scholarly journals Cyclometalated Iridium-Coumarin Ratiometric Oxygen Sensors: Improved Signal Resolution and Tunable Dynamic Ranges

Author(s):  
Yanyu Wu ◽  
Gregory D. Sutton ◽  
Michael D. S. Halamicek ◽  
Thomas S. Teets

In this work we introduce a new series of ratiometric oxygen sensors for hypoxic environments based on phosphorescent cyclometalated iridium centers partnered with organic coumarin fluorophores. Three different cyclometalating ligands and two different pyridyl-containing coumarin types were used to prepare six target complexes with tunable excited-state energies. Some of the complexes exhibit only phosphorescence originating from the cyclometalated Ir moiety, as a result of excited-state energy transfer from the coumarin to the Ir-centered excited states. Three of the complexes display dual emission, with fluorescence arising from the coumarin ligands and phosphorescence from the cyclometalated iridium synthons, and hence function as ratiometric oxygen sensors. Oxygen quenching experiments with these complexes demonstrate that the iridium centered phosphorescence is quenched under O₂ while fluorescence is unaffected. These sensors have good signal resolution, and the sensitivity and dynamic range, measured with Stern-Volmer analysis, span two orders of magnitude. This work demonstrates that this simple, modular approach for conjoining fluorescent and phosphorescent molecules can produce effective oxygen sensors with a wide range of attributes.

2021 ◽  
Author(s):  
Yanyu Wu ◽  
Gregory D. Sutton ◽  
Michael D. S. Halamicek ◽  
Thomas S. Teets

In this work we introduce a new series of ratiometric oxygen sensors for hypoxic environments based on phosphorescent cyclometalated iridium centers partnered with organic coumarin fluorophores. Three different cyclometalating ligands and two different pyridyl-containing coumarin types were used to prepare six target complexes with tunable excited-state energies. Some of the complexes exhibit only phosphorescence originating from the cyclometalated Ir moiety, as a result of excited-state energy transfer from the coumarin to the Ir-centered excited states. Three of the complexes display dual emission, with fluorescence arising from the coumarin ligands and phosphorescence from the cyclometalated iridium synthons, and hence function as ratiometric oxygen sensors. Oxygen quenching experiments on these complexes demonstrate that the iridium centered phosphorescence is quenched under O₂ while fluorescence is unaffected. These sensors have good signal resolution, and the sensitivity and dynamic range, measured with Stern-Volmer analysis, span two orders of magnitude. This work demonstrates that this simple, modular approach for conjoining fluorescent and phosphorescent molecules can produce effective oxygen sensors with a wide range of attributes.


2007 ◽  
Vol 06 (05) ◽  
pp. 383-387
Author(s):  
T. V. TORCHYNSKA ◽  
E. VELÁZQUEZ LOZADA ◽  
M. DYBIEC ◽  
S. OSTAPENKO ◽  
P. G. ELISEEV ◽  
...  

This paper presents the photoluminescence study at 12 K and scanning photoluminescence spectroscopy investigation of the ground and excited states at 80 and 300 K on InAs QDs inserted in In 0.15 Ga 0.85 As / GaAs QW structures and created at different QD growth temperatures. It is shown that investigated structures are characterized by the long range variation of an average QD size in QD ensemble across the wafer. This long range QD size inhomogeneity was used for investigation of the multi-excited state energy trend versus ground state energy (or QD sizes).


2021 ◽  
Author(s):  
Weixuan Zeng ◽  
Ouissam El Bakouri ◽  
Dariusz Szczepanik ◽  
Hugo Bronstein ◽  
Henrik Ottosson

The exact energies of the lowest singlet and triplet excited states in organic chromophores are crucial to their performance in optoelectronic devices. The possibility of utilizing singlet fission to enhance the performance of photovoltaic devices has resulted in a wide demand for tuneable, stable organic chromophores with wide S<sub>1</sub> – T<sub>1</sub> energy gaps (>1 eV). Cibalackrot-type compounds were recently considered to have favorably positioned excited state energies for singlet fission, and they were found to have a degree of aromaticity in the lowest triplet excited state (T<sub>1</sub>). This work reports on a revised and deepened theoretical analysis taking into account the excited state Hückel-aromatic (instead of Baird-aromatic) as well as diradical characters, with the aim to design new organic chromophores based on this scaffold in a rational way starting from qualitative theory. We demonstrate that the substituent strategy can effectively adjust the spin populations on the chromophore moieties and thereby manipulate the excited state energy levels. Additionally, the improved understanding of the aromatic characters enables us to demonstrate a feasible design strategy to vary the excited state energy levels by tuning the number and nature of Hückel-aromatic units in the excited state. Finally, our study elucidates the complications and pitfalls of the excited state aromaticity and antiaromaticity concepts, highlighting that quantitative results from quantum chemical calculations of various aromaticity indices must be linked with qualitative theoretical analysis of the character of the excited states.


2021 ◽  
Author(s):  
Weixuan Zeng ◽  
Ouissam El Bakouri ◽  
Dariusz Szczepanik ◽  
Hugo Bronstein ◽  
Henrik Ottosson

The exact energies of the lowest singlet and triplet excited states in organic chromophores are crucial to their performance in optoelectronic devices. The possibility of utilizing singlet fission to enhance the performance of photovoltaic devices has resulted in a wide demand for tuneable, stable organic chromophores with wide S<sub>1</sub> – T<sub>1</sub> energy gaps (>1 eV). Cibalackrot-type compounds were recently considered to have favorably positioned excited state energies for singlet fission, and they were found to have a degree of aromaticity in the lowest triplet excited state (T<sub>1</sub>). This work reports on a revised and deepened theoretical analysis taking into account the excited state Hückel-aromatic (instead of Baird-aromatic) as well as diradical characters, with the aim to design new organic chromophores based on this scaffold in a rational way starting from qualitative theory. We demonstrate that the substituent strategy can effectively adjust the spin populations on the chromophore moieties and thereby manipulate the excited state energy levels. Additionally, the improved understanding of the aromatic characters enables us to demonstrate a feasible design strategy to vary the excited state energy levels by tuning the number and nature of Hückel-aromatic units in the excited state. Finally, our study elucidates the complications and pitfalls of the excited state aromaticity and antiaromaticity concepts, highlighting that quantitative results from quantum chemical calculations of various aromaticity indices must be linked with qualitative theoretical analysis of the character of the excited states.


2019 ◽  
Vol 216 ◽  
pp. 395-413 ◽  
Author(s):  
T. Northey ◽  
T. Keane ◽  
J. Eng ◽  
T. J. Penfold

Excited state energy transfer in disordered systems has attracted significant attention owing to the importance of this phenomenon in both artificial and natural systems that operate in electronically excited states.


2012 ◽  
Vol 11 (03) ◽  
pp. 1250026 ◽  
Author(s):  
CHENG-SHUN WANG ◽  
YU-FANG CHEN ◽  
JING-JIN XIAO

Properties of the excited state of strong-coupling impurity bound polaron in an asymmetric quantum dot are studied by using linear combination operator and unitary transformation methods. The first internal excited state energy, the excitation energy and the transition frequency between the first internal excited and the ground states of the impurity bound polaron as functions of the transverse and the longitudinal effective confinement lengths of the dot, the electron–phonon coupling strength and the Coulomb bound potential were derived. Our numerical results show that they will increase with decreasing the effective confinement lengths, due to interesting quantum size confining effects. But they are an increasing functions of the Coulomb bound potential. The first internal excited state energy is a decreasing function of the electron–phonon coupling strength whereas the transition frequency and the excitation energy are an increasing one of the electron–phonon coupling strength.


2003 ◽  
Vol 42 (21) ◽  
pp. 6629-6647 ◽  
Author(s):  
Lianhe Yu ◽  
Kannan Muthukumaran ◽  
Igor V. Sazanovich ◽  
Christine Kirmaier ◽  
Eve Hindin ◽  
...  

2020 ◽  
Author(s):  
Florian Chotard ◽  
Vasily Sivchik ◽  
Mikko Linnolahti ◽  
Manfred Bochmann ◽  
Alexander Romanov

New luminescent “carbene-metal-amide” (CMA) Cu, Ag and Au complexes based on monocyclic (C6) or bicyclic six-ring (BIC6) cyclic (alkyl)(amino)carbene ligands illustrates the effects of LUMO energy stabilization, conformational flexibility and excited state energy on the photoemission properties, leading to near-quantitative quantum yields, short excited state lifetimes Cu > Au > Ag down to 0.5 µs and high radiative rates of 10<sup>6</sup> s<sup>–1</sup>.


2017 ◽  
Vol 56 (40) ◽  
pp. 12097-12101 ◽  
Author(s):  
Francesca Arcudi ◽  
Volker Strauss ◽  
Luka Đorđević ◽  
Alejandro Cadranel ◽  
Dirk M. Guldi ◽  
...  

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