Repozytorium

Quenching of the Eu3+ luminescence by Cu2+ ions in the nanosized hydroxyapatite designed for future bio-detection.

Autorzy

Katarzyna Szyszka

Sara Targońska

Agnieszka Lewińska

Adam Watras

Rafał J. Wiglusz

Rok wydania

2021

Czasopismo

Nanomaterials

Numer woluminu

11

Strony

464/1-464/17

DOI

10.3390/nano11020464

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

The hydroxyapatite nanopowders of the Eu3+-doped, Cu2+-doped, and Eu3+/Cu2+-co-doped Ca10(PO4)6(OH)2 were prepared by a microwave-assisted hydrothermal method. The structural and morphological properties of the products were investigated by X-ray powder diffraction (XRD), transmission electron microscopy techniques (TEM), and infrared spectroscopy (FT-IR). The average crystal size and the unit cell parameters were calculated by a Rietveld refinement tool. The absorption, emission excitation, emission, and luminescence decay time were recorded and studied in detail. The 5D0 → 7F2 transition is the most intense transition. The Eu3+ ions occupied two independent crystallographic sites in these materials exhibited in emission spectra: one Ca(1) site with C3 symmetry and one Ca(2) sites with Cs symmetry. The Eu3+ emission is strongly quenched by Cu2+ ions, and the luminescence decay time is much shorter in the case of Eu3+/Cu2+ co-doped materials than in Eu3+-doped materials. The luminescence quenching mechanism as well as the schematic energy level diagram showing the Eu3+ emission quenching mechanism using Cu2+ ions are proposed. The electron paramagnetic resonance (EPR) technique revealed the existence of at least two different coordination environments for copper(II) ion.

Słowa kluczowe

apatite, europium ions, cooper ions, photoluminescence spectroscopy, EPR spectroscopy

Licencja otwartego dostępu

CC-BY

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Pełny tekst licencji: https://creativecommons.org/licenses/by/3.0/pl/legalcode

Adres publiczny

http://dx.doi.org/10.3390/nano11020464

Strona internetowa wydawcy

http://www.mdpi.com/journal/metals

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