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有机发光二极管(OLED)作为新一代显示技术已广泛商用, 但蓝光有机发光二极管在效率和稳定性等方面仍存在不足, 虽用磷光染料能明显地提高效率, 其制作成本之高却限制了产业化发展. 因此, 本文对蓝色荧光有机发光二极管中的效率滚降现象进行了深入探究. 首先, 从稳态和瞬态两个角度研究了电子电流和空穴电流对单极器件光致发光行为的影响, 表明空穴对激子的淬灭效果更显著. 实验证明激子-电荷相互作用是荧光OLED中效率滚降的主要机制, 且激子主要是被束缚电荷淬灭而非移动电荷. 另一方面制备了不同掺杂浓度的有机发光二极管器件以探究掺杂浓度对激子-极化子相互作用的影响, 得到了综合性能较好的蓝色有机荧光器件, 分析表明调控发光层电荷俘获可以平衡界面堆积电荷和发光层束缚电荷对激子的淬灭. 本文完善了激子-极化子淬灭的内在机制,给减缓蓝色荧光有机发光二极管的效率滚降提供了有益参考.OLEDs are popular as display technology nowadays, which have been widely used in commercial application. However, there are still some problems that blue light devices are not as efficient or stable as red and green light devices. Although the use of phosphorescent dyes can significantly improve the internal quantum efficiency, the high production cost and unstable performance limit the industrialization of phosphorescent OLEDs. In the development of OLEDs, the researchers found that OLEDs suffered from a decline in their efficiency at high brightness levels, a behavior known as “efficiency roll-off”. The efficiency roll-off is more pronounced in phosphorescent devices due to the longer lifetime of triplet exciton than singlet exciton, so that it has been widely investigated in recent years. Little is known, still, about fluorescent devices. Accordingly, unraveling the exciton loss mechanism in blue fluorescent OLEDs is particularly important, as it is a limiting factor for the improvement of efficiency. In this work, the efficiency roll-off in blue fluorescent OLEDs is investigated by observing the quenching of DPAVBI excitons. Firstly, the effects of electron current and hole current on photoluminescence(PL) behavior of unipolar devices are studied by steady-state and transient-state measurements, and we analyze PL spectrum and calculate the exciton quenching rate constant according to the transient PL decay curves to clarify the exciton quenching dynamics. The results show that the holes are much more efficient in quenching the excitons when the host is a hole transport material. This is different from the general understanding that exciton-polaron quenching effect with higher carrier mobility is weaker. Because the existence of bound charges produces additional charge density, and it is inferred that the exciton is mainly quenched by trapped charge rather than moving charge. We also exclude the effect of exciton–exciton annihilation and electric-field-induced dissociation on the efficiency degradation of the OLEDs. It is confirmed experimentally that exciton-polaron interaction is the dominant mechanism of the efficiency roll-off in fluorescent OLEDs. We then fabricate organic light-emitting diode devices with different doping concentrations to figure out the effect of doping concentration on exciton-polaron interaction, and obtain a blue fluorescence device with good comprehensive performance. We also summarize some feasible methods to optimize the efficiency of the OLEDs. In this paper, our findings about exciton-polaron interaction might provide a viable source for efficiency improvement by regulating charge trapping in light emitting layer.
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图 1 能级结构图 (a) 单极空穴器件; (b) 单极电子器件
Fig. 1. Energy level diagrams of (a) hole-only device and (b) electron-only device.
图 2 (a) 单极电子器件的归一化发光光谱; (b) 单极空穴器件的归一化发光光谱
Fig. 2. (a) Normalized PL spectra of electron-only device; (b) normalized PL spectra of hole-only device.
图 3 (a) 归一化光致发光亮度随电流密度的变化曲线; (b) 电流密度随电压的变化曲线
Fig. 3. (a) Normalized PL intensity versus current density; (b) J–V characteristics.
图 4 (a) 单极电子器件的瞬态衰减曲线; (b) 单极空穴器件的瞬态衰减曲线
Fig. 4. (a) Transient PL decay curves of electron-only device; (b) transient PL decay curves of hole-only device.
图 6 不同掺杂浓度下器件的电流效率随电流密度的变化曲线
Fig. 6. Current efficiency vs current density in devices with mCBP:DPABI, 5%—15% guest concentration.
图 7 (a) 电流密度随电压变化曲线; (b) 发光强度随电压变化曲线; (c) 电流效率随电流密度变化曲线; (d) 外量子效率随发光强度变化曲线
Fig. 7. (a) J-V characteristics; (b) L-V characteristics; (c)η-J characteristics; (d) EQE-L characteristics.
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[1] 汪津, 赵毅, 谢文法, 段羽, 陈平, 刘式墉 2011 60 579
Google Scholar
Wang J, Zhao Y, Xie W F, Duan Y, Chen P, Liu S Y 2011 Acta Phys. Sin. 60 579
Google Scholar
[2] Song W, Lee J Y 2017 Org. Electron. 51 1
Google Scholar
[3] 崔荣朕, 唐艳茹, 马玉芹, 杨秀云, 耿丽华, 李云辉 2015 应用化学 32 855
Google Scholar
Cui R L, Tang Y R, Ma Y Q, Yang X Y, Gen L H, Li Y H 2015 Chin. J. Appl. Chem. 32 855
Google Scholar
[4] Xu Z, Tang B Z, Wang Y, Ma D G 2020 J. Mater. Chem. C 8 2614
Google Scholar
[5] Song D D, Zhao S L, Luo Y C, Aziz H 2010 Appl. Phys. Lett. 97 3
Google Scholar
[6] Luo Y C, Aziz H, Xu G, Popovic Z D 2007 Chem. Mater. 19 2288
Google Scholar
[7] Guo K, Li W, Zhang J, Zhang X, Wang X, Chen G, Xu T, Yang L, Zhu W, Wei B 2016 RSC Adv. 6 55626
Google Scholar
[8] Wang Q, Oswald I W H, Perez M R, Jia H, Gnade B E, Omary M A 2013 Adv. Funct. Mater. 23 5420
Google Scholar
[9] Reineke S, Walzer K, Leo K 2007 Phys. Rev. B 75 13
Google Scholar
[10] Baldo M A, Adachi C, Forrest S R 2000 Phys. Rev. B 62 10967
Google Scholar
[11] Giebink N C, Forrest S R 2008 Phys. Rev. B 77 9
Google Scholar
[12] Fukuda T, Okada T, Wei B, Ichikawa M, Taniguchi Y 2007 Appl. Phys. Lett. 90 3
Google Scholar
[13] 王利顺 2010 硕士学位论文 (保定: 河北大学)
Wang L S 2010 M. S. Thesis (Baoding: Hebei University) (in Chinese)
[14] Seo J A, Jeon S K, Lee J Y 2016 Org. Electron. 34 33
Google Scholar
[15] Baldo M A, Holmes R J, Forrest S R 2002 Phys. Rev. B 66 16
Google Scholar
[16] Murawski C, Leo K, Gather M C 2013 Adv. Mater. 25 6801
Google Scholar
[17] Song W, Kim T, Lee Y, Lee J Y 2017 Org. Electron. 43 82
Google Scholar
[18] Tan Y, Wang Z, Wei C, Liu Z, Bian Z, Huang C 2019 Org. Electron. 69 77
Google Scholar
[19] 廖立敏, 邓兵, 雷光东 2017 光谱学与光谱分析 37 636
Google Scholar
Liao L M, Deng B, Lei G D 2017 Spectrosc. Spect. Anal. 37 636
Google Scholar
[20] 林娜 2016 博士学位论文 (北京: 清华大学)
Lin N 2016 Ph. D. Dissertation (Beijing: Tsinghua University) (in Chinese)
[21] Patil V V, Lee K H, Lee J Y 2020 J. Mater. Chem. C 8 3051
Google Scholar
[22] Wu Z G, Zheng Y X, Zhou L, Wang Y, Pan Y 2017 Org. Electron. 42 141
Google Scholar
[23] Lee J H, Huang C L, Hsiao C H, Leung M K, Yang C C, Chao C C 2009 Appl. Phys. Lett. 94 3
Google Scholar
[24] Song W, Lee J Y 2017 Org. Electron. 49 152
Google Scholar
[25] Liu Z J, Zheng W Y, Wei P, Xu Z, Song D D, Qiao B, Zhao S L 2020 RSC Adv. 10 13215
Google Scholar
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