In this study, we investigate the real-time evolution of photoluminescence (PL) in MoS 2 samples modified with L63MS molecules during controlled thermal treatment, unveiling a unique laser-induced molecular agglomeration process. By integrating a heater into our microscopy setup, we monitored in situ changes and discovered that between 120 °C and 180 °C, focused laser irradiation induces the formation of molecular agglomerates with heights ranging from 5 to 20 nm (as confirmed by atomic force microscopy (AFM)). Notably, after subsequent heating to 320 °C, while non-agglomerated molecules desorb, these agglomerates remain stable. Raman spectroscopy reveals that the MoS 2 lattice beneath the agglomerates experiences minimal phonon mode shifts—demonstrating a protective effect—and PL measurements show a redshift in the exciton A peak due to localized strain and charge transfer effects. In contrast to previous studies on the real-time PL evolution of MoS 2 , our work uniquely demonstrates that controlled agglomerate formation via laser exposure not only modulates optical properties but also provides a pathway for localized functionalization of MoS 2 , opening new avenues for optoelectronic device engineering.
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Brkić et al. (2025) studied this question.
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