CdSe and CsPbBr3 Quantum Dots Co-doped Monolithic Glasses as Tunable Wavelength Convertors

CdSe and CsPbBr3 quantum dots are well studied photoluminescent materials due to their extraordinary emission properties. However, their vulnerability against environmental conditions limits their integration into further applications. At this point, glass encapsulation offers promising durability features due to its robust and dense structure. In this study, CdSe and CsPbBr3 QDs are successfully synthesized in the same glass host through melt-quenching technique followed by a single heat-treatment process. Excitation wavelength dependent photoluminescence properties are investigated and emission color tunability of monolithic glasses from yellow-green to red is demonstrated. Favorable quantum yield values are obtained as 21.78% and 16.63% under 345 and 365 nm excitation wavelengths, respectively. Prepared glasses demonstrate high potential to be used as tunable wavelength convertors for state-of-the-art photonic and opto-electronic applications.

Photocatalytic Degradation of Tobacco Tar Using CsPbBr3 Quantum Dots Modified Bi2WO6 Composite Photocatalyst

Polycyclic aromatic hydrocarbons (PAHs) in tobacco tar are regarded as a significant threat to human health. PAHs are formed due to the incomplete combustion of organics in tobacco and cigarette paper. Herein, for the first time, we extended the application of CsPbBr3 quantum dots (CsPbBr3) to the photocatalytic degradation of tobacco tar, which was collected from used cigarette filters. To optimize the photoactivity, CsPbBr3 was coupled with Bi2WO6 for the construction of a type-II photocatalyst. The photocatalytic performance of the CsPbBr3/Bi2WO6 composite was evaluated by the degradation rate of PAHs from tobacco tar under simulated solar irradiation. The results revealed that CsPbBr3/Bi2WO6 possesses a large specific surface area, outstanding absorption ability, good light absorption and rapid charge separation. As a result, in addition to good stability, the composite photocatalyst performed remarkably well in degrading PAHs (over 96% were removed in 50 mins of irradiation by AM 1.5 G). This study sheds light on promising novel applications of halide perovskite.