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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Tamm Plasmon Resonance-Enhanced Infrared Sensor for Hydrogen Detection: Numerical and Experimental Insights
Miguel A S Almeida1,2, João P M Carvalho1,2, André D Santos1,2
1INESC TEC - Institute of Systems and Computer Engineering, Technology and Science (Centre for Applied Photonics), and Department of Physics, Faculty of Sciences, University of Porto, Rua do Campo Alegre, Porto 4169-007, Portugal.
Abstract:
Hydrogen (H2) detection has become extremely important in recent years due to the increasing need for sustainable alternative energy sources. In this field, optical sensors can contribute significantly due to remote interrogation capabilities and the absence of ignition sources. Among the different H2 optical sensors, plasmonic sensors appear to be a very sensitive technology; however, they require expensive plasmonic materials like gold or silver, which, together with a palladium-sensitive layer, can increase the sensor cost. In addition, plasmonic bands are usually outside the ideal infrared range for remote interrogation, between 1500 and 1600 nm. This work presents a polymer-protected Tamm Plasmon Resonance (TPR) sensor with a well-defined resonance band at 1572 nm composed of SiO2, TiO2 layers, and palladium as a sensitive layer. This architecture can reduce the production cost of sensing structures, replacing plasmonic films with dielectric materials, while offering improved resonance definition at longer wavelengths. First, numerical calculations were carried out using the Transfer-Matrix Method to study the impact of the thickness of each layer, incidence angle, and light polarization on the resonance band wavelength and H2 sensitivity. The optimized structure was then fabricated, exhibiting a wavelength shift of 9.5 nm to 4 vol % of H2, a response time of 30 s, and no cross-sensitivity to methane or ammonia. The sensor also demonstrated high stability and resistance to environmental degradation up to eight days. These results emphasize the advantages of TPR structures for gas sensing in the infrared spectral range, opening new avenues for remote plasmonic sensing.
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