattering and four-wave mixing.

 

Solid-state defect qubit systems with spin-photon interfaces show great promise for quantum information and metrology applications. Photon collection efficiency, however, presents a major challenge for defect qubits in high refractive index host materials. Inverse-design optimization of photonic devices enables unprecedented flexibility in tailoring critical parameters of a spin-photon interface including spectral response, photon polarization, and collection mode. Further, the design process can incorporate additional constraints, such as fabrication tolerance and material processing limitations. Here, we design and demonstrate a compact hybrid gallium phosphide on diamond inverse-design planar dielectric structure coupled to single near-surface nitrogen-vacancy centers formed by implantation and annealing. We observe up to a 14-fold broadband enhancement in photon extraction efficiency, in close agreement with simulations. We expect that such inverse-designed devices will enable realization of scalable arrays of single-photon emitters, rapid characterization of new quantum emitters, efficient sensing, and heralded entanglement schemes.

 

Nearly all thermal radiation phenomena involving materials with linear response can be accurately described via semi-classical theories of light. Here, we go beyond these traditional paradigms to study anonlinearsystem that, as we show, requires quantum theory of damping. Specifically, we analyze thermal radiation from a resonant system containing aχ⁽²⁾nonlinear medium and supporting resonances at frequenciesω₁andω₂ ≈ 2ω₁, where both resonators are driven only by intrinsic thermal fluctuations. Within our quantum formalism, we reveal new possibilities for shaping the thermal radiation. We show that the resonantly enhanced nonlinear interaction allows frequency-selective enhancement of thermal emission through upconversion, surpassing the well-known blackbody limits associated with linear media. Surprisingly, we also find that the emitted thermal light exhibits non-trivial statistics (g⁽²⁾(0) ≠ ~2) and biphoton intensity correlations (at twodistinctfrequencies). We highlight that these features can be observed in the near future by heating a properly designed nonlinear system, without the need for any external signal. Our work motivates new interdisciplinary inquiries combining the fields of nonlinear photonics, quantum optics and thermal science.

 

Recent advances in measuring van der Waals (vdW) interactions have probed forces on molecules at nanometric separations from metal surfaces and demonstrated the importance of infrared nonlocal polarization response and temperature effects, yet predictive theories for these systems remain lacking. We present a theoretical framework for computing vdW interactions among molecular structures, accounting for geometry, short-range electronic delocalization, dissipation, and collective nuclear vibrations (phonons) at atomic scales, along with long-range electromagnetic interactions in arbitrary macroscopic environments. We primarily consider experimentally relevant low-dimensional carbon allotropes, including fullerenes, carbyne, and graphene, and find that phonons couple strongly with long-range electromagnetic fields depending on molecular dimensionality and dissipation, especially at nanometric scales, creating delocalized phonon polaritons that substantially modify infrared molecular response. These polaritons, in turn, alter vdW interaction energies between molecular and macroscopic structures, producing nonmonotonic power laws and nontrivial temperature variations at nanometric separations feasible in current experiments.