4.1 Article

Highly conductive and tough double-network hydrogels for smart electronics

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SMARTMAT
卷 -, 期 -, 页码 -

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WILEY
DOI: 10.1002/smm2.1160

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conducting polymers; double-network hydrogels; smart electronics; supercapacitors

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The development and understanding of highly mechanically robust and electronically conducting hydrogels is crucial for energy-based applications. Traditional methods of mixing conductive additives with hydrophilic polymers limit the mechanical strength and electronic conductivity of the hydrogels. This study presents a double-network (DN) engineering strategy to fabricate PVA/PPy DN hydrogels with superior mechanical and electrochemical properties. The integration of ionic-/electrical-conductive materials into DN hydrogels opens up new possibilities for smart-soft electronics and surpasses the commonly used PEDOT:PSS-based hydrogels.
Development and understanding of highly mechanically robust and electronically conducting hydrogels are extremely important for ever-increasing energy-based applications. Conventional mixing/blending of conductive additives with hydrophilic polymer network prevents both high mechanical strength and electronic conductivity to be presented in polymer hydrogels. Here, we proposed a double-network (DN) engineering strategy to fabricate PVA/PPy DN hydrogels, consisting of a conductive PPy-PA network via in-situ ultrafast gelation and a tough PVA network via a subsequent freezing/thawing process. The resultant PVA/PPy hydrogels exhibited superior mechanical and electrochemical properties, including electrical conductivity of similar to 6.8 S/m, mechanical strength of similar to 0.39 MPa, and elastic moduli of similar to 0.1 MPa. Upon further transformation of PVA/PPy hydrogels into supercapacitors, they demonstrated a high capacitance of similar to 280.7 F/g and a cycle life of 2000 galvanostatic charge/discharge cycles with over 94.3% capacity retention at the current density of 2 mA/cm(2) and even subzero temperatures of -20 degrees C. Such enhanced mechanical performance and electronic conductivity of hydrogels are mainly stemmed from a synergistic combination of continuous electrically conductive PPy-PA network and the two interpenetrating DN structure. This in-situ gelation strategy is applicable to the integration of ionic-/electrical-conductive materials into DN hydrogels for smart-soft electronics, beyond the most commonly used PEDOT:PSS-based hydrogels.

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