Iridium-Based Time-Resolved Luminescent Sensor for Ba<sup>2+</sup> Detection

We present a new time-resolved chemosensor for the detection of Ba<sup>2+</sup> ions. Our sensor is based on an iridium(III) compound with dual (fluorescent and phosphorescent) emission. The nature of the luminescence response of the sensor depends on its state; specifically, the phosphorescence emission of the free state at long wavelengths is strongly suppressed, while that of the Ba<sup>2+</sup>-chelated compound is strongly enhanced. Furthermore, the residual phosphorescence emission of the free compound decays with two short decay constants, τ<sub>free</sub><sup>1</sup> ∼ 3.5 ns (88%) and τ<sub>free</sub><sup>2</sup> ∼ 209 ns (12%), while the chelated compound decays with two long decay constants, τ<sub>bound</sub><sup>1</sup> ∼ 429 ns (21%) and τ<sub>bound</sub><sup>2</sup> ∼ 1128 ns (76%). This exceptional behavior, supported by quantum chemical calculations, allows a time-based separation between the signals of the free and the chelated species. Among other applications, our sensor could be the basis of a Ba<sup>2+</sup> tagging detector for neutrinoless double beta decay searches in xenon.

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Journal
ACS Sensors
Published
2025-04-11
DOI
https://doi.org/10.1021/acssensors.4c01892
Citations
2
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
1.61

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article

Iridium-Based Time-Resolved Luminescent Sensor for Ba2+ Detection

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ACS Sensors
Advanced biosensing and bioanalysis techniques
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article

Iridium-Based Time-Resolved Luminescent Sensor for Ba2+ Detection

Zoraida Freixa, Claire Tonnelé, Fernando P. Cossío, Celia Rogero, A. I. Aranburu, Ariadna Pazos, F. Monrabal, J.J. Gómez-Cadenas, P. Herrero-Gómez, Jose Eduardo Barcelon, Gabriel Molina‐Terriza, A. Brodolin, P. R. G. Valle, Mikel Elorza
article en
2 citations

Abstract

We present a new time-resolved chemosensor for the detection of Ba<sup>2+</sup> ions. Our sensor is based on an iridium(III) compound with dual (fluorescent and phosphorescent) emission. The nature of the luminescence response of the sensor depends on its state; specifically, the phosphorescence emission of the free state at long wavelengths is strongly suppressed, while that of the Ba<sup>2+</sup>-chelated compound is strongly enhanced. Furthermore, the residual phosphorescence emission of the free compound decays with two short decay constants, τ<sub>free</sub><sup>1</sup> ∼ 3.5 ns (88%) and τ<sub>free</sub><sup>2</sup> ∼ 209 ns (12%), while the chelated compound decays with two long decay constants, τ<sub>bound</sub><sup>1</sup> ∼ 429 ns (21%) and τ<sub>bound</sub><sup>2</sup> ∼ 1128 ns (76%). This exceptional behavior, supported by quantum chemical calculations, allows a time-based separation between the signals of the free and the chelated species. Among other applications, our sensor could be the basis of a Ba<sup>2+</sup> tagging detector for neutrinoless double beta decay searches in xenon.

ACS SensorsVol. 10(4)
Ikerbasque (ES), University of the Basque Country (ES), Hebrew University of Jerusalem (IL), FZU ‒ Institute of Physics of the Academy of Sciences of the Czech Republic (CZ), Material Physics Center (ES), Donostia International Physics Center (ES)
U.S. Department of Energy, Welch Foundation, “la Caixa” Foundation, Hezkuntza, Hizkuntza Politika Eta Kultura Saila, Eusko Jaurlaritza, Eusko Jaurlaritza, Generalitat Valenciana, Euskal Herriko Unibertsitatea, Israel Science Foundation, PAZY Foundation, Horizon 2020 Framework Programme, European Research Council, Fundação para a Ciência e a Tecnologia, European Regional Development Fund, Agencia Estatal de Investigación, Division of Chemistry
Openalex Percentile: Top 18%
Advanced biosensing and bioanalysis techniques
1.61
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