磷光
自愈水凝胶
丙烯酰胺
材料科学
极限抗拉强度
聚合
余辉
化学工程
复合材料
聚合物
高分子化学
单体
物理
伽马射线暴
量子力学
天文
工程类
荧光
作者
Ruixia Liu,Hongda Guo,Shouxin Liu,Jian Li,Shujun Li,Tony D. James,Zhijun Chen
标识
DOI:10.1038/s41467-024-55025-z
摘要
Room temperature phosphorescent (RTP) hydrogels exhibit great potential but show poor mechanical performance (Tensile strengthen <1 MPa) and non-tunable RTP performance, hindering their practical applications. Here, we develop wood hydrogel (W-hydrogel) by the in situ polymerization of acrylamide in the presence of delignified wood. As a result of the molecular interactions between the components of delignified wood and polyacrylamide, the W-hydrogel exhibit a tensile strengthen of 38.4 MPa and green RTP emission with a lifetime of 32.5 ms. Moreover, the tensile strength and RTP lifetime are increased to 153.8 MPa and 69.7 ms, upon treating W-hydrogel with ethanol. Significantly, the mechanical and RTP performance of W-hydrogel is switched by alternating "ethanol and water" treatments. Additionally, W-hydrogel is used as energy donor in order to produce red afterglow emission using RhB via an energy transfer process. Taking advantage of these properties, W-hydrogel is processed into multiple hydrogel-based luminescent materials. Hydrogels with room temperature phosphorescence have potential in a number of applications, but mechanical properties can limit the potential. Here, the authors report a wood-based hydrogel with room temperature phosphorescence, by polymerization of acrylamide with delignified wood.
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