Ultrasensitive Luminescence Switching of Zeolite Y Confined Silver Clusters for Dual‐Channel Oxygen Sensing.

Designing photoluminescence sensing devices for gaseous oxygen that combine ease of acquisition with efficient performance is a critical yet challenging task. Herein, a novel oxygen‐sensing probe based on zeolite Y confined silver clusters prepared via a simple approach, is proposed. The large Ag6 clusters formed after hydrogenation exhibit a bright orange emission. They are characterized by a high photoluminescence quantum yield (≈31%) and a long luminescence decay time (>500 µs). A possible formation mechanism of these clusters, which are for the first time observed in Faujasite zeolites, is proposed. Luminescence switching‐off, triggered by oxygen, can be detected in a dual‐channel combination of linear emission‐quenching and lifetime‐reduction, enabling a visual and ultrasensitive (limit of detection of 58 Pa) quantitative detection of oxygen in a wide pressure range (0–100 kPa) with fast response (<1 s), reversibility and reproducibility. A more detailed analysis shows that this high sensitivity is due to the long decay time of the orange emission and the high affinity of the zeolite for O2 adsorption rather than to a high rate constant for quenching. This work contributes to the development of optical oxygen sensing technology and lays the foundation for the design of silver cluster‐based zeolites for photo‐functional applications. [ABSTRACT FROM AUTHOR]