Issue 36, 2022

Dual-mode nanophotonic upconversion oxygen sensors

Abstract

Nanophotonic biosensors capable of being excited in the NIR spectrum have applications in various sectors. Here, we develop a 980 nm-excitable nanophotonic sensor for real-time oxygen detection in both water and air by analyzing the photoluminescence lifetime and intensity using a nanocomposite of lanthanide-doped NaYF4:Yb3+,Tm3+ upconversion nanoparticles and a PtTFPP platinum porphyrin complex in a polystyrene matrix. Excellent overlap between the emission of the upconversion nanoparticles and the excitation band of the PtTFPP guarantees 68% efficient excitation of the PtTFPP molecules with a 980 nm NIR laser. For the first time, the oxygen sensitivity of the upconversion nanoparticles alone was reported, and it was demonstrated that the PL lifetime-based sensitivity slope was boosted more than 10 times by adding PtTFPP oxygen-sensitive molecules due to the energy transfer from the upconversion nano-emitters. In addition, the functionality of the upconversion-based sensor was investigated by analyzing its sensitivity, stability, reversibility, and temperature-dependent lifetime in both water and air, and its performance was compared with that of the sensor exposed to direct excitation at 410 nm. More importantly, the sensor was implanted under the skin of a chicken, and it was demonstrated that the PL intensity was amplified more than 12 times by employing the 980 nm excitation laser instead of 410 nm laser light. Therefore, excellent emission of the sensor under the skin paves the way for the development of implantable oxygen sensor platforms.

Graphical abstract: Dual-mode nanophotonic upconversion oxygen sensors

Supplementary files

Article information

Article type
Paper
Submitted
21 Apr 2022
Accepted
09 Aug 2022
First published
02 Sep 2022

Nanoscale, 2022,14, 13362-13372

Dual-mode nanophotonic upconversion oxygen sensors

E. Heydari, J. AmirAhmadi, N. Ghazyani, G. Bai, H. Zare-Behtash and M. MajlesAra, Nanoscale, 2022, 14, 13362 DOI: 10.1039/D2NR02193E

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