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Please use this identifier to cite or link to this item: https://libeldoc.bsuir.by/handle/123456789/58539
Title: Metal oxide hybridization enhances room temperature phosphorescence of carbon dots–SiO2 matrix for information encryption and anti-counterfeiting
Authors: Qing Yao
Zeyu Wang
Gaponenko, N. V.
Jindou Shi
Zheyuan Da
Chen Zhang
Junnan Wang
Minqiang Wang
Keywords: публикации ученых;lead-free double perovskites;carbon dot materials;composites;optoelectronic devices
Issue Date: 2024
Publisher: Royal Society of Chemistry
Citation: Metal oxide hybridization enhances room temperature phosphorescence of carbon dots–SiO2 matrix for information encryption and anti-counterfeiting / Qing Yao, Zeyu Wang, N. V. Gaponenko [et al.] // Nanoscale. – 2024. – Vol. 16, № 23. – P. 11310–11317.
Abstract: Room temperature phosphorescent (RTP) carbon dot (CD) materials have been widely used in various fields, but it is difficult to achieve a long lifetime, high stability and easy synthesis. In particular, realizing the phosphorescence emission of CDs using a metal oxide (MO) matrix is a challenge. Here, solid gels are synthesized via in situ hydrolysis, and then RTP CDs are synthesized based on a SiO2 matrix (CDs@SiO2) and hybridized with a MO matrix (CDs@SiO2-MO) by high-temperature calcination. Among the materials synthesized, Al2O3 matrix RTP CDs (CDs@SiO2-Al2O3) have a long phosphorescence lifetime of 689 ms and can exhibit yellow-green light visible to the naked eye for 9 s after the UV light (365 nm) is turned off. Compared with the green phosphorescence of CDs@SiO2, the yellow-green phosphorescence lifetime of CDs@SiO2-Al2O3 is enhanced by 420 ms. In addition, CDs@SiO2-Al2O3 maintains good stability of phosphorescence emission in water, strongly oxidizing solutions and organic solvents. As a result, CDs@SiO2- Al2O3 can be applied to the field of information encryption and security anti-counterfeiting, and this work provides a new, easy and efficient synthesis method for MO as an RTP CD matrix.
URI: https://libeldoc.bsuir.by/handle/123456789/58539
DOI: https://doi.org/ 10.1039/d4nr01380h
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