Arel: Investigating [Eu(H2O)9]3+Photophysics and Creating a Method to Bypass Luminescence Quantum Yield Determinations
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Arel : Investigating [Eu(H2O)9]3+Photophysics and Creating a Method to Bypass Luminescence Quantum Yield Determinations. / Kofod, Nicolaj; Nawrocki, Patrick; Sørensen, Thomas Just.
I: Journal of Physical Chemistry Letters, Bind 13, Nr. 13, 2022, s. 3096-3104.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Arel
T2 - Investigating [Eu(H2O)9]3+Photophysics and Creating a Method to Bypass Luminescence Quantum Yield Determinations
AU - Kofod, Nicolaj
AU - Nawrocki, Patrick
AU - Sørensen, Thomas Just
N1 - Funding Information: The authors thank Carlsbergfondet, Villum Fonden (Grant No. 14922), the University of Copenhagen, the Danish Chemical Society, and Fulbright Denmark for support. Publisher Copyright: © 2022 American Chemical Society. All rights reserved.
PY - 2022
Y1 - 2022
N2 - Lanthanide luminescence has been treated separate from molecular photophysics, although the underlying phenomena are the same. As the optical transitions observed in the trivalent lanthanide ions are forbidden, they do belong to the group that molecular photophysics has yet to conquer, yet the experimental descriptors remain valid. Herein, the luminescence quantum yields (φlum), luminescence lifetimes (τobs), oscillator strengths (f), and the rates of nonradiative (knr) and radiative (krA) deactivation of [Eu(H2O)9]3+were determined. Further, it was shown that instead of a full photophysical characterization, it is possible to relate changes in transition probabilities to the relative parameter Arel, which does not require reference data. While Areldoes not afford comparisons between experiments, it resolves emission intensity changes due to emitter properties from intensity changes due to environmental effects and differences in the number of photons absorbed. When working with fluorescence this may seem trivial; when working with lanthanide luminescence it is not.
AB - Lanthanide luminescence has been treated separate from molecular photophysics, although the underlying phenomena are the same. As the optical transitions observed in the trivalent lanthanide ions are forbidden, they do belong to the group that molecular photophysics has yet to conquer, yet the experimental descriptors remain valid. Herein, the luminescence quantum yields (φlum), luminescence lifetimes (τobs), oscillator strengths (f), and the rates of nonradiative (knr) and radiative (krA) deactivation of [Eu(H2O)9]3+were determined. Further, it was shown that instead of a full photophysical characterization, it is possible to relate changes in transition probabilities to the relative parameter Arel, which does not require reference data. While Areldoes not afford comparisons between experiments, it resolves emission intensity changes due to emitter properties from intensity changes due to environmental effects and differences in the number of photons absorbed. When working with fluorescence this may seem trivial; when working with lanthanide luminescence it is not.
U2 - 10.1021/acs.jpclett.2c00418
DO - 10.1021/acs.jpclett.2c00418
M3 - Journal article
C2 - 35357175
AN - SCOPUS:85127850071
VL - 13
SP - 3096
EP - 3104
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
SN - 1948-7185
IS - 13
ER -
ID: 307333158