摘要
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 CsPbBr 3 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 CsPbBr 3 QD decorated Ti 3 C 2 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 CsPbBr 3 QDs can be retarded due to a relatively lower total energy during the adsorption of precursors on Ti 3 C 2 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 CsPbBr 3 QDs and Ti 3 C 2 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.
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