详细信息
Muscle-like self-strengthening poly(vinyl alcohol)/cellulose/MXene composite hydrogel by mechanical training for wearable electronics ( EI收录)
文献类型:期刊文献
英文题名:Muscle-like self-strengthening poly(vinyl alcohol)/cellulose/MXene composite hydrogel by mechanical training for wearable electronics
作者:Lu, Chuanwei[1] Gong, Sijie[1] Xia, Yu[1] Xu, Ning[1] Yu, Juan[1] Wang, Chunpeng[2] Wang, Jifu[2] Yong, Qiang[1] Chu, Fuxiang[2]
第一作者:Lu, Chuanwei
机构:[1] Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, International Innovation Center for Forest Chemicals and Materials, College of Chemical Engineering, Nanjing Forestry University, Nanjing, 210037, China; [2] National Key Laboratory for Development and Utilization of Forest Food Resources, Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing, 210042, China
年份:2025
卷号:322
外文期刊名:International Journal of Biological Macromolecules
收录:EI(收录号:20253318974879);Scopus(收录号:2-s2.0-105012945221)
语种:英文
外文关键词:Bearings (machine parts) - Chains - Electronic equipment - Hydrogels - Hydrogen bonds - Muscle - Nanocrystals - Strengthening (metal) - Wearable sensors
摘要:The development of mechanically tunable and self-strengthening hydrogels for advanced electronic applications is highly desirable but remains a challenge. Muscles, as force-bearing tissues, could autonomously grow to adapt to the surrounding environment through cyclic disassembly and reconstruction of muscle fibers by mechanical training. Inspired by this biological feature, we presented a mechanical training enhancement strategy for preparing self-strengthening conductive composite hydrogels. The polyvinyl alcohol (PVA) acted as the hydrogel matrix, MXene serving as conductive medium realized high conductivity (679.6 mS/m), and the incorporation of carboxymethyl cellulose (CMC) not only prevented MXene self-stacking but also strengthened hydrogen bonding interactions and chain entanglement density. During mechanical training process, the nanocrystalline domains of the PVA chain were reoriented into a highly ordered structure, while the decrease in average distance between neighboring nanocrystalline domains increased the density of nanocrystalline domains in the cross-section. As a result, the prestretched composite hydrogel demonstrated enhanced tensile strength of 1356.1 kPa and toughness of 2962.2 kJ/m3, which were 4.4 and 6.4 times of the initial composite hydrogel, respectively. The composite hydrogels were successfully employed as strain sensors for monitoring human motions. This work demonstrated a promising approach to developing self-strengthening soft materials for advanced applications. ? 2025 Elsevier B.V.
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