Erbium excited state deactivation is studied for two fluorinated complexes based on N-(P,P-ditetrafluorophosphinoyl-P,P-ditetrafluorophenyl phosphinimidates and N-(P,P-dipentafluoro phosphinoyl)-P,P-dipentafluorophenyl phosphinimidates ligands. We show that the substitution of a fluorine atom in para-position by an hydrogen atom on each phenyl ring of the perfluorinated organic ligand results in a decrease in near infrared luminescence lifetimes from 800 µs to 70 µs when measured under vacuum on sublimated powder samples. These experiments show that the introduction of C-H bonds, although outside the first coordination sphere of the erbium ion, can still induce a one order of magnitude decrease in its excited state lifetime. The found lifetime however is still longer than most reported partially fluorinated complexes, which opens the way for new functionalized complexes.

We present a systematic study of photo- and cathodoluminescence measurements in the visible of Terbium doped SiC:H and AlN thin films. The Terbium atomic concentrations vary from 0.9 to 10% for the SiC:H and from 0.8 to 6% for the AlN samples. For both materials the increase of the emission intensity with concentration and the subsequent quenching effect can be seen. The optimal concentration for the highest light emission is found. Photoluminescence excitation spectroscopy addresses the enhancement light emission mechanisms of the principal emission electronic transition of Terbium at ∼542 nm.