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Título: | Theory of SERS enhancement: general discussion |
Autor: | Graham, Duncan; Goodacre, Roy; Arnolds, Heike; Masson, Jean-Francois; Schatz, George; Baumberg, Jeremy J.; Kim, Dong-Ho; Aizpurua, Javier CSIC ORCID ; Lum, William; Silvestri, Alessandro CSIC ORCID; Nijs, Bart de; Xu, Yikai; Di Martino, Giuliana; Natan, Michael; Schlücker, Sebastian; Wuytens, Pieter; Bruzas, Ian; Kuttner, Christian; Hardy, Mike; Chikkaraddy, Rohit; Martín Sabanés, Natalia; Delfino, Ines; Dawson, Paul; Gawinkowski, Sylwester; Bontempi, Nicolò; Mahajan, Sumeet; Reich, Stephanie; Hourahine, Ben; Bell, Steven; Krolikowska, Agata; Porter, Marc; Keeler, Alex; Kamp, Marlous; Fountain, Augustus; Fasolato, Claudia; Giorgis, Fabrizio; Otero, Juan C.; Matricardi, Cristiano; Van Duyne, Richard; Lombardi, John R.; Deckert, Volker; Velleman, Leonora | Fecha de publicación: | 2017 | Editor: | Royal Society of Chemistry (UK) | Citación: | Faraday Discussions 205: 173-211 (2017) | Resumen: | Rohit Chikkaraddy opened the discussion of the Introductory Lecture: Regarding quantifying the chemical enhancement, you showed a systematic change in the SERS enhancement for halide substituted molecules due to charge transfer from the metal. Is the extra enhancement due to an inherent increase in the Raman cross-section of the molecule? How do you go about referencing, as the charge transfer changes the vibrational frequency? Richard Van Duyne answered: The extra enhancement is not due to an increase in the Raman cross section, as that is ratioed out in the calculation of the enhancement factor. The charge transfer (CT) process does not transfer a complete electron, it is a fractional degree of CT. Thus the change in vibrational frequency is small. DFT calculations that provide eigenvectors allow one to reference the vibrational modes of the free molecule with those of the adsorbed molecule. Sylwester Gawinkowski asked: You have shown that the enhancement factor curve is redshifted relative to the plasmon resonance band and has a maximum at about 800 nm. This means that the SERS signal should be strongest for excitations in the near infrared spectral region. Why do most SERS reports, particularly related to single molecule SERS, have the excitation in the green or red spectral range and not in the near infrared? | Descripción: | The first page of this article is displayed as the abstract. | Versión del editor: | https://doi.org/10.1039/C7FD90095C | URI: | http://hdl.handle.net/10261/177351 | DOI: | 10.1039/C7FD90095C | Identificadores: | doi: 10.1039/C7FD90095C issn: 1359-6640 e-issn: 1364-5498 |
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