材料科学
吸收(声学)
电介质
光电子学
氢
催化作用
钯
图层(电子)
光路
光学
可见光谱
光学腔
纳米技术
吸收光谱法
光路长度
领域(数学)
三维光学数据存储
光场
光学现象
作者
Hyeonbin Woo,Taehyun Kim,Min‐Joong Kim,Seung‐Yeol Lee,Jahyun Koo,Minah Seo,Junsuk Rho,Myung‐Ki Kim,Yong‐Sang Ryu
摘要
Chemical reactions offer a powerful strategy for generating visible optical responses through localized changes in absorption, dielectric environment, and interfacial wetting. A palladium (Pd)-embedded Fabry-Perot cavity is introduced as a reaction-active optical platform in which structural color is governed by intracavity absorption coupled with reaction-induced dielectric perturbation. Positioning Pd within the dielectric spacer creates a spatially controllable reactive absorber whose vertical location relative to the standing-wave field dictates wavelength-selective absorption within the cavity. The morphology of the embedded Pd layer provides an additional design parameter by modulating both optical loss and interfacial wetting. Under hydrogen exposure in the presence of oxygen, catalytic water formation at the Pd/polymer interface generates localized dielectric heterogeneity and interfacial water droplets, thereby perturbing the optical path length and amplifying the visible response. As a result, the cavity exhibits pronounced, morphology-dependent color transitions that are inaccessible through dielectric-layer engineering or Pd/PdH refractive-index changes alone, enabling direct visual hydrogen sensing under ambient light, as well as flexible optical devices capable of large-area patterning. These findings establish a design framework for reaction-active optical cavities that translate localized chemistry into a colorimetric hydrogen sensing mechanism.
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