Abstract
Nonlinear chiroptical response, particularly nonlinear circular dichroism (CD), holds significant potential for advancing nanotechnology, biophotonics, and molecular imaging. While conventional approaches rely on intrinsic chiral materials, we demonstrate a novel strategy to engineer this effect by transforming achiral two-dimensional (2D) transition-metal dichalcogenides (TMDs) into chiral nanostructures. By scrolling monolayer TMDs into geometrically chiral nanoscrolls, we achieve pronounced nonlinear CD (up to 0.8), evidenced by circular-polarization-dependent second-harmonic generation (SHG). Notably, the SHG-CD degree is tailored by controlling the nanoscrolls’ scrolling axes, demonstrating, for the first time, programmable chirality-dependent nonlinear responses in TMD nanoscrolls. Furthermore, the confined electromagnetic fields within the scrolled geometry amplify the SHG intensity by up to 100-fold compared to monolayers. This chiral nanoscrolling is anticipated to enable innovative functionalities in the realm of compact nonlinear light sources and modulators, heralding a new era of advanced photonic applications.
| Original language | English | 
|---|---|
| Pages (from-to) | 8399-8406 | 
| Number of pages | 8 | 
| Journal | Nano Letters | 
| Volume | 25 | 
| Issue number | 20 | 
| DOIs | |
| Publication status | Published - 21 May 2025 | 
Keywords
- Mie resonance
 - SHG
 - chirality
 - nonlinear circular dichroism
 - transition-metal dichalcogenides