Organic Excitonic State Management by Surface Metallic Coupling of Inorganic Lanthanide Nanocrystals

The ability to harness charges and spins for control of organic excitonic states is critical in developing high-performance organic luminophores and optoelectronic devices. Here we report a facile strategy to efficiently manipulate the electronic energy states of various organic phosphors by coupling them with inorganic lanthanide nanocrystals. We show that the metallic atoms exposed on the nanocrystal surface can introduce strong coupling effects to 9-(4-ethoxy-6-phenyl-1,3,5-triazin-2-yl)-9H-carbazole (OCzT) and some organic chromophores with carbazole functional groups when the organics are approaching the nanocrystals. This unconventional organic-inorganic hybridization enables a nearly 100 % conversion of the singlet excitation to fast charge transfer luminescence that does not exist in pristine organics, which broadens the utility of organic phosphors in hybrid systems. A facile strategy to manipulate the electronic energy states of organic phosphors by coupling with inorganic lanthanide nanocrystals NaGdF4 is reported. The metallic atoms introduce strong spin-orbit coupling effects to organic chromophores. The result demonstrates the ability of charge transfer mechanism to broaden the utility of organic phosphors.+image

Automated summary

Researchers report a facile strategy to efficiently manipulate the electronic energy states of organic phosphors by coupling them with inorganic lanthanide nanocrystals. This unconventional organic-inorganic hybridization enables the conversion of singlet excitation to fast charge transfer luminescence.