Tunable Multicolor Fluorescence of Perovskite-Based Composites for Optical Steganography and Light-Emitting Devices.

Multicolor fluorescence of mixed halide perovskites enormously enables their applications in photonics and optoelectronics. However, it remains an arduous task to obtain multicolor emissions from perovskites containing single halogen to avoid phase segregation. Herein, a fluorescent composite containing Eu-based metal-organic frameworks (MOFs), 0D Cs4PbBr6, and 3D CsPbBr3 is synthesized. Under excitations at 365 nm and 254 nm, the pristine composite emits blue (B) and red (R) fluorescence, which are ascribed to radiative defects within Cs4PbBr6 and 5D0→7FJ transitions of Eu3+, respectively. Interestingly, after light soaking in the ambient environment, the blue fluorescence gradually converts into green (G) emission due to the defect repairing and 0D-3D phase conversion. This permanent and unique photochromic effect enables anticounterfeiting and microsteganography with increased security through a micropatterning technique. Moreover, the RGB luminescence is highly stable after encapsulation by a transparent polymer layer. Thus, trichromatic light-emitting modules are fabricated by using the fluorescent composites as color-converting layers, which almost fully cover the standard color gamut. Therefore, this work innovates a strategy for construction of tunable multicolor luminescence by manipulating the radiative defects and structural dimensionality.

Identification of Lattice Oxygen in Few-Layer Black Phosphorous Exfoliated in Ultrahigh Vacuum and Largely Improved Ambipolar Field-Effect Mobilities by Hydrogenation and Phosphorization.

Black phosphorus (BP) has recently attracted considerable attention due to its unique structure and fascinating optical and electronic properties as well as possible applications in photothermal agents. However, its main drawback is rapid degradation in ambient environments of H2O and O2, which has led to much research on the improvement of its stability. Unfortunately, this research has not shown great improvement in carrier mobilities. Here, we perform scanning tunneling microscopy observations of few-layer BP (FLBP) sheets exfoliated in ultrahigh vacuum and reveal, for the first time, the existence of lattice oxygen introduced during crystal growth. As a proof-of-concept application, hydrogenation is conducted to remove the lattice oxygen atoms followed by phosphorization, which repairs the phosphorous vacancies caused by mechanical exfoliation and hydrogenation. The resulting FLBP sheets show high ambipolar field-effect mobilities of 1374 cm2 V-1 s-1 for holes and 607 cm2 V-1 s-1 for electrons at 2 K. After storage in air for 3 days, the hole and electron mobilities only decrease to 1181 and 518 cm2 V-1 s-1, respectively, and no structural degradation is observed. This work suggests an effective means to improve both the mobility and stability of BP sheets rendering practical application of FLBP sheets possible.