A stimuli responsive lanthanide-based hydrogel possessing tunable luminescence by efficient energy transfer pathways
A stimuli responsive lanthanide-based hydrogel possessing tunable luminescence by efficient energy transfer pathways作者机构:Tianjin Key Laboratory of Chemical Process SafetySchool of Chemical Engineering and TechnologyNational-Local Joint Engineering Laboratory for Energy Conservation in Chemical Process Integration and Resources UtilizationHebei University of TechnologyTianjin 300130China
出 版 物:《Journal of Rare Earths》 (稀土学报(英文版))
年 卷 期:2022年第40卷第5期
页 面:696-701,I0001页
核心收录:
学科分类:081702[工学-化学工艺] 0709[理学-地质学] 0819[工学-矿业工程] 08[工学] 0817[工学-化学工程与技术] 0708[理学-地球物理学] 0703[理学-化学]
基 金:Project supported by the National Natural Science Foundation of China(21771050) the Natural Science Foundation of Hebei Province(B2018202134,B2016202149,B2016202147) Outstanding Innovative Topics of Hebei Province(220056)。
主 题:Energy transfer Lanthanides Stimuli-responsive hydrogel Luminescence Rare earths
摘 要:Energy transfer as an important component in light-harvesting antenna systems can mimic effectively natural photosynthesis processes,showing great potential in optoelectronic devices.Herein,we report a responsive polymeric hydrogel based on the combination of excited state intramolecular proton transfer(ESIPT) molecule(Salicylic acid,Sal) and terbium(Ⅲ)(Tb^(3+)),as enabled by external stimuli to construct artificial light-harvesting antenna systems.Benefiting from unique photophysical properties of Sal,the synthesized hydrogel displays a temperature-dependent reversible opaque?transparent states transition,accompanied with an interesting photoluminescence behavior.Moreover,by further incorporating europium(Ⅲ)(Eu^(3+)) into the hydrogel,we demonstrate well-defined cascades of energy transfer that provides a tunable optical output from the collection of lanthanides by the excitation of a common sensitizer(Sal) upon base vapor stimulation.Efficient energy transfer efficiency from Tb^(3+) to Eu^(3+),as high as 97.8%,was also obtained as established by the time-resolved fluorescence spectroscopy analysis.