23 research outputs found

    Stretchable Self-Healable Semiconducting Polymer Film for Active-Matrix Strain-Sensing Array

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    Skin-like sensory devidces shoud be stretchable and self-healable to meet the demands for future electronic skin applications. Despite recent notable advances in skin-inspired electronic materials, it remains challenging to confer these desired functionalities to an active semiconductor. Here, we report a strain-sensitive, stretchable, and autonomously self-healable semiconducting film achieved through blending of a polymer semiconductor and a self-healable elastomer, both of which are dynamically cross-linked by metal coordination. We observed that by controlling the percolation threshold of the polymer semiconductor, the blend film became strain sensitive, with a gauge factor of 5.75 x 105 at 100% strain in a stretchable transistor. The blend film is also highly stretchable (fracture strain, \u3e1300%) and autonomously self-healable at room temperature. We proceed to demonstrate a fully integrated 5 x 5 stretchable active-matrix transistor sensor array capable of detecting strain distribution through surface deformation

    Construction of Palladium Nanoparticles Modified Covalent Triazine Frameworks towards Highly-Efficient Dehydrogenation of Dipentene for p-Cymene Production

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    The generation of p-cymene from the catalytic dehydrogenation of dipentene is one of the most vital approaches for the synthesis of p-cymene in the chemical industry. Herein, CTF polymer was synthesized by an ionothermal method via using terephthalonitrile as monomer and NaCl-KCl-ZnCl2 ternary mixture as catalyst and solvent, and Pd/CTF catalyst was prepared by loading CTF matrix with Pd nanoparticles via a chemical reduction method. The as-obtained Pd/CTF catalyst with the loading amount of 5 wt% Pd showed remarkable catalytic activity in the dehydrogenation of dipentene to p-cymene with a high conversion rate of 100% and a high selectivity of 96% at the reaction temperature of 220 °C in a stainless-steel autoclave containing 0.1 MPa of Ar gas, and also exhibited good stability in the recycling tests. The strong interaction between Pd nanoparticles and CTF and the enhanced electron transfer at the metal-semiconductor interface contribute to the outstanding catalytic performance of Pd/CTF for the dehydrogenation of dipentene to p-cymene. This work demonstrates that the metal-semiconductor catalysts possessed excellent potential in the production of high-value-added chemical products from terpenes conversion

    Fabrication of a Selective and Sensitive Sensor Based on Molecularly Imprinted Polymer/Acetylene Black for the Determination of Azithromycin in Pharmaceuticals and Biological Samples.

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    A new selective and sensitive sensor based on molecularly imprinted polymer/acetylene black (MIP/AB) was developed for the determination of azithromycin (AZM) in pharmaceuticals and biological samples. The MIP of AZM was synthesized by precipitation polymerization. MIP and AB were then respectively introduced as selective and sensitive elements for the preparation of MIP/AB-modified carbon paste (MIP/ABP) electrode. The performance of the obtained sensor was estimated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. Compared with non-molecularly imprinted polymer (NIP) electrodes, NIP/ABP electrodes, and MIP-modified carbon paste electrodes, MIP/ABP electrode exhibited excellent current response toward AZM. The prepared sensor also exhibited good selectivity for AZM in comparison with structurally similar compounds. The effect of electrode composition, extraction parameters, and electrolyte conditions on the current response of the sensor was investigated. Under the optimized conditions, the prepared sensor showed two dynamic linear ranges of 1.0 × 10-7 mol L-1 to 2.0 × 10-6 mol L-1 and 2.0 × 10-6 mol L-1 to 2.0 × 10-5 mol L-1, with a limit of detection of 1.1 × 10-8 mol L-1. These predominant properties ensured that the sensor exhibits excellent reliability for detecting AZM in pharmaceuticals and biological fluids without the assistance of any separation techniques. The results were validated by the high-performance liquid chromatography-tandem mass spectrometry method

    Hole-Transporting Low-Dimensional Perovskite for Enhancing Photovoltaic Performance

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    Halide perovskites with low-dimensionalities (2D or quasi-2D) have demonstrated outstanding stabilities compared to their 3D counterparts. Nevertheless, poor charge-transporting abilities of organic components in 2D perovskites lead to relatively low power conversion efficiency (PCE) and thus limit their applications in photovoltaics. Here, we report a novel hole-transporting low-dimensional (HT2D) perovskite, which can form a hole-transporting channel on the top surface of 3D perovskite due to self-assembly effects of metal halide frameworks. This HT2D perovskite can significantly reduce interface trap densities and enhance hole-extracting abilities of a heterojunction region between the 3D perovskite and hole-transporting layer. Furthermore, the posttreatment by HT2D can also reduce the crystal defects of perovskite and improve film morphology. As a result, perovskite solar cells (PSCs) can effectively suppress nonradiative recombination, leading to an increasement on photovoltage to >1.20 V and thus achieving >20% power conversion efficiency and >500 h continuous illumination stability. This work provides a pathway to overcome charge-transporting limitations in low-dimensional perovskites and delivers significant enhancements on performance of PSCs

    DTBP-Endocrinology-Supplemental Materials.pdf

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    Supplemental materials supporting the manuscript entitled, "2,4-Di-tert-butylphenol Induces Adipogenesis in Human Mesenchymal Stem Cells by Activating Retinoid X Receptors" This file includes Figure S1, Figure S2, Figure S3 and Table S1</p
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