Fabrication

Pathology

Nanotechnology

Organic chemistry

Selenide

Heterojunction

Vicinal

Chemistry

Metallurgy

Materials science

Alternative medicine

Chemical vapor deposition

Stacking

Optoelectronics

Selenium

Medicine

Nature

An approach is developed for the continuous fabrication of lateral multi-junction heterostructures of transition-metal dichalcogenides, in which the sequential formation of heterojunctions is achieved solely by changing the composition of the reactive gas environment in the presence of water vapour. Growing lateral heterostructures of two-dimensional (2D) dichalcogenide structures via chemical vapour deposition opens up new opportunities for building 2D electronic and optoelectronic devices. But it is challenging to make multiple spatially defined lateral heterostructures. This paper reports a straightforward one-pot approach to growing 2D multi-junction heterostructures by switching the gas environment in the presence of water vapour flowing over the solid sources of both MoX2 and WX2 powders placed in the same boat. The gas environment regulates the precursor species in the vapour phase via precursor volatilization and water-induced oxidation and can thus control their preferential deposition. Humberto Gutiérrez and colleagues use this technique to create multiple heterostructures of MoX2 and WX2 in one reactor and to make alloyed sulfide/selenide heterostructures. Two-dimensional heterojunctions of transition-metal dichalcogenides1,2,3,4,5,6,7,8,9,10,11,12,13,14,15 have great potential for application in low-power, high-performance and flexible electro-optical devices, such as tunnelling transistors5,6, light-emitting diodes2,3, photodetectors2,4 and photovoltaic cells7,8. Although complex heterostructures have been fabricated via the van der Waals stacking of different two-dimensional materials2,3,4,14, the in situ fabrication of high-quality lateral heterostructures9,10,11,12,13,15 with multiple junctions remains a challenge. Transition-metal-dichalcogenide lateral heterostructures have been synthesized via single-step9,11,12, two-step10,13 or multi-step growth processes15. However, these methods lack the flexibility to control, in situ, the growth of individual domains. In situ synthesis of multi-junction lateral heterostructures does not require multiple exchanges of sources or reactors, a limitation in previous approaches9,10,11,12,13,15 as it exposes the edges to ambient contamination, compromises the homogeneity of domain size in periodic structures, and results in long processing times. Here we report a one-pot synthetic approach, using a single heterogeneous solid source, for the continuous fabrication of lateral multi-junction heterostructures consisting of monolayers of transition-metal dichalcogenides. The sequential formation of heterojunctions is achieved solely by changing the composition of the reactive gas environment in the presence of water vapour. This enables selective control of the water-induced oxidation16 and volatilization17 of each transition-metal precursor, as well as its nucleation on the substrate, leading to sequential edge-epitaxy of distinct transition-metal dichalcogenides. Photoluminescence maps confirm the sequential spatial modulation of the bandgap, and atomic-resolution images reveal defect-free lateral connectivity between the different transition-metal-dichalcogenide domains within a single crystal structure. Electrical transport measurements revealed diode-like responses across the junctions. Our new approach offers greater flexibility and control than previous methods for continuous growth of transition-metal-dichalcogenide-based multi-junction lateral heterostructures. These findings could be extended to other families of two-dimensional materials, and establish a foundation for the development of complex and atomically thin in-plane superlattices, devices and integrated circuits18.

One-pot growth of two-dimensional lateral heterostructures via sequential edge-epitaxy