Zugriffsnummer 42845
Dokumenttyp Zeitschriftenartikel
Peer Review mit Peer Review
Sprache Englisch
Titel Quantifying the contribution of chemical enhancement to SERS: A model based on the analysis of light-induced degradation processes
Autor(in); Institution
Liu, Bo; TU Braunschweig, Institute for Condensed Matter Physics, Braunschweig, GERMANY
Thielert, Bonito; TU Braunschweig, Institute for Condensed Matter Physics, Braunschweig, GERMANY
Reutter, Andreas; TU Braunschweig, Institute for Condensed Matter Physics, Braunschweig, GERMANY
Stosch, Rainer; 3.1, Allgemeine und Anorganische Chemie, PTB-Braunschweig
Lemmens, Peter; TU Braunschweig, Institute for Condensed Matter Physics, Laboratory for Emerging Nanometrology LENA, Braunschweig, GERMANY
Quelle/Jahr Journal of Physical Chemistry C: 123 (2019), 31, 19119 - 19124
ISSN 1932-7447 (PRINT) ; 1932-7455 (ONLINE)
DOI
Verlag Washington, DC: ACS Publications
Zusammenfassung Surface-enhanced Raman scattering (SERS) is of growing importance in different fields, from clinical analysis/chemistry to food industry. For a better insight into the complex light-matter interaction processes that are underlying the intensity enhancement, it is essential to experimentally distinguish and quantify the contributions based on the chemical mechanism (CM) with respect to the electromagnetic mechanism. Here, we present a model to estimate the relative CM response of Raman modes by analyzing light-induced degradation of target molecules on designed metal/semiconductor SERS substrates. The resulting intensity evolution is described by a biexponential function with two model parameters that allow a differentiation of the enhancement processes. Our work thereby provides a means for a better understanding of CM and will be advantageous for an application of intensity-based quantitative SERS techniques.

Zitierung

Liu, B., Thielert, B., Reutter, A., Stosch, R., & Lemmens, P. (2019). Quantifying the contribution of chemical enhancement to SERS: A model based on the analysis of light-induced degradation processes. Journal of Physical Chemistry C, 123(31), 19119–19124. https://doi.org/10.1021/acs.jpcc.9b04526

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