Abstract

A viable technology for liquid phosphor-based light-emitting diodes (LEDs) with emission color tuneability is described. These devices are based on Tris(bipyridine)ruthenium(II) chloride but can be constructed from other similar metal coordination charge transfer complexes. The Frank-Condon excited state generated upon the absorption of blue (450 nm) pump photons has a large electric dipole moment due to intramolecular metal-to-ligand charge transfer from the ruthenium atom to one specific bipyridyl ligand. Polar solvents respond to the dipole field creating a solvatochromic shift that is solvent dependent. The devices were fully sealed in either a long path length or a short path length configuration. The latter encapsulating the luminescing medium in hollow silica spheres that can be easily applied like a slurry on top of InGaN/GaN LED dies. The devices were optically, thermally and environmentally stable. Also discussed is the possibility of using solvatochromic emitters for achieving color temperature tuneability in white LEDs.

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