Optical bound states in the continuum (BICs) provide a way to engineer resonant response in photonic crystals with giant quality factors. The extended interaction time in such systems is particularly promising for enhancement of nonlinear optical processes and development of a new generation of active optical devices. However, the achievable interaction strength is limited by the purely photonic character of optical BICs. Here, 1 arXiv:1905.13505v1 [cond-mat.mes-hall] 31 May 2019 we mix optical BIC in a photonic crystal slab with excitons in atomically thin transition metal dichalcogenide MoSe 2 via strong coupling to form exciton-polaritons with Rabi splitting exceeding 27 meV. We experimentally show BIC-like behavior of both upper and lower polariton branches, with complete suppression of radiation into far-field at the BIC wavevector and strongly varying Q-factor in its vicinity. Owing to an effective disorder averaging through motional narrowing, we achieve small polariton linewidth of 2 meV and demonstrate linewidth control via angle and temperature tuning. Our results pave the way towards developing tunable BIC-based polaritonic devices for sensing, lasing, and nonlinear optics. Optical bound states in the continuum (BICs), supported by photonic crystal structures of certain geometries, have received much attention recently as a novel approach to generating extremely spectrally narrow resonant responses. 1,2 Since BICs are uncoupled from the radiation continuum through symmetry protection 3 or resonance trapping, 4 their high quality factors, while reaching 10 5 − 10 6 , can be robust to perturbations of photonic crystal geometric parameters. This enables a broad range of practical applications, including recently demonstrated spectral filtering, 5 chemical and biological sensing, 6,7 and lasing. 4Providing an efficient light-trapping mechanism, optical BICs are particularly attractive for enhancing nonlinear optical effects, with recent theoretical proposals discussing enhanced bistability 8 and Kerr-type focusing nonlinearity. 9 However, for practical realization of these proposals, a significantly stronger material nonlinear susceptibility is needed than generally available in dielectric-based photonic crystals.An attractive approach to the enhancement of effective nonlinearity is through the use of exciton-polaritons -hybrid quasi-particles that inherit both the coherent properties of photonic modes and interaction strength of excitons. 10,11 Hybrid nanophotonic systems incorporating atomically thin transition metal dichalcogenides (TMDs) have proven to be a particularly promising platform owing to their ease of fabrication and possibility of room temperature operation. [12][13][14] In addition to conventional microcavity-based designs, TMD

present the results of magnetoluminescence study of ZnSe:CdMnSe quantum dots samples in a magnetic field up to 11 T both in the Faraday and Voigt geometries at liquid He temperatures and various levels of laser excitation. We found that the intensity of the quantum dot photoluminescence strongly increases (up to two orders of magnitude) in the Faraday geometry and only slightly (∼ 1.5 times) in the Voigt geometry within the range of B=0-11 T. We explain the strong increase of the photoluminescence in the Faraday geometry within the frame of the spin-dependent Auger recombination of excitons through Mn ions. We relate the observed anisotropy of the quantum dot emission with the high anisotropy of the hole spins in QDs. We present a theoretical model which allows us to obtain selection rules for the Auger transition and thoroughly explains experimental results. The selections rules allow to explain characteristic fitures in single quantum dot spectra.

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