Issue 48, 2023

Enhanced interactions of excitonic complexes in free-standing WS2

Abstract

Excitonic complexes, bound states of electrons and holes, provide a promising platform in monolayer transition-metal dichalcogenide (TMDC) semiconductors for investigating diverse many-body interaction phenomena. The surrounding dielectric environment has been found to strongly influence the excitonic properties of the TMDC monolayers. While the impact of different dielectric surroundings on two-dimensional semiconductor materials and their strong correlations have been well studied, the effects on exciton formation and its properties resulting from a further reduction in dielectric screening remain elusive. In this study, we examined free-standing tungsten disulfide (WS2) monolayers, where the efficient generation of higher-order correlated excitonic complexes is readily observed. This phenomenon arises from the effective mutual interactions among excitons and internal carriers, attributed to the modulated exciton dynamics generated by the further reduced dielectric screening effect in the freestanding structure. The formation efficiency of excitonic complexes is enhanced and the multiple biexciton species (five particles such as charged biexcitons and acceptor/donor-bound biexcitons) are successfully induced under low excitation intensity and moderate temperature conditions. Our findings offer valuable insights into the influence of the dielectric environment on exciton interactions and enable a productive avenue for exploring fundamental many-body interactions, providing new possibilities for dielectric engineering of atomic thin semiconductors.

Graphical abstract: Enhanced interactions of excitonic complexes in free-standing WS2

Supplementary files

Article information

Article type
Paper
Submitted
12 Sep 2023
Accepted
23 Oct 2023
First published
24 Oct 2023

Nanoscale, 2023,15, 19533-19545

Enhanced interactions of excitonic complexes in free-standing WS2

X. Sun, Z. Lu and Y. Lu, Nanoscale, 2023, 15, 19533 DOI: 10.1039/D3NR04594C

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