Abstract

The development of photonic-based gas sensors using metal–organic frameworks (MOFs) and other microporous solids is often a multistep, complex process, typically involving MOF synthesis, purification, and attachment of microcrystals to an optical fiber end face. This study introduces a one-step method that integrates MOF synthesis and sensor head fabrication directly onto the fiber end face, forming an extrinsic Fabry–Perot interferometer (EFPI) with a thin film of MOF microcrystals. The resulting film, only 3–10-μm-thick, enhances sensor response by enabling rapid gas detection within seconds. Utilizing a pendant micro-droplet evaporation technique, this method forms a microporous MOF layer in situ, allowing unreacted molecular components to act as an adhesive that secures the MOF crystallites to the optical fiber, potentially also contributing to the film's adsorption properties. This process, demonstrated with the HKUST-1 MOF as a model system, optimizes both the fabrication speed and sensor response times by reducing the film formation process to 24 s under nitrogen and 90 s in ambient conditions. In situ Raman spectroscopy, X-ray diffraction (XRD), thermogravimetry (TGA), and energy dispersive X-ray spectroscopy (EDS) were used to validate the composition of the sensor head, confirming the presence of MOF crystallites as the primary sensing component within the EFPI film and characterizing additional film components that may enhance stability, selectivity, and response. This bottom-up approach holds significant promise for the scalable production of fiber-optic sensors that leverage MOF's gas adsorption properties.

Department(s)

Electrical and Computer Engineering

Comments

Army Research Office, Grant W911NF-21-2-0280

Keywords and Phrases

chemical adsorption; crystallization; crystal–polymer composite layer; HKUST-1; material characterization; metal−organic framework (MOF); optical fiber (OF)─extrinsic Fabry−Perot interferometer (EFPI) sensors; polymerization

International Standard Serial Number (ISSN)

2379-3694

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2025 American Chemical Society, All rights reserved.

Publication Date

26 Sep 2025

PubMed ID

40824761

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