📝 SummarXiv

Abstract

Plasmonic metasurfaces play a crucial role in resonance-driven photocatalytic reactions by effectively enhancing reactivity via localized surface plasmon resonances. Catalytic activity can be selectively modulated by tuning the strength of plasmonic resonances through two primary non-thermal mechanisms: near-field enhancement and hot carrier injection, which govern the population of energetic carrier excited or injected into unoccupied molecular orbitals. We developed a set of polarization-sensitive metasurfaces consisting of elliptical Au-TiO2 nanopillars, specifically designed to plasmonically modulate the reactivity of a model reaction: the photocatalytic degradation of methylene blue. Surface-enhanced Raman spectroscopy reveals a polarization-dependent reaction yield in real-time, modulating from 4.7 (transverse electric polarization) to 9.98 (transverse magnetic polarization) in 10 s period, as quantified by the integrated area of the 480 cm-1 Raman peak and correlated with enhanced absorption at 633 nm. The single metasurface configuration enables continuous tuning of photocatalytic reactivity via active control of plasmonic resonance strength, as evidenced by the positive correlation between measured absorption and product yield. This dynamic approach provides a route to selectively enhance or suppress resonance-driven reactions, which can be further leveraged to achieve selectivity in multibranch reactions, guiding product yields toward desired outcomes.