自愈水凝胶
胶束
荧光
吸光度
材料科学
螺吡喃
异构化
甲基丙烯酸酯
化学工程
光化学
聚合物
纳米技术
共聚物
光致变色
化学
高分子化学
有机化学
色谱法
水溶液
催化作用
复合材料
光学
工程类
物理
作者
Junheng Gao,Fu Tang,Yuting Li,L. L. Zhang,An Hu,Shuo Li,Lidong Li
标识
DOI:10.1002/adom.202403352
摘要
Abstract Fluorescent hydrogels have immense potential and are widely studied for on demand displays. Response rate of fluorophores upon stimuli within the hydrogel matrix is a key role to improve the timely responsiveness, but rare reports are elaborated on it. In this work, the photoisomeric spiropyran methacrylate (SPMA) is introduced into the poly (2‐hydroxyethyl methacrylate) hydrogel to fabricate a stimuli‐responsive fluorescent hydrogel. Interestingly, the photoresponse rate of SPMA in the hydrogel is greatly accelerated at the presence of F127 micelles than without it. Both of the absorbance and fluorescence intensity of the hydrogels at the photostationary state are improved obviously with micelles. Besides, the normalized absorbance and the fluorescence kinetic studies indicated a more than 2 times quicker isomerization process. The absolute fluorescence quantum yields of SPMA in the hydrogel is also increased. These can be attributed to the hydrophobic microenvironment provided by the F127 micelles that facilitated the conformation transition of SPMA. Thus, the synergetic effect of the increased amount of activable SPMA and the promoted speed of isomerization contributed to the accelerated photoresponse of the prepared hydrogel. Taking advantage of these virtues, a timely and multi‐responsive on‐demand information encryption system is realized.
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