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Bio-derived optoelectronic material is captivating and sustainable research as it reduces the environmental toxicity and comforting the wearable aspects. Our research involves the synthesis of series of bio-derived polyfluorene-block-poly(delta-decanolactone) (PF-b-PDL) conjugated block copolymers through smart one-pot procedure that involves simple purification for fabricating touch-responsive light-emitting diode (LED) devices. Compared with PF homopolymer, the block copolymers exhibit higher photoluminescence quantum yields and higher exciton binding energies. PF18-b-PDL13 specifically exhibits external quantum efficiency (EQE %) (similar to 6 times higher than PF homopolymer). Moreover, because of coily PDL block inducing a highly stable bound state in block copolymer generating the increment in PL lifetime and exciton binding energies than the homopolymer. Furthermore, the diblock copolymers device exhibits fully solution processability, higher carrier recombination efficiency, flex-stretch stability, good structural integrity and mechanical endurance highlighting the brighter potential of our bio-derived block copolymers for fabricating highly durable wearable stretchable nano and microelectronic devices.

We demonstrated a novel strategy for the preparation of light down-converter by combining rod-coil block copolymers with perovskite quantum dots (QDs) through electrospinning. Reports have shown that polymer deformability can be enhanced by incorporating a soft segment and controlled by varying the rod/coil ratio. Therefore, we first synthesized the rod-coil block copolymer through the click reaction of polyfluorene (PF) and poly(n-butyl acrylate) (PBA). Next, the CsPbBr3@PF8k-b-PBA(12k) composite fibers were fabricated by blending perovskite through electrospinning. Optical spectral evidence demonstrated the success of the strategy, as light down-converters were prepared through the controlled variance of QD/polymer ratios to achieve tunable color and stretchability. This result reveals the potential of using rod-coil block copolymers to fabricate color-tunable perovskite light down-converters.

Cesium lead halide perovskite quantum dots (QDs) have drawn extensive attention due to their excellent optical properties. However, their use is limited by poor stability. To enhance their stability, we electrospun perovskite-embedded fibers from composite CsPbX3 (X = Cl, Br, and I) perovskite QDs, blending with three polymers, poly(styrene-butadiene-styrene) (SBS), poly(methyl methacrylate) (PMMA), or polystyrene (PS), for the light-emitting diode (LED) applications. We found that the stretchable CsPbBr3@SBS fibers revealed the highest photoluminescence quantum yield, the CsPbBr3@PMMA fibers demonstrated a high thermal stability, and the CsPbBr3@PS fibers exhibited the best water-resistant stability. The photoluminescence intensity maintained 83% of its initial intensity for more than 3 months in water. Furthermore, the LED devices are manufactured from the blue chips and packaged with the core/shell red and green perovskite-based fibers by using biaxial electrospinning exhibited stable and highly efficient white luminescence. The luminance and efficiency are higher than 400% of the values of multilayered structures. (C) 2019 Author(s).

Amphiphilic molecules are well-known for their ability to self-assemble in water to form structures such as micelles and vesicles. In comparison, much less is known about amphiphilic self-assembly in nonpolar organic liquids. Such "reverse" self assembly can produce many of the counterparts to structures found in water. In this dissertation, we focus on the formation and dynamics of such reverse structures. We seek to obtain fundamental insight into the driving forces for reverse self-assembly processes. Three specific types of reverse structures are studied: (a) reverse wormlike micelles, i.e., long, flexible micellar chains; (b) reverse vesicles, i.e., hollow containers enclosed by reverse bilayers; and (c) organogel networks. While our focus is on the fundamentals, we note that reverse structures can be useful in a variety of applications ranging from drug delivery, controlled release, hosts for enzymatic reactions, and templates for nanomaterials synthesis. In the first part of this study, we describe a new route for forming reverse wormlike micelles in nonpolar organic liquids. This route involves the addition of trace amounts of a bile salt to solutions of the phospholipid, lecithin. We show that bile salts, due to their unique "facially amphiphilic" structure, can promote the aggregation of lecithin molecules into these reverse micellar chains. The resulting samples are viscoelastic and show interesting rheological properties. Unusual trends are seen in the temperature dependence of their rheology, which indicates the importance of hydrogen-bonding interactions in the formation of these micelles. Another remarkable feature of their rheology is the presence of strain-stiffening, where the material becomes stiffer at high deformations. Strain-stiffening has been seen before for elastic gels of biopolymers; here, we demonstrate the same properties for viscoelastic micellar solutions. The second reverse aggregate we deal with is the reverse vesicle. We present a