Chiral electroluminescence from thin-film perovskite metacavities.

Chiral light sources realized in ultracompact device platforms are highly desirable for various applications. Among active media used for thin-film emission devices, lead-halide perovskites have been extensively studied for photoluminescence due to their exceptional properties. However, up to date, there have been no demonstrations of chiral electroluminescence with a substantial degree of circular polarization (DCP) based on perovskite materials, being critical for the development of practical devices. Here, we propose a concept of chiral light sources based on a thin-film perovskite metacavity and experimentally demonstrate chiral electroluminescence with a peak DCP approaching 0.38. We design a metacavity created by a metal and a dielectric metasurface supporting photonic eigenstates with a close-to-maximum chiral response. Chiral cavity modes facilitate asymmetric electroluminescence of pairs of left and right circularly polarized waves propagating in the opposite oblique directions. The proposed ultracompact light sources are especially advantageous for many applications requiring chiral light beams of both helicities.

Topological Control of 2D Perovskite Emission in the Strong Coupling Regime.

Momentum space topology can be exploited to manipulate radiation in real space. Here we demonstrate topological control of 2D perovskite emission in the strong coupling regime via polaritonic bound states in the continuum (BICs). Topological polarization singularities (polarization vortices and circularly polarized eigenstates) are observed at room temperature by measuring the Stokes parameters of photoluminescence in momentum space. Particularly, in symmetry-broken structures, a very large degree of circular polarization (DCP) of ∼0.835 is achieved in the perovskite emission, which is the largest in perovskite materials to our knowledge. In the strong coupling regime, lower polariton modes shift to the low-loss spectral region, resulting in strong emission enhancement and large DCP. Our reciprocity analysis reveals that DCP is limited by material absorption at the emission wavelength. Polaritonic BICs based on 2D perovskite materials combine unique topological features with exceptional material properties and may become a promising platform for active nanophotonic devices.

Circularly Polarized Emission from Organic-Inorganic Hybrid Perovskites via Chiral Fano Resonances.

Organic-inorganic hybrid perovskites hold great potential for various optoelectronic devices with exceptional properties. Although the direct generation of circularly polarized emission from perovskites would enable various compact devices, achieving a large degree of circular polarization (DCP) at room temperature still remains challenging. Herein, we demonstrate that DCP can be strongly enhanced at the narrow mode position of chiral Fano resonances. In our design, a perovskite film is spin-coated on a symmetry-broken structure with a relatively large feature size. A large DCP of more than 0.5 is achieved at room temperature without the direct patterning of the perovskite layer. Reciprocity calculation reveals that chiral field enhancement enables the emission of opposite helicity to couple into counter-propagating slab modes and leads to a large DCP. Our design is very general and scalable. Our work may lead to circularly polarized light sources based on various perovskite materials.

Enhancement of sub-bandgap light absorption in perovskite semiconductor films via critical coupling.

Light absorption in semiconductors is a fundamental problem that has broad impact on a wide range of fields. However, it is intrinsically limited by the bandgap energy of the semiconductor. Herein, we study the enhancement of sub-bandgap light absorption in inorganic-organic hybrid perovskite semiconductor films via critical coupling. This is achieved at large incidence angles by balancing radiative and nonradiative decay rates in a planar multilayer structure. We found that a very small loss in the semiconductor layer can result in substantial light absorption. This simple but general method can be used to enhance the optical and optoelectronic responses of semiconductors below the bandgap energy.

3D printing of twisting and rotational bistable structures with tuning elements.

Three-dimensional (3D) printing is ideal for the fabrication of various customized 3D components with fine details and material-design complexities. However, most components fabricated so far have been static structures with fixed shapes and functions. Here we introduce bistability to 3D printing to realize highly-controlled, reconfigurable structures. Particularly, we demonstrate 3D printing of twisting and rotational bistable structures. To this end, we have introduced special joints to construct twisting and rotational structures without post-assembly. Bistability produces a well-defined energy diagram, which is important for precise motion control and reconfigurable structures. Therefore, these bistable structures can be useful for simplified motion control in actuators or for mechanical switches. Moreover, we demonstrate tunable bistable components exploiting shape memory polymers. We can readjust the bistability-energy diagram (barrier height, slope, displacement, symmetry) after printing and achieve tunable bistability. This tunability can significantly increase the use of bistable structures in various 3D-printed components.

Theoretical investigations on microwave Fano resonances in 3D-printable hollow dielectric resonators.

High-index dielectric structures have recently been studied intensively for Mie resonances at optical frequencies. These dielectric structures can enable extreme light manipulation, similar to that which has been achieved with plasmonic nanostructures. In the microwave region, dielectric resonators and metamaterials can be fabricated directly using 3D printing, which is advantageous for fabricating structurally complicated 3D geometries. It is therefore especially suitable for the fabrication of subwavelength structures. Here we report theoretical investigations on microwave Fano resonances in 3D-printable dielectric materials and structures. In particular, we propose and analyse 3D-printable, hollow, dielectric resonators with relatively low refractive indices, which exhibit sharp Fano resonances. We can control the interaction between bright and dark modes in a coupled dielectric particle pair by adjusting the inner-hole size, and thus we can increase the radiative Q factors further. We also find that Fano resonances in these hollow dielectric resonators are very sensitive to an index change in the surrounding medium, which could be useful for long-distance environmental sensing. New possibilities and opportunities are opening up with the rapid development of 3D-printing technologies. Our findings and the detailed investigations reported here can provide useful guidelines for future photonic devices based on 3D-printable materials and structures.

Active switching and tuning of sharp Fano resonances in the mid-infrared spectral region.

We propose and analyze a scheme for active switching and spectral tuning of mid-infrared Fano resonances. We consider dielectric resonators made of semiconductor cylinder arrays and block pairs, and theoretically investigate their optical response change due to carrier generation. Owing to sharp optical resonances in these structures and large dielectric constant variations with carrier densities, the significant spectral tuning of Fano resonances is achievable. Furthermore, selective optical pumping in coupled semiconductor structures can even enable dynamic switching of Fano resonances. This leads to a drastic change in the scattering spectra as well as in the near-field intensity. We also observe a stark difference between Fano resonances in cylinder arrays and block pairs. To understand this unusual behavior, we adopt the two coupled oscillator model, and extract the relevant Fano resonance parameters that explain this difference. Our findings and in-depth analyses can be useful for molecular sensors and switching devices in the technologically important mid-infrared spectral region.