The necessity for new sources for greener and cleaner energy production to replace the existing ones has been increasingly growing in recent years. Of those new sources, the hydrogen evolution reaction has a large potential. In this work, for the first time, MoSe /Mo core-shell 3D-hierarchical nanostructures are created, which are derived from the Mo 3D-hierarchical nanostructures through a low-temperature plasma-assisted selenization process with controlled shapes grown by a glancing angle deposition system.

Zero dimensional perovskite Cs4PbBr6 has attracted considerable attention recently not only because of its highly efficient green photoluminescence (PL), but also its two highly debated opposing mechanisms of the luminescence: embedded CsPbBr3 nanocrystals versus intrinsic Br vacancy states. After a brief discussion on the root cause of the controversy, we provide sensitive but noninvasive methods that can not only directly correlate luminescence with the underlying structure, but also distinguish point defects from embedded nanostructures. We first synthesized both emissive and non-emissive Cs4PbBr6 crystals, obtained the complete Raman spectrum of Cs4PbBr6 and assigned all Raman bands based on density functional theory simulations. We then used correlated Raman-PL as a passive structure-property method to identify the difference between emissive and non-emissive Cs4PbBr6 crystals and revealed the existence of CsPbBr3 nanocrystals in emissive Cs4PbBr6. We finally employed a diamond anvil cell to probe the response of luminescence centers to hydrostatic pressure. The observations of fast red-shifting, diminishing and eventual disappearance of both green emission and Raman below Cs4PbBr6 phase transition pressure of ~3 GPa is compatible with CsPbBr3 nanocrystal inclusions as green PL emitters and cannot be explained by Br vacancies. The resolution of this long-lasting controversy paves the way for further device applications of low dimensional perovskites, and our comprehensive optical technique integrating structure-property with dynamic pressure response is generic and can be applied to other emerging optical materials to understand the nature of their luminescent centers.

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HIGHLIGHTS • The controllable fabrication methods, the unique properties, and relative applications of 2D heterostructures were summarized. • The generation and detection of interlayer excitons in 2D heterostructures with type II band alignment indicate a longer lifetime and larger binding energy than intralayer excitons. • The advances in magnetic tunneling junctions based on 2D heterostructures can be applied in spintronic devices to realize spin filtering. ABSTRACT With a large number of researches being conducted on two-dimensional (2D) materials, their unique properties in optics, electrics, mechanics, and magnetics have attracted increasing attention. Accordingly, the idea of combining distinct functional 2D materials into heterostructures naturally emerged that provides unprecedented platforms for exploring new physics that are not accessible in a single 2D material or 3D heterostructures. Along with the rapid development of controllable, scalable, and programmed synthesis techniques of high-quality 2D heterostructures, various heterostructure devices with extraordinary performance have been designed and fabricated, including tunneling transistors, photodetectors, and spintronic devices. In this review, we present a summary of the latest progresses in fabrications, properties, and applications of different types of 2D heterostructures, followed by the discussions on present challenges and perspectives of further investigations.