4.6 Article

Interlayer exciton emission in a MoS2/VOPc inorganic/organic van der Waals heterostructure

Journal

MATERIALS HORIZONS
Volume 9, Issue 4, Pages 1253-1263

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1mh01622a

Keywords

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Funding

  1. National Natural Science Foundation of China [62090030/62090031, 51872257, 51672244]
  2. Zhejiang Province Natural Science Foundation of China [LZ20F040001]

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Heterostructures built from two-dimensional materials and organic semiconductors have unique advantages in addressing fundamental physics and constructing functional devices. We report the interlayer exciton emission in a heterostructure of pyramidal VOPc and transition metal dichalcogenide monolayer MoS2, which provides a new avenue to tune the optoelectronic properties of heterojunctions consisting of 2D materials and organic semiconductors.
Heterostructures built from two-dimensional (2D) materials and organic semiconductors offer a unique platform for addressing many fundamental physics and construction of functional devices by taking advantage of both the 2D materials and organic semiconductors. We report interlayer exciton emission in the near infrared range around 1.54 eV (similar to 805 nm) from the heterostructure of pyramidal VOPc (p-type) and transition metal dichalcogenide monolayer MoS2 (VOPc/MoS2). This contrasts the observation of photoluminescence (PL) from the SnCl2Pc/MoS2 heterostructure despite both being type-II heterostructures. We attribute the exciton emission to the carrier transition from the generated interface mid-gap states of VOPc to the ground states of MoS2 in the heterostructure system as predicted from density functional theory (DFT) calculations. Furthermore, the observed PL signal of the VOPc/MoS2 heterostructure shows blue shift, while the PL peak of the SnCl2Pc/MoS2 heterostructure shows red shift. Our finding opens up a new avenue to tune the optoelectronic properties of the van der Waals heterojunctions consisting of 2D materials and organic semiconductors for optoelectronic applications.

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