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1. 北京交通大学, 光电子技术研究所, 北京, 100044
2. 北京交通大学, 发光与光信息技术教育部重点实验室 北京,100044
3. 河北师范大学, 化学与材料科学学院,河北 石家庄,050016
收稿日期:2005-12-20,
修回日期:2006-03-03,
纸质出版日期:2006-11-20
移动端阅览
程宝妹, 邓振波, 梁春军, 徐登辉, 王瑞芬. 一种新型铽、钆稀土配合物的发光特性[J]. 发光学报, 2006,27(6): 882-886
CHENG Bao-mei, DENG Zhen-bo, LIANG Chun-jun, XU Deng-hui, WANG Rui-fen. Emitting Characteristics of a New Rare Earth Complex Doped into Ploy N-vinylcarbazole[J]. Chinese Journal of Luminescence, 2006,27(6): 882-886
合成了一种新型的铽、钆稀土配合物TbGd(BA)
6
(bipy)
2
把它作为发光材料应用于有机电致发光器件中。为改善稀土配合物的载流子传输能力并避免其在真空蒸发时的热分解
实验中将铽、钆稀土配合物TbGd(BA)
6
(bipy)
2
掺入高分子导电聚合物Poly(N-vinycarbazole)(PVK)中
用旋涂的方式制备发光层
并制成电致发光器件。通过测量器件的光致和电致发光光谱
均得到纯正的、明亮的Tb
3+
离子的绿光发射
四个特征峰分别位于489
545
585
620nm
分别对应着能级
5
D
4
→
7
F
J
(
J
=6
5
4
3)的跃迁。讨论了共混体系的发光特性和能量传递机理。稀土配合物的光致发光是由于外部直接激发及PVK到稀土配合物的能量传递。电致发光有两个途径
PVK到稀土配合物的能量传递及载流子的直接俘获。在双层器件中
发光区域随Alq
3
厚度变化
尤其是在高电压下
激子复合区域移向Alq
3
一侧。优化后
多层器件在电压为13V时
达到最高亮度183cd/m
2
得到明亮的铽的绿色发光。
Anew rare earth complex TbGd(BA)
6
(bipy)
2
was synthesized
which was used as an emitting material in OLEDs. By doping into poly N-vinylcarbazole(PVK)
stability and conductivity of terbium complex are improved. As can be seen from photoluminescence spectra of the blended film
the emission peaks at 405
489
545
585
620 nm respond to PVK and
5
D
4
→
7
F
J
(
J
=6
5
4
3) transition of Tb
3+
ions respectively. The photoluminescence of PVK
terbium complex and their co-system indicated that energy transferred from PVK to terbium complex is respected as both the ratio of their blend and the state of terbium complex dispersed into PVK. When the
m
(PVK):
m
(TbGd(BA)
6
(bipy)
2
) is 5:1
the energy transferred from PVKto terbium complex completely. In order to study electroluminescence mechanism of the terbium complex
two series devices were fabricated with structures:(1)ITO/PVK:TbGd(BA)
6
(bipy)
2
/Al;(2)ITO/PVK:TbGd-(BA)
6
(bipy)
2
/Alq
3
/LiF/Al. The emitting film was prepared by spin coating PVK:TbGd(BA)
6
(bipy)
2
chloroform solution with mass ratio 5:1 onto the clean dry ITO glass. Then
the layers of Alq
3
LiF and Al were deposited by vacuum deposition. For single-layer and double-layer devices
the emission of PVK is completely restrained
and only the green emission from Tb
3+
is observed in electroluminescence
which is different from that in photoluminescence. The characteristics of these devices are investigated that not only energy transfer but also direct sequential charge trapping appeared to be the operating mechanism. In the charge trapping process
PVK is a hole transporting material and terbium complexes play a role as electron trapping centers. Terbium complexes trap electrons and holes
which enable direct recombination on terbium com- plexes. In the double-layer devices
holes and electrons were recombinated at the interface of emitting-layer/electron-transporting-layer. With increasing the thickness of Alq
3
especially at highly electric field
exciton recombination region transferred closely to electron transporting layer. From the optimized double-layer device
bright and green emission from terbium complex had been obtained with the highest brightness of 183 cd/m
2
at 13 V.
0
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