Synthesis and spectral investigation of alkyl methacrylates with halogenated carbazolyl pendant groups for photonics applications

The alkyl methacrylates with halogenated carbazolyl pendant groups were prepared, and the analysis of their absorption and emission spectra showed that the polymers containing monohalogenatged carbazole rings were capable of exhibiting a high singlet‐triplet (S‐T) conversion. The reasons that mainly triplet excitons could be observed in such polymers and additional bands appearance in the spectra of the polymers with dihalogenated carbazole rings are discussed. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1650–1656, 2002; DOI 10.1002/app.10469     

环糊精和表面活性剂在室温磷光中的应用

介绍了环糊精和表面活性剂作为有序介质在室温磷光中的研究进展．并对各种方法的特点和应用情况作了简要概括。认为环糊精和表面活性剂混合介质能大大提高发光物质的室温磷光．而且操作简便．应用前景广阔。     

铝基原料对磷光粉SrAl2O4：Eu^2＋，Dy3＋发光性能的影响

采用高温固相反应法,分别以高纯氧化铝、自制纯净铝酸钠溶液及精制工业铝酸钠溶液为原料合成了黄绿色SrAl2O4：Eu^2＋Dy^3＋磷光粉,通过测量其激发光谱、发射光谱及余辉时间,考察了不同铝基原料对磷光材料发光性能的影响．结果表明,所制备的3种磷光粉的激发光谱和发射光谱的波长基本一致,激发光谱位于300-450nm之间,主发射波长在510nm左右．用工业铝酸钠溶液制备出的长余辉材料的发射强度不低于用另外两种原料制备的长余辉材料,余辉时间比用另外两种原料制备的长余辉材料稍长,效果较好,采用工业铝酸钠溶液制备铝酸盐基长余辉材料,可以降低能耗、节约成本．     

Ultraefficient Non-Doped Deep Blue Fluorescent OLED: Achieving a High EQE of 10.17% at 1000 cd m−2 with CIEy<0.08

The pursuit for efficient deep blue material is an ever-increasing issue in organic optoelectronics field. It is a long-standing challenge to achieve high external quantum efficiency (EQE) exceed 10% at brightness of 1000 cd m⁻² with a Commission International de L'Eclairage (CIE_y) <0.08 in non-doped organic light-emitting diodes (OLEDs). Herein, this study reports a deep blue luminogen, PPITPh, by bonding phenanthro[9,10-d]imidazole moiety with m-terphenyl group via benzene bridge. The non-doped OLED based on PPITPh exhibits an exceptionally high EQE of 11.83% with a CIE coordinate of (0.15, 0.07). The EQE still maintains 10.17% at the brightness of 1000 cd m⁻², and even at a brightness as high as 10000 cd m⁻², an EQE of 7.5% is still remained, representing the record-high result among non-doped deep-blue OLEDs at 1000 cd m⁻². The unprecedented device performance is attributed to the reversed intersystem crossing process through hot exciton mechanism. Besides, the maximum EQE of orange phosphorescent OLED with PPITPh as host is 32.02%, and remains 31.17% at the brightness of 1000 cd m⁻². Such minimal efficiency roll-off demonstrates that PPITPh is also an excellent phosphorescent host material. The result offers a new design strategy for the enrichment of high-efficiency deep blue luminogen.     

Frontiers in Circularly Polarized Phosphorescent Materials

Circularly polarized luminescence (CPL) materials have received increasing attention in recent years. Amongst various CPL materials, circularly polarized phosphorescence (CPP) materials featuring long life-time represent a novel research frontier and exhibit promising applications in various fields. Herein, the state-of-the-art advances of CPP materials are systematically summarized, as classified into transition metal complexes, organic small molecules, polymers, and organic/inorganic hybrid materials. Besides, the recent applications of CPP materials in organic light-emitting diodes and encryption display are also summarized. Furthermore, the current challenges and future perspectives are put forward. It is expected that this review will offer more inspirations for the future rational design of advanced CPP materials, thus further promoting their future practical applications.     

Intrinsically Flexible and Aging Resistant Fluorene-Based Rod-Coil Copolymer for Bendable Deep-Blue PLEDs

In the field of flexible light-emitting display, goal-oriented intelligent molecular design is used to control various behaviors of molecules, which provides potential for the development of flexible light-emitting conjugated polymers (LCPs). The introduction of non-conjugated units into polymer molecules is a key prerequisite for realizing the intrinsic flexibility, but its easy interchain slip will also lead to the formation of interchain excited states, which is detrimental to the efficiency of light-emitting diodes. Herein, two kinds of fluorene-based rod-coil copolymer with stable deep blue emission characteristics is presented and with Commission Internationale de L'Eclairage (CIE) coordinates of (0.18, 0.14) and (0.15, 0.09), respectively. Surprisingly, the copolymer films show efficient blue emission even at 100% tension. Meanwhile, the rod-coil copolymer possesses better aging resistance compared to rigid π-conjugated counterparts. Finally, both rigid and flexible light-emitting diodes based on rod-coil copolymer exhibit stable deep blue emission, and the G2-based PLED with CIE coordinates of (0.16, 0.08), which approach National Television System Committee standard blue specification. These results confirm the validity of rod-coil copolymer design strategy in constructing inherently flexible polymers with deep blue emission, which have great application potential in flexible PLEDs.     

硼铝酸锶长余辉发光玻璃的制备及发光性能研究

采用一步合成法制备了硼铝酸锶长余辉发光玻璃,系统研究了热处理温度、热处理时间、冷却制度等条件对长余辉玻璃发光性能的影响.结果表明:在N2气氛下,热处理温度为1300℃、保温时间为3h、试样随炉冷却的制备工艺可得到发光性能优良的长余辉玻璃,该玻璃的长余辉特性源自在玻璃基体中均匀分布的Eu2 、Dy3 共掺杂的SrAl2O4微晶.     

稀土离子掺杂对长余辉发光玻璃发光性能的影响

选择制备了系列Eu^2＋，Dy^3＋共掺杂的硼铝酸锶长余辉发光玻璃。利用发光光谱、余辉衰减曲线、热释光谱系统研究了稀土离子掺杂对长余辉玻璃发光性能的影响。研究结果表明，不同掺量组合的Eu^2＋及Dy^3＋对长余辉玻璃发光性能有不同影响，在Eu^2＋及Dy^3＋掺量比为l：l（摩尔比）的情形下，随Eu^2＋离子掺量的增多，发光性能下降；在Eu^2＋及Dy^3＋掺量比为1：2的情形下，随Eu^2＋离子掺量的增多，发光性能增强。在此实验基础上，围绕缺陷形态及其与稀土离子间的能量传递，提出了可能的长余辉机制。     

A New Yellow Long Lasting Phosphor Y2O2S∶Ti

A new kind of doped rare earth free phosphor Y2O2S∶xTi(0＜x≤0.10) with doped Ti as activative center was synthesized by solid state reaction and sintered at 1200 ℃ for 2.5 h under reducing atmosphere. XRD patterns, photoluminescence spectra, time-resolved phosphorescence spectra and decay curves of the phosphor were investigated. XRD results reveal that a single Y2O2S phase exists with Ti content up to 6%(mol fraction). Yellow long lasting phosphorescence for present materials was observed in the dark with naked eye after the removal of the excitation light. From the time-resolved phosphorescence spectra the broad emission band centered at 565 nm was confirmed to be responsible for the long lasting phosphorescence which could maintain above 1 h. The possible mechanism responsible for the long lasting phosphorescence of the Y2O2S∶Ti phosphor was proposed.