Search

Robust amorphous glass protected CsPbBr3 (CsPbBr3@glass) perovskite quantum dots (PeQDs) with ultra‐pure green emission and superior long‐term stability are highly desirable for developing wide‐color‐gamut liquid crystal displays. However, most of the reported CsPbBr3@glass nanocomposites are subject to low external quantum efficiency (EQE). This work demonstrates that ZrO2 additive has an "accumulation" effect on the borosilicate glass network structure to promote in situ nucleation/growth of PeQDs inside glass rather than self‐crystallization. This effect is beneficial in reducing surface defects, improving the quality of PeQDs, and thus boosting radiative recombination of excitons. As a consequence, the as‐prepared CsPbBr3@glass shows a record EQE of up to 75% and can pass the accelerated aging tests at 85 °C/85% RH for 1000 h and blue light irradiation over 2000 h. Finally, a prototype display using CsPbBr3@glass‐based straight‐down backlit unit is designed and gains more favorable responses in blind selection tests for its high brightness of 2647 cd m−2 and high color purity of 88%. The findings will pave the way for realizing the commercial application of CsPbBr3@glass nanocomposite in PeQDs‐converted backlit display. [ABSTRACT FROM AUTHOR]

The complex and high‐precision patterning of perovskite quantum dots (PeQDs) is of vital importance for exploring their new functionalities and device applications. In this work, a strategy based on the combination femtosecond (fs) laser‐irradiation and humidity‐control is reported to construct patterns of cyan CsPb(Cl/Br)3 PeQDs in a transparent glass medium. Benefiting from their ionic crystal feature and low formation energy, CsPb(Cl/Br)3 PeQDs can be locally crystallized and decomposed via fs laser irradiation without further heat‐treatment. More notably, it is found that a water molecule is able to affect the growth of CsPb(Cl/Br)3 PeQDs in glass. By modulation of relative humidity in air, the selectively decomposed perovskite structure is spontaneously regenerated, and the highly emissive CsPb(Cl/Br)3 PeQDs can be in situ manufactured in the confined glass region. This allows for reversible luminescence from the same patterns of laser printing‐erasing‐recovering, and the process can be repeated for multiple cycles without destruction of optical performance and robustness. The results provide a flexible method to develop new encryption/decryption technology for information security and anti‐counterfeiting. [ABSTRACT FROM AUTHOR]

A novel approach has been developed to synthesize slightly fluorinated graphene quantum dots (GQDs-F) through thermal cutting of highly fluorinated graphene. The fluorinated graphene with substantial structure defects is fragile and is readily attacked. The direct evaporation of abundant CFn (n = 2, 3) groups near structure defects lead to the loss of adjacent skelton C atoms, and the fluorinated graphene can be thermally cut into GQDs-F with a relatively uniform nanosize in pyrolysis at 810 K. The GQDs-F with a low F/C atomic ratio of ca. 0.03 exhibit excitation wavelength-dependent properties with multicolor photoluminescence (PL) from blue to green. At the same time, F adatoms that are most likely located at the edges of GQDs-F have a high efficiency of introducing paramagnetic centres, and GQDs-F show a strong paramagnetism because of sp3-type defects and magnetic zigzag edges. The graphene quantum dots with such multimodal capabilities should have great applied value in material science. [ABSTRACT FROM AUTHOR]