铈掺杂KSrY(BO3)2的合成与发光

Y.A. Zholdas, A. Bolatov, A. Kuznetsov, K. Kokh, B. Uralbekov, A. Kokh
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The mixture of the starting materials after grinding in an agate mortar has been calcined at 700°C in a platinum crucible for 12 hours. The calcination temperature has been increased in steps of 50°C with re-ground of the mixture at each stage. The KSrY0.95(BO3)2:0.05Ce3+sample has been annealed in hydrogen at 900°C for 8 hours. Results and discussion. The X-ray phase analysis has shown that the new compound crystallizes in the monoclinic space group P21/m. The calculated unit cell parameters for KSrY0.95(BO3)2:0.05Ce3+are: a = 9.2861(23) Å, b = 5.3654(6) Å, c = 6.5854(14) Å, V = 289.7(1) Å3. In the crystal structure of KSrY(BO3)2, each B atom is connected to three O atoms, forming a BO3 triangle. The planar groups (BO3)3 are distributed layer by layer in the plane. The Y atoms are surrounded by six oxygen atoms, forming an octahedral structure and occupying interlayer positions.Ce3+ ions in the crystal lattice mainly replace the Y+3positions based on the similarity of the ionic radius and valency of Y+3 (r = 0.90 Å, CN = VI), Ce3+ (r = 1.01 Å, CN = VI). Conclusion. At a wavelength of 440 nm, the excitation spectrum exhibits one absorption band with the 2F7/2 → 5D1 energy transition, which corresponds to the excitation of the cerium ion from the ground state to the excited state. 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However, the main problem of such compounds, in addition to the concentration quenching, is the presence in the matrix of both the trivalent Ce3+ and tetravalent Ce4+ states of cerium ions. The goal. Study of the luminescent properties of the new KSrY0.95(BO3)2:0.05Ce3+ compound. Experimental. New phosphors based on complex borate KSrY(BO3)2 doped with cerium ions have been obtained by the solid-phase synthesis. The mixture of the starting materials after grinding in an agate mortar has been calcined at 700°C in a platinum crucible for 12 hours. The calcination temperature has been increased in steps of 50°C with re-ground of the mixture at each stage. The KSrY0.95(BO3)2:0.05Ce3+sample has been annealed in hydrogen at 900°C for 8 hours. Results and discussion. The X-ray phase analysis has shown that the new compound crystallizes in the monoclinic space group P21/m. 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摘要

稀土硼酸盐化合物广泛应用于各种科学技术领域,如固态激光器,led和等离子体面板。蓝色发光荧光粉的开发通常涉及掺杂各种基质的铈离子,显示出led的高光致发光量子产率。然而,这些化合物的主要问题,除了浓度猝灭外,是在基体中同时存在三价Ce3+和四价Ce4+的铈离子状态。我们的目标。新型KSrY0.95(BO3)2:0.05Ce3+化合物的发光性能研究。实验。采用固相合成方法制备了掺杂铈离子的配合硼酸盐KSrY(BO3)2荧光粉。在玛瑙砂浆中研磨后的原料混合物在700°C铂坩埚中煅烧12小时。煅烧温度以50°C为阶梯提高,每一阶段对混合物进行再磨。将KSrY0.95(BO3)2:0.05Ce3+样品在900℃的氢气中退火8小时。结果和讨论。x射线相分析表明,该化合物在单斜空间群P21/m中结晶。计算得到KSrY0.95(BO3)2:0.05Ce3+的胞元参数为:a = 9.2861(23) Å, b = 5.3654(6) Å, c = 6.5854(14) Å, V = 289.7(1) Å3。在KSrY(BO3)2的晶体结构中,每个B原子与三个O原子相连,形成BO3三角形。平面基团(BO3)3在平面上逐层分布。Y原子被6个氧原子包围,形成八面体结构,占据层间位置。基于Y+3 (r = 0.90 Å, CN = VI)和Ce3+ (r = 1.01 Å, CN = VI)的离子半径和价的相似性,Ce3+离子在晶格中主要取代Y+3的位置。在440 nm波长处,激发光谱呈现出一条2F7/2→5D1能级跃迁的吸收带,对应于铈离子从基态激发到激发态。KSrY0.95(BO3)2:0.05Ce3+样品退火3小时后发光强度下降。
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SYNTHESIS AND LUMINESCENCE OF CERIUM DOPED KSrY(BO3)2
The rare-earth borate compounds are widely used in various fields of science and technology as solid-state lasers, LEDs, and plasma panels. Development of blue emitting phosphors typically involves doping with cerium ions various matrices, exhibiting high photoluminescence quantum yields for LEDs. However, the main problem of such compounds, in addition to the concentration quenching, is the presence in the matrix of both the trivalent Ce3+ and tetravalent Ce4+ states of cerium ions. The goal. Study of the luminescent properties of the new KSrY0.95(BO3)2:0.05Ce3+ compound. Experimental. New phosphors based on complex borate KSrY(BO3)2 doped with cerium ions have been obtained by the solid-phase synthesis. The mixture of the starting materials after grinding in an agate mortar has been calcined at 700°C in a platinum crucible for 12 hours. The calcination temperature has been increased in steps of 50°C with re-ground of the mixture at each stage. The KSrY0.95(BO3)2:0.05Ce3+sample has been annealed in hydrogen at 900°C for 8 hours. Results and discussion. The X-ray phase analysis has shown that the new compound crystallizes in the monoclinic space group P21/m. The calculated unit cell parameters for KSrY0.95(BO3)2:0.05Ce3+are: a = 9.2861(23) Å, b = 5.3654(6) Å, c = 6.5854(14) Å, V = 289.7(1) Å3. In the crystal structure of KSrY(BO3)2, each B atom is connected to three O atoms, forming a BO3 triangle. The planar groups (BO3)3 are distributed layer by layer in the plane. The Y atoms are surrounded by six oxygen atoms, forming an octahedral structure and occupying interlayer positions.Ce3+ ions in the crystal lattice mainly replace the Y+3positions based on the similarity of the ionic radius and valency of Y+3 (r = 0.90 Å, CN = VI), Ce3+ (r = 1.01 Å, CN = VI). Conclusion. At a wavelength of 440 nm, the excitation spectrum exhibits one absorption band with the 2F7/2 → 5D1 energy transition, which corresponds to the excitation of the cerium ion from the ground state to the excited state. A decrease in the luminescence intensity of the KSrY0.95(BO3)2:0.05Ce3+ sample has been found for 3 hours after its annealing.
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