Highly efficient color-tunable organic co-crystals unveiling polymorphism, isomerism, delayed fluorescence for optical waveguides and cell-imaging.

Photofunctional co-crystal engineering strategies based on donor-acceptor π-conjugated system facilitates expedient molecular packing, consistent morphology, and switchable optical properties, conferring synergic 'structure-property relationship' for optoelectronic and biological functions. In this work, a series of organic co-crystals were formulated using a twisted aromatic hydrocarbon (TAH) donor and three diverse planar acceptors, resulting in color-tunable solid and aggregated state emission via variable packing and through-space charge-transfer interactions. While, adjusting the strength of acceptors, a structural transformation into hybrid stacking modes ultimately results in color-specific polymorphs, a configurational cis-isomer with very high photoluminescence quantum yield. The cis-isomeric co-crystal exhibits triplet-harvesting thermally activated delayed fluorescence (TADF) characteristics, presenting a key discovery in hydrocarbon-based multicomponent systems. Further, 1D-microrod-shaped co-crystal acts as an efficient photon-transducing optical waveguides, and their excellent dispersibility in water endows efficient cellular internalization with bright cell imaging performances. These salient approaches may open more avenues for the design and applications of TAH based co-crystals.

Dimension Engineering of Stimuli-Responsive 1D Molecular Crystals into Unusual 2D and 3D Zigzag Waveguides.

We demonstrate an innovative technique to achieve organic 2D and 3D waveguides with peculiar shapes from an acicular, stimuli-responsive molecular crystal, (2Z,2'Z)-3,3'-(anthracene-9,10-diyl)bis(2-(3,5-bis(trifluoromethyl)phenylacrylonitrile), Ant-CF3 . The greenish-yellow fluorescent (FL) Ant-CF3 molecular crystals exhibit laser power-dependent permanent mechanical bending in 2D and 3D. Investigation of a single-crystal using spatially-resolved Raman/FL/electron microscopy, and theoretical calculations revealed photothermal (Z,E)/(E,E) isomerization-assisted transition from crystalline to amorphous phase at the laser-exposed regions. This phenomenon facilitates the dimension engineering of a 1D crystal waveguide into 2D waveguide on a substrate or a 3D waveguide in free space. The bends can be used as interconnection points to couple different optical elements. The presented technique has broader implications in organic photonics and other crystal-related photonic technologies.

Hot-exciton harvesting via through-space single-molecule based white-light emission and optical waveguides.

Through-space donor-alkyl bridge-acceptor (D-σ-A) luminogens are developed as new organic single-molecule white light emitters (OSMWLEs) involving multiple higher lying singlet (S n ) and triplet (T m ) states (hot-excitons). Experimental and theoretical results confirm the origin of white light emission due to the co-existence of prompt fluorescence from locally excited states, thermally activated delayed fluorescence (TADF), and fast/slow dual phosphorescence color mixing simultaneously. Notably, the fast phosphorescence was observed due to trace amounts of isomeric impurities from commercial carbazole, while H-/J-aggregation resulted in slow phosphorescence. Crystal structure-packing-property analysis revealed that the alkyl chain length induced supramolecular self-assembly greatly influenced the solid-state optical properties. Remarkably, the 1D-microrod crystals of OSMWLEs demonstrated the first examples of triplet harvesting waveguides by self-guiding the generated phosphorescence through light propagation along their longitudinal axis. This work thus highlights an uncommon design strategy to achieve multi-functional OSMWLEs with in-depth mechanistic insights and optical waveguiding applications making them a potentially new class of white emissive materials.

Polarised Optical Emission from Organic Anisotropic Microoptical Waveguides Grown by Ambient Pressure Vapour-deposition.

Ambient pressure chemical vapour deposition of 5,5'-bis((2-(trifluoromethyl)phenyl)ethynyl)-2,2'-bithiophene provides ultrapure needle-shaped crystals. The crystal's supramolecular structure consists of an array of hydrogen bonds and π-π interactions leading to anisotropic arrangements. The cyan emitting crystals exhibit an optical waveguiding tendency with guided polarised optical emissions due to anisotropic molecular arrangements.

Mechanical Processing of Naturally Bent Organic Crystalline Microoptical Waveguides and Junctions.

Precise mechanical processing of optical microcrystals involves complex microscale operations viz. moving, bending, lifting, and cutting of crystals. Some of these mechanical operations can be implemented by applying mechanical force at specific points of the crystal to fabricate advanced crystalline optical junctions. Mechanically compliant flexible optical crystals are ideal candidates for the designing of such microoptical junctions. A vapor-phase growth of naturally bent optical waveguiding crystals of 1,4-bis(2-cyanophenylethynyl)benzene (1) on a surface forming different optical junctions is presented. In the solid-state, molecule 1 interacts with its neighbors via CH⋅⋅⋅N hydrogen bonding and π-π stacking. The microcrystals deposited at a glass surface exhibit moderate flexibility due to substantial surface adherence energy. The obtained network crystals also display mechanical compliance when cut precisely with sharp atomic force microscope cantilever tip, making them ideal candidates for building innovative T- and Δ-shaped optical junctions with multiple outputs. The presented micromechanical processing technique can also be effectively used as a tool to fabricate single-crystal integrated photonic devices and circuits on suitable substrates.

Mechanophotonics: Flexible Single-Crystal Organic Waveguides and Circuits.

We present the one-dimensional optical-waveguiding crystal dithieno[3,2-a:2',3'-c]phenazine with a high aspect ratio, high mechanical flexibility, and selective self-absorbance of the blue part of its fluorescence (FL). While macrocrystals exhibit elasticity, microcrystals deposited at a glass surface behave more like plastic crystals due to significant surface adherence, making them suitable for constructing photonic circuits via micromechanical operation with an atomic-force-microscopy cantilever tip. The flexible crystalline waveguides display optical-path-dependent FL signals at the output termini in both straight and bent configurations, making them appropriate for wavelength-division multiplexing technologies. A reconfigurable 2×2-directional coupler fabricated via micromanipulation by combining two arc-shaped crystals splits the optical signal via evanescent coupling and delivers the signals at two output terminals with different splitting ratios. The presented mechanical micromanipulation technique could also be effectively extended to other flexible crystals.

Micromanipulation of Mechanically Compliant Organic Single-Crystal Optical Microwaveguides.

Flexible organic single crystals are evolving as new materials for optical waveguides that can be used for transfer of information in organic optoelectronic microcircuits. Integration in microelectronics of such crystalline waveguides requires downsizing and precise spatial control over their shape and size at the microscale, however that currently is not possible due to difficulties with manipulation of these small, brittle objects that are prone to cracking and disintegration. Here we demonstrate that atomic force microscopy (AFM) can be used to reshape, resize and relocate single-crystal microwaveguides in order to attain spatial control over their light output. Using an AFM cantilever tip, mechanically compliant acicular microcrystals of three N-benzylideneanilines were bent to an arbitrary angle, sliced out from a bundle into individual crystals, cut into shorter crystals of arbitrary length, and moved across and above a solid surface. When excited by using laser light, such bent microcrystals act as active optical microwaveguides that transduce their fluorescence, with the total intensity of transduced light being dependent on the optical path length. This micromanipulation of the crystal waveguides using AFM is non-invasive, and after bending their emissive spectral output remains unaltered. The approach reported here effectively overcomes the difficulties that are commonly encountered with reshaping and positioning of small delicate objects (the "thick fingers" problem), and can be applied to mechanically reconfigure organic optical waveguides in order to attain spatial control over their output in two and three dimensions in optical microcircuits.

Direct micro-scale monitoring of molecular aggregation, its growth and diffusion via aggregation-induced emission.

Time-dependent monitoring of aggregation-induced fluorescence of a model compound namely, (Z)-3-(3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-4-yl)-2-(4-bromophenyl)acrylonitrile unearth hitherto unknown molecular level events such as onset of molecular aggregation, their growth, size, and diffusion dynamics. The presented generalized approach can also be extended to in situ monitoring and controlling of various biological aggregation processes down to a single-cell level and all aspects of materials chemistry, as well.

Mechanical Actuation and Patterning of Rewritable Crystalline Monomer-Polymer Heterostructures via Topochemical Polymerization in a Dual-Responsive Photochromic Organic Material.

The dark-orange monomer single crystals of 1,1'-dioxo-1H-2,2'-biindene-3,3'-diyldidodecanoate (BIT-dodeca2) convert to a transparent single-crystalline polymer (PBIT-dodeca2) material via a single-crystal-to-single-crystal (SCSC) polymerization reaction under sunlight, which then undergoes reverse thermal transformation into BIT-dodeca2 single crystals, leading to reversible photo-/thermochromism, coupled with mechanical actuation. We exploit the properties of this unique material to demonstrate the formation of monomer-polymer heterostructures in selected regions of single crystals with micrometer-scale precision using a laser. This is the first example of heterostructure patterning involving monomer-polymer domains in single crystals. We reveal that the speed of photomechanical bending induced by the polymerization reaction in this example is comparable to those of the well-known diarylethene derivatives, in which electrocyclic ring-closing-ring-opening reactions operate. Furthermore, we characterize the distinct mechanical properties of the monomer and polymer using a quantitative nanoindentation technique as well as demonstrate photopatterning on a monomer-coated paper for potential use in security devices. These crystals with several advantages, such as photomechanical bending (weight lifting) even when the crystal size is large, responsiveness to both UV and visible light, distinct solubilities (the polymer is insoluble, whereas the monomer is soluble in most organic solvents) and colors, provide unique opportunities for their use at different length scales of the sample (µm to mm) for various purposes.

Mechanophotonics: precise selection, assembly and disassembly of polymer optical microcavities via mechanical manipulation for spectral engineering.

The advancement of nanoscience and technology relies on the development and utility of innovative techniques. Precise manipulation of photonic microcavities is one of the fundamental challenges in nanophotonics. This challenge impedes the construction of optoelectronic and photonic microcircuits. As a proof-of-principle, we demonstrate here that an atomic force microscopy cantilever and confocal microscopy can be used together to mechanically micromanipulate polymer-based whispering gallery mode microcavities or microresonators into well-ordered geometries. The micromanipulation technique efficiently assembles or disassembles resonators and also produces well-ordered dimer, trimer, tetramer, and pentamer assemblies of resonators in linear and bent geometries. Interestingly, an intricate L-shaped coupled-resonator optical waveguide (CROW) comprising a pentamer assembly effectively transduces light through a 90° bend angle. The presented new research direction, which combines mechanical manipulation and nanophotonics, is also expected to open up a plethora of opportunities in nano and microstructure-based research areas including nanoelectronics and nanobiology.

Vapour-Phase Epitaxial Growth of Dual-Colour-Emitting DCM-Perylene Micro-Heterostructure Optical Waveguides.

Organic micro-heterostructures (MHS) with dual optical emissions are essential to produce miniaturized optical waveguides for wavelength division multiplexing technologies. The bimolecular MHS produced by solution-based bottom-up self-assembly technique often leads to poor surface smoothness, edge imperfection, defects, and unwanted thin films deposits. Conversely, sequential sublimation technique at ambient pressure facilitates effective integration of α-perylene micro-square with dicyanomethylene-2-methyl-6-(p-dimethylaminostyryl) 4H-pyran (DCM) microrods in an epitaxial manner to produce MHS. The obtained DCM/perylene MHS act as optical waveguides to produce red (λmax ≈670 nm) or/and yellow (λmax ≈607 nm) dual optical outputs via an energy transfer mechanism depending upon the heterostructures geometry and optical excitation positions. The presented dual-color emitting MHS optical waveguides are essential for the integrated nano-photonic and optoelectronic device structures.