We report that incandescent beams patterned with amplitude depressions (dips) suffer instability in a photopolymerizable system and organize into lattices of black and bright self-trapped beams propagating respectively, through self-induced black and bright waveguides. Such optochemically organized lattices emerge when beams embedded with a hexagonal or square array of dips initiate free-radical polymerization and corresponding changes in refractive index (Δn) along their propagation paths. Under these nonlinear conditions, the dips evolve into a hexagonal or square lattice of black beams, while their bright interstitial regions become unstable and divide spontaneously into multiple filaments of light.
View Article and Find Full Text PDFWe report that a self-trapped black optical beam that is spatially and temporally incoherent forms spontaneously in a nascent photopolymerization system. The black beam inscribes a permanent cylindrical channel, which prevents the propagation of visible light even under passive conditions (in the absence of polymerization). The finding opens a powerful new mechanism to manipulate light signals from incoherent sources such as LEDs through selective suppression of light propagation.
View Article and Find Full Text PDFWe report that a beam of spatially and temporally incoherent white light self-traps by initiating free-radical polymerization in an organosiloxane medium. Refractive index changes due to polymerization lead to the formation of a narrow channel waveguide that traps and guides the entire multimode, broadband beam without diffraction. The response time of the system, which is determined by the inherently slow rate of free-radical polymerization, exceeds by several orders of magnitude the femtosecond-scale random phase fluctuations that characterize white light.
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