Morphology‐Encoded Colorimetric Hydrogen Sensing Using Embedded Reactive Pd Absorbers in Fabry–Perot Cavities

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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Publication Details

Journal
Advanced Materials
Published
2026-09-01
DOI
https://doi.org/10.1002/adma.74886
Primary Topic
Photonic Crystals and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Morphology‐Encoded Colorimetric Hydrogen Sensing Using Embedded Reactive Pd Absorbers in Fabry–Perot Cavities

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Advanced Materials
Photonic Crystals and Applications
article

Morphology‐Encoded Colorimetric Hydrogen Sensing Using Embedded Reactive Pd Absorbers in Fabry–Perot Cavities

Yong‐Sang Ryu, Junsuk Rho, Minah Seo, Myung‐Ki Kim, Hyeonbin Woo, Jahyun Koo, Taehyun Kim, Seung‐Yeol Lee, Min‐Joong Kim
article en

Abstract

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.

Advanced Materials
Pohang University of Science and Technology (KR), Sogang University (KR), Korea University (KR), Kyungpook National University (KR), Institute of Public Health (AL), Korea University (JP)
National Research Foundation, Korea Health Industry Development Institute
Clean water and sanitation
Openalex Percentile: Top 13%
Photonic Crystals and Applications
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