ABSTRACT
Visible light guiding optical fibers with underwater operational capability are highly desired for subaquatic communication and sensing technologies. Herein, we present mechanically flexible, blue-violet fluorescent (4,4'-bis(2,6-di(1H-pyrazol-1-yl)pyridin-4-yl)biphenyl) (BPP) crystal waveguides with high-aspect ratio. These milli-meter-long BPP crystals guide light actively and passively in ambient and underwater conditions demonstrating their amphibian-like character. Due to the crystal's high flexibility, the optical fiber's output light direction in submerged and ambient states can be altered mechanically for high-precision lighting and sensing applications. The development of such multi-environment-compatible and mechanically flexible organic optical fibers acting as sensing materials possess enormous potential for short-range underwater photonic technologies.
ABSTRACT
We report the construction of an organic crystal multiplexer using three chemically and optically different acicular, flexible organic crystals for a broadband, visible light signal transportation. The mechanical integration of a highly flexible crystal waveguide of (Z)-2-(3,5-bis(trifluoromethyl)phenyl)-3-(7-methoxybenzo[c][1,2,5]thiadiazol-4-yl)acrylonitrile (BTD2CF3 ) displaying bright yellow (λ1 ) fluorescence with blue-emitting (λ2 ) BPP and cyan emitting (λ3 ) DBA crystals using AFM-tip provides a composite organic crystal multiplexer. The constructed hybrid single crystal multiplexer effectively transduces three optical signals (λ1 +λ2 +λ3 ) covering the 420-750â nm region as a composite output signal. The presented proof-of-principle experiment demonstrates the real potential of organic flexible crystal waveguides for visible light communication technologies.
ABSTRACT
Flexible organic crystals (elastic and plastic) are important materials for optical waveguides, tunable optoelectronic devices, and photonic integrated circuits. Here, we present highly elastic organic crystals of a Schiff base, 1-((E)-(2,5-dichlorophenylimino)methyl)naphthalen-2-ol (1), and an azine molecule, 2,4-dibromo-6-((E)-((E)-(2,6-dichlorobenzylidene)hydrazono)methyl)phenol (2). These microcrystals are highly flexible under external mechanical force, both in the macroscopic and the microscopic regimes. The mechanical flexibility of these crystals arises as a result of weak and dispersive C-Hâ â â Cl, Clâ â â Cl, Brâ â â Br, and πâ â â π stacking interactions. Singly and doubly-bent geometries were achieved from their straight shape by a micromechanical approach using the AFM cantilever tip. Crystals of molecules 1 and 2 display a bright-green and red fluorescence (FL), respectively, and selective reabsorption of a part of their FL band. Crystals 1 and 2 exhibit optical-path-dependent low loss emissions at the termini of crystal in their straight and even in extremely bent geometries. Interestingly, the excitation position-dependent optical modes appear in both linear and bent waveguides of crystals 1 and 2, confirming their light-trapping ability.
ABSTRACT
We demonstrate mechanically-powered rolling locomotion of a twisted-microcrystal optical-waveguide cavity on the substrate, rotating the output signal's linear-polarization. Self-assembly of (E)-2-bromo-6-(((4-methoxyphenyl)imino)methyl)-4-nitrophenol produces naturally twisted microcrystals. The strain between several intergrowing, orientationally mismatched nanocrystalline fibres dictates the pitch lengths of the twisted crystals. The crystals are flexible, perpendicular to twisted (001) and (010) planes due to πâ â â π stacking, C-Hâ â â Br, N-Hâ â â O and C-Hâ â â O interactions. The twisted crystals in their straight and bent geometries guide fluorescence along their body axes and display optical modes. Depending upon the degree of mechanical rolling locomotion, the crystal-waveguide cavity correspondingly rotates the output signal polarization. The presented twisted-crystal cavity with a combination of mechanical locomotion and photonic attributes unfolds a new dimension in mechanophotonics.
ABSTRACT
Nonlinear microresonators are very desired for a wide variety of applications. Up-conversion processes responsible for the transformation of IR laser radiation into visible are intensity-dependent and thus rather sensitive to all involved effects, which can mask each other. In this work we study the phenomena that are the most important for possible lasing in 4-(dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4 H-pyran dye spherical microresonators: the two-photon absorption and photobleaching. Based on the suggested model of the threshold-like dependence of the two-photon luminescence (TPL) on pump power, we demonstrate the role of intensity-dependent photobleaching in the appearance of the TPL and find a good agreement with the experiment. This finding is important for the analysis of lasing in nonlinear dye-based resonators.