Deciphering and quantifying linear light upconversion in molecular erbium complexes

Abstract

Single-center light upconversion corresponds to the piling up of low-energy photons <i>via</i> successive linear absorptions: a phenomenon commonly observed in lanthanide-doped low-phonon ionic solids or nanoparticles. Its ultimate miniaturization in molecular complexes opens challenging perspectives in terms of improved reproducibility, chemical control and optical programming. However, high-energy vibrations inherent in coordination complexes severely limit the efficiency of successive excited-state absorptions (ESAs) responsible for the gain in photon energy. By carefully wrapping three polyaromatic ligand strands around trivalent erbium, we managed to induce low-power room temperature near-infrared (<i>λ</i> _exc = 801 nm or 966 nm) to visible green (<i>λ</i> _em = 522 nm and 545 nm) light upconversion within mononuclear coordination complexes [Er(<b>L<i>k</i></b> )₃]³⁺ operating either in the solid state or in non-deuterated solution. The calculated upconversion quantum yields set the zero-level of an elemental erbium-centered molecular ESA mechanism, a value which favorably compares with cooperative upconversion (CU) previously implemented in sophisticated multisite Yb₂Tb supramolecular assemblies. The various dependences of the upconverted emission on the incident excitation power imply different mechanisms, which can be tuned by molecular design.