High-Efficiency Polycrystalline Perovskite Light-Emitting Diodes Based on Mixed Cations.

We have achieved high-efficiency polycrystalline perovskite light-emitting diodes (PeLEDs) based on formamidinium (FA) and cesium (Cs) mixed cations without quantum dot synthesis. Uniform single-phase FA1- xCs xPbBr3 polycrystalline films were fabricated by one-step formation with various FA:Cs molar proportions; then the influences of chemical composition on film morphology, crystal structure, photoluminescence (PL), and electroluminescence (EL) were systematically investigated. Incorporation of Cs+ cations in FAPbBr3 significantly reduced the average grain size (to 199 nm for FA:Cs = 90:10) and trap density; these changes consequently increased PL quantum efficiency (PLQE) and PL lifetime of FA1- xCs xPbBr3 films and current efficiency (CE) of PeLEDs. Further increase in Cs molar proportion from 10 mol % decreased crystallinity and purity, increased trap density, and correspondingly decreased PLQE, PL lifetime, and CE. Incorporation of Cs also increased photostability of FA1- xCs xPbBr3 films, possibly due to suppressed formation of light-induced metastable states. FA1- xCs xPbBr3 PeLEDs show the maximum CE = 14.5 cd A-1 at FA:Cs = 90:10 with very narrow EL spectral width (21-24 nm); this is the highest CE among FA-Cs-based PeLEDs reported to date. This work provides an understanding of the influences of Cs incorporation on the chemical, structural, and luminescent properties of FAPbBr3 polycrystalline films and a breakthrough to increase the efficiency of FA1- xCs xPbBr3 PeLEDs.

Facile Fabrication of Ultra-Stretchable Metallic Nanocluster Films for Wearable Electronics.

With recent progress in flexible electronics, developing facile one-step techniques for fabricating stretchable conductors and interconnects remain essential. It is also desirable for these processes to have a small number of processing steps, incorporate micropatterning, and be capable of being effortlessly implemented for manufacturing of wearable logic circuits. A low vacuum flash evaporation of Au nanoclusters is proposed as a facile method to fabricate highly stretchable conductors capable of fulfilling all such requirements. High metal-elastomer adhesion on textured substrates ensures low surface resistances (100% strain ≈ 25 Ω-sq-1) where thin film Au accommodate strain like a "bellow". Stretchability for conductors deposited on non-prestretched textured substrates up to 150% and smooth PDMS substrates up to 200% are shown. The system is modeled on a microscopic system calculating 2-D current continuity equations. Devising low cost techniques for fabricating stretchable conductors remains essential and in that direction stretchable circuits, heating elements have been demonstrated.

Organic soluble and uniform film forming oligoethylene glycol substituted BODIPY small molecules with improved hole mobility.

Judiciously chosen side chains of conjugated molecules have a positive impact on charge transport properties when used as the active material in organic electronic devices. Amongst the side chains, oligoethylene glycols (OEGs) have been relatively unexplored due to their hydrophilic nature. OEGs also affect the smooth film formation of conjugated molecules, which preclude device fabrication. However, X-ray diffraction studies have shown that OEGs facilitate intermolecular contact, which is a desirable property for the fabrication of organic electronic devices. Thus the challenge is to design and synthesize organic solvent soluble and uniform film forming conjugated molecules with OEG side chains. We have designed and synthesized conjugated small molecules (CSMs) comprising BODIPY as acceptor and triphenylamine as donor with an OEG side chain. This molecule forms smooth films when processed from organic solvents. In order to understand the impact of the OEG side chain, we have also synthesized alkyl chain analogs. All the molecules exhibit exactly the same HOMO and LUMO energy levels, but the packing in the solid state is different. CSM with methyl side chains exhibit an inter planar distance of 4.15 Å. Contrary to this, the OEG side chain containing CSM showed an inter planar spacing of 4.30 Å, which is 0.2 Å less than the alkyl side chain comprising CSMs. Please note that the length of the hydrophobic and hydrophilic side chains is the same. Interestingly, the OEG side chain comprising CSM showed two orders of higher hole carrier mobilities compared to all the other derivatives. The same molecule also showed an extremely low threshold voltage of -0.27 V indicating the OEG side chains' favourable interaction between substrate as well as between molecules.

Neuronal differentiation of embryonic stem cell derived neuronal progenitors can be regulated by stretchable conducting polymers.

Electrically conducting polymers are prospective candidates as active substrates for the development of neuroprosthetic devices. The utility of these substrates for promoting differentiation of embryonic stem cells paves viable routes for regenerative medicine. Here, we have tuned the electrical and mechanical cues provided to the embryonic stem cells during differentiation by precisely straining the conducting polymer (CP) coated, elastomeric-substrate. Upon straining the substrates, the neural differentiation pattern occurs in form of aggregates, accompanied by a gradient where substrate interface reveals a higher degree of differentiation. The CP domains align under linear stress along with the formation of local defect patterns leading to disruption of actin cytoskeleton of cells, and can provide a mechano-transductive basis for the observed changes in the differentiation. Our results demonstrate that along with biochemical and mechanical cues, conductivity of the polymer plays a major role in cellular differentiation thereby providing another control feature to modulate the differentiation and proliferation of stem cells.