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      Multi-band Metasurface-Driven Surface-Enhanced Infrared Absorption Spectroscopy for Improved Characterization of in-Situ Electrochemical Reactions

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          Abstract

          Surface-enhanced spectroscopy techniques are the method-of-choice to characterize adsorbed intermediates occurring during electrochemical reactions, which are crucial in realizing a green and sustainable future. Characterizing species with low coverage or short lifetimes has so far been limited by low signal enhancement. Recently, single-band metasurface-driven surface-enhanced infrared absorption spectroscopy (SEIRAS) has been pioneered as a promising technology to monitor a single vibrational mode during electrochemical CO oxidation. However, electrochemical reactions are complex, and their understanding requires the simultaneous monitoring of multiple adsorbed species in situ, hampering the adoption of nanostructured electrodes in spectro-electrochemistry. Here, we develop a multi-band nanophotonic-electrochemical platform that simultaneously monitors in situ multiple adsorbed species emerging during cyclic voltammetry scans by leveraging the high resolution offered by the reproducible nanostructuring of the working electrode. Specifically, we studied the electrochemical reduction of CO 2 on a Pt surface and used two separately tuned metasurface arrays to monitor two adsorption configurations of CO with vibrational bands at ∼2030 and ∼1840 cm –1. Our platform provides a ∼40-fold enhancement in the detection of characteristic absorption signals compared to conventional broadband electrochemically roughened platinum films. A straightforward methodology is outlined starting with baselining our system in a CO-saturated environment and clearly detecting both configurations of adsorption. In contrast, during the electrochemical reduction of CO 2 on platinum in K 2CO 3, CO adsorbed in a bridged configuration could not be detected. We anticipate that our technology will guide researchers in developing similar sensing platforms to simultaneously detect multiple challenging intermediates, with low surface coverage or short lifetimes.

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          Most cited references40

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          Optical properties of metallic films for vertical-cavity optoelectronic devices.

          We present models for the optical functions of 11 metals used as mirrors and contacts in optoelectronic and optical devices: noble metals (Ag, Au, Cu), aluminum, beryllium, and transition metals (Cr, Ni, Pd, Pt, Ti, W). We used two simple phenomenological models, the Lorentz-Drude (LD) and the Brendel-Bormann (BB), to interpret both the free-electron and the interband parts of the dielectric response of metals in a wide spectral range from 0.1 to 6 eV. Our results show that the BB model was needed to describe appropriately the interband absorption in noble metals, while for Al, Be, and the transition metals both models exhibit good agreement with the experimental data. A comparison with measurements on surface normal structures confirmed that the reflectance and the phase change on reflection from semiconductor-metal interfaces (including the case of metallic multilayers) can be accurately described by use of the proposed models for the optical functions of metallic films and the matrix method for multilayer calculations.
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            • Record: found
            • Abstract: not found
            • Article: not found

            Imaging-based molecular barcoding with pixelated dielectric metasurfaces

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              • Record: found
              • Abstract: found
              • Article: not found

              Understanding cation effects in electrochemical CO 2 reduction

              Field-sensitive electrochemical reactions are controlled by electrode charging which is sensitive to the size of the electrolyte containing cations. Solid–liquid interface engineering has recently emerged as a promising technique to optimize the activity and product selectivity of the electrochemical reduction of CO 2 . In particular, the cation identity and the interfacial electric field have been shown to have a particularly significant impact on the activity of desired products. Using a combination of theoretical and experimental investigations, we show the cation size and its resultant impact on the interfacial electric field to be the critical factor behind the ion specificity of electrochemical CO 2 reduction. We present a multi-scale modeling approach that combines size-modified Poisson–Boltzmann theory with ab initio simulations of field effects on critical reaction intermediates. The model shows an unprecedented quantitative agreement with experimental trends in cation effects on CO production on Ag, C 2 production on Cu, CO vibrational signatures on Pt and Cu as well as Au(111) single crystal experimental double layer capacitances. The insights obtained represent quantitative evidence for the impact of cations on the interfacial electric field. Finally, we present design principles to increase the activity and selectivity of any field-sensitive electrochemical process based on the surface charging properties: the potential of zero charge, the ion size, and the double layer capacitance.
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                Author and article information

                Journal
                ACS Photonics
                ACS Photonics
                ph
                apchd5
                ACS Photonics
                American Chemical Society
                2330-4022
                26 January 2024
                21 February 2024
                : 11
                : 2
                : 714-722
                Affiliations
                []Department of Physics, Technical University of Munich , Garching 85748, Germany
                []Chair in Hybrid Nanosystems, Nanoinstitute Munich, and Center for NanoScience, Faculty of Physics, Ludwig-Maximilians-University Munich , Königinstraße 10, München 80539, Germany
                [§ ]School of Physics and Astronomy, Monash University , Clayton, VIC 3800, Australia
                []Department of Physics, Imperial College London , London SW7 2AZ, United Kingdom
                Author notes
                Author information
                https://orcid.org/0000-0002-9052-1680
                https://orcid.org/0000-0001-6558-5618
                https://orcid.org/0000-0001-9704-7902
                https://orcid.org/0000-0003-3191-7164
                Article
                10.1021/acsphotonics.3c01592
                10885203
                38405393
                fd6dc625-571d-40ba-b4c9-5d518fbb16a4
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 02 November 2023
                : 20 December 2023
                : 19 December 2023
                Funding
                Funded by: Solar Technologies go Hybrid, doi 10.13039/100012027;
                Award ID: NA
                Funded by: European Union, doi NA;
                Award ID: NEHO, 101046329
                Funded by: EPSRC Physical Sciences Programme Grant Interview Panel, doi NA;
                Award ID: EPSRC (EP/W017075/1)
                Funded by: Center for NanoScience, Ludwig-Maximilians-Universität München, doi 10.13039/501100007153;
                Award ID: NA
                Funded by: Deutsche Forschungsgemeinschaft, doi 10.13039/501100001659;
                Award ID: TI 1063/1
                Funded by: Deutsche Forschungsgemeinschaft, doi 10.13039/501100001659;
                Award ID: EXC 2089/1390776260
                Funded by: HORIZON EUROPE European Research Council, doi 10.13039/100019180;
                Award ID: ERC, METANEXT, 101078018
                Categories
                Article
                Custom metadata
                ph3c01592
                ph3c01592

                nanophotonics,metasurfaces,surface-enhanced infrared absorption spectroscopy,electrochemical co2 reduction,in situ spectro-electrochemistry

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