Energy-Relay-Engineered Upconversion Emission with Intrinsic Environmental Responsiveness.
basic_science · Level V
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- Record sourced from PubMed, PMID 41848555.
- Also identified by DOI 10.1002/adma.72806.
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Abstract
Lanthanide-based upconversion nanoparticles (UCNPs) offer excellent photostability and large anti-Stokes shifts but are often limited by poor environmental responsiveness, hindering sensing applications. To address this challenge, we developed an energy-relay strategy by integrating near-infrared (NIR) dyes with Er<sup>3+</sup>/Tm<sup>3+</sup> doped UCNPs. Under 980 nm excitation, Yb<sup>3+</sup> transfers energy to Tm<sup>3+</sup> and Er<sup>3+</sup>, excited Tm<sup>3+</sup> ions then pass their energy to NIR dyes such as Cy7.5, which subsequently relay it back to Yb<sup>3+</sup> ions, enabling a second Yb<sup>3+</sup>-to-Er<sup>3+</sup> energy transfer. This cascade process amplifies Er<sup>3+</sup> emission while quenching Tm<sup>3</sup> <sup>+</sup> emission. In Cy7.5-modified Er<sup>3+</sup>/Tm<sup>3+</sup> doped UCNPs (NaYbF<sub>4</sub>:Er@NaYbF<sub>4</sub>@NaYbF<sub>4</sub>:Tm@NaYbF<sub>4</sub>@NaLuF<sub>4</sub>), the energy-relay effect enhances the Er<sup>3+</sup>/Tm<sup>3+</sup> ratiometric signal by two orders of magnitude. The process is highly dependent on the dopant architecture, as swapping Er<sup>3+</sup> and Tm<sup>3+</sup> positions disrupts the relay. The generality of this strategy is supported by similar energy-relay observed with Cy7 and IR806. Despite the incorporation of dyes, our energy-relay design retains the excellent photostability characteristic of lanthanide upconversion while introducing environmental responsiveness. As a proof of concept, the energy-relay nanoprobe demonstrated high sensitivity in both thermal and chemical sensing. Our findings establish energy-relay engineering as a versatile design principle for designing stable, efficient, and responsive upconversion nanoprobe platforms.