Zusammenfassung
The design of photoluminescence-quenching probes for molecular oxygen (O-2) is always a large space to explore. Luminescent semiconductor nanocrystals (NCs) have been proposed as emerging oxygen-responsive probes, but the inherent O-2 sensing of phosphorescent semiconductor NCs has not been reported so far. Here, we demonstrate the O-2 sensing capability of Mn-II-doped CsPbCl3 nanocrystals ...
Zusammenfassung
The design of photoluminescence-quenching probes for molecular oxygen (O-2) is always a large space to explore. Luminescent semiconductor nanocrystals (NCs) have been proposed as emerging oxygen-responsive probes, but the inherent O-2 sensing of phosphorescent semiconductor NCs has not been reported so far. Here, we demonstrate the O-2 sensing capability of Mn-II-doped CsPbCl3 nanocrystals (Mn:CsPbCl3 NCs) and reveal the role of O-2 on the optical de-excitation process of such perovskite nanocrystals (PNCs). By adjusting the amount and distribution of Mn-II dopants, as well as the host-dopant energy transfer process in PNCs, we highlight that O-2 can reversibly quench the Mn-II emission due to the temporary disturbance to the ligand field of near-surface Mn-II dopants in PNCs. In phosphorescence mode, the photoluminescence intensity of the Mn:CsPbCl3 NCs is quenched by 53% on increasing O-2 concentration from 0 to 100%. The Stern-Volmer plot shows a good linear in the 0-12% O-2 concentration range. High sensing reversibility and rapid signal response are also achieved. In our perception, the mechanism study makes our PNCs candidates for the optical probes of O-2, and it is enlightening to explore more possibilities of the inherent O-2 sensing based on the semiconductor-doped NCs (not restricted to Mn-II-doped PNCs) with phosphorescence emission.
Altmetric