TY - JOUR
T1 - Correction Due to Nonthermally Coupled Emission Bands and Its Implications on the Performance of Y2O3:Yb3+/Er3+Single-Particle Thermometers
AU - Pessoa, Allison R.
AU - Galindo, Jefferson A.O.
AU - Dos Santos, Luiz F.
AU - Gonçalves, Rogéria R.
AU - Maier, Stefan A.
AU - De S. Menezes, Leonardo
AU - Amaral, Anderson M.
N1 - Funding Information:
The authors thank the financial support from the Brazilian science funding agencies Coordenação de Aperfeiçoamento Pessoal de Nível Superior (CAPES), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (FACEPE) and the National Photonics Institute - INFo/CNPq. L.F.S. acknowledges Funcação de Amparo à Pesquisa do Estado de São Paulo (FAPESP - Grant Number 2020/04157-5). R.R.G. acknowledges CNPq (Grant Number 303110/2019-8) and FAPESP (Grant Number 2020/05319-9, 2017/11301-2, and 2021/08111-2) for financial support. S.A.M. acknowledges the EPSRC (EP/W017075/1) and the Lee-Lucas Chair in Physics.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/5/25
Y1 - 2023/5/25
N2 - Lanthanide-doped single dielectric nanoparticles have been exploited toward the realization of temperature sensing in the nanoscale with high spatial, temporal, and thermal resolution. However, due to the relatively small number of emitters when compared with suspensions or powders, the luminescence readouts in individual nanocrystals usually require higher excitation power densities to keep an acceptable signal-to-noise ratio. Since in numerous cases these thermometers work by exploiting upconversion excitation pathways, higher excitation powers can lead to higher-order photon emissions that can overlap with the luminescent bands used to perform the temperature measurements. This work shows that the performance and the characterization of ∼400 nm Y2O3: Yb3+/Er3+ single-particle thermometers vary depending on the excitation irradiance if higher-order spectrally overlapping bands are not properly taken into account. We apply a recently developed method to separate these bands based on their different power-law, without the need for multiple wavelength excitation, resulting in a correction procedure that reduces the temperature readout uncertainty from 0.6 to 0.3 K in the specific case of the thermometer investigated in this work. Additionally, power-excitation-related thermal artifacts on the order of 10 °C were detected and corrected with the presented method.
AB - Lanthanide-doped single dielectric nanoparticles have been exploited toward the realization of temperature sensing in the nanoscale with high spatial, temporal, and thermal resolution. However, due to the relatively small number of emitters when compared with suspensions or powders, the luminescence readouts in individual nanocrystals usually require higher excitation power densities to keep an acceptable signal-to-noise ratio. Since in numerous cases these thermometers work by exploiting upconversion excitation pathways, higher excitation powers can lead to higher-order photon emissions that can overlap with the luminescent bands used to perform the temperature measurements. This work shows that the performance and the characterization of ∼400 nm Y2O3: Yb3+/Er3+ single-particle thermometers vary depending on the excitation irradiance if higher-order spectrally overlapping bands are not properly taken into account. We apply a recently developed method to separate these bands based on their different power-law, without the need for multiple wavelength excitation, resulting in a correction procedure that reduces the temperature readout uncertainty from 0.6 to 0.3 K in the specific case of the thermometer investigated in this work. Additionally, power-excitation-related thermal artifacts on the order of 10 °C were detected and corrected with the presented method.
UR - http://www.scopus.com/inward/record.url?scp=85160679385&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.3c00522
DO - 10.1021/acs.jpcc.3c00522
M3 - Article
AN - SCOPUS:85160679385
SN - 1932-7447
VL - 127
SP - 9673
EP - 9680
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 20
ER -