To expand inorganic aggregation-induced emission systems, we demonstrate a universal solution-phase strategy for lanthanide(III) ions (Tb3+, Sm3+ and Dy3+) via electronic-vibrational decoupling: concentration-driven ligand-sphere reorganization and solvent deuteration suppress multiphonon quenching, boosting the Ln3+ emission intensity, lifetime, and photoluminescence quantum yield.
Wang et al. (Thu,) studied this question.