Apparent self-heating of individual upconverting nanoparticle thermometers

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...

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Veröffentlicht in:Nature communications 2018-11, Vol.9 (1), p.4907-12, Article 4907
Hauptverfasser: Pickel, Andrea D., Teitelboim, Ayelet, Chan, Emory M., Borys, Nicholas J., Schuck, P. James, Dames, Chris
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Sprache:eng
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Zusammenfassung: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 NaYF 4 :Yb 3+ ,Er 3+ 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 NaYF 4 :Yb 3+ ,Er 3+ 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 Er 3+ energy levels. This study has important implications for single-particle thermometry. Nanoparticles are often used as nanothermometers by measuring their luminescence from upconverted energy under illumination. The authors uncover the artificial appearance of a temperature rise at high excitation intensities due to effects involving higher energy states.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-018-07361-0