Related Experiment Video
Updated: Jun 4, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Activating efficient phosphorescence from purely organic materials by crystal design
Onas Bolton1, Kangwon Lee, Hyong-Jun Kim
1Department of Materials Science and Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Abstract:
Phosphorescence is among the many functional features that, in practice, divide pure organic compounds from organometallics and inorganics. Considered to be practically non-phosphorescent, purely organic compounds (metal-free) are very rarely explored as emitters in phosphor applications, despite the emerging demand in this field. To defy this paradigm, we describe novel design principles to create purely organic materials demonstrating phosphorescence that can be turned on by incorporating halogen bonding into their crystals. By designing chromophores to contain triplet-producing aromatic aldehydes and triplet-promoting bromine, crystal-state halogen bonding can be made to direct the heavy atom effect to produce surprisingly efficient solid-state phosphorescence. When this chromophore is diluted into the crystal of a bi-halogenated, non-carbonyl analogue, ambient phosphorescent quantum yields reach 55%. Here, using this design, a series of pure organic phosphors are colour-tuned to emit blue, green, yellow and orange. From this initial discovery, a directed heavy atom design principle is demonstrated that will allow for the development of bright and practical purely organic phosphors.
Related Concept Videos
Photoluminescence: Applications
Variables Affecting Phosphorescence and Fluorescence
Photoluminescence: Fluorescence and Phosphorescence
A pair of electrons in a...
Fluorescence and Phosphorescence: Instrumentation
Determination of Crystal Structures
Deactivation Processes: Jablonski Diagram

