Structure and color-tunable luminescence properties of Sm3+ singly- and Dy3+/Sm3+ co-doped CaLaGa3O7 phosphors

IF 3.6 3区 物理与天体物理 Q2 OPTICS Journal of Luminescence Pub Date : 2025-05-01 Epub Date: 2025-01-30 DOI:10.1016/j.jlumin.2025.121117
Fei Pan , Yunyun Liu , Chaoyang Tu
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Abstract

Sm3+ singly- and Dy3+/Sm3+ co-doped CaLaGa3O7 phosphors were synthesized successfully by a traditional high-temperature solid-state reaction method. Their structure was determined by X-ray diffraction (XRD) measurements, confirming the tetragonal phase of the samples with space group P 4 21m. For Sm3+: CaLaGa3O7 samples, the excitation spectra show that the phosphors could be excited by 403 nm light. The strongest emission peak is at 598 nm, which is assigned to the transition from Sm3+: 4G5/2 level to 6H7/2 state. The CIE color coordinate with optimal Sm3+ doping concentration was calculated to be (0.5882, 0.4110), which is located in the orange-red area. For Dy3+/Sm3+: CaLaGa3O7 phosphors, the excitation spectra show that the obtained samples could be effective pumped by 348 nm or 403 nm. Regardless of the excitation wavelength, the emission spectrum contains the characteristic emission peaks of Dy3+ and Sm3+. The relative emission intensity of Dy3+ and Sm3+ could be adjusted by modifying the concentration of Sm3+ and the exciting wavelength, indicating that the luminescence color is tunable for Dy3+/Sm3+ co-doped samples. The luminescence performance and fluorescence lifetime jointly prove that mutual energy transfers between Dy3+ and Sm3+ take place in the Dy3+/Sm3+: CaLaGa3O7 phosphors. The CIE color coordinates and correlated color temperature were calculated for varying rare-earth concentration as well as excitation wavelength to ascertain their potential applications in light emission devices.
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Sm3+单掺杂和Dy3+/Sm3+共掺杂CaLaGa3O7荧光粉的结构和可调色发光性能
采用传统的高温固相反应法制备了Sm3+单掺杂和Dy3+/Sm3+共掺杂的CaLaGa3O7荧光粉。通过x射线衍射(XRD)测量确定了它们的结构,确认了具有p4 - 21m空间群的样品的四方相。Sm3+: CaLaGa3O7样品的激发光谱表明,403 nm光可以激发Sm3+: CaLaGa3O7。最强发射峰在598 nm处,属于Sm3+: 4G5/2态向6H7/2态转变。计算出Sm3+掺杂浓度最优的CIE颜色坐标为(0.5882,0.4110),位于橙红色区域。对于Dy3+/Sm3+: CaLaGa3O7荧光粉,激发光谱表明所获得的样品可以被348 nm或403 nm的有效泵浦。无论激发波长如何,发射光谱都包含Dy3+和Sm3+的特征发射峰。通过改变Sm3+的浓度和激发波长,可以调节Dy3+和Sm3+的相对发射强度,表明Dy3+/Sm3+共掺杂样品的发光颜色是可调的。发光性能和荧光寿命共同证明了Dy3+/Sm3+: CaLaGa3O7荧光粉发生了Dy3+和Sm3+之间的能量相互转移。计算了不同稀土浓度和激发波长下的CIE色坐标和相关色温,以确定其在发光器件中的潜在应用。
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
期刊介绍: The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid. We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.
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