In recent years, organic room‐temperature phosphorescence (RTP) has been widely investigated owing to its fascinating afterglow characteristics. Consequently, it has been applied in anti‐counterfeiting and information security. However, these applications are limited by cost, substrates, and technological processes. Hence, a simple and environmentally friendly adsorption‐induced RTP system containing sulfonic acid groups is designed for convenient and efficient application. A pure organic compound of (1,1″‐biphenyl)‐4,4″‐disulfonic acid can be easily ionized and dispersed in water. When it is adsorbed on different types of paper and cloth substrates rich in hydroxyl groups, bright RTP emissions with maximum lifetimes of ≈1.1 s are achieved after drying the substrates. The destructive effect of H2O on the intermolecular hydrogen bonds between the phosphor and substrates makes the RTP emissions responsive to the stimuli of water and heat. Furthermore, a white afterglow is realized after doping with Rhodamine B for energy transfer. On the account of the adsorption‐induced RTP effect, four economical applications are demonstrated, wherein one dollar's worth of the phosphor can be used for anti‐counterfeiting 7692 banknotes, printing and dyeing 1538 graphs on cloth, making 196 Chinese knots, and producing 385 writes of encryption information, promoting the further development and commercialization of RTP materials.
No matter photoinduced organic radicals have been reported frequently, they are usually non‐luminescent at ambient conditions. The internal mechanism on stability and electronic transitions of photoinduced radicals, is thus crucial for the development of relevant materials. Herein, a series of photoinduced radical emission systems were developed conveniently through doping benzoic acids into the hydrogen donor polyvinyl alcohol (PVA) matrix. Visual photoinduced radical emission and photochromism could be observed on Ph‐3COOH@PVA film with the formation of cyclohexadienyl‐type structure. For the first time, radical afterglow appeared with energy transfer from triplet state. The appropriate introduction of carboxylic groups to three nonadjacent carbon atoms on the benzene ring was the best for decreasing spin population and promoting electronic transitions of the radical. This study largely expands the radical emission property from both internal mechanism and practical application.
Fabric it is not an impermeable substrate because of fiber porosity. To study the solvent diffusion mechanism of coated fabric in the curing process, the drying model of PMMA/acetone coated glass fiber fabric was established. This drying model was verified by confocal Raman spectroscopy. Finally, the impact of fabric structure, thickness and porosity on the solvent diffusion process in coated fabrics was studied by the model. It was shown that the predicted solvent concentrations by the model were consistent with the experimental values. This model can be used to quantitatively calculate the solvent concentration at any position and at any time inside the coating film during the drying process. Moreover, it can also predict the curing time and residual solvent concentration of the coating fabric required to reach drying equilibrium. Compared with coated 3/1 twill, 5/3 satin and 2/1 twill, the solvent diffusion of coated plain fabric was faster during curing. Under the same environmental conditions, the thinner the fabric was and the greater the porosity was, the shorter the curing time was. The fitting equations for fabric thickness, fabric porosity and drying time were obtained, which can provide a theoretical guidance for the preparation, performance research and drying conditions optimization of PMMA coated textile materials.
No matter photoinduced organic radicals have been reported frequently, they are usually non-luminescent at ambient conditions. The internal mechanism on stability and electronic transitions of photoinduced radicals, is thus crucial for the development of relevant materials. Herein, a series of photoinduced radical emission systems were developed conveniently through doping benzoic acids into the hydrogen donor polyvinyl alcohol (PVA) matrix. Visual photoinduced radical emission and photochromism could be observed on Ph-3COOH@PVA film with the formation of cyclohexadienyl-type structure. For the first time, radical afterglow appeared with energy transfer from triplet state. The appropriate introduction of carboxylic groups to three nonadjacent carbon atoms on the benzene ring was the best for decreasing spin population and promoting electronic transitions of the radical. This study largely expands the radical emission property from both internal mechanism and practical application.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.