Experimental study demonstrates spatial separation suppresses back energy transfer in upconversion nanoparticles, highlighting a strategy to produce exceptionally bright optical nanomaterials.
Lanthanide-doped upconversion nanoparticles are promising for applications ranging from biosensing, bioimaging to solid-state lasing. However, their brightness remains limited by the concentration quenching effect of lanthanide activator ions, which greatly restricts their utility. Here, we develop a heterogeneous core-shell-shell nanostructure based on hexagonal NaYF₄, in which Tm³⁺ activator and Yb³⁺ sensitizer are separated into the core and inner shell, while the outmost shell is used to suppress surface quenching effects. We show that this design can alleviate the activator concentration quenching effect, resulting in optimal Tm³⁺ concentration increasing from 1% to 8% at sub-100 W/cm² irradiance, compared with the canonical core-only NaYF₄:Yb³⁺/Tm³⁺. Moreover, under high excitation irradiance (20 MW/cm²), the optimal Tm³⁺ concentration could be further increased to 50%. Mechanistic investigations reveal that the spatial separation of sensitizer and activator effectively suppresses the back energy transfer from Tm³⁺ to Yb³⁺, driving the increase of optimal activator concentration. These findings enhance our understanding of lanthanide concentration quenching effect, unleashing opportunities for developing bright upconverting materials.
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Huang et al. (2025) studied this question.
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