Repozytorium

Evaluating NaNdF₄:x%Yb3+ (x = 5, 7, 10, 20) nanoheating properties by NaYF4:Yb3+, Er3+ luminescent thermometer: The impact of shell type

Autorzy

K. Maciejewska

M. Krzystek-Korpacka

I. Krauze

Mirosław Karbowiak

Rok wydania

2025

Czasopismo

Journal of Alloys and Compounds

Numer woluminu

1044

Strony

183190/1-183190/10

DOI

10.1016/j.jallcom.2025.183190

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

In this study, we investigated the heating properties of NaNdF₄ nanoparticles (NPs) co-doped with Yb³⁺ ions (NaNdF₄:x%Yb³⁺, x = 5, 7, 10, 20), focusing on the impact of different surface coatings; silica (SiO₂), polyethylene glycol (PEG), and cetyltrimethylammonium bromide micelles (CTAB) on their photothermal conversion efficiency. Luminescent NaYF₄:18%Yb³⁺,2%Er³⁺ NPs were employed as thermometric sensors, enabling the quantitative determination of heat generation by monitoring the luminescence intensity ratio of thermally coupled up-conversion emission bands. The study demonstrates that both the surface coating and Yb³⁺ ion concentration significantly influence the rate and magnitude of the temperature increase. The highest temperature rise (ΔT = 10.0°C) was observed for NaNdF₄:7%Yb³⁺ NPs coated with SiO₂, attributed to effective core isolation and high thermal conductivity of the SiO₂ layer. Lower ΔT values were recorded for NPs coated with PEG (7.9°C) and CTAB (5.9°C), reflecting reduced environmental isolation and less efficient energy transfer between ions. Additionally, we found that the coating type strongly affects the kinetics of temperature increase, which is crucial for potential applications in photothermal therapy and biomedical nanotechnology. These findings highlight the importance of precise control over nanoparticle surface structures to optimize their functional properties for applications in luminescent thermometry and nanomedicine.

Słowa kluczowe

luminescent NPs, luminescent thermometry, Nd3 +based nanoheating

Adres publiczny

http://dx.doi.org/10.1016/j.jallcom.2025.183190

Strona internetowa wydawcy

http://www.elsevier.com

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