Centre for Organic Photonics & Electronics, School of Chemistry and Molecular Biosciences, The University of Queensland , Brisbane, QLD 4072, Australia.
Australian Nuclear Science and Technology Organisation , Locked Bag 2001, Kirrawee DC, NSW 2232, Australia.
ACS Appl Mater Interfaces. 2018 Jan 31;10(4):3848-3855. doi: 10.1021/acsami.7b15542. Epub 2018 Jan 22.
Organic light-emitting devices containing solution-processed emissive dendrimers can be highly efficient. The most efficient devices contain a blend of the light-emitting dendrimer in a host and one or more charge-transporting layers. Using neutron reflectometry measurements with in situ photoluminescence, we have investigated the structure of the as-formed film as well as the changes in film structure and dendrimer emission under thermal stress. It was found that the as-formed film stacks comprising poly(3,4-ethylenedioxythiophene):polystyrene sulfonate/host:dendrimer/1,3,5-tris(N-phenylbenzimidazol-2-yl)benzene (where the host was deuterated 4,4'-N,N'-di(carbazolyl)biphenyl or tris(4-carbazol-9-ylphenyl)amine, the host:dendrimer layer was solution-processed, and the 1,3,5-tris(N-phenylbenzimidazol-2-yl)benzene evaporated) had well-defined interfaces, indicating good wetting of each of the layers by the subsequently deposited layer. Upon thermal annealing, there was no change in the poly(3,4-ethylenedioxythiophene):polystyrene sulfonate/host:dendrimer interface, but once the temperature reached above the T of the host:dendrimer layer, it became a supercooled liquid into which 1,3,5-tris(N-phenylbenzimidazol-2-yl)benzene dissolved. When the film stacks were held at a temperature just above the onset of the diffusion process, they underwent an initial relatively fast diffusion process before reaching a quasi-stable state at that temperature.
含有溶液处理发光树突的有机发光器件可以具有高效率。最有效的器件包含发光树突在主体中的混合物和一个或多个电荷传输层。使用具有原位光致发光的中子反射测量法,我们已经研究了形成的膜的结构以及在热应力下膜结构和树突发射的变化。发现由聚(3,4-亚乙基二氧噻吩):聚苯乙烯磺酸盐/主体:树突/1,3,5-三(N-苯基苯并咪唑-2-基)苯(其中主体是氘代 4,4'-N,N'-二(咔唑基)联苯或三(4-咔唑基-9-基苯基)胺,主体:树突层是溶液处理的,而 1,3,5-三(N-苯基苯并咪唑-2-基)苯蒸发)具有明确定义的界面,表明各层之间具有良好的润湿性。在热退火时,聚(3,4-亚乙基二氧噻吩):聚苯乙烯磺酸盐/主体:树突界面没有变化,但是一旦温度达到主体:树突层的 T 以上,它就变成了过冷液体,其中 1,3,5-三(N-苯基苯并咪唑-2-基)苯溶解。当膜叠层在刚好高于扩散过程起始温度的温度下保持时,它们在达到该温度下的准稳定状态之前经历了初始的相对较快的扩散过程。