Zhong Yu, Wang Zhiqi, Quan Lingqi, Wu Yiqiang, Hu Dongying, Cheng Jun, Zheng Yanjie, Cheng Fangchao
State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, School of Resources, Environment and Materials, Guangxi University, Nanning 530004, China.
College of Material Science and Engineering, Central South University of Forestry and Technology, Changsha 410004, China.
J Colloid Interface Sci. 2025 Feb;679(Pt A):393-402. doi: 10.1016/j.jcis.2024.09.204. Epub 2024 Sep 27.
The rapid development of anti-counterfeiting technology has brought new challenges to the repeatability and stability of reversible fluorescence/photochromic switching hydrogels. To address this issue, a series of chemical cross-linked cellulose-based intelligent responsive hydrogels were synthesized by free-radical graft copolymerization in a hydrothermal process. This strategy allows for the creation of a chemical cross-linked three-dimensional structure that anchors photochromic ammonium molybdate and fluorescent carbon dots together, resulting in enhanced stability and mechanical properties. Especially, the tensile and compressive strength of hydrogel reached a maximum value of 280 kPa and 560 kPa, respectively, which far exceeds that of some reported hydrogels. The resultant hydrogels exhibited desired reversible fluorescence/photochromic switching, reversible printing and erasing of patterns, and information encryption/decryption. Notably, the change of photochromism from yellow to green can be realized, and the self-fading process can be shortened to 25 min at 60 °C instead of 6 h at room temperature. More importantly, the fluorescence quenching phenomenon of the hydrogel occurs gradually after 2 min of continuous irradiation, and it can be recovered by selective treatment with ethanol. Overall, this study provides a simple strategy for the preparation of environmentally friendly reversible fluorescence/photochromic switching cellulose-based hydrogels for information encryption.
防伪技术的快速发展给可逆荧光/光致变色开关水凝胶的重复性和稳定性带来了新的挑战。为了解决这个问题,通过水热过程中的自由基接枝共聚合成了一系列化学交联的纤维素基智能响应水凝胶。这种策略允许创建一种化学交联的三维结构,将光致变色钼酸铵和荧光碳点锚定在一起,从而提高稳定性和机械性能。特别是,水凝胶的拉伸强度和压缩强度分别达到最大值280 kPa和560 kPa,远远超过一些报道的水凝胶。所得水凝胶表现出所需的可逆荧光/光致变色开关、图案的可逆打印和擦除以及信息加密/解密。值得注意的是,可以实现从黄色到绿色的光致变色变化,并且在60°C下自褪色过程可以缩短到25分钟,而不是在室温下需要6小时。更重要的是,水凝胶在连续照射2分钟后会逐渐出现荧光猝灭现象,并且可以通过用乙醇进行选择性处理来恢复。总的来说,这项研究为制备用于信息加密 的环保型可逆荧光/光致变色开关纤维素基水凝胶提供了一种简单的策略。