Deciphering and quantifying linear light upconversion in molecular erbium complexes. Issue 28 (14th June 2019)

• Record Type: Journal Article
• Authors: Golesorkhi, Bahman; Fürstenberg, Alexandre; Nozary, Homayoun; Piguet, Claude
• Is Part Of: Chemical science. Volume 10:Issue 28(2019)
• Page Start: 6876
• Page End: 6885
• Publication Date: 2019-06-14
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c9sc02068c
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Single-center linear excited state absorption (ESA) can be implemented in isolated mononuclear erbium(iii ) coordination complexes, thus fixing the zero-level of quantum yields for lanthanide-based molecular light upconversion. Abstract : Single-center light upconversion corresponds to the piling up of low-energy photons via 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 ( λ exc = 801 nm or 966 nm) to visible green ( λ em = 522 nm and 545 nm) light upconversion within mononuclear coordination complexes [Er(L k )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 Yb2 Tb supramolecular assemblies. The various dependences of the upconverted emission on the incident excitation power imply different mechanisms, which can be tuned by molecular design.