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用于可持续全凝胶超级电容器的水触发可重构甘油凝胶

Water-Triggered Reconfigurable Glycerogels for Sustainable All-Gel Supercapacitors.

作者信息

Mredha Md Tariful Islam, Rama Varma Adith Varma, Gupta Tanish, Jeon Insu

机构信息

School of Mechanical Engineering, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju, 61186, Republic of Korea.

出版信息

Adv Sci (Weinh). 2025 Jan;12(4):e2411847. doi: 10.1002/advs.202411847. Epub 2024 Dec 4.

DOI:10.1002/advs.202411847
PMID:39630938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11775550/
Abstract

The polymeric structures of synthetic gels are typically static, which makes them damage-prone and nonrecyclable. Inspired by the dynamic reconfigurability of biological tissues, which eliminate old/damaged cells and regenerate new ones via biological triggers/signals, a reconfigurable biopolymer gel is presented based on a glycerol-mediated supramolecular gelation strategy. In response to an eco-friendly triggering agent water, this gel undergoes on-demand molecular-level reconfiguration. The versatility of the approach enables the development of reconfigurable gels with modulated functionality. As a proof-of-concept, a reconfigurable glycerogel electrode and electrolyte are developed and used to prototype an all-gel supercapacitor that exhibits exceptional self-healing, degradation, and rebuilding abilities. Furthermore, it can tolerate extreme mechanical deformations (e.g., stretching, bending, and twisting) and temperatures (-20 to 80 °C). The device exhibits excellent energy storage performance, with a maximum areal capacitance of 450 mF cm (at 0.035 mA cm) and remarkable capacitance retention of 89% following 20 000 charge/discharge cycles (at 0.35 mA cm). Moreover, following self-healing and rebuilding, the capacitance remains at 91% and 110% (at 0.35 mA cm) of the original value, respectively. This generalized strategy for preparing multifunctional reconfigurable gels will facilitate the development of high-performance flexible and wearable devices with improved durability and recyclability.

摘要

合成凝胶的聚合物结构通常是静态的,这使得它们容易受损且不可回收。受生物组织动态可重构性的启发,生物组织通过生物触发因素/信号消除旧的/受损的细胞并再生新细胞,基于甘油介导的超分子凝胶化策略,提出了一种可重构的生物聚合物凝胶。响应于环保触发剂水,这种凝胶会进行按需分子水平的重构。该方法的多功能性使得能够开发具有调制功能的可重构凝胶。作为概念验证,开发了一种可重构的甘油凝胶电极和电解质,并用于制作全凝胶超级电容器的原型,该超级电容器具有出色的自愈、降解和重建能力。此外,它可以承受极端的机械变形(例如拉伸、弯曲和扭转)以及温度(-20至80°C)。该器件表现出优异的储能性能,最大面积电容为450 mF/cm²(在0.035 mA/cm²时),在20000次充放电循环后(在0.35 mA/cm²时)电容保持率高达89%。此外,在自愈和重建后,电容分别保持在原始值的91%和110%(在0.35 mA/cm²时)。这种制备多功能可重构凝胶的通用策略将有助于开发具有更高耐久性和可回收性的高性能柔性和可穿戴设备。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/7c290f9774f2/ADVS-12-2411847-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/e6845477a795/ADVS-12-2411847-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/1f558d309f9b/ADVS-12-2411847-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/b46182cd7284/ADVS-12-2411847-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/b1c7cc3ab21a/ADVS-12-2411847-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/a9ad0be8ef30/ADVS-12-2411847-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/7c290f9774f2/ADVS-12-2411847-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/e6845477a795/ADVS-12-2411847-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/1f558d309f9b/ADVS-12-2411847-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/b46182cd7284/ADVS-12-2411847-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/b1c7cc3ab21a/ADVS-12-2411847-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/a9ad0be8ef30/ADVS-12-2411847-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8e/11775550/7c290f9774f2/ADVS-12-2411847-g004.jpg

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