Optical and electrical probing of plasmonic metal-molecule interactions

Plasmonic nanostructures enable efficient light-to-chemical energy conversion by concentrating optical energy into nanoscale volumes. A key mechanism in this process is chemical interface damping (CID), where surface plasmons are damped by adsorbed molecules, enabling the transfer of charge to adsorbed molecules. Here, we investigate the relationship between CID and adsorbate-induced changes in dc electrical resistivity for four molecular adsorbates on gold surfaces. Our results reveal two distinct CID regimes. On one hand, CID takes place via direct resonant electronic transitions to the lowest unoccupied molecular orbital. This mechanism is dependent on plasmon energy. In the second regime, plasmon damping takes place through inelastic electron scattering at the metal-molecule interface. This regime shows a weaker dependency on plasmon energy. This mechanism also leads to adsorbate-induced changes in dc resistivity. These findings provide previously unidentified insights into the microscopic origins of plasmon damping and offer a unified framework for understanding metal-adsorbate energy transfer.

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Publication Details

Journal
Science Advances
Published
2025-12-12
DOI
https://doi.org/10.1126/sciadv.aea0585
Citations
1
Primary Topic
Gold and Silver Nanoparticles Synthesis and Applications
Type
article
Field-Weighted Citation Impact
0.43

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article

Optical and electrical probing of plasmonic metal-molecule interactions

Peter Nordlander, Johannes Lischner, Toby Severs Millard, Pilar Carro et al.
1 citations
Science Advances
Gold and Silver Nanoparticles Synthesis and Applications
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article

Optical and electrical probing of plasmonic metal-molecule interactions

Peter Nordlander, Johannes Lischner, Toby Severs Millard, Pilar Carro, Ross C. Schofield, Ming Fu, Rupert F. Oulton, Emiliano Cortés, Andrei Ştefancu, Naomi J. Halas, J. L. Edwards, Wenxuan Tang
article en
1 citations

Abstract

Plasmonic nanostructures enable efficient light-to-chemical energy conversion by concentrating optical energy into nanoscale volumes. A key mechanism in this process is chemical interface damping (CID), where surface plasmons are damped by adsorbed molecules, enabling the transfer of charge to adsorbed molecules. Here, we investigate the relationship between CID and adsorbate-induced changes in dc electrical resistivity for four molecular adsorbates on gold surfaces. Our results reveal two distinct CID regimes. On one hand, CID takes place via direct resonant electronic transitions to the lowest unoccupied molecular orbital. This mechanism is dependent on plasmon energy. In the second regime, plasmon damping takes place through inelastic electron scattering at the metal-molecule interface. This regime shows a weaker dependency on plasmon energy. This mechanism also leads to adsorbate-induced changes in dc resistivity. These findings provide previously unidentified insights into the microscopic origins of plasmon damping and offer a unified framework for understanding metal-adsorbate energy transfer.

Science AdvancesVol. 11(50)
Universidad de La Laguna (ES), Imperial College London (GB), Technical University of Munich (DE), Rice University (US), Ludwig-Maximilians-Universität München (DE)
Alexander von Humboldt-Stiftung, Solar Technologies go Hybrid, Deutsche Forschungsgemeinschaft, Technische Universität München
Openalex Percentile: Top 33%
Gold and Silver Nanoparticles Synthesis and Applications
0.43
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