Abstract
With the development of high-resolution display technologies with vision health consideration, the absent emission wavelengths on the long-wavelength blue light (460 nm to 480 nm) of CsPbBr3 quantum dots (QDs) has become a crucial hindrance for the wide color gamut displays, and the tunable emission wavelengths via size control can unfortunately suffer from the ligand shedding. In the light of chlorophylls, the CsPbBr3 QD decorated Ti3C2 nanosheets (CQDTs) are in-situ synthesized with a controllable emission wavelength range from 455 nm to 505 nm at room temperature. The growth rate of CsPbBr3 QDs can be retarded due to a relatively lower total energy during the adsorption of precursors on Ti3C2 nanosheets, thus the improved monodispersity of resulting QDs in turn results in the photoluminescence quantum yield at 505 nm (∼100%) and at 455 nm (∼42%). Providing with the strong binding energy between CsPbBr3 QDs and Ti3C2 nanosheets, the decomposition of perovskite can be efficiently hindered, endowing an excellent stability. The enhanced stability of the flexible light-emitting films fabricated with CQDT is witnessed with a remained luminescence intensity of 77% (pristine is 45%) after 40 000 bending cycles, and the CQDT LED possesses the chromatic coordinates of (0.06, 0.61), (0.71, 0.28), (0.12, 0.06) with a ∼107% NTSC color gamut.
| Original language | English |
|---|---|
| Journal | Nano Materials Science |
| DOIs | |
| State | Accepted/In press - 2026 |
| Externally published | Yes |
Keywords
- CsPbBr
- MXene
- Perovskite quantum dots
- Tunable luminescence
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