Abstract

Individual luminescent nanoparticles enable thermometry with sub-diffraction limited spatial resolution, but potential self-heating effects from high single-particle excitation intensities remain largely uninvestigated because thermal models predict negligible self-heating. Here, we report that the common “ratiometric” thermometry signal of individual NaYF4:Yb3+,Er3+ nanoparticles unexpectedly increases with excitation intensity, implying a temperature rise over 50 K if interpreted as thermal. Luminescence lifetime thermometry, which we demonstrate for the first time using individual NaYF4:Yb3+,Er3+ nanoparticles, indicates a similar temperature rise. To resolve this apparent contradiction between model and experiment, we systematically vary the nanoparticle’s thermal environment: the substrate thermal conductivity, nanoparticle-substrate contact resistance, and nanoparticle size. The apparent self-heating remains unchanged, demonstrating that this effect is an artifact, not a real temperature rise. Using rate equation modeling, we show that this artifact results from increased radiative and non-radiative relaxation from higher-lying Er3+ energy levels. This study has important implications for single-particle thermometry.

Highlights

  • Individual luminescent nanoparticles enable thermometry with sub-diffraction limited spatial resolution, but potential self-heating effects from high single-particle excitation intensities remain largely uninvestigated because thermal models predict negligible self-heating

  • Lanthanide-doped upconverting nanoparticles (UCNPs) are popular non-contact luminescent thermometers due to their excellent photostability[1], good thermal sensitivity allowing for sub-1 K temperature resolution[2,3], and biocompatibility[4,5]

  • We study faceted hexagonal 50 × 50 × 50 nm[3] and cylindrical 20 × 20 × 40 nm[3] NaYF4 particles doped with 20% Yb3+ and 2% Er3+, the most common UCNP composition

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Summary

Introduction

Individual luminescent nanoparticles enable thermometry with sub-diffraction limited spatial resolution, but potential self-heating effects from high single-particle excitation intensities remain largely uninvestigated because thermal models predict negligible self-heating. In sharp contrast with a conservative thermal estimate, we show that increasing the excitation intensity causes an apparent temperature rise of more than 50 K as measured by two independent thermometry methods. This effect is remarkably insensitive to systematic manipulation of the relevant heat dissipation pathways or the number of absorbing Yb3+ ions. The modeled relative increase in r is similar to our experimental results, confirming that such intensity-dependent photophysics, rather than thermal effects, is responsible for the apparent temperature rise

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