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Register a new userTailoring the Local Density of Optical States and directionality of light emission by symmetry-breaking
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We present a method to simultaneously engineer the energy-momentum dispersion and the local density of optical states. Using vertical symmetry-breaking in high-contrast gratings, we enable the mixing of modes with different parities, thus producing hybridized modes with controlled dispersion. By tuning geometric parameters, we control the coupling between Bloch modes, leading to flatband, M- and W-shaped dispersion as well as Dirac dispersion. Such a platform opens up a new way to control the direction of emitted photons, and to enhance the spontaneous emission into desired modes. We then experimentally demonstrate that this method can be used to redirect light emission from weak emitters -- defects in Silicon -- to optical modes with adjustable density of states and angle of emission.
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We uncover that the breaking point of the PT-symmetry in optical waveguide arrays has a dramatic impact on light localization induced by the off-diagonal disorder. Specifically, when the gain/loss control parameter approaches a critical value at which PT-symmetry breaking occurs, a fast growth of the coupling between neighboring waveguides causes diffraction to dominate to an extent that light localization is strongly suppressed and statistically averaged width of the output pattern substantially increases. Beyond the symmetry-breaking point localization is gradually restored, although in this regime the power of localized modes grows upon propagation. The strength of localization monotonically increases with disorder at both, broken and unbroken PT-symmetry.
We present experimental evidence for the different mechanisms driving the fluctuations of the local density of states (LDOS) in disordered photonic systems. We establish a clear link between the microscopic structure of the material and the frequency correlation function of LDOS accessed by a near-field hyperspectral imaging technique. We show, in particular, that short- and long-range frequency correlations of LDOS are controlled by different physical processes (multiple or single scattering processes, respectively) that can be---to some extent---manipulated independently. We also demonstrate that the single scattering contribution to LDOS fluctuations is sensitive to subwavelength features of the material and, in particular, to the correlation length of its dielectric function. Our work paves a way towards a complete control of statistical properties of disordered photonic systems, allowing for designing materials with predefined correlations of LDOS.
We propose a method to break the chiral symmetry of light in traveling wave resonators by coupling the optical modes to a lossy channel. Through the engineered dissipation, an indirect dissipative coupling between two oppositely propagating modes can be realized. Combining with reactive coupling, it can break the chiral symmetry of the resonator, allowing light propagating only in one direction. The chiral symmetry breaking is numerically verified by the simulation of an electromagnetic field in a micro-ring cavity, with proper refractive index distributions. This work provokes us to emphasize the dissipation engineering in photonics, and the generalized idea can also be applied to other systems.
The study of the non-linear response of matter to high electric fields has recently encompassed harmonic generation in solids at near-infrared (NIR) driving wavelengths. Interest has been driven by the prospect of ultrafast signal processing and all-optical mapping of electron wave-functions in solids. Engineering solid-state band structures to control the non-linear process has already been highlighted theoretically. Here, we show experimentally for the first time that second harmonic generation (SHG) can be enhanced by doping crystals of magnesium oxide (MgO) with chromium (Cr) atoms. We show that the degree of enhancement depends non-linearly on dopant concentration. The SHG efficiency is shown to increase when Cr dopants are introduced into pure MgO. A physical picture of the effect of Cr dopants is aided by density functional theory (DFT) calculations of the electronic structure for pure and doped samples. This work shows an unambiguous enhancement of the SHG efficiency by modifying the electronic structure. The observed effects are consistent with an electronic structure that facilitates the surface induced SHG and demonstrates a minimal angular dependence. This work highlights the potential of manipulating the electronic structure of solids to control or test theories of their non-linear optical response.
Forward and backward THz emission by ionizing two-color laser pulses in gas is investigated by means of a simple semi-analytical model based on Jefimenkos equation and rigorous Maxwell simulations in one and two dimensions. We find the emission in backward direction having a much smaller spectral bandwidth than in forward direction and explain this by interference effects. Forward THz radiation is generated predominantly at the ionization front and thus almost not affected by the opacity of the plasma, in excellent agreement with results obtained from a unidirectional pulse propagation model.
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