4.7 Article

Ultra-stable dual-color phosphorescence Carbon-Dot@Silica material for advanced anti-counterfeiting

Journal

DYES AND PIGMENTS
Volume 208, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2022.110827

Keywords

Room temperature phosphorescence; Photostability; Carbon dots; Silica; Dual-color phosphorescence; Anti-counterfeiting

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This article introduces a universal method for the fabrication of a carbon-dot@silica composite with ultralong lifetime, high phosphorescence quantum efficiency, excellent luminescence stability, and dual-color phosphorescence emission. The triplet excited states of carbon dots are stabilized by the rigid network of silica and the stable covalent bonding between carbon dots and silica. The carbon-dot@silica exhibit ultralong lifetimes of 1.33 s and 0.38 s under excitation at 254 nm and 365 nm, respectively. Moreover, the phosphorescence color of the carbon-dot@silica can change from cyan to yellow when the exciting wavelength switches from 254 nm to 365 nm. The obtained carbon-dot@silica also show outstanding characteristics of anti-photobleaching and phosphorescence stability in an aqueous solution. Based on the unique phosphorescent properties of the carbon-dot@silica, a stable and dual-color phosphorescence security label is designed for advanced information encryption.
Room temperature phosphorescence (RTP) materials have motivated massive attention due to their great ad-vantages in anti-counterfeiting and optical encryption. However, the commonly used carbon-based RTP mate-rials suffer from drawbacks of photobleaching, quenching and single phosphorescence color outputs, which obstruct their performance in high-level anti-counterfeiting techniques. Herein, we present a universal method for the fabrication of a carbon-dot@silica (CDs@SiO2) composite that possesses ultralong lifetime, high phos-phorescence quantum efficiency (PQE), excellent luminescence stability, and dual-color phosphorescence emission. Taking advantage of the restriction by rigid network of SiO2 and stable covalent bonding between CDs and SiO2, the triplet excited states of CDs are stabilized. As a result, the CDs@SiO2 exhibit ultralong lifetime of 1.33 s and 0.38 s under excitation at 254 nm and 365 nm, respectively. Furthermore, the phosphorescence color of CDs@SiO2 can change from cyan to yellow when the exciting wavelength switches from 254 nm to 365 nm. The obtained CDs@SiO2 also exhibit outstanding characteristics of anti-photobleaching and phosphorescence stability in an aqueous solution. Based on the unique phosphorescent properties of the CDs@SiO2, a stable and dual-color phosphorescence security label is designed for advanced information encryption.

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