Guardado en:
| Autores principales: | , , , , , , , |
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| Formato: | Preprint |
| Publicado: |
2026
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| Materias: | |
| Acceso en línea: | https://arxiv.org/abs/2604.09293 |
| Etiquetas: |
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- Phase change materials provide a powerful platform for dynamically modulating optical responses in nanophotonic systems. While plasmonic metasurfaces have been widely employed to enhance photocatalytic efficiency and promote particular light-driven reactions, active and dynamical control over reaction pathways within a single device remains challenging. Here, we report a phase-induced tunable metasurface that tailors photoexcited electron populations through mode hybridization, enabling selective control over the reactivity of light-driven chemical processes. By exploiting thermally induced refractive-index switching in a Sb2S3 cavity, the plasmonic resonance strength of Au nanodisks is actively tuned via cavity-plasmon hybridization. This reconfiguration modulates the product yield of methylene blue degradation by a factor of 2.4, suppressing to 0.45 in the crystalline phase and enhancing to 1.09 in the amorphous phase. Importantly, this reconfigurable platform enables dynamic control of the reaction yield using a single metasurface architecture under identical illumination conditions. Our approach establishes a dynamically programmable light-driven reaction platform capable of precisely manipulating reaction reactivity, offering new opportunities for selective photocatalysis in complex multibranch reaction systems.