No abstract

Adding 2-phenoxyethylamine (POEA) into a CH NH PbBr precursor solution can modulate the organic-inorganic hybrid perovskite structure from bulk to layered, with a photoluminescence and electroluminescence shift from green to blue. Meanwhile, POEA can passivate the CH NH PbBr surface and help to obtain a pure CH NH PbBr phase, leading to an improvement of the external quantum efficiency to nearly 3% in CH NH PbBr LED.

Two novel evaporation- and solution-process-feasible thermally activated delayed fluorescence emitters, green-light-emission ACRDSO2 and yellow-light-emission PXZDSO2, based on a brand-new electron-acceptor moiety thianthrene-9,9',10,10'-tetraoxide, are developed for organic light-emitting diodes. The solution-processed devices, without any hole-transport layer, exhibit competitive performance and reduced efficiency roll-off compared with corresponding vacuum-deposited devices.

The rate constant of reverse intersystem crossing was found to be the “rate-limited step” in thermally activated delayed fluorescence lifetime governing.

We report a soluble yet crystalline covalent organic framework (COF) by regulation of inter-layer interactions, which endows the COF with remarkable solubility and processability of thin films for optoelectronic devices that exhibit high yet anisotropic conductivities and outperform all the other COF-based semiconductors.