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This research leverages nitrogen-vacancy centers in nanodiamonds as nanoscale sensors to perform in-situ monitoring of radical species during liquid-phase chemical reactions. By utilizing optical spin readout, the study achieves sensitive detection in the nanomolar range without requiring complex sample preparation or invasive probes. The work represents a significant advancement in applying quantum sensing principles to fundamental chemical physics and reaction kinetics.
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Towards Application of Nanodiamonds for in-situ Monitoring of Radicals in Liquid Phase Chemical Reactions

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arXiv:2604.19433v2 Announce Type: replace-cross Abstract: In many chemical reactions, short-lived radical intermediates play a crucial role, while detecting such short-lived species in-situ remains challenging. The optically readable electronic spin of nitrogen-vacancy (NV) centers in diamond is a nanoscale sensor for such radical species: its longitudinal spin relaxation time (T$_{1}$) reacts to magnetic fluctuations from the unpaired electrons of radical species in its local environment. In this setting, we demonstrate the successful in-situ detection of the nitroxide radical 2,2,6,6-Tetramethylpiperidinyloxyl (TEMPO) using NV center-based T$_1$ relaxometry after depositing nanodiamonds onto the inner wall of a glass cuvette. A significant concentration-dependent shortening of the relaxation time was observed, from 197\:\textmu s $\pm$ 21\:\textmu s without radical to 66\:\textmu s $\pm$ 30\:\textmu s at a concentration of 1\:M TEMPO. At the same time, the nanodiamonds remain firmly attached to the cuvette even after the solution under investigation has been exchanged. The detection is sensitive in the nanomolar (nM) range and the determined signal-to-noise ratio is between 1.6 and 3.

Abstract:In many chemical reactions, short-lived radical intermediates play a crucial role, while detecting such short-lived species in-situ remains challenging. The optically readable electronic spin of nitrogen-vacancy (NV) centers in diamond is a nanoscale sensor for such radical species: its longitudinal spin relaxation time (T$_{1}$) reacts to magnetic fluctuations from the unpaired electrons of radical species in its local environment. In this setting, we demonstrate the successful in-situ detection of the nitroxide radical 2,2,6,6-Tetramethylpiperidinyloxyl (TEMPO) using NV center-based T$_1$ relaxometry after depositing nanodiamonds onto the inner wall of a glass cuvette. A significant concentration-dependent shortening of the relaxation time was observed, from 197\:\textmu s $\pm$ 21\:\textmu s without radical to 66\:\textmu s $\pm$ 30\:\textmu s at a concentration of 1\:M TEMPO. At the same time, the nanodiamonds remain firmly attached to the cuvette even after the solution under investigation has been exchanged. The detection is sensitive in the nanomolar (nM) range and the determined signal-to-noise ratio is between 1.6 and 3.

Mesoscale and Nanoscale Physics (cond-mat.mes-hall); Chemical Physics (physics.chem-ph); Quantum Physics (quant-ph)

arXiv:2604.19433 [cond-mat.mes-hall]

(or arXiv:2604.19433v2 [cond-mat.mes-hall] for this version)

https://doi.org/10.48550/arXiv.2604.19433 Focus to learn more arXiv-issued DOI via DataCite

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