Dynamic photo-enhanced polyacrylic acid-based room temperature phosphorescence materials with persistent long-wavelength and even near-infrared luminescence via Förster resonance energy transfer

磷光 聚丙烯酸 发光 持续发光 材料科学 光化学 光电子学 费斯特共振能量转移 罗丹明B 兴奋剂 接受者 罗丹明 光致发光 化学 光学 聚合物 荧光 光催化 有机化学 物理 复合材料 热释光 催化作用 凝聚态物理
作者
Liuqi Kong,Shaochen Sun,Yan Zhu,Hongye Li,Tianyu Li,Huiying Li,Fei Li,Farong Tao,Liping Wang,Guang Li
出处
期刊:Dyes and Pigments [Elsevier]
卷期号:226: 112131-112131 被引量:3
标识
DOI:10.1016/j.dyepig.2024.112131
摘要

Stimulus-responsive organic room temperature phosphorescence (RTP) materials have attracted widespread attention in chemical sensors, bioimaging and information security. In this work, a dynamic photo-enhanced RTP material is prepared by doping 1,8-naphthalic anhydride (NA) into the polyacrylic acid (PAA) matrix. After 10 min irradiation of 302 nm UV light, the RTP properties of the doping systems PAA-NA are significantly enhanced and the photo-enhanced performances show excellent reversibility. More interestingly, PAA-NA as energy donor and the commercial dye rhodamine B (RhB) as energy acceptor are used to construct the ternary doping systems PAA-NA-RhB, which exhibit color-tunable long afterglow from orange to red through the triplet-to-singlet Förster resonance energy transfer (TS-FRET) process. Significantly, RhB as the intermediate and near infrared (NIR) dye Nile blue (NiB) as energy acceptor are codoped into energy donor PAA-NA matrices to facilely prepare the quaternary doping systems PAA-NA-RhB-NiB, and persistent NIR luminescence is realized successfully via the stepwise FRET process after 10 min irradiation of 302 nm UV light. The great application potential of the prepared photo-enhanced PAA-based RTP materials in high-level information encryption has been confirmed due to their excellent RTP performance. This study broadens the range of photo-enhanced polymer-based RTP materials and extends the persistent luminescence of PAA-based RTP materials to the long-wavelength and NIR regions.
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