Exploring the photophysics of carbene metal amides (Conference Presentation)

Saul T. E. Jones, D. Credgington
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Abstract

Light emission in organic semiconductors is governed by the spin of excitons formed upon electrical excitation. Conventionally, 25% of excitons form as emissive singlets and 75% form non-emissive triplets. Exceeding this limit for OLEDs requires designing new materials. Developments in molecular design have allowed utilization of triplet excitons through either direct phosphorescence (1) or secondary processes converting a triplet into a singlet via a spin flip, creating “delayed” fluorescence. (2) Thermally Activated Delayed Fluorescence (TADF) has provided guidelines for creating donor-acceptor molecules, but the effects governing spin dynamics are still being explored. Increasingly, there is consensus that intersystem crossing,(ISC) cannot be understood from a static picture of the molecules; a more dynamic approach is necessary. Carbene Metal Amide (CMA) emitters (3) provide an excellent example, displaying large spectral shifts due to conformational reorganisation and highly variable intersystem crossing rates. In solid films, they have produced solution processed green OLEDs with record efficiencies. Here we show, starting from the green CMA archetypes, we can alter the molecular design to probe the effects of steric hindrance, spin-orbit coupling, and dipole strength on the emission properties. Using fast time resolved cryogenic PL spectroscopy we demonstrate the impact of changing the metal bridge atom on ISC, and explore high molecular weight variants for flexible electronics. We demonstrate these emitters can be tuned across the visible spectrum whilst retaining similar photophysical properties, and achieve efficient OLED devices via both solution and vacuum processing. We discuss their structure property relationships for emission, explore a new set of high efficiency OLED dopants, and provide fundamental insight into their spin conversion mechanism. From these studies we derive the first set of design rules for this new class of organometallic TADF emitters. 1) Very high-efficiency green organic light-emitting devices based on electrophosphorescence, Baldo et al. Appl. Phys. Lett. 1999 2) Highly efficient organic light-emitting diodes from delayed fluorescence. Uoyama et al. Nature 2012 3) High-performance light-emitting diodes based on carbene-metal-amides, Di et al. Science, 2017
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探讨碳金属酰胺的光物理性质(会议报告)
有机半导体中的光发射是由电激发形成的激子自旋控制的。通常,25%的激子形成发射单重态,75%形成非发射三重态。如果要超过这个限制,就需要设计新的材料。分子设计的发展使得三重态激子可以通过直接磷光(1)或通过自旋翻转将三重态转化为单线态的二次过程来利用,从而产生“延迟”荧光。(2)热激活延迟荧光(TADF)为创造给受体分子提供了指导,但控制自旋动力学的效应仍在探索中。越来越多的人一致认为,系统间交叉(ISC)不能从分子的静态图像中理解;一种更加动态的方法是必要的。卡本金属酰胺(CMA)发射体(3)就是一个很好的例子,由于构象重组和高度可变的系统间交叉速率,显示出较大的光谱位移。在固体薄膜方面,他们已经生产出了效率创纪录的溶液处理绿色有机发光二极管。在这里,我们表明,从绿色的CMA原型开始,我们可以改变分子设计来探测空间位阻、自旋轨道耦合和偶极子强度对发射特性的影响。利用快速时间分辨低温PL光谱,我们展示了改变金属桥原子对ISC的影响,并探索了柔性电子的高分子量变异体。我们证明了这些发射器可以在可见光光谱上调谐,同时保持相似的光物理性质,并通过溶液和真空处理实现高效的OLED器件。我们讨论了它们的发射结构性质关系,探索了一套新的高效OLED掺杂剂,并对其自旋转换机制提供了基本的见解。从这些研究中,我们得出了这种新型有机金属TADF发射器的第一套设计规则。1)基于电磷光的非常高效的绿色有机发光器件,Baldo等。达成。理论物理。Lett. 19992)延迟荧光的高效有机发光二极管。Uoyama等人。基于碳金属酰胺的高性能发光二极管,Di等。科学,2017
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