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arXiv 2604.09293physics.optics
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通过相变材料基底调节等离子体超材料以调节光驱动反应的反应性

Tuning Plasmonic Metasurfaces via Phase Change Material Substrates for Modulating Reactivity in Light-Driven Reactions

Friedrich-Schiller-Universität Jena(耶拿弗里德里希·席勒大学);Australian National University(澳大利亚国立大学);Xi’an University of Posts and Telecommunications(西安邮电大学);University of Applied Sciences Landshut(兰茨胡特应用科学大学)

Ning Lyu, Anjalie Edirisooriya, Dawei Liu, Zelio Fusco, Shenyou Zhao, Lan Fu, Fiona J. Beck, Christin David

AI总结:

本文通过相变材料基底调节等离子体超材料,利用模式混合法调控光激发电子群体,实现对光驱动化学反应反应性的选择性控制,实验显示产物产率在晶态和非晶态下分别降低和提高。

摘要:

相变材料提供了一个强大的平台,用于在纳米光子系统中动态调节光学响应。尽管等离子体超材料已被广泛用于增强光催化效率并促进特定的光驱动反应,但在单一设备中对反应路径进行主动和动态控制仍具有挑战性。本文报告了一种相诱导可调超材料,通过模式混合法调控光激发电子群体,从而实现对光驱动化学过程反应性的选择性控制。通过利用热诱导折射率切换的Sb2S3腔体,利用腔体-等离子体混合法调节Au纳米盘的等离子体共振强度。这种重新配置使亚甲基蓝降解产物产率提高了2.4倍,在晶态下抑制至0.45,在非晶态下增强至1.09。重要的是,这种可重构平台在相同的照明条件下,通过单一超材料架构实现了反应产率的动态控制。我们的方法建立了一个动态可编程的光驱动反应平台,能够精确操控反应活性,为复杂多分支反应系统中的选择性光催化提供了新的机会。

英文摘要:

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.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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