新一代oled的可扭曲电荷转移态(会议报告)

D. Credgington
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引用次数: 0

摘要

有机发光二极管(oled)的基本科学挑战是成功地管理电子自旋。激发态只有衰变到自旋为0的基态才能发光。在过去的三十年里,寻找从自旋-1激发中收集光的方法塑造了OLED技术,因为实现这一目标的策略选择必然会影响材料设计、器件架构和限制器件寿命的工艺。在这里,我们展示了一种快速三联体收获的新方法。我们介绍了一种新型的线性给体-桥体-受体发光分子,它们在激发态中扭曲,改变电子和空穴之间的耦合。(1)这些使掺杂聚合物led即使在高亮度下也具有接近100%的内部量子效率。(2)我们的溶液处理oled的电流效率,功率效率和亮度可与最先进的真空沉积oled和量子点led相比较或超过。利用时间分辨光谱,我们确定在环境温度下,经过系统间反向交叉到单重态后,三重态发光发生在100ns的时间尺度上。我们发现这种情况的发生是因为分子的几何结构使得单线态和三重态的能隙(交换能)接近于零,使得快速的相互转换成为可能。与其他低交换能量系统不同,大量振荡器强度在这一点上得到维持。我们描述了这些材料发射的最新实验和理论证据,并展示了它如何强烈地依赖于旋转能量学、温度、振荡器强度和发射层纳米形貌之间的相互作用。这给了我们新的工具来控制发射颜色和速率。这样做,我们将排放从绿色调整为天蓝色,并在1000 cdm-2时达到近30%的EQE。基于这一分子基序,我们实现了在可见光谱范围内实现亚微秒三重态发射和低滚降的分子发射器的新设计。A. S. Romanov等,具有亚微秒光辐射的铜和金环(烷基)(氨基)碳配合物:结构和取代基对氧化还原和发光性能的影响。化学。——欧元。[j] .中国农业科学,2016,32(5):555 - 557。D. Di等人,基于碳金属酰胺的高性能发光二极管。科学通报,35(6),39 - 43(2017)。
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Twistable charge-transfer states for next generation OLEDs (Conference Presentation)
The fundamental scientific challenge for organic light emitting diodes (OLEDs) is to successfully manage electronic spin. The excited state can only give out light if it can decay to the spin-0 ground state. Finding ways of harvesting light from spin-1 excitations has shaped OLED technology for the last three decades, since the choice of strategy to achieve this necessarily impacts materials design, device architecture, and the processes limiting device lifetime. Here we demonstrate a new approach to rapid triplet harvesting. We introduce a novel class of linear donor-bridge-acceptor light-emitting molecules which twist in their excited states, changing the coupling between electron and hole.(1) These enable doped polymer LEDs with near-100% internal quantum efficiency even at high brightness.(2) Our solution-processed OLEDs achieve current efficiency, power efficiency and brightness comparable to or exceeding those of state-of-the-art vacuum-deposited OLEDs and quantum dot LEDs. Using time-resolved spectroscopy, we establish that luminescence via triplets occurs on 100s of ns timescales at ambient temperature, after reverse intersystem crossing to singlets. We find this occurs because molecular geometries exist at which the singlet-triplet energy gap (exchange energy) is close to zero, such that rapid interconversion is possible. Unlike other low exchange energy systems, substantial oscillator strength is sustained at this point. We describe recent experimental and theoretical evidence for emission from these materials and show how it depends strongly in the interplay between rotational energetics, temperature, oscillator strength and the nanomorphology of the emissive layer. This gives us new tools to control emission colour and rate. Doing so, we tune emission from green to sky-blue, and achieve EQE at 1000 cdm-2 of nearly 30%. Based on this molecular motif, we realise new designs for molecular emitters realising sub-microsecond triplet emission and low roll-off in devices across the visible spectral range. 1. A. S. Romanov et al., Copper and Gold Cyclic (Alkyl)(amino)carbene Complexes with Sub-Microsecond Photoemissions: Structure and Substituent Effects on Redox and Luminescent Properties. Chem. - A Eur. J. 23, 4625–4637 (2017). 2. D. Di et al., High-performance light-emitting diodes based on carbene-metal-amides. Science. 356, 159–163 (2017).
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