Multifunctional polyurethane hydrogel based on a phenol-carbamate network and an Fe3+-polyphenol coordination bond toward NIR light triggered actuators and strain sensors

JOURNAL OF MATERIALS CHEMISTRY A(2022)

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摘要
Multifunctional smart hydrogels have been extensively used in wearable devices, soft robotics, tissue engineering, and information storage, especially those with good mechanical properties, desired stimuli-responsiveness, high strain sensitivity, and recyclability. Herein, a novel synergistic dual-network polyurethane hydrogel was prepared through two steps, that is, tannic acid (TA) was firstly incorporated into a polyurethane backbone comprising thermosensitive polyethylene glycol/polypropylene glycol (PEG/PPG) blocks to obtain TA-based polyurethane (TAPU) bearing a phenol-carbamate network; subsequently, TAPU film was immersed in FeCl3 aqueous solution to obtain a TAPU/Fe hydrogel bearing an Fe3+-polyphenol network. The prepared TAPU/Fe hydrogel exhibited a high tensile strength of 0.75 MPa, and large elongation at break of 550%. Benefiting from the thermosensitivity of PEG/PPG blocks and the photothermal effect of the Fe3+/TA complex, the TAPU/Fe hydrogel showed ideal near-infrared (NIR) light triggered actuating behavior and photothermal stability. Under the irradiation of NIR light, the flower-shaped hydrogel actuator can bend upward vertical to the horizontal plane within 2 min. Furthermore, Fe3+ incorporated into the hydrogel matrix can endow the TAPU/Fe hydrogel sensor with high strain sensitivity, which can be used for real-time, stable and repeated monitoring of human movement, and can also be designed as a light-driven switch to light an LED bulb. Built on the reversible cross-linked networks, the TAPU/Fe hydrogel with good biocompatibility can be recycled. Unexpectedly, the TAPU hydrogel showed blue fluorescence under UV light (365 nm) irradiation, and the fluorescence could be quenched (with Cu2+) and recovered (with ethylenediaminetetraacetic acid), resembling rewritable papers.
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