Xin Cong , Kaide Ou , Xuelin Dong , Jiao Ma , Hang Chen , Yonggui Liao , Yajiang Yang , Hong Wang
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引用次数: 0
Abstract
In this study, a multicolor luminescent material (TSS) was prepared by lanthanide ions (Tb3+) with 2-hydroxybenzoic acid (SA) and spiropyran (SP). TSS exhibited dynamically tunable dual-mode color (optical and fluorescent colors). The absorption and fluorescence spectra revealed that the changes in dual-mode color of TSS depended on the duration of the visible (Vis) irradiation time (t) and excitation wavelength (λ). Consequently, the optical color of TSS can be modulated from orange to colorless with varying t, while its fluorescent color changed from red to green and blue to cyan under 365- and 254-nm ultraviolet (UV) lamp, respectively. The combined effects of fluorescence resonance energy transfer (FRET) between SP and Tb3+ and the inner filter effect (IFE) between SP and SA contributed to the rich multicolor of TSS. Moreover, the cascade effect of FRET and IFE imparted TSS with fine and tunable time-related features. By employing the color difference value (ΔE) to measure the changes in the dual-mode color of TSS, a binary output logic gate based on ΔE was proposed to realize accurate information encryption and decryption. Furthermore, the ΔE-based encryption strategy enhances the information encryption capacity of multicolor materials through the subdivision of ΔE. This approach provides a cost-effective means of achieving high-capacity information output. Thus, the ΔE-based encryption strategy significantly improves the efficiency of multicolor material utilization. This study demonstrates significant potential for further accurate and low-cost encryption.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.