Hybrid tip-enhanced nano-spectroscopy and -imaging of monolayer WSe2 with local strain control

TL;DR

This study combines tip-enhanced nano-spectroscopy and nano-imaging to analyze and control local strain effects on excitonic properties in monolayer WSe2, revealing nanoscale correlations and reversible/irreversible bandgap tuning.

Contribution

It introduces a hybrid nano-optical and nano-mechanical approach to systematically study strain and defect effects in 2D materials at nanoscale resolution.

Findings

Resolved nanoscale correlations of PL intensity and shifts near edges and twin boundaries.

Achieved reversible bandgap tuning up to 24 meV and irreversible up to 48 meV via active tip interaction.

Demonstrated the ability to distinguish strain effects from defect influences on optical properties.

Abstract

Many classes of two-dimensional (2D) materials have emerged as potential platforms for novel electronic and optical devices. However, the physical properties are strongly influenced by nanoscale heterogeneities in the form of edges, grain boundaries, and nucleation sites. Using combined tip-enhanced Raman scattering (TERS) and photoluminescence (TEPL) nano-spectroscopy and -imaging, we study the associated effects on the excitonic properties in monolayer WSe2 grown by physical vapor deposition (PVD). With <15 nm spatial resolution we resolve nonlocal nanoscale correlations of PL spectral intensity and shifts with crystal edges and internal twin boundaries associated with the expected exciton diffusion length. Through an active atomic force tip interaction we can control the crystal strain on the nanoscale, and tune the local bandgap in reversible (up to 24 meV shift) and irreversible (up to 48 meV shift) fashion. This allows us to distinguish the effect of strain from the dominant influence of defects on the PL modification at the different structural heterogeneities. Hybrid nano-optical and nano-mechanical imaging and spectroscopy thus enables the systematic study of the coupling of structural and mechanical degrees of freedom to the nanoscale electronic and optical properties in layered 2D materials.