Abstract

2D vertical van der Waals (vdW) heterostructures with atomically sharp interfaces have attracted tremendous interest in 2D photonic and optoelectronic applications. Band alignment engineering in 2D heterostructures provides a perfect platform for tailoring interfacial charge transfer behaviors, from which desired optical and optoelectronic features can be realized. Here, by developing a two‐step chemical vapor deposition strategy, direct vapor growth of monolayer PbI2 on monolayer transition metal dichalcogenides (TMDCs) (WS2, WSe2, or alloying WS2(1− x )Se2 x), forming bilayer vertical heterostructures, is demonstrated. Based on the calculated electron band structures, the interfacial band alignments of the obtained heterostructures can be gradually tuned from type‐I (PbI2/WS2) to type‐II (PbI2/WSe2). Steady‐state photoluminescence (PL) and time‐resolved PL measurements reveal that the PL emissions from the bottom TMDC layers can be modulated from apparently enhanced (for WS2) to greatly quenched (for WSe2) compared to their monolayer counterparts, which can be attributed to the band alignment–induced distinct interfacial charge transfer behaviors. The band alignment nature of the heterostructures is further demonstrated by the PL excitation spectroscopy and interlayer exciton investigation. The realization of 2D vertical heterostructures with tunable band alignments will provide a new material platform for designing and constructing multifunctional optoelectronic devices.

Highlights

  • The photoluminescence (PL) emission from the bottom transition metal dichalcogenides (TMDCs) layers can be modulated from apparently enhanced to greatly quenched compared to their pristine monolayer counterparts, which can be attributed to the band alignment–induced distinct interfacial charge transfer behaviors

  • PbI2/TMDC vertical heterostructures were synthesized via a two-step chemical vapor deposition (CVD) strategy (Figure 1a)

  • The substrate with as-grown TMDC monolayers was rapidly transferred to the downstream of the other furnace with a quartz boat loaded with PbI2 powder placed at the heating zone

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Summary

Introduction

By tuning different x values in the bottom alloying TMDC monolayers, the band alignment of these heterostructures emerges a transition from type-I (PbI2/WS2, x = 0) to type-II (PbI2/WSe2, x = 1), with a transition point at x = 0.67 (PbI2/WS0.67Se1.33). The photoluminescence (PL) emission from the bottom TMDC layers can be modulated from apparently enhanced (for WS2) to greatly quenched (for WSe2) compared to their pristine monolayer counterparts, which can be attributed to the band alignment–induced distinct interfacial charge transfer behaviors.

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