A new type of luminescence switching behavior based on phosphorescence enhancement from a series of metal‐free organic phosphors doped polymers by UV‐irradiation is investigated. This phenomenon is observed only from pairs of organic phosphors and polymer matrices having a combination of appropriate triplet exciton lifetime and oxygen permeability. Systematic investigation reveals that the luminescence switching behavior of organic phosphors embedded in a specific polymeric matrix stems from the conversion of triplet oxygens to singlet oxygens by UV‐irradiation, leading to the unique phosphorescence enhancement of organic phosphors. Visualization of latent information by UV‐irradiation is demonstrated toward novel secure information communication applications.
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Yu, Youngchang ; Kwon, Min Sang ; Jung, Jaehun ; Zeng, Yingying ; Kim, Mounggon ; Chung, Kyeongwoon ; Gierschner, Johannes ; Youk, Ji Ho ; Borisov, Sergey M. ; Kim, Jinsang ( , Angewandte Chemie International Edition)
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Yu, Youngchang ; Kwon, Min Sang ; Jung, Jaehun ; Zeng, Yingying ; Kim, Mounggon ; Chung, Kyeongwoon ; Gierschner, Johannes ; Youk, Ji Ho ; Borisov, Sergey M. ; Kim, Jinsang ( , Angewandte Chemie)
Abstract The highly sensitive optical detection of oxygen including dissolved oxygen (DO) is of great interest in various applications. We devised a novel room‐temperature‐phosphorescence (RTP)‐based oxygen detection platform by constructing core–shell nanoparticles with water‐soluble polymethyloxazoline shells and oxygen‐permeable polystyrene cores crosslinked with metal‐free purely organic phosphors. The resulting nanoparticles show a very high sensitivity for DO with a limit of detection (LOD) of 60 n
m and can be readily used for oxygen quantification in aqueous environments as well as the gaseous phase.