Nonuniform Chemical Passivation Dynamics in Monolayer MoS 2 from Real-Time Photoluminescence Imaging
Year: 2026
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Postchemical treatment is a major strategy for improving the optical and electronic performance of two-dimensional transition-metal dichalcogenides (TMDs), where surface defects and unintentional doping limit radiative recombination. Despite its broad application, the passivation dynamics in both time and space remain insufficiently understood. Here, we employ real-time, spatially resolved photoluminescence (PL) imaging to track the evolution of PL emission from monolayer MoS 2 during the Li-TFSI treatment. The PL intensity increases gradually over 4.7 min, indicating reaction-limited passivation kinetics. At the same time, the spatial variation in PL becomes more pronounced, revealing position-dependent reactivity and heterogeneous treatment across the flake. Pixel-level PL statistics compared with noise-based simulations confirm that this broadening originates from the intrinsic spatial heterogeneity of the material. These results demonstrate that chemical treatment enhances radiative recombination while simultaneously amplifying pre-existing spatial differences, establishing real-time PL imaging as a sensitive approach to probing heterogeneous surface reactions in 2D semiconductors.
Institutions: University of Cambridge, Uppsala University
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
Awards: G2780060105, G2941617128, G42369779, Engineering low power tunnel transistors based on two-dimensional semiconductors, Harnessing vibration-induced enhancement of transport in functional materials with soft structural dynamics, G4901095167, Photon Management for Solar Energy Harvesting with Hybrid Excitonics, G5162491134, Spin-Exchange and Energy Transfer at Hybrid Molecular/Lanthanide Nanoparticle Interfaces to Control Triplet Excitons, G662877069
OpenAlex ID: W7162109111
