Polarization-sensitive photodetection in a broad spectrum range is highly desired due to the great significance in military and civilian applications. Palladium diselenide (PdSe2), a newly explored air-stable, group 10 two-dimensional (2D) noble metal dichalcogenide with a puckered pentagonal structure, holds promise for polarization-sensitive photodetection. Herein, we report a highly polarization-sensitive, broadband, self-powered photodetector based on graphene/PdSe2/germanium heterojunction. Owing to the enhanced light absorption of the mixed-dimensional van der Waals heterojunction and the effective carrier collection with graphene transparent electrode, the photodetector exhibits superior device performance in terms of a large photoresponsivity, a high specific detectivity, a fast response speed to follow nanosecond pulsed light signal, and a broadband photosensitivity ranging from deep ultraviolet (DUV) to mid-infrared (MIR). Significantly, highly polarization-sensitive broadband photodetection with an ultrahigh polarization sensitivity of 112.2 is achieved, which represents the best result for 2D layered material-based photodetectors. Further, we demonstrated the high-resolution polarization imaging based on the heterojunction device. This work reveals the great potential of 2D PdSe2 for high-performance, air-stable, and polarization-sensitive broadband photodetectors.

Recently, a pressing requirement of solid-state lighting sources with high performance and low cost has motivated increasing research in metal halide perovskites. However, the relatively low emission efficiency and poor operation stability of perovskite light-emitting diodes (LEDs) are still critical drawbacks. In this study, a strategy of solution-processed all-inorganic heterostructure was proposed to overcome the emission efficiency and operation stability issues facing the challenges of perovskite LEDs. Solution-processed n-ZnO nanoparticles and p-NiO are used as the carrier injectors to fabricate all-inorganic heterostructured CsPbBr quantum dot LEDs, and a high-efficiency green emission is achieved with maximum luminance of 6093.2 cd/m, external quantum efficiency of 3.79%, and current efficiency of 7.96 cd/A. More importantly, the studied perovskite LEDs possess a good operation stability after a long test time in air ambient. Typically, the devices can endure a high humidity (75%, 12 h) and a high working temperature (393 K, three heating/cooling cycles) even without encapsulation, and the operation stability is better than any previous reports. It is anticipated that this work will provide an effective strategy for the fabrication of high-performance perovskite LEDs with good stability under ambient and harsh conditions, making practical applications of such LEDs a real possibility.

The high-performance broadband photodetectors have attracted intensive scientific interests due to their potential applications in optoelectronic systems. Despite great achievements in two-dimensional (2D) materials based photodetectors such as graphene and black phosphorus, obvious disadvantages such as low optical absorbance and instability preclude their usage for the broadband photodetectors with the desired performance. An alternative approach is to find promising 2D materials and fabricate heterojunction structures for multifunctional hybrid photodetectors. In this work, 2D WS 2 /Si heterojunction with a type-II band alignment is formed in situ. This heterojunction device produced a high I on /I off ratio over 10, 6 responsivity of 224 mA/W, specific detectivity of 1.5 × 10 12 Jones, high polarization sensitivity, and broadband response up to 3043 nm. Furthermore, a 4 × 4 device array of WS 2 /Si heterojunction device is demonstrated with high stability and reproducibility. These results suggest that the WS 2 /Si type-II heterojunction is an ideal photodetector in broadband detection and integrated optoelectronic system.

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White light‐emitting diodes (WLEDs) are promising next‐generation solid‐state light sources. However, the commercialization route for WLED production suffers from challenges in terms of insufficient color‐rendering index (CRI), color instability, and incorporation of rare‐earth elements. Herein, a new two‐component strategy is developed by assembling two broadband emissive materials with self‐trapped excitons (STEs) for high CRI and stable WLEDs. The strategy addresses effectively the challenging issues facing current WLEDs. Based on first‐principles thermodynamic calculations, copper‐based ternary halides composites, CsCu2I3@Cs3Cu2I5, are synthesized by a facile one‐step solution approach. The composites exhibit an ideal white‐light emission with a cold/warm white‐light tuning and a robust stability against heat, ultraviolet light, and environmental oxygen/moisture. A series of cold/warm tunable WLEDs is demonstrated with a maximum luminance of 145 cd m−2 and an external quantum efficiency of 0.15%, and a record high CRI of 91.6 is achieved, which is the highest value for lead‐free WLEDs. Importantly, the fabricated device demonstrates an excellent operation stability in a continuous current mode, exhibiting a long half‐lifetime of 238.5 min. The results promise the use of the hybrids of STEs‐derived broadband emissive materials for high‐performance WLEDs.

Silica coated magnetite (Fe3O4@SiO2) core-shell nanoparticles (NPs) with controlled silica shell thicknesses were prepared by a modified Stöber method using 20 nm hydrophilic Fe3O4 NPs as seeds. The core-shell NPs were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), selected area electron diffraction (SAED), and UV-Vis adsorption spectra (UV-Vis). The results imply that NPs consist of a crystalline magnetite core and an amorphous silica shell. The silica shell thickness can be controlled from 12.5 nm to 45 nm by varying the experimental parameters. The reaction time, the ratio of TEOS/Fe3O4, and the concentration of hydrophilic Fe3O4 seeds were found to be very influential in the control of silica shell thickness. These well-dispersed core-shell Fe3O4@SiO2 NPs show superparamagnetic properties at room temperature.

High-performance perovskite photodetectors based on solution-processed all-inorganic CsPbBr3 thin films were fabricated with a high photoresponsivity and on/off photocurrent ratio.

Monolayer and bilayer graphene sheets have been produced by a solvothermal-assisted exfoliation process in a highly polar organic solvent, acetonitrile, using expanded graphite (EG) as the starting material. It is proposed that the dipole-induced dipole interactions between graphene and acetonitrile facilitate the exfoliation and dispersion of graphene. The facile and effective solvothermal-assisted exfoliation process raises the low yield of graphene reported in previous syntheses to 10 wt% 12 wt%. By means of centrifugation at 2000 rpm for 90 min, monolayer and bilayer graphene were separated effectively without the need to add a stabilizer or modifi er. Electron diffraction and Raman spectroscopy indicate that the resulting graphene sheets are high quality products without any signifi cant structural defects.