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Table · dataset · 2026

Spatially Confined Liquid-Precursor CVD Enables Direct Growth of WS<sub>2</sub>/MoS<sub>2</sub> Twisted Heterostructures

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The performance of two-dimensional transition metal dichalcogenide (TMD) heterostructures is profoundly influenced by their interlayer coupling with modulating twist angles.

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However, it is still a great challenge to achieve thermodynamically unfavorable twisted TMD heterostructures. Herein, WS<sub>2</sub>/MoS<sub>2</sub> heterostructures with unfavorable twist angles from 0° to 100° were directly synthesized by a spatially confined liquid-precursor-assisted CVD growth.

Spectroscopic analyses reveal that non-0° twisted heterostructures exhibit weakened interlayer coupling with the redshift of the Raman A<sub>1g</sub> mode. Low-temperature photoluminescence indicates the resonance energy transfer from the MoS<sub>2</sub> B exciton to the WS<sub>2</sub> A exciton, enhancing WS<sub>2</sub> emission. The thermodynamically unfavorable (20°, 30°, and 90°) twisted heterostructures are found to possess much larger interfacial work function difference and longer exciton lifetimes, indicating more efficient interfacial charge transfer.

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This work clarifies the fundamental role of twist angle in modulating the built-in electric field and exciton dynamics of WS<sub>2</sub>/MoS<sub>2</sub> heterostructures and underscores their great potential for practical optoelectronic applications.

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ZivaHuboai:figshare.com:article/3402108810 d agoJSON v1
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