Rational synthesis of Eu3+ and Yb3+ single −doped and co-doped Ba0.5Sr0.5TiO3 phosphors for dynamic anti-counterfeiting and fingerprint recognition applications
Jingyi Yang , Shifa Wang , Yuanyuan Zhang , Peilin Mo , Xianlun Yu , Lei Hu , Huajing Gao , Chaoli Chen , Leiming Fang , V. Jagadeesha Angadi , M. Atif , Ashok Kumar
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引用次数: 0
Abstract
The Eu3+ and Yb3+ ions single −doped and co-doped Ba0.5Sr0.5TiO3 (BST5) phosphors were prepared by a polyacrylamide gel method. The effects of rare earth ion concentration and ion type on the phase structure, microstructure, optical, color properties and photoluminescence properties of the BST5 phosphor were investigated by various characterization methods. Since the concentration of doped ions is less than 1 %, and Eu3+ and Yb3+ ions occupy the Ba/Sr site of the BST5 phosphor, the phase structure of the BST5 phosphor is not changed. Microstructure characterization confirmed that the co-doping of Eu3+ and Yb3+ with BST5 phosphor made the rhomboid particles more uniform in size. In addition to the band absorption of the BST5 phosphor, all phosphors also have two absorption peaks at 371 and 445 nm caused by Eu3+ ion ground state 7F0 to excited states 5L6 and 5D2, respectively. Simultaneously, the co-doping changes the lattice constant and crystal structure stability of BST5, resulting in a slight shift in the absorption peak. When the excitation wavelength is 395 nm, BST5:Eu and BST5: 0.25 %Eu:Yb phosphor have the strongest emission peaks at 595 and 598 nm, respectively. The photoluminescence mechanism confirmed that the existence of superexchange between Eu3+-O-Ti4+ and energy transfer between Eu3+ and Yb3+ enhanced the photoluminescence performance of the BST5:0.25 % Eu:Yb phosphor. The practical application shows that the BST5: Eu/Yb phosphor has a potential application prospect in the field of photoluminescence, dynamic anti-counterfeiting and fingerprint recognition.
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.