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绿色低成本碱-多酚协同自催化体系用于制备可自供电摩擦纳米发电机的可自愈自粘导电水凝胶的快速凝胶化

Green and Low-Cost Alkali-Polyphenol Synergetic Self-Catalysis System Access to Fast Gelation of Self-Healable and Self-Adhesive Conductive Hydrogels for Self-Powered Triboelectric Nanogenerators.

作者信息

Zhang Hongmei, Xue Kai, Xu Xihang, Wang Xiaohui, Wang Bing, Shao Changyou, Sun Runcang

机构信息

Liaoning Key Laboratory of Lignocellulose Chemistry and BioMaterials, Liaoning Collaborative Innovation Center for Lignocellulosic Biorefinery, College of Light Industry and Chemical Engineering, Dalian Polytechnic University, Dalian, 116034, China.

State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, 510641, China.

出版信息

Small. 2024 Mar;20(10):e2305502. doi: 10.1002/smll.202305502. Epub 2023 Oct 25.

Abstract

Biomass-based hydrogels have attracted great attention in flexible and sustainable self-powered power sources but struggled to fabricate in a green, high-efficiency, and low-cost manner. Herein, a novel and facile alkali-polyphenol synergetic self-catalysis system is originally employed for the fast gelation of self-healable and self-adhesive lignin-based conductive hydrogels, which can be regarded as hydrogel electrodes of flexible triboelectric nanogenerators (TENGs). This synergy self-catalytic system comprises aqueous alkali and polyphenol-containing lignin, in which alkali-activated ammonium persulfate (APS) significantly accelerates the generation of radicals and initiates the polymerization of monomers, while polyphenol acts as a stabilizer to avoid bursting polymerization from inherent radical scavenging ability. Furthermore, multiple hydrogen bonds between lignin biopolymers and polyacrylamide (PAM) chains impart lignin-based hydrogels with exceptional adhesiveness and self-healing properties. Intriguingly, the alkaline conditions not only contribute to the solubility of lignin but also impart superior ionic conductivity of lignin-based hydrogel that is applicable to flexible TENG in self-powered energy-saving stair light strips, which holds great promise for industrial applications of soft electronics.

摘要

生物质基水凝胶在柔性且可持续的自供电电源领域备受关注,但难以以绿色、高效和低成本的方式制备。在此,一种新型且简便的碱 - 多酚协同自催化体系首次被用于可自愈合和自粘附的木质素基导电水凝胶的快速凝胶化,该水凝胶可被视为柔性摩擦纳米发电机(TENG)的水凝胶电极。这种协同自催化体系由碱水溶液和含多酚的木质素组成,其中碱活化的过硫酸铵(APS)显著加速自由基的产生并引发单体聚合,而多酚作为稳定剂,凭借其固有的自由基清除能力避免爆聚。此外,木质素生物聚合物与聚丙烯酰胺(PAM)链之间的多个氢键赋予木质素基水凝胶出色的粘附性和自愈合性能。有趣的是,碱性条件不仅有助于木质素的溶解性,还赋予木质素基水凝胶优异的离子导电性,适用于自供电节能楼梯灯带中的柔性TENG,这为软电子的工业应用带来了巨大希望。

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