Zhenyu Lei , Junxin Wang , Bin Hui , Han Si , Zixin Liu , Cuijiao Zhao , Peng Cao , Dechao Yu , Saifang Huang
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引用次数: 0
摘要
制造高性能白光发光二极管(LED)急需热稳定的荧光粉。本文采用固态反应法成功合成了 Sr2SiO4:0.02Ce3+,xDy3+,(0.02+x)Na+荧光粉,并对其发光特性进行了研究。相分析表明,当 x 大于 0.006 时,制备出了单相的 α-Sr2SiO4,而在 x 为 0.006 或以下的样品中则得到了 α-Sr2SiO4 和 β-Sr2SiO4 的混合相。当在 344 纳米波长处激发时,在 380-500 纳米波长处有一个主要的发射带,对应于 Ce3+ 的 5d-4f 转变,还有其他发射峰,其中在 575 纳米波长处有一个主要的发射峰,对应于 Dy3+ 的 4F9/2-6H13/2 转变。研制成功的 Sr2SiO4:Ce3+,Dy3+,Na+ 荧光粉具有极佳的热稳定性。具体来说,在 300 °C 时,425 纳米和 572 纳米的强度保持率分别高达 103.6 % 和 89.2 %。此外,利用该共激活荧光粉和商用绿光及红光荧光粉组装出了近紫外(nUV)芯片泵浦白光 LED 原型,证明了其在固态照明应用的大功率白光 LED 方面的巨大潜力。
α-Sr2SiO4:Ce3+, Dy3+, Na+ phosphors with abnormal thermal quenching properties for solid-state lighting applications
There is urgent need of thermally stable phosphors for fabricating high-performance white light emitting diodes (LEDs). In this paper, Sr2SiO4:0.02Ce3+,xDy3+, (0.02+x)Na+ phosphors were successfully synthesized by the solid-state reaction method and their luminescence properties were studied. Phase analysis shows that single-phasic α-Sr2SiO4 was prepared when x was greater than 0.006, while a mixed phase of α-Sr2SiO4 and β-Sr2SiO4 were obtained in the samples with x of 0.006 or less. When excited at 344 nm, there is a major emission band at 380–500 nm corresponding to the 5d-4f transition of Ce3+, and other emission peaks with a dominated one at 575 nm corresponding to the 4F9/2-6H13/2 transition of Dy3+. The as-developed Sr2SiO4:Ce3+,Dy3+,Na+ phosphors exhibit excellent thermal stability. To be specific, the intensity retention rate of 425 and 572 nm at 300 °C is as high as 103.6 % and 89.2 %, respectively. Furthermore, near-ultraviolet (nUV) chip-pumped white LED prototypes were assembled using the co-activated phosphor and commercial green and red phosphors, which demonstrate its great potential in high-power white LEDs for solid-state lighting applications.
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.